Lanopepden MesylateProduct ingredient for Lanopepden

Name
Lanopepden Mesylate
Drug Entry
Lanopepden

Lanopepden has been used in trials studying the treatment of Pneumonia, Infections, Bacterial, Skin Diseases, Infectious, and Skin Infections, Bacterial.

Accession Number
DBSALT002104
Structure
Thumb
Synonyms
Not Available
UNII
YW25HPP501
CAS Number
1441390-17-5
Weight
Average: 575.66
Monoisotopic: 575.253745929
Chemical Formula
C23H38FN7O7S
InChI Key
UNGNACZMQRGYNV-URBRKQAFSA-N
InChI
InChI=1S/C22H34FN7O4.CH4O3S/c1-15-24-20(19(23)21(25-15)29-7-6-28-8-9-34-13-18(28)12-29)26-27-22(32)17(11-30(33)14-31)10-16-4-2-3-5-16;1-5(2,3)4/h14,16-18,33H,2-13H2,1H3,(H,27,32)(H,24,25,26);1H3,(H,2,3,4)/t17-,18+;/m1./s1
IUPAC Name
N-[(2R)-2-(N'-{6-[(9aS)-octahydropyrazino[2,1-c][1,4]oxazin-8-yl]-5-fluoro-2-methylpyrimidin-4-yl}hydrazinecarbonyl)-2-(cyclopentylmethyl)ethyl]-N-hydroxyformamide; methanesulfonic acid
SMILES
CS(O)(=O)=O.CC1=NC(NNC(=O)[C@H](CC2CCCC2)CN(O)C=O)=C(F)C(=N1)N1CCN2CCOC[C@@H]2C1
External Links
ChemSpider
31389940
ChEMBL
CHEMBL3301616
Predicted Properties
PropertyValueSource
Water Solubility0.304 mg/mLALOGPS
logP1.6ALOGPS
logP1.64ChemAxon
logS-3.2ALOGPS
pKa (Strongest Acidic)8.42ChemAxon
pKa (Strongest Basic)7.09ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area123.16 Å2ChemAxon
Rotatable Bond Count8ChemAxon
Refractivity126 m3·mol-1ChemAxon
Polarizability50.6 Å3ChemAxon
Number of Rings4ChemAxon
Bioavailability1ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon