Phosphodiesterase 3

Target ID: CHEMBL2094125

Organism: Homo sapiens

Type: PROTEIN FAMILY

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
INAMRINONE Nc1cc(-c2ccncc2)c[nH]c1=O Mean ED50: 0.389 mg kg-1
CIPAMFYLLINE Nc1nc2c([nH]1)c(=O)n(CC1CC1)c(=O)n2CC1CC1 Inhibition: 5.0 %
ZAPRINAST CCCOc1ccccc1-c1nc2[nH]nnc2c(=O)[nH]1 IC50: 1750000.0 nM
THEOPHYLLINE Cn1c(=O)c2[nH]cnc2n(C)c1=O ED50: 18.5 mg.kg-1
SILDENAFIL CCCc1nn(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)nc12 Pc: 87000000.0 cm s-1
ZARDAVERINE COc1cc(-c2ccc(=O)[nH]n2)ccc1OC(F)F IC50: 10000.0 nM
ISOMAZOLE COc1cc([S+](C)[O-])ccc1-c1nc2cnccc2[nH]1 ED50: 0.05 dp/dt
CILOMILAST COc1ccc([C@]2(C#N)CC[C@@H](C(=O)O)CC2)cc1OC1CCCC1 IC50: 100.0 nM
LODENAFIL CCCc1nn(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(CCO)CC4)ccc3OCC)nc12 IC50: 460.0 nM
CILOSTAMIDE CN(C(=O)CCCOc1ccc2[nH]c(=O)ccc2c1)C1CCCCC1 EC50: 1200.0 nM
ROLIPRAM COc1ccc(C2CNC(=O)C2)cc1OC1CCCC1 IC50: 1000.0 nM
SULMAZOLE COc1cc([S+](C)[O-])ccc1-c1nc2cccnc2[nH]1 Delta: 163.0 %
VARDENAFIL HYDROCHLORIDE CCCc1nc(C)c2c(O)nc(-c3cc(S(=O)(=O)N4CCN(CC)CC4)ccc3OCC)nn12.Cl IC50: 180.0 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*]O[3*] 5.79 273
[3*]OC 6.0 195
[12*]S(=O)(=O)c1ccc([16*])c([16*])c1 6.54 117
[8*]CCC 6.54 117
[4*]CC 6.54 117