U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H20F2N2O4
Molecular Weight 426.4127
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GARENOXACIN

SMILES

C[C@H]1NCC2=CC(=CC=C12)C3=CC=C4C(=O)C(=CN(C5CC5)C4=C3OC(F)F)C(O)=O

InChI

InChIKey=NJDRXTDGYFKORP-LLVKDONJSA-N
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

HIDE SMILES / InChI

Molecular Formula C23H20F2N2O4
Molecular Weight 426.4127
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including, http://www.shijiebiaopin.com/upload/product/201233119022430.pdf

Garenoxacin is an antibacterial agent active against a range of aerobic Gram-positive and Gram-negative bacteria. It exerts its action by inhibiting bacterial DNA gyrase and topoisomerase IV. The drug was withdrawn from the market in Europe and was never approved in the USA. Garenoxacin is still marketed in Japan under the name Geninax.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
GARENOXACIN MESYLATE

Approved Use

Acute bacterial exacerbation of chronic bronchitis, Acute bacterial sinusitis, Community-acquired pneumonia, Uncomplicated skin and skin structures infections, Complicated skin and skin structure infections including diabetic foot infections, Complicated intra-abdominal infections, including post-surgical and acute pelvic infections.
Curative
GARENOXACIN MESYLATE

Approved Use

Laryngopharyngitis, Tonsillitis (including peritonsillitis and peritonsillar abscess), Acute bronchitis, Pneumonia, Secondary infection in chronic respiratory lesion, Otitis media, Sinusitis
Curative
GARENOXACIN MESYLATE

Approved Use

Acute bacterial exacerbation of chronic bronchitis, Acute bacterial sinusitis, Community-acquired pneumonia, Uncomplicated skin and skin structures infections, Complicated skin and skin structure infections including diabetic foot infections, Complicated intra-abdominal infections, including post-surgical and acute pelvic infections.
Curative
GARENOXACIN MESYLATE

Approved Use

Acute bacterial exacerbation of chronic bronchitis, Acute bacterial sinusitis, Community-acquired pneumonia, Uncomplicated skin and skin structures infections, Complicated skin and skin structure infections including diabetic foot infections, Complicated intra-abdominal infections, including post-surgical and acute pelvic infections.
Curative
GARENOXACIN MESYLATE

Approved Use

Acute bacterial exacerbation of chronic bronchitis, Acute bacterial sinusitis, Community-acquired pneumonia, Uncomplicated skin and skin structures infections, Complicated skin and skin structure infections including diabetic foot infections, Complicated intra-abdominal infections, including post-surgical and acute pelvic infections.
Curative
GENINAX

Approved Use

Laryngopharyngitis, Tonsillitis (including peritonsillitis and peritonsillar abscess), Acute bronchitis, Pneumonia, Secondary infection in chronic respiratory lesion, Otitis media, Sinusitis

Launch Date

2006
Curative
GENINAX

Approved Use

Laryngopharyngitis, Tonsillitis (including peritonsillitis and peritonsillar abscess), Acute bronchitis, Pneumonia, Secondary infection in chronic respiratory lesion, Otitis media, Sinusitis

Launch Date

2006
Curative
GENINAX

Approved Use

Laryngopharyngitis, Tonsillitis (including peritonsillitis and peritonsillar abscess), Acute bronchitis, Pneumonia, Secondary infection in chronic respiratory lesion, Otitis media, Sinusitis

Launch Date

2006
PubMed

PubMed

TitleDatePubMed
The in vitro activity of BMS-284756, a new des-fluorinated quinolone.
2002 Jan
Mycobacterium tuberculosis DNA gyrase: interaction with quinolones and correlation with antimycobacterial drug activity.
2004 Apr
In vitro susceptibility of Mycobacterium tuberculosis clinical isolates to garenoxacin and DA-7867.
2005 Oct
Torsades de Pointes induced by a combination of garenoxacin and disopyramide and other cytochrome P450, family 3, subfamily A polypeptide-4-influencing drugs during hypokalemia due to licorice.
2010 Apr
Patents

Patents

Sample Use Guides

The usual adult dosage is 400 mg once daily.
Route of Administration: Oral
The MICs was 0.025-0.78 ug/ml against aerobic and facultative anaerobic Gram-positive bacteria, 0.00313-12.5 ug/ml against aerobic and facultative anaerobic Gram-negative bacteria, 0.1-3.13 ug/ml against obligate anaerobic Gram-positive bacteria and 0.05-0.78 ug/ml for obligate Gram-negative bacteria. The MICs against C. pneumoniae, C. psittaci, M. pneumoniae and Legionella spp., were 0.008, 0.002, 0.016, 0.0313 and 0.0039-0.0313 ug/ml, respectively.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:38:20 GMT 2023
Edited
by admin
on Sat Dec 16 17:38:20 GMT 2023
Record UNII
V72H9867WB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GARENOXACIN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
GARENOXACIN [MI]
Common Name English
GARENOXACIN [MART.]
Common Name English
Garenoxacin [WHO-DD]
Common Name English
T-3811
Code English
garenoxacin [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01MA19
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
NCI_THESAURUS C795
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
WHO-ATC J01MA19
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
Code System Code Type Description
SMS_ID
100000091588
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
MERCK INDEX
m5672
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY Merck Index
CAS
194804-75-6
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
INN
8237
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
FDA UNII
V72H9867WB
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
WIKIPEDIA
Garenoxacin
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
NCI_THESAURUS
C65800
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
EVMPD
SUB25475
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID30173135
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
DRUG CENTRAL
4053
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL215303
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
MESH
C419689
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
DRUG BANK
DB06160
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
PUBCHEM
124093
Created by admin on Sat Dec 16 17:38:22 GMT 2023 , Edited by admin on Sat Dec 16 17:38:22 GMT 2023
PRIMARY
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