Compound ID | 1425

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Quabodepistat

Synonym(s): OPC-167832

Class: Small molecule antibacterial agent

Agent Type: Semisynthetic; Small molecule; Direct acting;
Spectrum of activity: Antimycobacterial
Mechanism of action: Mycolic acid synthesis inhibitor. Decaprenylphosphoryl-B-d-ribose 2′-oxidase inhibitor (DprE1 inhibitor)
Target Pathogen: Active against Mycobacterium tuberculosis
Description: A 3,4-dihydrocarbostyril derivative
Institute where first reported: Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan
Year first mentioned: 2020
Highest development stage: Phase 2 (NCT05221502)
Development status: Active
Chemical structure(s):
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Molecular weight: 456.84
Iso. SMILES: C1CC(=O)NC2=C(C=CC(=C21)OC[C@@]3(CCN(C[C@H]3O)C4=C(C=C(C=C4F)Cl)F)O)F
InChI Key: XZISSTDXPBUCJA-DYESRHJHSA-N
Can. SMILES: C1CC(=O)NC2=C1C(=CC=C2F)OC[C@@]3(CCN(C[C@H]3O)C4=C(C=C(C=C4F)Cl)F)O
InChI: InChI=1S/C21H20ClF3N2O4/c22-11-7-14(24)20(15(25)8-11)27-6-5-21(30,17(28)9-27)10-31-16-3-2-13(23)19-12(16)1-4-18(29)26-19/h2-3,7-8,17,28,30H,1,4-6,9-10H2,(H,26,29)/t17-,21-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/118904282
Guide to Pharmacology: quabodepistat
Citations:
  • https://aac.asm.org/content/63/8/e00603-19
  • https://aac.asm.org/content/64/6/e02020-19

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