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49 similar compounds to monomer 50077278

Compile data set for download or QSAR
Wt: 1024.1
BDBM85490
Wt: 1808.1
BDBM50132596
Wt: 755.9
BDBM50013634
Wt: 1166.4
BDBM50063809
Wt: 1192.4
BDBM50063815
Wt: 1218.4
BDBM50063817
Wt: 1192.4
BDBM50063838
Wt: 1145.3
BDBM50077267
Wt: 1113.3
BDBM50077272
Wt: 1102.2
BDBM50077273
Wt: 1257.2
BDBM50077281
Wt: 1257.2
BDBM50077286
Wt: 1102.2
BDBM50077295
Wt: 1145.3
BDBM50077297
Wt: 1246.2
BDBM50077304
Displayed 1 to 15 (of 49 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 67 hits for monomerid = 85490,50132596,50013634,50063809,50063815,50063817,50063838,50077267,50077272,50077273,50077281,50077286,50077295,50077297,50077304   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Oxytocin receptor


(RAT)
BDBM50013634
PNG
(24-(1H-5-imidazolylmethyl)-16-(1H-3-indolylmethyl)...)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]2CCCCN2C(=O)[C@@H]2CCCCN2C1=O
Show InChI InChI=1S/C40H53N9O6/c1-3-24(2)34-40(55)49-17-9-7-14-33(49)39(54)48-16-8-6-13-31(48)37(52)45-30(20-26-22-41-23-43-26)38(53)47-18-10-15-32(47)36(51)44-29(35(50)46-34)19-25-21-42-28-12-5-4-11-27(25)28/h4-5,11-12,21-24,29-34,42H,3,6-10,13-20H2,1-2H3,(H,41,43)(H,44,51)(H,45,52)(H,46,50)/t24-,29-,30-,31+,32+,33-,34-/m0/s1
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7.80n/an/an/an/an/an/an/an/a



Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of [3H]- oxytocin binding to rat uterine Oxytocin receptor


J Med Chem 33: 1843-5 (1990)


Article DOI: 10.1021/jm00169a001
BindingDB Entry DOI: 10.7270/Q2JS9PDK
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077281
PNG
(CHEMBL438726 | H-Pfp-cyclo[DCys-D2Pal-DTrp-Lys-Val...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33+,34-,35+,46+/m0/s1
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34n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077297
PNG
(CHEMBL415201 | H-Fpa-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-35-16-19-37-11-3-4-12-38(37)24-35)32-81-80-31-48(69-52(73)42(61)25-34-17-20-40(59)21-18-34)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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35n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077295
PNG
(CHEMBL406491 | H-2Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1F)C(N)=O)NC(=O)[C@@H](N)Cc1ccccc1F
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-12-4-7-15-35(30)54)26-77-76-25-42(65-46(69)36(56)19-29-11-3-6-14-34(29)53)51(74)64-41(22-32-24-58-27-60-32)49(72)63-40(21-31-23-59-37-16-8-5-13-33(31)37)48(71)61-38(47(70)67-44)17-9-10-18-55/h3-8,11-16,23-24,27-28,36,38-44,59H,9-10,17-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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37n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Gastrin-Releasing peptide


(RAT)
BDBM85490
PNG
(DPhe6,Leu13,Psi(CH2NH),Cpa14-Bn(6-14))
Show SMILES CC(C)C[C@@H](CN[C@@H](C#N)C(N)=O)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](N)Cc1ccccc1)C(C)C
Show InChI InChI=1S/C50H69N15O9/c1-27(2)17-33(24-57-40(21-51)44(54)68)61-49(73)39(20-32-23-55-26-59-32)62-42(67)25-58-50(74)43(28(3)4)65-45(69)29(5)60-48(72)38(19-31-22-56-36-14-10-9-13-34(31)36)64-47(71)37(15-16-41(53)66)63-46(70)35(52)18-30-11-7-6-8-12-30/h6-14,22-23,26-29,33,35,37-40,43,56-57H,15-20,24-25,52H2,1-5H3,(H2,53,66)(H2,54,68)(H,55,59)(H,58,74)(H,60,72)(H,61,73)(H,62,67)(H,63,70)(H,64,71)(H,65,69)/t29-,33-,35+,37-,38-,39-,40-,43-/m0/s1
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42n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by PDSP Ki Database




Biochemistry 38: 7307-20 (1999)


Article DOI: 10.1021/bi990204w
BindingDB Entry DOI: 10.7270/Q29022BG
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077273
PNG
(CHEMBL411556 | H-3Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(F)c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(F)c1
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-10-8-12-33(54)18-30)26-77-76-25-42(65-46(69)36(56)19-29-9-7-11-32(53)17-29)51(74)64-41(22-34-24-58-27-60-34)49(72)63-40(21-31-23-59-37-14-4-3-13-35(31)37)48(71)61-38(47(70)67-44)15-5-6-16-55/h3-4,7-14,17-18,23-24,27-28,36,38-44,59H,5-6,15-16,19-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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60n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077267
PNG
(CHEMBL385689 | H-Nal-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-34-17-20-40(59)21-18-34)32-81-80-31-48(69-52(73)42(61)25-35-16-19-37-11-3-4-12-38(37)24-35)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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69n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077304
PNG
(CHEMBL414598 | H-Pfp-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C52H57F10N13O8S2/c1-20(2)44-52(83)74-33(50(81)70-29(45(65)76)14-25-36(55)40(59)43(62)41(60)37(25)56)18-85-84-17-32(73-46(77)26(64)13-24-34(53)38(57)42(61)39(58)35(24)54)51(82)72-31(12-22-16-66-19-68-22)49(80)71-30(11-21-15-67-27-8-4-3-7-23(21)27)48(79)69-28(47(78)75-44)9-5-6-10-63/h3-4,7-8,15-16,19-20,26,28-33,44,67H,5-6,9-14,17-18,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t26-,28-,29-,30+,31-,32-,33-,44+/m0/s1
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69n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077281
PNG
(CHEMBL438726 | H-Pfp-cyclo[DCys-D2Pal-DTrp-Lys-Val...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33+,34-,35+,46+/m0/s1
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93n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077273
PNG
(CHEMBL411556 | H-3Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(F)c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(F)c1
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-10-8-12-33(54)18-30)26-77-76-25-42(65-46(69)36(56)19-29-9-7-11-32(53)17-29)51(74)64-41(22-34-24-58-27-60-34)49(72)63-40(21-31-23-59-37-14-4-3-13-35(31)37)48(71)61-38(47(70)67-44)15-5-6-16-55/h3-4,7-14,17-18,23-24,27-28,36,38-44,59H,5-6,15-16,19-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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103n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077272
PNG
(CHEMBL412561 | H-DFpa-cyclo[DCys-Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C54H66F2N12O8S2/c1-30(2)46-54(76)67-45(52(74)63-41(47(59)69)23-32-14-18-36(56)19-15-32)29-78-77-28-44(66-48(70)38(58)22-31-12-16-35(55)17-13-31)53(75)64-42(24-33-8-7-21-60-26-33)50(72)65-43(25-34-27-61-39-10-4-3-9-37(34)39)51(73)62-40(49(71)68-46)11-5-6-20-57/h3-4,7-10,12-19,21,26-27,30,38,40-46,61H,5-6,11,20,22-25,28-29,57-58H2,1-2H3,(H2,59,69)(H,62,73)(H,63,74)(H,64,75)(H,65,72)(H,66,70)(H,67,76)(H,68,71)/t38-,40+,41-,42+,43-,44+,45-,46-/m1/s1
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106n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077304
PNG
(CHEMBL414598 | H-Pfp-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C52H57F10N13O8S2/c1-20(2)44-52(83)74-33(50(81)70-29(45(65)76)14-25-36(55)40(59)43(62)41(60)37(25)56)18-85-84-17-32(73-46(77)26(64)13-24-34(53)38(57)42(61)39(58)35(24)54)51(82)72-31(12-22-16-66-19-68-22)49(80)71-30(11-21-15-67-27-8-4-3-7-23(21)27)48(79)69-28(47(78)75-44)9-5-6-10-63/h3-4,7-8,15-16,19-20,26,28-33,44,67H,5-6,9-14,17-18,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t26-,28-,29-,30+,31-,32-,33-,44+/m0/s1
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124n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077267
PNG
(CHEMBL385689 | H-Nal-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-34-17-20-40(59)21-18-34)32-81-80-31-48(69-52(73)42(61)25-35-16-19-37-11-3-4-12-38(37)24-35)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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166n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077286
PNG
(CHEMBL437057 | H-Pfp-cyclo[DCys-2Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33-,34-,35+,46+/m0/s1
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170n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077295
PNG
(CHEMBL406491 | H-2Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1F)C(N)=O)NC(=O)[C@@H](N)Cc1ccccc1F
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-12-4-7-15-35(30)54)26-77-76-25-42(65-46(69)36(56)19-29-11-3-6-14-34(29)53)51(74)64-41(22-32-24-58-27-60-32)49(72)63-40(21-31-23-59-37-16-8-5-13-33(31)37)48(71)61-38(47(70)67-44)17-9-10-18-55/h3-8,11-16,23-24,27-28,36,38-44,59H,9-10,17-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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176n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077297
PNG
(CHEMBL415201 | H-Fpa-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-35-16-19-37-11-3-4-12-38(37)24-35)32-81-80-31-48(69-52(73)42(61)25-34-17-20-40(59)21-18-34)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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271n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077297
PNG
(CHEMBL415201 | H-Fpa-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-35-16-19-37-11-3-4-12-38(37)24-35)32-81-80-31-48(69-52(73)42(61)25-34-17-20-40(59)21-18-34)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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287n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077267
PNG
(CHEMBL385689 | H-Nal-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-34-17-20-40(59)21-18-34)32-81-80-31-48(69-52(73)42(61)25-35-16-19-37-11-3-4-12-38(37)24-35)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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376n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077295
PNG
(CHEMBL406491 | H-2Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1F)C(N)=O)NC(=O)[C@@H](N)Cc1ccccc1F
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-12-4-7-15-35(30)54)26-77-76-25-42(65-46(69)36(56)19-29-11-3-6-14-34(29)53)51(74)64-41(22-32-24-58-27-60-32)49(72)63-40(21-31-23-59-37-16-8-5-13-33(31)37)48(71)61-38(47(70)67-44)17-9-10-18-55/h3-8,11-16,23-24,27-28,36,38-44,59H,9-10,17-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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382n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077273
PNG
(CHEMBL411556 | H-3Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(F)c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(F)c1
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-10-8-12-33(54)18-30)26-77-76-25-42(65-46(69)36(56)19-29-9-7-11-32(53)17-29)51(74)64-41(22-34-24-58-27-60-34)49(72)63-40(21-31-23-59-37-14-4-3-13-35(31)37)48(71)61-38(47(70)67-44)15-5-6-16-55/h3-4,7-14,17-18,23-24,27-28,36,38-44,59H,5-6,15-16,19-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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397n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077297
PNG
(CHEMBL415201 | H-Fpa-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-35-16-19-37-11-3-4-12-38(37)24-35)32-81-80-31-48(69-52(73)42(61)25-34-17-20-40(59)21-18-34)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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484n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077286
PNG
(CHEMBL437057 | H-Pfp-cyclo[DCys-2Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33-,34-,35+,46+/m0/s1
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568n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077304
PNG
(CHEMBL414598 | H-Pfp-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C52H57F10N13O8S2/c1-20(2)44-52(83)74-33(50(81)70-29(45(65)76)14-25-36(55)40(59)43(62)41(60)37(25)56)18-85-84-17-32(73-46(77)26(64)13-24-34(53)38(57)42(61)39(58)35(24)54)51(82)72-31(12-22-16-66-19-68-22)49(80)71-30(11-21-15-67-27-8-4-3-7-23(21)27)48(79)69-28(47(78)75-44)9-5-6-10-63/h3-4,7-8,15-16,19-20,26,28-33,44,67H,5-6,9-14,17-18,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t26-,28-,29-,30+,31-,32-,33-,44+/m0/s1
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637n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077281
PNG
(CHEMBL438726 | H-Pfp-cyclo[DCys-D2Pal-DTrp-Lys-Val...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33+,34-,35+,46+/m0/s1
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692n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077272
PNG
(CHEMBL412561 | H-DFpa-cyclo[DCys-Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C54H66F2N12O8S2/c1-30(2)46-54(76)67-45(52(74)63-41(47(59)69)23-32-14-18-36(56)19-15-32)29-78-77-28-44(66-48(70)38(58)22-31-12-16-35(55)17-13-31)53(75)64-42(24-33-8-7-21-60-26-33)50(72)65-43(25-34-27-61-39-10-4-3-9-37(34)39)51(73)62-40(49(71)68-46)11-5-6-20-57/h3-4,7-10,12-19,21,26-27,30,38,40-46,61H,5-6,11,20,22-25,28-29,57-58H2,1-2H3,(H2,59,69)(H,62,73)(H,63,74)(H,64,75)(H,65,72)(H,66,70)(H,67,76)(H,68,71)/t38-,40+,41-,42+,43-,44+,45-,46-/m1/s1
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694n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077273
PNG
(CHEMBL411556 | H-3Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(F)c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(F)c1
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-10-8-12-33(54)18-30)26-77-76-25-42(65-46(69)36(56)19-29-9-7-11-32(53)17-29)51(74)64-41(22-34-24-58-27-60-34)49(72)63-40(21-31-23-59-37-14-4-3-13-35(31)37)48(71)61-38(47(70)67-44)15-5-6-16-55/h3-4,7-14,17-18,23-24,27-28,36,38-44,59H,5-6,15-16,19-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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734n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50077272
PNG
(CHEMBL412561 | H-DFpa-cyclo[DCys-Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C54H66F2N12O8S2/c1-30(2)46-54(76)67-45(52(74)63-41(47(59)69)23-32-14-18-36(56)19-15-32)29-78-77-28-44(66-48(70)38(58)22-31-12-16-35(55)17-13-31)53(75)64-42(24-33-8-7-21-60-26-33)50(72)65-43(25-34-27-61-39-10-4-3-9-37(34)39)51(73)62-40(49(71)68-46)11-5-6-20-57/h3-4,7-10,12-19,21,26-27,30,38,40-46,61H,5-6,11,20,22-25,28-29,57-58H2,1-2H3,(H2,59,69)(H,62,73)(H,63,74)(H,64,75)(H,65,72)(H,66,70)(H,67,76)(H,68,71)/t38-,40+,41-,42+,43-,44+,45-,46-/m1/s1
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838n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 3


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077286
PNG
(CHEMBL437057 | H-Pfp-cyclo[DCys-2Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33-,34-,35+,46+/m0/s1
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918n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077304
PNG
(CHEMBL414598 | H-Pfp-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C52H57F10N13O8S2/c1-20(2)44-52(83)74-33(50(81)70-29(45(65)76)14-25-36(55)40(59)43(62)41(60)37(25)56)18-85-84-17-32(73-46(77)26(64)13-24-34(53)38(57)42(61)39(58)35(24)54)51(82)72-31(12-22-16-66-19-68-22)49(80)71-30(11-21-15-67-27-8-4-3-7-23(21)27)48(79)69-28(47(78)75-44)9-5-6-10-63/h3-4,7-8,15-16,19-20,26,28-33,44,67H,5-6,9-14,17-18,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t26-,28-,29-,30+,31-,32-,33-,44+/m0/s1
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926n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077295
PNG
(CHEMBL406491 | H-2Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1F)C(N)=O)NC(=O)[C@@H](N)Cc1ccccc1F
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-12-4-7-15-35(30)54)26-77-76-25-42(65-46(69)36(56)19-29-11-3-6-14-34(29)53)51(74)64-41(22-32-24-58-27-60-32)49(72)63-40(21-31-23-59-37-16-8-5-13-33(31)37)48(71)61-38(47(70)67-44)17-9-10-18-55/h3-8,11-16,23-24,27-28,36,38-44,59H,9-10,17-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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972n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077273
PNG
(CHEMBL411556 | H-3Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(F)c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(F)c1
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-10-8-12-33(54)18-30)26-77-76-25-42(65-46(69)36(56)19-29-9-7-11-32(53)17-29)51(74)64-41(22-34-24-58-27-60-34)49(72)63-40(21-31-23-59-37-14-4-3-13-35(31)37)48(71)61-38(47(70)67-44)15-5-6-16-55/h3-4,7-14,17-18,23-24,27-28,36,38-44,59H,5-6,15-16,19-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50077286
PNG
(CHEMBL437057 | H-Pfp-cyclo[DCys-2Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33-,34-,35+,46+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 2


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077272
PNG
(CHEMBL412561 | H-DFpa-cyclo[DCys-Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C54H66F2N12O8S2/c1-30(2)46-54(76)67-45(52(74)63-41(47(59)69)23-32-14-18-36(56)19-15-32)29-78-77-28-44(66-48(70)38(58)22-31-12-16-35(55)17-13-31)53(75)64-42(24-33-8-7-21-60-26-33)50(72)65-43(25-34-27-61-39-10-4-3-9-37(34)39)51(73)62-40(49(71)68-46)11-5-6-20-57/h3-4,7-10,12-19,21,26-27,30,38,40-46,61H,5-6,11,20,22-25,28-29,57-58H2,1-2H3,(H2,59,69)(H,62,73)(H,63,74)(H,64,75)(H,65,72)(H,66,70)(H,67,76)(H,68,71)/t38-,40+,41-,42+,43-,44+,45-,46-/m1/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077267
PNG
(CHEMBL385689 | H-Nal-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-34-17-20-40(59)21-18-34)32-81-80-31-48(69-52(73)42(61)25-35-16-19-37-11-3-4-12-38(37)24-35)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077272
PNG
(CHEMBL412561 | H-DFpa-cyclo[DCys-Pal-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C54H66F2N12O8S2/c1-30(2)46-54(76)67-45(52(74)63-41(47(59)69)23-32-14-18-36(56)19-15-32)29-78-77-28-44(66-48(70)38(58)22-31-12-16-35(55)17-13-31)53(75)64-42(24-33-8-7-21-60-26-33)50(72)65-43(25-34-27-61-39-10-4-3-9-37(34)39)51(73)62-40(49(71)68-46)11-5-6-20-57/h3-4,7-10,12-19,21,26-27,30,38,40-46,61H,5-6,11,20,22-25,28-29,57-58H2,1-2H3,(H2,59,69)(H,62,73)(H,63,74)(H,64,75)(H,65,72)(H,66,70)(H,67,76)(H,68,71)/t38-,40+,41-,42+,43-,44+,45-,46-/m1/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077295
PNG
(CHEMBL406491 | H-2Fpa-cyclo[DCys-His-DTrp-Lys-Val-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1F)C(N)=O)NC(=O)[C@@H](N)Cc1ccccc1F
Show InChI InChI=1S/C52H65F2N13O8S2/c1-28(2)44-52(75)66-43(50(73)62-39(45(57)68)20-30-12-4-7-15-35(30)54)26-77-76-25-42(65-46(69)36(56)19-29-11-3-6-14-34(29)53)51(74)64-41(22-32-24-58-27-60-32)49(72)63-40(21-31-23-59-37-16-8-5-13-33(31)37)48(71)61-38(47(70)67-44)17-9-10-18-55/h3-8,11-16,23-24,27-28,36,38-44,59H,9-10,17-22,25-26,55-56H2,1-2H3,(H2,57,68)(H,58,60)(H,61,71)(H,62,73)(H,63,72)(H,64,74)(H,65,69)(H,66,75)(H,67,70)/t36-,38-,39-,40+,41-,42-,43-,44+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077304
PNG
(CHEMBL414598 | H-Pfp-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C52H57F10N13O8S2/c1-20(2)44-52(83)74-33(50(81)70-29(45(65)76)14-25-36(55)40(59)43(62)41(60)37(25)56)18-85-84-17-32(73-46(77)26(64)13-24-34(53)38(57)42(61)39(58)35(24)54)51(82)72-31(12-22-16-66-19-68-22)49(80)71-30(11-21-15-67-27-8-4-3-7-23(21)27)48(79)69-28(47(78)75-44)9-5-6-10-63/h3-4,7-8,15-16,19-20,26,28-33,44,67H,5-6,9-14,17-18,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t26-,28-,29-,30+,31-,32-,33-,44+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50077297
PNG
(CHEMBL415201 | H-Fpa-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(F)cc1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-35-16-19-37-11-3-4-12-38(37)24-35)32-81-80-31-48(69-52(73)42(61)25-34-17-20-40(59)21-18-34)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 4


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50077267
PNG
(CHEMBL385689 | H-Nal-cyclo[DCys-Pal-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc(F)cc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C58H69FN12O8S2/c1-33(2)50-58(79)70-49(56(77)66-45(51(62)72)26-34-17-20-40(59)21-18-34)32-81-80-31-48(69-52(73)42(61)25-35-16-19-37-11-3-4-12-38(37)24-35)57(78)67-46(27-36-10-9-23-63-29-36)54(75)68-47(28-39-30-64-43-14-6-5-13-41(39)43)55(76)65-44(53(74)71-50)15-7-8-22-60/h3-6,9-14,16-21,23-24,29-30,33,42,44-50,64H,7-8,15,22,25-28,31-32,60-61H2,1-2H3,(H2,62,72)(H,65,76)(H,66,77)(H,67,78)(H,68,75)(H,69,73)(H,70,79)(H,71,74)/t42-,44-,45-,46-,47+,48-,49+,50+/m0/s1
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1.06E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 1


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Bombesin 4


(Frog)
BDBM85490
PNG
(DPhe6,Leu13,Psi(CH2NH),Cpa14-Bn(6-14))
Show SMILES CC(C)C[C@@H](CN[C@@H](C#N)C(N)=O)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](N)Cc1ccccc1)C(C)C
Show InChI InChI=1S/C50H69N15O9/c1-27(2)17-33(24-57-40(21-51)44(54)68)61-49(73)39(20-32-23-55-26-59-32)62-42(67)25-58-50(74)43(28(3)4)65-45(69)29(5)60-48(72)38(19-31-22-56-36-14-10-9-13-34(31)36)64-47(71)37(15-16-41(53)66)63-46(70)35(52)18-30-11-7-6-8-12-30/h6-14,22-23,26-29,33,35,37-40,43,56-57H,15-20,24-25,52H2,1-5H3,(H2,53,66)(H2,54,68)(H,55,59)(H,58,74)(H,60,72)(H,61,73)(H,62,67)(H,63,70)(H,64,71)(H,65,69)/t29-,33-,35+,37-,38-,39-,40-,43-/m0/s1
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1.29E+3n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by PDSP Ki Database




