Bloom syndrome protein

Target ID: CHEMBL1293237

Organism: Homo sapiens

Type: SINGLE PROTEIN

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
METHOTREXATE CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(C(=O)N[C@@H](CCC(=O)O)C(=O)O)cc1 ID50: 6.2 nM
GENISTEIN O=c1c(-c2ccc(O)cc2)coc2cc(O)cc(O)c12 IC50: 1000.0 nM
HYDROXYPROGESTERONE CC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C Remaining activity: 89.0 %
MIFEPRISTONE CC#C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(N(C)C)cc3)C[C@@]21C IC50: 0.028 nM
ZAPRINAST CCCOc1ccccc1-c1nc2[nH]nnc2c(=O)[nH]1 IC50: 1750000.0 nM
ACETAZOLAMIDE CC(=O)Nc1nnc(S(N)(=O)=O)s1 Ki: 250.0 nM
BRIMONIDINE Brc1c(NC2=NCCN2)ccc2nccnc12 pC25: 1.55 uM kg-1
AMIFOSTINE NCCCNCCSP(=O)(O)O LD50: 1049.0 mg.kg-1
2-METHOXYESTRADIOL COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)CC[C@@H]12 GI50: 700.0 nM
SEMAXANIB Cc1cc(C)c(/C=C2\C(=O)Nc3ccccc32)[nH]1 IC50: 700.0 nM
QUERCETIN O=c1c(O)c(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12 IC50: 32870.0 nM
DAIDZEIN O=c1c(-c2ccc(O)cc2)coc2cc(O)ccc12 Suppression: 22.0 %
ZARDAVERINE COc1cc(-c2ccc(=O)[nH]n2)ccc1OC(F)F IC50: 10000.0 nM
TRIMETHOPRIM COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC IC50: 12000.0 nM
RALOXIFENE HYDROCHLORIDE Cl.O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12 IC50: 0.4 nM
AMINOPTERIN Nc1nc(N)c2nc(CNc3ccc(C(=O)N[C@@H](CCC(=O)O)C(=O)O)cc3)cnc2n1 Ki: 0.0037 nM
ESTRADIOL C[C@]12CC[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CC[C@@H]2O IC50: 1.5 nM
CILOSTAMIDE CN(C(=O)CCCOc1ccc2[nH]c(=O)ccc2c1)C1CCCCC1 EC50: 1200.0 nM
ASPARTIC ACID N[C@@H](CC(=O)O)C(=O)O KA: 48.0 uM
ROLIPRAM COc1ccc(C2CNC(=O)C2)cc1OC1CCCC1 IC50: 1000.0 nM
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
PINACIDIL ANHYDROUS CC(N/C(=N\C#N)Nc1ccncc1)C(C)(C)C IC50: 800.0 nM
DIPYRIDAMOLE OCCN(CCO)c1nc(N2CCCCC2)c2nc(N(CCO)CCO)nc(N3CCCCC3)c2n1 IC50: 500.0 nM
MILRINONE Cc1[nH]c(=O)c(C#N)cc1-c1ccncc1 Mean ED50: 0.037 mg kg-1

Top Fragments

SMILES Avg pKi Count Structure
[3*]OC 5.48 147
[3*]O[3*] 5.79 146
[16*]c1ccc([16*])cc1 9.9 138
[5*]N[5*] 8.82 119
[16*]c1ccc(O)cc1 7.45 97