Hypoxia-inducible factor 1 alpha

Target ID: CHEMBL4261

Organism: Homo sapiens

Type: SINGLE PROTEIN

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
HEXACHLOROPHENE Oc1c(Cl)cc(Cl)c(Cl)c1Cc1c(O)c(Cl)cc(Cl)c1Cl Control current: 237.4 %
GENTIAN VIOLET CN(C)c1ccc(C(=C2C=CC(=[N+](C)C)C=C2)c2ccc(N(C)C)cc2)cc1.[Cl-] Lysis: 100.0 %
ETHACRYNIC ACID C=C(CC)C(=O)c1ccc(OCC(=O)O)c(Cl)c1Cl mequiv of Na+/kg: 4.14 0-5h
EMETINE CC[C@H]1CN2CCc3cc(OC)c(OC)cc3[C@@H]2C[C@@H]1C[C@H]1NCCc2cc(OC)c(OC)cc21 IC50: 40.0 nM
DIETHYLSTILBESTROL CC/C(=C(/CC)c1ccc(O)cc1)c1ccc(O)cc1 EC50: 9.0 nM
AZARIBINE CC(=O)OC[C@H]1O[C@@H](n2ncc(=O)[nH]c2=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O Potency: 562.3 nM
BITHIONOL Oc1c(Cl)cc(Cl)cc1Sc1cc(Cl)cc(Cl)c1O Control current: 198.6 %
OXATOMIDE O=c1[nH]c2ccccc2n1CCCN1CCN(C(c2ccccc2)c2ccccc2)CC1 A10: 0.014 mg l-1
ESTRONE C[C@]12CC[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CCC2=O EC50: 1135.0 nM

Top Fragments

SMILES Avg pKi Count Structure
[4*]C([8*])[8*] None 39
[16*]c1ccccc1 None 39
[5*]N1CCN([5*])CC1 None 39
[9*]n1c(=O)[nH]c2ccccc21 None 39
[4*]CCC[8*] None 39