ID: ALA2426577

Max Phase: Preclinical

Molecular Formula: C15H15N5OS2

Molecular Weight: 345.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cccc(-c2nc(CSc3nc(N)cc(N)n3)cs2)c1

Standard InChI:  InChI=1S/C15H15N5OS2/c1-21-11-4-2-3-9(5-11)14-18-10(7-22-14)8-23-15-19-12(16)6-13(17)20-15/h2-7H,8H2,1H3,(H4,16,17,19,20)

Standard InChI Key:  MWNSGZIJSDEJKP-UHFFFAOYSA-N

Associated Targets(non-human)

Deoxycytidine kinase 72 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: 345.45Molecular Weight (Monoisotopic): 345.0718AlogP: 3.07#Rotatable Bonds: 5
Polar Surface Area: 99.94Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.75CX LogP: 2.91CX LogD: 2.41
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.54Np Likeness Score: -1.92

References

1. Murphy JM, Armijo AL, Nomme J, Lee CH, Smith QA, Li Z, Campbell DO, Liao HI, Nathanson DA, Austin WR, Lee JT, Darvish R, Wei L, Wang J, Su Y, Damoiseaux R, Sadeghi S, Phelps ME, Herschman HR, Czernin J, Alexandrova AN, Jung ME, Lavie A, Radu CG..  (2013)  Development of new deoxycytidine kinase inhibitors and noninvasive in vivo evaluation using positron emission tomography.,  56  (17): [PMID:23947754] [10.1021/jm400457y]

Source