ID: ALA1650759

Max Phase: Preclinical

Molecular Formula: C9H12FN2O5P

Molecular Weight: 278.18

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1[nH]c(=O)n(C/C=C/CCP(=O)(O)O)cc1F

Standard InChI:  InChI=1S/C9H12FN2O5P/c10-7-6-12(9(14)11-8(7)13)4-2-1-3-5-18(15,16)17/h1-2,6H,3-5H2,(H,11,13,14)(H2,15,16,17)/b2-1+

Standard InChI Key:  KCTKUURHXFRJGJ-OWOJBTEDSA-N

Associated Targets(Human)

Thymidylate kinase 169 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: 278.18Molecular Weight (Monoisotopic): 278.0468AlogP: -0.20#Rotatable Bonds: 5
Polar Surface Area: 112.39Molecular Species: ACIDHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.81CX Basic pKa: CX LogP: -0.64CX LogD: -3.04
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.51Np Likeness Score: -0.20

References

1. Topalis D, Pradère U, Roy V, Caillat C, Azzouzi A, Broggi J, Snoeck R, Andrei G, Lin J, Eriksson S, Alexandre JA, El-Amri C, Deville-Bonne D, Meyer P, Balzarini J, Agrofoglio LA..  (2011)  Novel antiviral C5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates.,  54  (1): [PMID:21128666] [10.1021/jm1011462]

Source