Thiosulfate sulfurtransferase

Target ID: CHEMBL4295835

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 %
ERGOCALCIFEROL C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)/C=C/[C@H](C)C(C)C)CC[C@@H]12 EC50: 3800.0 nM
ETHACRYNIC ACID C=C(CC)C(=O)c1ccc(OCC(=O)O)c(Cl)c1Cl mequiv of Na+/kg: 4.14 0-5h
CANDESARTAN CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 T1/2: 9.0 hr
AMPICILLIN CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O MIC: 5.0 ug.mL-1
BITHIONOL Oc1c(Cl)cc(Cl)cc1Sc1cc(Cl)cc(Cl)c1O Control current: 198.6 %

Top Fragments

SMILES Avg pKi Count Structure
[8*]C[8*] None 35
[16*]c1ccc([16*])cc1 None 34
[3*]O[3*] None 32
c1ccc(Cc2ccccc2)cc1 None 23
[16*]c1c(O)c(Cl)cc(Cl)c1Cl None 23