Biochemistry 38: 7307-20 (1999)


Article DOI: 10.1021/bi990204w
BindingDB Entry DOI: 10.7270/Q29022BG
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50077281
PNG
(CHEMBL438726 | H-Pfp-cyclo[DCys-D2Pal-DTrp-Lys-Val...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccccn2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1c(F)c(F)c(F)c(F)c1F)C(N)=O)NC(=O)[C@@H](N)Cc1c(F)c(F)c(F)c(F)c1F
Show InChI InChI=1S/C54H58F10N12O8S2/c1-22(2)46-54(84)75-35(52(82)71-31(47(67)77)18-27-38(57)42(61)45(64)43(62)39(27)58)21-86-85-20-34(74-48(78)28(66)17-26-36(55)40(59)44(63)41(60)37(26)56)53(83)73-33(16-24-9-6-8-14-68-24)51(81)72-32(15-23-19-69-29-11-4-3-10-25(23)29)50(80)70-30(49(79)76-46)12-5-7-13-65/h3-4,6,8-11,14,19,22,28,30-35,46,69H,5,7,12-13,15-18,20-21,65-66H2,1-2H3,(H2,67,77)(H,70,80)(H,71,82)(H,72,81)(H,73,83)(H,74,78)(H,75,84)(H,76,79)/t28-,30-,31-,32+,33+,34-,35+,46+/m0/s1
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1.38E+3n/an/an/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
The compound was tested for binding affinity against human Somatostatin receptor type 5


J Med Chem 42: 1863-71 (1999)


Article DOI: 10.1021/jm9806289
BindingDB Entry DOI: 10.7270/Q2XW4J03
More data for this
Ligand-Target Pair
Vasopressin V2 Receptor


(Rattus norvegicus (Rat))
BDBM50013634
PNG
(24-(1H-5-imidazolylmethyl)-16-(1H-3-indolylmethyl)...)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]2CCCCN2C(=O)[C@@H]2CCCCN2C1=O
Show InChI InChI=1S/C40H53N9O6/c1-3-24(2)34-40(55)49-17-9-7-14-33(49)39(54)48-16-8-6-13-31(48)37(52)45-30(20-26-22-41-23-43-26)38(53)47-18-10-15-32(47)36(51)44-29(35(50)46-34)19-25-21-42-28-12-5-4-11-27(25)28/h4-5,11-12,21-24,29-34,42H,3,6-10,13-20H2,1-2H3,(H,41,43)(H,44,51)(H,45,52)(H,46,50)/t24-,29-,30-,31+,32+,33-,34-/m0/s1
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1.80E+3n/an/an/an/an/an/an/an/a



Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of [3H]-arginine vasopressin binding to rat kidney medulla Vasopressin V2 receptor


J Med Chem 33: 1843-5 (1990)


Article DOI: 10.1021/jm00169a001
BindingDB Entry DOI: 10.7270/Q2JS9PDK
More data for this
Ligand-Target Pair
Vasopressin V1 receptor


(RAT)
BDBM50013634
PNG
(24-(1H-5-imidazolylmethyl)-16-(1H-3-indolylmethyl)...)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]2CCCCN2C(=O)[C@@H]2CCCCN2C1=O
Show InChI InChI=1S/C40H53N9O6/c1-3-24(2)34-40(55)49-17-9-7-14-33(49)39(54)48-16-8-6-13-31(48)37(52)45-30(20-26-22-41-23-43-26)38(53)47-18-10-15-32(47)36(51)44-29(35(50)46-34)19-25-21-42-28-12-5-4-11-27(25)28/h4-5,11-12,21-24,29-34,42H,3,6-10,13-20H2,1-2H3,(H,41,43)(H,44,51)(H,45,52)(H,46,50)/t24-,29-,30-,31+,32+,33-,34-/m0/s1
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2.20E+3n/an/an/an/an/an/an/an/a



Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of [3H]arginine vasopressin binding to rat liver Vasopressin V1 receptor


J Med Chem 33: 1843-5 (1990)


