ID: ALA4562253

Max Phase: Preclinical

Molecular Formula: C18H16F2N2O2S

Molecular Weight: 362.40

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@H](NC(=O)N1C(=O)C[C@@H]1Sc1ccc(F)cc1F)c1ccccc1

Standard InChI:  InChI=1S/C18H16F2N2O2S/c1-11(12-5-3-2-4-6-12)21-18(24)22-16(23)10-17(22)25-15-8-7-13(19)9-14(15)20/h2-9,11,17H,10H2,1H3,(H,21,24)/t11-,17-/m0/s1

Standard InChI Key:  OKCBIQMGUWDPNS-GTNSWQLSSA-N

Associated Targets(non-human)

Moraxella catarrhalis 3334 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium tuberculosis 203094 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: 362.40Molecular Weight (Monoisotopic): 362.0901AlogP: 4.09#Rotatable Bonds: 4
Polar Surface Area: 49.41Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.82CX Basic pKa: CX LogP: 3.80CX LogD: 3.80
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.83Np Likeness Score: -1.20

References

1. Kuskovsky R, Lloyd D, Arora K, Plotkin BJ, Green JM, Boshoff HI, Barry C, Deschamps J, Konaklieva MI..  (2019)  C4-Phenylthio β-lactams: Effect of the chirality of the β-lactam ring on antimicrobial activity.,  27  (20): [PMID:31474471] [10.1016/j.bmc.2019.115050]

Source