gemifloxacin mesylate
The mesylate salt of gemifloxacin.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C18H20FN5O4.CH4O3S |
|---|---|
| Charge | 0 |
| Average mass | 485.494 Da |
| Monoisotopic mass | 485.13805 Da |
| Source | ChEBI |
| InChIKey | JIYMVSQRGZEYAX-CWUUNJJBSA-N |
CO/N=C1\CN(c2nc3c(cc2F)c(=O)c(C(=O)O)cn3C2CC2)CC1CN.CS(=O)(=O)O
InChI=1S/C18H20FN5O4.CH4O3S/c1-28-22-14-8-23(6-9(14)5-20)17-13(19)4-11-15(25)12(18(26)27)7-24(10-2-3-10)16(11)21-17;1-5(2,3)4/h4,7,9-10H,2-3,5-6,8,20H2,1H3,(H,26,27);1H3,(H,2,3,4)/b22-14+;
Also called
- 7-[3-(aminomethyl)-4-(methoxyimino)pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid methanesulfonate
Cross-references
- beilstein:9176911
- cas:210353-53-0
Drug registries
Activity roles
- antimicrobial agent
CHEBI:33281
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:53749 |
gemifloxacin mesylate | antibioticmech:chebi-71b5be365d |
2026-08-30 |
Mechanism summary
- Mode of action
- NUCLEIC_ACID_SYNTHESIS_INHIBITION microbial target
- Clinical status
- APPROVED
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories