ID: ALA1650755

Max Phase: Preclinical

Molecular Formula: C8H10FN2O5P

Molecular Weight: 264.15

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C8H10FN2O5P/c9-6-5-11(8(13)10-7(6)12)3-1-2-4-17(14,15)16/h1-2,5H,3-4H2,(H,10,12,13)(H2,14,15,16)/b2-1+

Standard InChI Key:  HQXXZZRCJPJFHM-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: 264.15Molecular Weight (Monoisotopic): 264.0311AlogP: -0.59#Rotatable Bonds: 4
Polar Surface Area: 112.39Molecular Species: ACIDHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.74CX Basic pKa: CX LogP: -0.92CX LogD: -3.32
Aromatic Rings: 1Heavy Atoms: 17QED Weighted: 0.50Np Likeness Score: -0.50

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