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Garenoxacin information


Garenoxacin
Clinical data
Routes of
administration
Oral
ATC code
  • J01MA19 (WHO)
Identifiers
IUPAC name
  • 1-Cyclopropyl-8-(difluoromethoxy)-7-[(1R)-1-methyl-2,3-dihydro-1H-isoindol-5-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
CAS Number
  • 194804-75-6 ☒N
PubChem CID
  • 124093
ChemSpider
  • 110579 ☒N
UNII
  • V72H9867WB
KEGG
  • D04031 checkY
ChEBI
  • CHEBI:131716 ☒N
CompTox Dashboard (EPA)
  • DTXSID30173135 Edit this at Wikidata
Chemical and physical data
FormulaC23H20F2N2O4
Molar mass426.420 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • FC(F)Oc1c(ccc2c1N(/C=C(\C2=O)C(=O)O)C3CC3)c4ccc5c(c4)CN[C@@H]5C
InChI
  • InChI=1S/C23H20F2N2O4/c1-11-15-5-2-12(8-13(15)9-26-11)16-6-7-17-19(21(16)31-23(24)25)27(14-3-4-14)10-18(20(17)28)22(29)30/h2,5-8,10-11,14,23,26H,3-4,9H2,1H3,(H,29,30)/t11-/m1/s1 ☒N
  • Key:NJDRXTDGYFKORP-LLVKDONJSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Garenoxacin (INN) is a quinolone antibiotic for the treatment of Gram-positive and Gram-negative bacterial infections.[1]

Garenoxacin was discovered by Toyama Chemical Co., Ltd. of Tokyo, Japan, and is currently being marketed in Japan under the tradename Geninax. Schering-Plough holds worldwide rights for garenoxacin, except for Japan, South Korea, and China.[citation needed]

On February 13, 2006, Schering-Plough announced that the United States Food and Drug Administration had accepted the New Drug Application (NDA) for garenoxacin, and had been granted a 10-month review.[2] As of 2015, however, it has not been approved in the US.[citation needed]

Schering-Plough later withdrew its application to the United States Food and Drug Administration, FDA, (August 20, 2006) for approval of the antibiotic Garenoxacin.[3]

The European Medicines Agency (EMA) had also been formally notified by Schering-Plough Europe (July 25, 2007) of its decision to withdraw the application for a centralized marketing authorization for garenoxacin as well.[4][5][6] Based on the CHMP review of the data regarding safety and efficacy (risk/benefit), the CHMP considered the application for garenoxacin to be unapprovable.[7]

  1. ^ Takagi H, Tanaka K, Tsuda H, Kobayashi H (December 2008). "Clinical studies of garenoxacin". International Journal of Antimicrobial Agents. 32 (6): 468–74. doi:10.1016/j.ijantimicag.2008.06.032. PMID 18790608.
  2. ^ "Drugs.com, Schering-Plough Reports Garenoxacin NDA Accepted for FDA Review". Retrieved 2008-03-25.
  3. ^ "Schering-Plough pulls its garenoxacin app".
  4. ^ "Schering-Plough Europe Withdraws Its Marketing Authorisation Application For Garenoxacin Mesylate". MediLexicon International Ltd. 28 July 2007. Archived from the original on 2007-08-08. Retrieved 2009-05-30.
  5. ^ "Garenoxacin mesylate: Withdrawn application". European Medicines Agency (EMA). 17 September 2018. Retrieved 13 July 2020.
  6. ^ "Schering-Plough Europe withdraws its marketing authorisation applicationfor Garenoxacin mesylate". European Medicines Agency (EMA) (Press release). Retrieved 13 July 2020.
  7. ^ "Withdrawal Assessment report for Garenoxacin Mesylate (garenoxacin)" (PDF). European Medicines Agency. 18 October 2007.

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Garenoxacin

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Garenoxacin (INN) is a quinolone antibiotic for the treatment of Gram-positive and Gram-negative bacterial infections. Garenoxacin was discovered by Toyama...

Word Count : 317

Quinolone antibiotic

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30 3.00 1.2 1.2 10.1 14.0 3.5 3.5 3.5 3.5 30 30 34 34 Yes Yes No No Garenoxacin 400 600 ND 92 5.0 10.4 ND 1.2 60 96.7 14.2 9.8 ND ND 75 ND 40 ND ND ND...

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ATC code J01

Last Update:

J01MA16 Gatifloxacin J01MA17 Prulifloxacin J01MA18 Pazufloxacin J01MA19 Garenoxacin J01MA21 Sitafloxacin J01MA22 Tosufloxacin J01MA23 Delafloxacin J01MA24...

Word Count : 1151

Prontosil

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Gatifloxacin Finafloxacin Gemifloxacin Moxifloxacin# Clinafloxacin† Garenoxacin‡ Prulifloxacin‡ Sitafloxacin‡ Trovafloxacin‡/Alatrofloxacin‡ Veterinary...

Word Count : 1603

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