ciprofloxacin hydrochloride hydrate
The monohydrate form of ciprofloxacin monohydrochloride.
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 | C17H18FN3O3.H2O.HCl |
|---|---|
| Charge | 0 |
| Average mass | 385.823 Da |
| Monoisotopic mass | 385.12046 Da |
| Source | ChEBI |
| InChIKey | ARPUHYJMCVWYCZ-UHFFFAOYSA-N |
Cl.O.O=C(O)c1cn(C2CC2)c2cc(N3CCNCC3)c(F)cc2c1=O
InChI=1S/C17H18FN3O3.ClH.H2O/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24;;/h7-10,19H,1-6H2,(H,23,24);1H;1H2
Also called
- 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrochloride—water (1/1)
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride hydrate
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride monohydrate
- Ciprofloxacin hydrochloride monohydrate
- ciprofloxacin hydrochloride
- ciprofloxacin hydrochloride monohydrate
- ciprofloxacin monohydrochloride monohydrate
Cross-references
Drug registries
Activity roles
- antibacterial drug
CHEBI:36047
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:59936 |
ciprofloxacin hydrochloride hydrate | antibioticmech:chebi-0ea4a4a49e |
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
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories