cyclopentyl N-{3-[(2-methoxy-4-{[4-(2H3)methyl(2H4)benzenesulfonyl]carbamoyl}phenyl)methyl]-1-methyl-1H-indol-5-yl}carbamate

• ChemBase ID: 179618
• Molecular Formular: C31H33N3O6S
• Molecular Mass: 575.67522
• Monoisotopic Mass: 575.20900679
• SMILES: c1c(cc2c(c1)n(cc2Cc1c(cc(cc1)C(=O)NS(=O)(=O)c1ccc(cc1)C)OC)C)NC(=O)OC1CCCC1
• Canonical SMILES: COc1cc(ccc1Cc1cn(c2c1cc(cc2)NC(=O)OC1CCCC1)C)C(=O)NS(=O)(=O)c1ccc(cc1)C
• InChI: InChI=1S/C31H33N3O6S/c1-20-8-13-26(14-9-20)41(37,38)33-30(35)22-11-10-21(29(17-22)39-3)16-23-19-34(2)28-15-12-24(18-27(23)28)32-31(36)40-25-6-4-5-7-25/h8-15,17-19,25H,4-7,16H2,1-3H3,(H,32,36)(H,33,35)
• InChIKey: HOOQJZTUMKGZMP-UHFFFAOYSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: cyclopentyl N-{3-[(2-methoxy-4-{[4-(^2H₃)methyl(^2H₄)benzenesulfonyl]carbamoyl}phenyl)methyl]-1-methyl-1H-indol-5-yl}carbamate
• IUPAC Traditional name: cyclopentyl N-{3-[(2-methoxy-4-{[4-(^2H₃)methyl(^2H₄)benzenesulfonyl]carbamoyl}phenyl)methyl]-1-methylindol-5-yl}carbamate
• Synonyms: N-[3-[[2-Methoxy-4-[[[(4-methylphenyl-d7)sulfonyl]amino]carbonyl]phenyl]methyl]-1-methyl-1H-indol-5-yl]carbamic Acid Cyclopentyl Ester; Zafirlukast Related Compound E-d7; Cyclopentyl 3-[2-Methoxy-4-[p-(tolyl-d7)sulfonylcarbamoyl)benzyl]-1-methylindol-5-ylcarbamate; Zafirlukast p-Tolyl Isomer-d7

Database IDs

• PubChem SID: 164235528
• PubChem CID: 71753009

CALCULATED PROPERTIES

• Acid pKa: 4.292288
• H Acceptors: 6
• H Donor: 2
• LogD (pH = 5.5): 5.6232
• LogD (pH = 7.4): 5.4634223
• Log P: 6.4037447
• Molar Refractivity: 158.5769 cm^3
• Polarizability: 61.800007 Å^3
• Polar Surface Area: 115.73 Å^2
• Rotatable Bonds: 8
• Lipinski's Rule of Five: false

DETAILS

Toronto Research Chemicals - Z125017

Labelled analogue of Zafirlukast p-Tolyl Isomer, a positional isomer and impurity of the cysteinyl leukotriene type 1 receptor antagonist, Zafirlukast (D226955).

REFERENCES

• Krishnaiah, C. et al.: Anal. Chem. Ind. J., 8, 471 (2009)
• Madhavi, A. et al.: Chromatographia, 70, 233 (2009)
• Goverdhan, G. et al.: J. Pharmac. Biomed. Anal., 49, 895 (2009)