ID: ALA4640290

Max Phase: Preclinical

Molecular Formula: C11H16F2N5O13P3

Molecular Weight: 557.19

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@]1(F)[C@H](n2cnc3c(=O)[nH]c(N)nc32)O[C@](F)(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@H]1O

Standard InChI:  InChI=1S/C11H16F2N5O13P3/c1-10(12)7(20)11(13,2-28-33(24,25)31-34(26,27)30-32(21,22)23)29-8(10)18-3-15-4-5(18)16-9(14)17-6(4)19/h3,7-8,20H,2H2,1H3,(H,24,25)(H,26,27)(H2,21,22,23)(H3,14,16,17,19)/t7-,8+,10+,11+/m0/s1

Standard InChI Key:  DSZXDHWOUTVAEA-SCVMZPAESA-N

Associated Targets(Human)

DNA polymerase alpha subunit 225 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA polymerase beta 23632 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hepatitis C virus NS5B RNA-dependent RNA polymerase 3026 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 557.19Molecular Weight (Monoisotopic): 556.9926AlogP: -0.67#Rotatable Bonds: 8
Polar Surface Area: 278.87Molecular Species: ACIDHBA: 13HBD: 7
#RO5 Violations: 3HBA (Lipinski): 18HBD (Lipinski): 8#RO5 Violations (Lipinski): 3
CX Acidic pKa: 0.89CX Basic pKa: 0.31CX LogP: -2.35CX LogD: -9.34
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.20Np Likeness Score: 0.79

References

1. Wang G, Dyatkina N, Prhavc M, Williams C, Serebryany V, Hu Y, Huang Y, Wu X, Chen T, Huang W, Rajwanshi VK, Deval J, Fung A, Jin Z, Stoycheva A, Shaw K, Gupta K, Tam Y, Jekle A, Smith DB, Beigelman L..  (2020)  Synthesis and Anti-HCV Activity of Sugar-Modified Guanosine Analogues: Discovery of AL-611 as an HCV NS5B Polymerase Inhibitor for the Treatment of Chronic Hepatitis C.,  63  (18): [PMID:32816483] [10.1021/acs.jmedchem.0c00935]

Source