Ciprofloxacin hydrochlorideProduct ingredient for Ciprofloxacin

Name
Ciprofloxacin hydrochloride
Drug Entry
Ciprofloxacin

Ciprofloxacin is a second generation fluoroquinolone that has spawned many derivative antibiotics.9 It is formulated for oral, intravenous, intratympanic, ophthalmic, and otic administration for a number of bacterial infections.18,19,20,21,22,23,24,25,26

The first ciprofloxacin containing product was FDA approved on 22 October 1987.17

Accession Number
DBSALT000293
Structure
Synonyms
Ciprofloxacin HCl / Ciprofloxacin hydrochloride / Ciprofloxacin hydrochloride hydrate / Ciprofloxacin hydrochloride monohydrate
External IDs
DRG-0110 / RX710
UNII
4BA73M5E37
CAS Number
86393-32-0
Weight
Average: 385.82
Monoisotopic: 385.120462
Chemical Formula
C17H21ClFN3O4
InChI Key
ARPUHYJMCVWYCZ-UHFFFAOYSA-N
InChI
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
IUPAC Name
1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrate hydrochloride
SMILES
O.Cl.OC(=O)C1=CN(C2CC2)C2=CC(N3CCNCC3)=C(F)C=C2C1=O
KEGG Drug
D02216
KEGG Compound
C13993
PubChem Compound
62999
ChemSpider
56700
ChEBI
59936
ChEMBL
CHEMBL4303345
Wikipedia
Ciprofloxacin
Predicted Properties
PropertyValueSource
Water Solubility1.35 mg/mLALOGPS
logP-0.57ALOGPS
logP-0.86Chemaxon
logS-2.4ALOGPS
pKa (Strongest Acidic)5.56Chemaxon
pKa (Strongest Basic)8.77Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area72.88 Å2Chemaxon
Rotatable Bond Count3Chemaxon
Refractivity87.94 m3·mol-1Chemaxon
Polarizability33.33 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon