Compile Data Set for Download or QSAR
maximum 50k data
Found 76 with Last Name = 'shagufta' and Initial = 'na'
TargetAngiotensin-converting enzyme 2(Homo sapiens (Human))TBA
LigandPNGBDBM50233798(CHEMBL398940 | N-(2-aminoethyl)-1-aziridine-ethana...)
Affinity DataKi:  4.59E+5nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123025(CHEMBL3623231)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123026(CHEMBL3623232)
Affinity DataIC50:  0.200nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50073850((S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyr...)
Affinity DataIC50:  2.5nMAssay Description:pA2 for NK2 receptor of human bladder IM9 cellsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123026(CHEMBL3623232)
Affinity DataIC50:  2.5nMAssay Description:Inhibition of steroid sulfatase in human JEG-3 cells using [6,7-3H]E1S as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM24306(Letrozole derivative, 40 | {2-bromo-4-[(4-cyanophe...)
Affinity DataIC50:  3nMAssay Description:Inhibition of aromatase in human JEG-3 cells using [1beta-3H]androstenedione as substrate after 1 hr by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50398452(CHEMBL2179110)
Affinity DataIC50:  12nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 2(Ovis aries (Sheep))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50324804((2-(4-(methylsulfonyl)phenyl)hex-1-ene-1,1-diyl)di...)
Affinity DataIC50:  14nMAssay Description:Inhibition of ovine COX2 using arachidonic acid as substrate assessed as reduction in PGF2alpha production preincubated for 5 mins followed by substr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50464567(CHEMBL4278683)
Affinity DataIC50:  20nMAssay Description:Binding affinity to estrogen receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50035204(4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50035204(4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50075009(1-Ethyl-5-[(4-fluoro-phenyl)-imidazol-1-yl-methyl]...)
Affinity DataIC50:  40nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM420297(acs.jmedchem.1c00409_ST.30 | med.21724, Compound 6...)
Affinity DataIC50:  40nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
Ligand InfoPurchasePDB
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50097366(4-((1H-imidazol-1-yl)methyl)-1-nitro-4aH-xanthen-9...)
Affinity DataIC50:  40nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123152(CHEMBL3219600)
Affinity DataIC50:  41nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123024(CHEMBL3623227)
Affinity DataIC50:  41nMAssay Description:Inhibition of human placental aromatase using [1,2,6,7-3H] androstenedione as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50097373(4-((1H-imidazol-1-yl)methyl)-9-oxo-9H-xanthene-1-c...)
Affinity DataIC50:  43nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM9475(4-(1H-Imidazol-1-ylmethyl)-7-phenoxy-2H-chromen-2-...)
Affinity DataIC50:  51nMAssay Description:Inhibition of human placental aromatase in presence of [1beta,2beta-3H] testosterone by Thompson and Siiteri methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM420296(Advanced SARS-CoV-2 Inhibitor 11a | MPI10 | acs.jm...)
Affinity DataIC50:  53nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
Ligand InfoPurchasePDB
LigandPNGBDBM50407514(CHEMBL1234732)
Affinity DataIC50:  100nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetEstrogen receptor(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  100nMAssay Description:Displacement of [3H]E2 from human recombinant ERalpha assessed as receptor binding after 45 mins by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123153(CHEMBL3623225)
Affinity DataIC50:  100nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123016(CHEMBL3623214)
Affinity DataIC50:  160nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Rattus norvegicus)
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)
Affinity DataIC50:  170nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123012(CHEMBL3623217)
Affinity DataIC50:  170nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM420283(alpha-ketoamide inhibitor 11r | med.21724, Compoun...)
Affinity DataIC50:  180nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123017(CHEMBL3623213)
Affinity DataIC50:  180nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123023(CHEMBL3623226)
Affinity DataIC50:  190nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50407515(CHEMBL5285968)
Affinity DataIC50:  200nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123019(CHEMBL3621226)
Affinity DataIC50:  220nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  222nMAssay Description:Inhibition of estrogen receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123020(CHEMBL3623209)
Affinity DataIC50:  250nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Rattus norvegicus)
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123022(CHEMBL169251)
Affinity DataIC50:  260nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123021(CHEMBL3623208)
Affinity DataIC50:  420nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme 2(Homo sapiens (Human))TBA
LigandPNGBDBM21489((2S)-2-{[(1S)-1-carboxy-2-{1-[(3,5-dichlorophenyl)...)
Affinity DataIC50:  440nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123151(CHEMBL3623223)
Affinity DataIC50:  470nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123030(CHEMBL3623219)
Affinity DataIC50:  480nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM7461(5,7-dihydroxy-2-phenyl-4H-chromen-4-one | 5,7-dihy...)
Affinity DataIC50:  500nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  500nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123014(CHEMBL3623215)
Affinity DataIC50:  510nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM50407519(CHEMBL5268979)
Affinity DataIC50:  670nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM420295(alpha-ketoamide inhibitor 13b | med.21724, Compoun...)
Affinity DataIC50:  670nMAssay Description:pA2 value against histamine h4 receptorMore data for this Ligand-Target Pair
Ligand InfoPurchase
In DepthDetails PubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123011(CHEMBL3623218)
Affinity DataIC50:  970nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123013(CHEMBL3623216)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM50407516(CHEMBL5280512)
Affinity DataIC50:  1.55E+3nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM50431275(CARMOFUR | Carm-ofur | Mifurol | med.21724, Compou...)
Affinity DataIC50:  1.82E+3nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM420293(alpha-ketoamide inhibitor 13a)
Affinity DataIC50:  2.39E+3nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetAromatase(Homo sapiens (Human))
American University Of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50123027(CHEMBL3623212)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of human placental aromatase assessed as conversion of 3H2O from [1beta,2beta-3H] testosterone after 20 mins by scintillation spectrometer...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)TBA
LigandPNGBDBM7781(4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione ...)
Affinity DataIC50:  2.50E+3nMAssay Description:Functional Histamine H3 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails PubMed
Displayed 1 to 50 (of 76 total ) | Next | Last >>
Jump to: