GABA-B receptor 1

Target ID: CHEMBL2064

Organism: Homo sapiens

Type: SINGLE PROTEIN

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
CAFFEINE Cn1c(=O)c2c(ncn2C)n(C)c1=O Vdss: 0.61 L.kg-1
VALDECOXIB Cc1onc(-c2ccccc2)c1-c1ccc(S(N)(=O)=O)cc1 Ki: 54000.0 nM
FLUVASTATIN CC(C)n1c(/C=C/C(O)CC(O)CC(=O)O)c(-c2ccc(F)cc2)c2ccccc21 IC50: 28.0 nM
BOSUTINIB COc1cc(Nc2c(C#N)cnc3cc(OCCCN4CCN(C)CC4)c(OC)cc23)c(Cl)cc1Cl IC50: 1.3 nM
TOFACITINIB C[C@@H]1CCN(C(=O)CC#N)C[C@@H]1N(C)c1ncnc2[nH]ccc12 IC50: 13.0 nM
VORINOSTAT O=C(CCCCCCC(=O)Nc1ccccc1)NO Inhibition: 100.0 %
AMILORIDE N=C(N)NC(=O)c1nc(Cl)c(N)nc1N Pc: 780000.0 cm s-1
HYDROCHLOROTHIAZIDE NS(=O)(=O)c1cc2c(cc1Cl)NCNS2(=O)=O IC50: 181970085860998.25 nM
SILDENAFIL CCCc1nn(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)nc12 Pc: 87000000.0 cm s-1
CANDESARTAN CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 T1/2: 9.0 hr
TOPIRAMATE CC1(C)O[C@@H]2[C@@H](CO[C@@]3(COS(N)(=O)=O)OC(C)(C)O[C@@H]23)O1 Ki: 250.0 nM
AMOXICILLIN CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccc(O)cc3)C(=O)N2[C@H]1C(=O)O MIC: 0.021 ug.mL-1

Top Fragments

SMILES Avg pKi Count Structure
[3*]O[3*] 8.89 90
[5*]N[5*] 8.89 85
[5*]N1CCN(C)CC1 8.89 78
[16*]c1ccccc1 4.27 73
[4*]CC None 51