Moxifloxacin hydrochloride monohydrateProduct ingredient for Moxifloxacin

Name
Moxifloxacin hydrochloride monohydrate
Drug Entry
Moxifloxacin

Moxifloxacin is a synthetic fluoroquinolone antibiotic agent. Bayer AG developed the drug (initially called BAY 12-8039) and it is marketed worldwide (as the hydrochloride) under the brand name Avelox (in some countries also Avalox) for oral treatment.

Accession Number
DBSALT002560
Structure
Synonyms
Not Available
UNII
B8956S8609
CAS Number
192927-63-2
Weight
Average: 455.91
Monoisotopic: 455.1623268
Chemical Formula
C21H27ClFN3O5
InChI Key
SKZIMSDWAIZNDD-WJMOHVQJSA-N
InChI
InChI=1S/C21H24FN3O4.ClH.H2O/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24;;/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28);1H;1H2/t11-,16+;;/m0../s1
IUPAC Name
7-[(4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrate hydrochloride
SMILES
O.Cl.[H][C@]12CN(C[C@@]1([H])NCCC2)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1OC)C(O)=O
ChemSpider
8065921
ChEMBL
CHEMBL2326947
Predicted Properties
PropertyValueSource
Water Solubility0.168 mg/mLALOGPS
logP0.01ALOGPS
logP-0.5Chemaxon
logS-3.4ALOGPS
pKa (Strongest Acidic)5.69Chemaxon
pKa (Strongest Basic)9.42Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count7Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area82.11 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity106.22 m3·mol-1Chemaxon
Polarizability41.29 Å3Chemaxon
Number of Rings5Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon