ID: ALA3120171

Max Phase: Preclinical

Molecular Formula: C26H33N6O8P

Molecular Weight: 588.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[C@@H](C)OC(=O)[C@H](C)NP(=O)(OC[C@H]1O[C@@](C#N)(c2ccc3c(N)ncnn23)[C@](C)(O)[C@@H]1O)Oc1ccccc1

Standard InChI:  InChI=1S/C26H33N6O8P/c1-5-16(2)38-24(34)17(3)31-41(36,40-18-9-7-6-8-10-18)37-13-20-22(33)25(4,35)26(14-27,39-20)21-12-11-19-23(28)29-15-30-32(19)21/h6-12,15-17,20,22,33,35H,5,13H2,1-4H3,(H,31,36)(H2,28,29,30)/t16-,17+,20-,22-,25-,26+,41?/m1/s1

Standard InChI Key:  WJHFJNXZGRLCEI-GZPOSPORSA-N

Associated Targets(Human)

Hepatocyte 2737 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver 3974 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Caco-2 12174 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Huh-7 12904 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Canis familiaris 36305 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Syrian golden hamster 1610 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hepatitis C virus 23859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 588.56Molecular Weight (Monoisotopic): 588.2097AlogP: 2.06#Rotatable Bonds: 11
Polar Surface Area: 203.55Molecular Species: NEUTRALHBA: 13HBD: 4
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.23CX Basic pKa: 0.65CX LogP: 1.45CX LogD: 1.45
Aromatic Rings: 3Heavy Atoms: 41QED Weighted: 0.19Np Likeness Score: 0.03

References

1. Cho A, Zhang L, Xu J, Lee R, Butler T, Metobo S, Aktoudianakis V, Lew W, Ye H, Clarke M, Doerffler E, Byun D, Wang T, Babusis D, Carey AC, German P, Sauer D, Zhong W, Rossi S, Fenaux M, McHutchison JG, Perry J, Feng J, Ray AS, Kim CU..  (2014)  Discovery of the first C-nucleoside HCV polymerase inhibitor (GS-6620) with demonstrated antiviral response in HCV infected patients.,  57  (5): [PMID:23547794] [10.1021/jm400201a]

Source