Radezolid hydrochlorideProduct ingredient for Radezolid

Name
Radezolid hydrochloride
Drug Entry
Radezolid

Radezolid has been used in trials studying the treatment of Abscess, Bacterial Skin Diseases, Streptococcal Infections, Infectious Skin Diseases, and Staphylococcal Skin Infections, among others.

Accession Number
DBSALT002178
Structure
Synonyms
Radezolid HCl
External IDs
RX-01 / RX-1741_667 / RX-1741667
UNII
37CW568NXL
CAS Number
869884-77-5
Weight
Average: 474.92
Monoisotopic: 474.1582445
Chemical Formula
C22H24ClFN6O3
InChI Key
UQKABVKLBIJYBI-FYZYNONXSA-N
InChI
InChI=1S/C22H23FN6O3.ClH/c1-14(30)25-12-19-13-29(22(31)32-19)18-6-7-20(21(23)8-18)16-4-2-15(3-5-16)9-24-10-17-11-26-28-27-17;/h2-8,11,19,24H,9-10,12-13H2,1H3,(H,25,30)(H,26,27,28);1H/t19-;/m0./s1
IUPAC Name
N-{[(5S)-3-[2-fluoro-4'-({[(1H-1,2,3-triazol-5-yl)methyl]amino}methyl)-[1,1'-biphenyl]-4-yl]-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide hydrochloride
SMILES
Cl.CC(=O)NC[C@H]1CN(C(=O)O1)C1=CC=C(C(F)=C1)C1=CC=C(CNCC2=CN=NN2)C=C1
ChemSpider
28530506
ChEMBL
CHEMBL2105651
Predicted Properties
PropertyValueSource
Water Solubility0.043 mg/mLALOGPS
logP1.23ALOGPS
logP1.29Chemaxon
logS-4ALOGPS
pKa (Strongest Acidic)8.56Chemaxon
pKa (Strongest Basic)7.46Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count3Chemaxon
Polar Surface Area112.24 Å2Chemaxon
Rotatable Bond Count8Chemaxon
Refractivity115.89 m3·mol-1Chemaxon
Polarizability45.2 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon