ID: ALA204762

Max Phase: Preclinical

Molecular Formula: C21H14FN3O2S

Molecular Weight: 391.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1[nH]sc2c1c(=O)c1cc(F)c(-c3cc4ccccc4[nH]3)cc1n2C1CC1

Standard InChI:  InChI=1S/C21H14FN3O2S/c22-14-8-13-17(9-12(14)16-7-10-3-1-2-4-15(10)23-16)25(11-5-6-11)21-18(19(13)26)20(27)24-28-21/h1-4,7-9,11,23H,5-6H2,(H,24,27)

Standard InChI Key:  OPJNSXZCMYVJIF-UHFFFAOYSA-N

Associated Targets(Human)

HEp-2 3859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Topoisomerase IV subunit A 110 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 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: 391.43Molecular Weight (Monoisotopic): 391.0791AlogP: 4.53#Rotatable Bonds: 2
Polar Surface Area: 70.65Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.81CX Basic pKa: CX LogP: 3.78CX LogD: 2.85
Aromatic Rings: 5Heavy Atoms: 28QED Weighted: 0.46Np Likeness Score: -0.51

References

1. Wiles JA, Song Y, Wang Q, Lucien E, Hashimoto A, Cheng J, Marlor CW, Ou Y, Podos SD, Thanassi JA, Thoma CL, Deshpande M, Pucci MJ, Bradbury BJ..  (2006)  Biological evaluation of isothiazoloquinolones containing aromatic heterocycles at the 7-position: In vitro activity of a series of potent antibacterial agents that are effective against methicillin-resistant Staphylococcus aureus.,  16  (5): [PMID:16337789] [10.1016/j.bmcl.2005.11.064]

Source