Gatifloxacin
Gatifloxacin
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Gatifloxacin

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Catalog Number PR112811593
CAS 112811-59-3
Description Gatifloxacin is an antibiotic of the fourth-generation fluoroquinolone family, that like other members of that family, inhibits the bacterial topoisomerase type-II enzymes. It has a role as an antiinfective agent, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor and an antimicrobial agent.
Synonyms Tequin; Gatiflo; Zymar
IUPAC Name 1-cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid
Molecular Weight 375.4
Molecular Formula C19H22FN3O4
InChI XUBOMFCQGDBHNK-UHFFFAOYSA-N
InChI Key InChI=1S/C19H22FN3O4/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26)
Documentation/Certification GMP
Drug Categories Anti-Bacterial Agents; Anti-Infective Agents; Antibacterials for Systemic Use; Antiinfectives for Systemic Use; Compounds used in a research, industrial, or household setting; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inhibitors (moderate); Cytochrome P-450 Enzyme Inhibitors; Enzyme Inhibitors; Fluoroquinolones; Heterocyclic Compounds, Fused-Ring; Hypoglycemia-Associated Agents; Ophthalmic Solutions; Ophthalmologicals; Pharmaceutical Preparations; Pharmaceutical Solutions; Potential QTc-Prolonging Agents; QTc Prolonging Agents; Quinolines; Quinolone Antimicrobial; Quinolones; Sensory Organs; Solutions; Topoisomerase II Inhibitors; Topoisomerase Inhibitors
Drug Interactions Acarbose-The therapeutic efficacy of Acarbose can be increased when used in combination with Gatifloxacin.
Aceclofenac-Aceclofenac may increase the neuroexcitatory activities of Gatifloxacin.
Acemetacin-Acemetacin may increase the neuroexcitatory activities of Gatifloxacin.
Acenocoumarol-The therapeutic efficacy of Acenocoumarol can be increased when used in combination with Gatifloxacin.
Acetaminophen-The metabolism of Acetaminophen can be decreased when combined with Gatifloxacin.
Half-Life 7-14 hours
Isomeric SMILES CC1CN(CCN1)C2=C(C=C3C(=C2OC)N(C=C(C3=O)C(=O)O)C4CC4)F
Type Small Molecule
Therapeutic Category Antibacterials
Pharmacology

Indications

Gatifloxacin is primarily indicated for the treatment of various bacterial infections, including·hitis, sinusitis, community-acquired pneumonia, and skin infections such as abscesses and wounds. This pharmaceutical agent is particularly effective against infections caused by bacteria such as S. pneumoniae, H. influenzae, S. aureus, M. pneumoniae, C. pneumoniae, L. pneumophila, and S. pyogenes.

Pharmacodynamics

Gatifloxacin is classified as a synthetic broad-spectrum 8-methoxyfluoroquinolone antibacterial agent available for both oral and intravenous administration. Its mechanism of action is bactericidal, relying·he inhibition of bacterial DNA replication. This is accomplished through the binding·he bacterial enzyme DNA gyrase, thereby preventing·he untwisting·he DNA double helix necessary for replication. This drug exhibits a notably higher affinity-100 times greater-for bacterial DNA gyrase compared to its affinity for mammalian equivalents. Gatifloxacin demonstrates broad-spectrum activity, targeting·h Gram-positive and Gram-negative bacteria, and should be reserved for infections that are confirmed or strong·have a bacterial origin.

Absorption

Upon oral administration, gatifloxacin is well absorbed from the gastrointestinal tract, exhibiting·his high level of absorption ensures that adequate therapeutic levels can be achieved systemically following·he human body. Less than 1% of the administered dose is metabolized and subsequently excreted in the urine as ethylenediamine and methylethylenediamine metabolites, indicating·hat the drug is largely excreted unchanged.

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