Article DOI: 10.1021/jm00169a001
BindingDB Entry DOI: 10.7270/Q2JS9PDK
More data for this
Ligand-Target Pair
NMB


(RAT)
BDBM85490
PNG
(DPhe6,Leu13,Psi(CH2NH),Cpa14-Bn(6-14))
Show SMILES CC(C)C[C@@H](CN[C@@H](C#N)C(N)=O)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](N)Cc1ccccc1)C(C)C
Show InChI InChI=1S/C50H69N15O9/c1-27(2)17-33(24-57-40(21-51)44(54)68)61-49(73)39(20-32-23-55-26-59-32)62-42(67)25-58-50(74)43(28(3)4)65-45(69)29(5)60-48(72)38(19-31-22-56-36-14-10-9-13-34(31)36)64-47(71)37(15-16-41(53)66)63-46(70)35(52)18-30-11-7-6-8-12-30/h6-14,22-23,26-29,33,35,37-40,43,56-57H,15-20,24-25,52H2,1-5H3,(H2,53,66)(H2,54,68)(H,55,59)(H,58,74)(H,60,72)(H,61,73)(H,62,67)(H,63,70)(H,64,71)(H,65,69)/t29-,33-,35+,37-,38-,39-,40-,43-/m0/s1
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2.70E+3n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by PDSP Ki Database




Biochemistry 38: 7307-20 (1999)


Article DOI: 10.1021/bi990204w
BindingDB Entry DOI: 10.7270/Q29022BG
More data for this
Ligand-Target Pair
BRS3


(Homo sapiens (Human))
BDBM85490
PNG
(DPhe6,Leu13,Psi(CH2NH),Cpa14-Bn(6-14))
Show SMILES CC(C)C[C@@H](CN[C@@H](C#N)C(N)=O)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](N)Cc1ccccc1)C(C)C
Show InChI InChI=1S/C50H69N15O9/c1-27(2)17-33(24-57-40(21-51)44(54)68)61-49(73)39(20-32-23-55-26-59-32)62-42(67)25-58-50(74)43(28(3)4)65-45(69)29(5)60-48(72)38(19-31-22-56-36-14-10-9-13-34(31)36)64-47(71)37(15-16-41(53)66)63-46(70)35(52)18-30-11-7-6-8-12-30/h6-14,22-23,26-29,33,35,37-40,43,56-57H,15-20,24-25,52H2,1-5H3,(H2,53,66)(H2,54,68)(H,55,59)(H,58,74)(H,60,72)(H,61,73)(H,62,67)(H,63,70)(H,64,71)(H,65,69)/t29-,33-,35+,37-,38-,39-,40-,43-/m0/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by PDSP Ki Database




Biochemistry 38: 7307-20 (1999)


Article DOI: 10.1021/bi990204w
BindingDB Entry DOI: 10.7270/Q29022BG
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50063809
PNG
(CHEMBL437081 | H-Nal-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C60H71N13O8S2/c1-34(2)52-60(81)72-51(58(79)68-47(53(63)74)26-36-19-21-38-12-4-6-14-40(38)24-36)32-83-82-31-50(71-54(75)44(62)25-35-18-20-37-11-3-5-13-39(37)23-35)59(80)70-49(28-42-30-64-33-66-42)57(78)69-48(27-41-29-65-45-16-8-7-15-43(41)45)56(77)67-46(55(76)73-52)17-9-10-22-61/h3-8,11-16,18-21,23-24,29-30,33-34,44,46-52,65H,9-10,17,22,25-28,31-32,61-62H2,1-2H3,(H2,63,74)(H,64,66)(H,67,77)(H,68,79)(H,69,78)(H,70,80)(H,71,75)(H,72,81)(H,73,76)/t44-,46+,47-,48-,49+,50+,51-,52-/m0/s1
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n/an/a 68n/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human somatostatin 3 (hsst) receptor


J Med Chem 41: 1146-54 (1998)


Article DOI: 10.1021/jm970730q
BindingDB Entry DOI: 10.7270/Q26W9BS9
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50063815
PNG
(CHEMBL440067 | H-Nal-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(c1)-c1ccccc1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C62H73N13O8S2/c1-36(2)54-62(83)74-53(60(81)70-49(55(65)76)28-37-13-12-18-42(25-37)39-14-4-3-5-15-39)34-85-84-33-52(73-56(77)46(64)27-38-22-23-40-16-6-7-17-41(40)26-38)61(82)72-51(30-44-32-66-35-68-44)59(80)71-50(29-43-31-67-47-20-9-8-19-45(43)47)58(79)69-48(57(78)75-54)21-10-11-24-63/h3-9,12-20,22-23,25-26,31-32,35-36,46,48-54,67H,10-11,21,24,27-30,33-34,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t46-,48+,49-,50-,51+,52+,53-,54-/m0/s1
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n/an/a 1.00E+3n/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human somatostatin 5 (hsst) receptor


