ID: ALA3088281

Max Phase: Preclinical

Molecular Formula: C24H25F3N4O2S

Molecular Weight: 490.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)c1sc(-c2ccccn2)nc1N1CCC(NCc2cccc(C(F)(F)F)c2)CC1

Standard InChI:  InChI=1S/C24H25F3N4O2S/c1-2-33-23(32)20-21(30-22(34-20)19-8-3-4-11-28-19)31-12-9-18(10-13-31)29-15-16-6-5-7-17(14-16)24(25,26)27/h3-8,11,14,18,29H,2,9-10,12-13,15H2,1H3

Standard InChI Key:  PZSJACZPGLTYND-UHFFFAOYSA-N

Associated Targets(non-human)

DNA gyrase subunit A/DNA gyrase subunit B 505 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

RAW264.7 28094 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium tuberculosis 203094 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA gyrase subunit B 445 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: 490.55Molecular Weight (Monoisotopic): 490.1650AlogP: 5.16#Rotatable Bonds: 7
Polar Surface Area: 67.35Molecular Species: BASEHBA: 7HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.29CX LogP: 5.27CX LogD: 3.39
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.46Np Likeness Score: -1.71

References

1. Jeankumar VU, Renuka J, Santosh P, Soni V, Sridevi JP, Suryadevara P, Yogeeswari P, Sriram D..  (2013)  Thiazole-aminopiperidine hybrid analogues: design and synthesis of novel Mycobacterium tuberculosis GyrB inhibitors.,  70  [PMID:24148991] [10.1016/j.ejmech.2013.09.025]

Source