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
- 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
Property Value Source Water Solubility 0.304 mg/mL ALOGPS logP 1.6 ALOGPS logP 1.64 Chemaxon logS -3.2 ALOGPS pKa (Strongest Acidic) 8.42 Chemaxon pKa (Strongest Basic) 7.09 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 9 Chemaxon Hydrogen Donor Count 3 Chemaxon Polar Surface Area 123.16 Å2 Chemaxon Rotatable Bond Count 8 Chemaxon Refractivity 126 m3·mol-1 Chemaxon Polarizability 50.6 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 1 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon