Page last updated: 2024-11-07

oxociprofloxacin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

oxociprofloxacin: structure given in first source; ciprofloxacin metabolite [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID128242
CHEBI ID192773
SCHEMBL ID9686037
MeSH IDM0166960

Synonyms (19)

Synonym
oxociprofloxacin
1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-oxo-1-piperazinyl)-3-quinolinecarboxylic acid
CHEBI:192773
103237-52-1
1-cyclopropyl-6-fluoro-4-oxo-7-(3-oxopiperazin-1-yl)quinoline-3-carboxylic acid
FT-0673360
3-quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-oxo-1-piperazinyl)-
bay-q 3542
4-oxociprofloxacin
unii-y901rq8cdm
y901rq8cdm ,
3'-oxociprofloxacin
3-quinolinecarboxylicacid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-oxo-1-piperazinyl)-
MYYZZOHRULFPOQ-UHFFFAOYSA-N
SCHEMBL9686037
DTXSID80145706
AKOS030241012
Q27294389
1-cyclopropyl-6-fluoro-4-oxo-7-(3-oxopiperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The pharmacokinetic parameters for ciprofloxacin were not significantly altered in cirrhotic patients."( The effect of cirrhosis on the steady-state pharmacokinetics of oral ciprofloxacin.
Frost, RW; Krol, G; Lasseter, KC; Lettieri, JT; Shamblen, EC, 1989
)
0.28

Dosage Studied

ExcerptRelevanceReference
" Therefore it appears from this study that no dosage adjustment is required in patients with hepatic cirrhosis."( The effect of cirrhosis on the steady-state pharmacokinetics of oral ciprofloxacin.
Frost, RW; Krol, G; Lasseter, KC; Lettieri, JT; Shamblen, EC, 1989
)
0.28
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
drug metabolitenull
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (5)

ClassDescription
N-arylpiperazine
piperazinone
cyclopropanesCyclopropane and its derivatives formed by substitution.
quinolinemonocarboxylic acidAny aromatic carboxylic acid that contains a quinoline moiety that is substituted by one carboxy substituent.
quinolone
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (2)

PathwayProteinsCompounds
Drug ADME6387
Ciprofloxacin ADME513

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (60.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (20.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other4 (80.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]