ID: ALA2431367

Max Phase: Preclinical

Molecular Formula: C26H30N2O4S

Molecular Weight: 466.60

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1c(/C=C/c2ccc(NS(C)(=O)=O)cc2)cc(-c2cc(C)c[nH]c2=O)cc1C(C)(C)C

Standard InChI:  InChI=1S/C26H30N2O4S/c1-17-13-22(25(29)27-16-17)20-14-19(24(32-5)23(15-20)26(2,3)4)10-7-18-8-11-21(12-9-18)28-33(6,30)31/h7-16,28H,1-6H3,(H,27,29)/b10-7+

Standard InChI Key:  SPKNRTZABWHHKN-JXMROGBWSA-N

Associated Targets(Human)

Hepatocyte 2737 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver microsomes 16955 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hepatocyte 2621 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hepatitis C virus 23859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rattus norvegicus 775804 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver microsomes 8692 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: 466.60Molecular Weight (Monoisotopic): 466.1926AlogP: 5.20#Rotatable Bonds: 6
Polar Surface Area: 88.26Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.91CX Basic pKa: CX LogP: 4.03CX LogD: 4.03
Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.49Np Likeness Score: -0.31

References

1. Schoenfeld RC, Bourdet DL, Brameld KA, Chin E, de Vicente J, Fung A, Harris SF, Lee EK, Le Pogam S, Leveque V, Li J, Lui AS, Najera I, Rajyaguru S, Sangi M, Steiner S, Talamas FX, Taygerly JP, Zhao J..  (2013)  Discovery of a novel series of potent non-nucleoside inhibitors of hepatitis C virus NS5B.,  56  (20): [PMID:24069953] [10.1021/jm401266k]

Source