iPPI-DB

Inhibitors of Protein-Protein Interaction Database

Compound 1835

Identifiers

  • Canonical SMILES: 
    Cc1cc(cc(C)c1O)-c1nc2sc3CCCCCc3c2c(=O)[nH]1
  • IUPAC name: 
    5-(4-hydroxy-3,5-dimethylphenyl)-8-thia-4,6-diazatricyclo[7.5.0.0^{2,7}]tetradeca-1(9),2(7),5-trien-3-one
  • InChi: 
    InChI=1S/C19H20N2O2S/c1-10-8-12(9-11(2)16(10)22)17-20-18(23)15-13-6-4-3-5-7-14(13)24-19(15)21-17/h8-9,22H,3-7H2,1-2H3,(H,20,21,23)
  • InChiKey: 
    UNXACKFLOUYIKN-UHFFFAOYSA-N

External links


137654107
CHEMBL4096544

External search

Bibliography (1)

Publication Name
Ouyang Liang, Zhang Lan, Liu Jie, Fu Leilei, Yao Dahong, Zhao Yuqian, Zhang Shouyue, Wang Guan, He Gu, Liu Bo. . Discovery of a Small-Molecule Bromodomain-Containing Protein 4 (BRD4) Inhibitor That Induces AMP-Activated Protein Kinase-Modulated Autophagy-Associated Cell Death in Breast Cancer Journal of Medicinal Chemistry. 7f

Pharmacological data

Biochemical tests Cellular tests PK tests Cytotoxicity tests
1 2 0 0

Targets

PPI family Best activity Diseases MMoA
Bromodomain / Histone 6.31 breast cancer Inhibition
Physicochemical filters
Descriptor Lipinski's RO5 Veber Pfizer's 3/75
Compliance
MW 340.12 g/mol
HBA 4
HBD 2
HBA + HBD 6
AlogP 5.33
TPSA 61.69
RB 1
Radar chart
PCA : iPPI-DB chemical space
PCA : Correlation circle
Efficiencies: iPPI-DB biplot LE versus LLE
Summary
Bibliographic ressources Biochemical tests Cellular tests PK tests Cytotoxicity tests
1 1 2 0 0
Pharmacological data
Bibliography Name Target Competition Assay type Assay name Cell line Activity type Activity
10.1021/acs.jmedchem.7b00275 7f BRD4
O60885 		H4
P62805 		Biochemical assay alphascreen BRD4 pIC50 (half maximal inhibitory concentration, -log10) 6.31
10.1021/acs.jmedchem.7b00275 7f BRD4
O60885 		H4
P62805 		Cellular assay Anti-proliferative MCF-7 MCF7 mammary carcinoma cells pIC50 (half maximal inhibitory concentration, -log10) 5.55
10.1021/acs.jmedchem.7b00275 7f BRD4
O60885 		H4
P62805 		Cellular assay Anti-proliferative MDA-MB-231 MDA-MB-231 breast pIC50 (half maximal inhibitory concentration, -log10) 5.08
Ta Structure Name Drugbank ID
0.7663 5,6,7,8-TETRAHYDRO[1]BENZOTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE DB08777
0.6533 3-(1H-tetrazol-5-ylmethyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one DB06889
0.6340 (5S)-5-(2-amino-2-oxoethyl)-4-oxo-N-[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)methyl]-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidine-2-carboxamide DB07397
0.4038 Sufugolix DB06494
0.3958 DDP-225 DB05642
0.3801 Relugolix DB11853
0.3677 Udenafil DB06267
0.3629 Sagopilone DB12391
0.3626 2-AMINO-4-(2,4-DICHLOROPHENYL)-N-ETHYLTHIENO[2,3-D]PYRIMIDINE-6-CARBOXAMIDE DB08789
0.3609 T-62 DB12919
0.3596 Pelitrexol DB12757
0.3584 CRA_16847 DB02063
0.3555 5-ethoxy-4-(1-methyl-7-oxo-3-propyl-6,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-5-yl)thiophene-2-sulfonamide DB08729
0.3496 Sildenafil DB00203
0.3481 2-amino-4-[2,4-dichloro-5-(2-pyrrolidin-1-ylethoxy)phenyl]-N-ethylthieno[2,3-d]pyrimidine-6-carboxamide DB06969