J Med Chem 41: 1146-54 (1998)


Article DOI: 10.1021/jm970730q
BindingDB Entry DOI: 10.7270/Q26W9BS9
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50063817
PNG
(CHEMBL429371 | H-Dip-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1cccc(c1)-c1ccccc1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(c1)-c1ccccc1
Show InChI InChI=1S/C64H75N13O8S2/c1-38(2)56-64(85)76-55(62(83)72-51(57(67)78)30-40-16-14-22-44(28-40)42-19-7-4-8-20-42)36-87-86-35-54(75-58(79)48(66)29-39-15-13-21-43(27-39)41-17-5-3-6-18-41)63(84)74-53(32-46-34-68-37-70-46)61(82)73-52(31-45-33-69-49-24-10-9-23-47(45)49)60(81)71-50(59(80)77-56)25-11-12-26-65/h3-10,13-24,27-28,33-34,37-38,48,50-56,69H,11-12,25-26,29-32,35-36,65-66H2,1-2H3,(H2,67,78)(H,68,70)(H,71,81)(H,72,83)(H,73,82)(H,74,84)(H,75,79)(H,76,85)(H,77,80)/t48-,50+,51-,52-,53+,54+,55-,56-/m0/s1
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n/an/a 669n/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human somatostatin 2 (hsst) receptor


J Med Chem 41: 1146-54 (1998)


Article DOI: 10.1021/jm970730q
BindingDB Entry DOI: 10.7270/Q26W9BS9
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50063809
PNG
(CHEMBL437081 | H-Nal-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C60H71N13O8S2/c1-34(2)52-60(81)72-51(58(79)68-47(53(63)74)26-36-19-21-38-12-4-6-14-40(38)24-36)32-83-82-31-50(71-54(75)44(62)25-35-18-20-37-11-3-5-13-39(37)23-35)59(80)70-49(28-42-30-64-33-66-42)57(78)69-48(27-41-29-65-45-16-8-7-15-43(41)45)56(77)67-46(55(76)73-52)17-9-10-22-61/h3-8,11-16,18-21,23-24,29-30,33-34,44,46-52,65H,9-10,17,22,25-28,31-32,61-62H2,1-2H3,(H2,63,74)(H,64,66)(H,67,77)(H,68,79)(H,69,78)(H,70,80)(H,71,75)(H,72,81)(H,73,76)/t44-,46+,47-,48-,49+,50+,51-,52-/m0/s1
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n/an/a 1.00E+3n/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human somatostatin 1 (hsst) receptor


J Med Chem 41: 1146-54 (1998)


Article DOI: 10.1021/jm970730q
BindingDB Entry DOI: 10.7270/Q26W9BS9
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50063838
PNG
(CHEMBL217216 | H-Dip-cyclo[DCys-His-DTrp-Lys-Val-C...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@@H](N)Cc1cccc(c1)-c1ccccc1
Show InChI InChI=1S/C62H73N13O8S2/c1-36(2)54-62(83)74-53(60(81)70-49(55(65)76)28-38-22-23-40-16-6-7-17-41(40)26-38)34-85-84-33-52(73-56(77)46(64)27-37-13-12-18-42(25-37)39-14-4-3-5-15-39)61(82)72-51(30-44-32-66-35-68-44)59(80)71-50(29-43-31-67-47-20-9-8-19-45(43)47)58(79)69-48(57(78)75-54)21-10-11-24-63/h3-9,12-20,22-23,25-26,31-32,35-36,46,48-54,67H,10-11,21,24,27-30,33-34,63-64H2,1-2H3,(H2,65,76)(H,66,68)(H,69,79)(H,70,81)(H,71,80)(H,72,82)(H,73,77)(H,74,83)(H,75,78)/t46-,48+,49-,50-,51+,52+,53-,54-/m0/s1
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n/an/a 1.01E+3n/an/an/an/an/an/a



Tulane University School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human somatostatin 1 (hsst) receptor


J Med Chem 41: 1146-54 (1998)


Article DOI: 10.1021/jm970730q
BindingDB Entry DOI: 10.7270/Q26W9BS9
More data for this
Ligand-Target Pair
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