cinoxacin

Trade name: cinobac

Small moleculeapproved

Approved

Jun 13, 1980

Cinoxacin is a synthetic antibacterial agent for oral administration. Cinoxacin mode of action involves the inhibiting of DNA gyrase, a type II topoisomerase, and topoisomerase IV. Adverse effects are nausea, anorexia, vomiting, abdominal cramps/pain, perverse taste, diarrhea, headache, dizziness, rash, urticaria, pruritus, edema and other. — NCATS

Clinical trial activity

0 trials · 0 clinical orgs · 2 marketing orgs

Phase 1
0
Phase 2
0
Phase 3
0
Phase 4
0

Timeline

1980s

  1. Jun 13, 1980

    Eli Lilly — Earliest FDA Approval

  2. Jun 13, 1980

    Eli Lilly — NDA Organization

1990s

  1. Feb 28, 1992

    Teva — Marketing Organization

Indications

Mechanism of action

Approval history

  • approvedJun 13, 1980

Chemistry & pharmacology

Loading structure…

SMILES

CCN1N=C(C(O)=O)C(=O)C2=C1C=C3OCOC3=C2
Mol. weight
262.2182 g/mol
Lipinski Ro5
Pass
Rule of 3
No
Chirality
Achiral Molecule
Inorganic
No
Polymer
No
Delivery
Oral
Availability
Discontinued

Oral

Yes

Parenteral

No

Topical

No

Sources

Also known as

  • 1-ethyl-6,7-methylenedioxy-4(1h)-oxocinnoline-3-carboxylic acid
  • 1-ethyl-6,7-methylenedioxy-4(1h)-oxocinnoline-3-carboxylic acid
  • 5-ethyl-8-oxo-5,8-dihydro-1,3-dioxa-5,6-diaza-cyclopenta[b]naphthalene-7-carboxylic acid
  • 5-ethyl-8-oxo-5,8-dihydro-1,3-dioxa-5,6-diaza-cyclopenta[b]naphthalene-7-carboxylic acid
  • 64716
  • cinobac
  • cinobac
  • cinobac
  • cinobac
  • cinobactin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacin
  • cinoxacine
  • cinoxacine
  • cinoxacino
  • cinoxacino
  • cinoxacinum
  • cinoxacinum

Organizations

Marketing (3)

OrganizationOrg typeRelationshipDate
Eli LillyFor profitSYNJun 13, 1980
Eli LillyFor profitNDAJun 13, 1980
TevaFor profitMKTGFeb 28, 1992