BDBM50020207 CHEMBL2369473::Gly-D-Ticc(-Cys-Tyr-D-Trp-Orn-Thr-Pen-)Thr-NH2

SMILES [H][C@]1(NC(=O)[C@H](CCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC(C)(C)[C@H](NC1=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)NC(=O)[C@H]1Cc2ccccc2CN1C(=O)CN)[C@@H](C)O

InChI Key InChIKey=ATYZDDGFJJQCCO-WGQWSGESSA-N

Data  3 IC50

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   Substructure
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50020207   

TargetDelta-type opioid receptor(Rattus norvegicus (rat))
University of Arizona

Curated by ChEMBL
LigandPNGBDBM50020207(CHEMBL2369473 | Gly-D-Ticc(-Cys-Tyr-D-Trp-Orn-Thr-...)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H]1NC(=O)[C@@H](NC(=O)[C@H](CCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC1(C)C)NC(=O)[C@H]1Cc2ccccc2CN1C(=O)CN)[C@@H](C)O)C(N)=O
Show InChI InChI=1S/C53H70N12O12S2/c1-27(66)42(45(56)70)62-52(77)44-53(3,4)79-78-26-39(61-50(75)40-22-30-10-5-6-11-31(30)25-65(40)41(69)23-55)49(74)59-37(20-29-15-17-33(68)18-16-29)47(72)60-38(21-32-24-57-35-13-8-7-12-34(32)35)48(73)58-36(14-9-19-54)46(71)63-43(28(2)67)51(76)64-44/h5-8,10-13,15-18,24,27-28,36-40,42-44,57,66-68H,9,14,19-23,25-26,54-55H2,1-4H3,(H2,56,70)(H,58,73)(H,59,74)(H,60,72)(H,61,75)(H,62,77)(H,63,71)(H,64,76)/t27-,28-,36+,37-,38+,39+,40-,42+,43+,44-/m1/s1
Affinity DataIC50: 5.35E+3nMAssay Description:Binding affinity in competition with [3H]- DPDPE in Opioid receptor delta 1 binding to rat brain membraneMore data for this Ligand-Target Pair
TargetSomatostatin receptor type 1/2/3/4/5(RAT)
University of Arizona

Curated by ChEMBL
LigandPNGBDBM50020207(CHEMBL2369473 | Gly-D-Ticc(-Cys-Tyr-D-Trp-Orn-Thr-...)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H]1NC(=O)[C@@H](NC(=O)[C@H](CCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC1(C)C)NC(=O)[C@H]1Cc2ccccc2CN1C(=O)CN)[C@@H](C)O)C(N)=O
Show InChI InChI=1S/C53H70N12O12S2/c1-27(66)42(45(56)70)62-52(77)44-53(3,4)79-78-26-39(61-50(75)40-22-30-10-5-6-11-31(30)25-65(40)41(69)23-55)49(74)59-37(20-29-15-17-33(68)18-16-29)47(72)60-38(21-32-24-57-35-13-8-7-12-34(32)35)48(73)58-36(14-9-19-54)46(71)63-43(28(2)67)51(76)64-44/h5-8,10-13,15-18,24,27-28,36-40,42-44,57,66-68H,9,14,19-23,25-26,54-55H2,1-4H3,(H2,56,70)(H,58,73)(H,59,74)(H,60,72)(H,61,75)(H,62,77)(H,63,71)(H,64,76)/t27-,28-,36+,37-,38+,39+,40-,42+,43+,44-/m1/s1
Affinity DataIC50: 1.94E+4nMAssay Description:Binding affinity in competition with [125I]- CGP-23996 in somatostatin receptor binding to rat brain membraneMore data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Arizona

Curated by ChEMBL
LigandPNGBDBM50020207(CHEMBL2369473 | Gly-D-Ticc(-Cys-Tyr-D-Trp-Orn-Thr-...)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H]1NC(=O)[C@@H](NC(=O)[C@H](CCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC1(C)C)NC(=O)[C@H]1Cc2ccccc2CN1C(=O)CN)[C@@H](C)O)C(N)=O
Show InChI InChI=1S/C53H70N12O12S2/c1-27(66)42(45(56)70)62-52(77)44-53(3,4)79-78-26-39(61-50(75)40-22-30-10-5-6-11-31(30)25-65(40)41(69)23-55)49(74)59-37(20-29-15-17-33(68)18-16-29)47(72)60-38(21-32-24-57-35-13-8-7-12-34(32)35)48(73)58-36(14-9-19-54)46(71)63-43(28(2)67)51(76)64-44/h5-8,10-13,15-18,24,27-28,36-40,42-44,57,66-68H,9,14,19-23,25-26,54-55H2,1-4H3,(H2,56,70)(H,58,73)(H,59,74)(H,60,72)(H,61,75)(H,62,77)(H,63,71)(H,64,76)/t27-,28-,36+,37-,38+,39+,40-,42+,43+,44-/m1/s1
Affinity DataIC50: 278nMAssay Description:Binding affinity in competition with [3H]- CTOP in Opioid receptor mu 1 binding to rat brain membraneMore data for this Ligand-Target Pair