ID: ALA3359163

Max Phase: Preclinical

Molecular Formula: C13H10F3N5OS

Molecular Weight: 341.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1nc2[nH]c(SCc3ccccc3C(F)(F)F)nc2c(=O)[nH]1

Standard InChI:  InChI=1S/C13H10F3N5OS/c14-13(15,16)7-4-2-1-3-6(7)5-23-12-18-8-9(20-12)19-11(17)21-10(8)22/h1-4H,5H2,(H4,17,18,19,20,21,22)

Standard InChI Key:  USLXLGBNYPWUAW-UHFFFAOYSA-N

Associated Targets(non-human)

2-amino-4-hydroxy-6-hydroxymethyldihydropteridin e pyrophosphokinase 89 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacterial dihydropteroate synthase 13 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: 341.32Molecular Weight (Monoisotopic): 341.0558AlogP: 2.54#Rotatable Bonds: 3
Polar Surface Area: 100.45Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.72CX Basic pKa: CX LogP: 2.66CX LogD: 2.52
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.64Np Likeness Score: -1.41

References

1. Dennis ML, Chhabra S, Wang ZC, Debono A, Dolezal O, Newman J, Pitcher NP, Rahmani R, Cleary B, Barlow N, Hattarki M, Graham B, Peat TS, Baell JB, Swarbrick JD..  (2014)  Structure-based design and development of functionalized Mercaptoguanine derivatives as inhibitors of the folate biosynthesis pathway enzyme 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Staphylococcus aureus.,  57  (22): [PMID:25357262] [10.1021/jm501417f]

Source