A quinolone antibiotic
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Ozenoxacin

Item No. 41837

Technical Information
Formal Name
1-cyclopropyl-1,4-dihydro-8-methyl-7-[5-methyl-6-(methylamino)-3-pyridinyl]-4-oxo-3-quinolinecarboxylic acid
CAS Number
245765-41-7
Synonyms
  • T-3912
Molecular Formula
C21H21N3O3
Formula Weight
Purity
≥98%
A solid
DMSO: Slightly soluble: 0.1-1 mg/ml
SMILES
O=C(C1=CN(C2CC2)C3=C(C)C(C4=CC(C)=C(NC)N=C4)=CC=C3C1=O)O
InChi Code
InChI=1S/C21H21N3O3/c1-11-8-13(9-23-20(11)22-3)15-6-7-16-18(12(15)2)24(14-4-5-14)10-17(19(16)25)21(26)27/h6-10,14H,4-5H2,1-3H3,(H,22,23)(H,26,27)
InChi Key
XPIJWUTXQAGSLK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Ozenoxacin is a quinolone antibiotic.1 It is active against clinical isolates of S. pyogenes, P aeruginosa, and P. acnes and clinical isolates of antibiotic-sensitive and -resistant S. aureus, S. epidermidis, and S. pneumoniae (MIC50s = 0.00625-1.56 mg/L). Ozenoxacin inhibits S. aureus DNA gyrase and topoisomerase IV (IC50s = 4.5 and 0.617 mg/L, respectively). It reduces insulin- or 5α-dihydroxy testosterone-induced triglyceride production and lipid droplet formation in primary hamster sebocytes when used at a concentration of 30 µM.2 Ozenoxacin (30 µg/ml) decreases heat-killed C. acnes-induced increases in IL-6 and IL-8 production in HEKa primary human keratinocytes and IL-1β, IL-6, IL-8, and TNF-α production in THP-1 monocytes.3 Topical application of ozenoxacin (1%) decreases skin lesion bacterial counts in a mouse model of burn infection caused by S. aureus.1 Formulations containing ozenoxacin have been used in the treatment of S. aureus- or S. pyogenes-associated impetigo.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Yamakawa, T., Mitsuyama, J., and Hayashi, K. In vitro and in vivo antibacterial activity of T-3912, a novel non-fluorinated topical quinolone. J. Antimicrob. Chemother. 49(3), 455-465 (2002).

    2. Kitano, T., Koiwai, T., Fujikawa, K., et alOzenoxacin suppresses sebum production by inhibiting mTORC1 activation in differentiated hamster sebocytes. J. Dermatol. 51(9), 1187-1198 (2024).

    3. Tabara, K., Tamura, R., Nakamura, A., et alAnti-inflammatory effects of ozenoxacin, a topical quinolone antimicrobial agent. J. Antibot. (Tokyo) 73(4), 247-254 (2020).