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Tacrolimus EP Impurity H

SZ目录编号 SZ-T005030
CAS 号 143210-33-7
分子式 C43H69NO11
分子量 776
投资状态 Custom Synthesis


化学名称: (1E,3S,4R,5S,8R,9E,12S,14S)-5-hydroxy-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-14-methoxy-14-[(2R,3S,5R)-3-methoxy-5-methyl-6-oxooxan-2-yl]-2,4,10,12-tetramethyl-7-oxo-8-(prop-2-en-1-yl)tetradeca-1,9-dien-3-yl (2S)-1-formylpiperidine-2- carboxylate (as per EP)

Solid state compatibility study and characterization of a novel degradation product of tacrolimus in formulation
Tanja Rozman Peterka∗, Rok Grahek, Jure Hren, Andrej Bastarda, Jure Bergles, Urosˇ Urleb
Journal of Pharmaceutical and Biomedical Analysis 110 (2015) 67–75
 
Forced degradation of tacrolimus and the development of a UHPLC method for impurities determination
Tanja Rozman Peterka 1 , Tina Trdan Lušin 1 , Jure Bergles 1 , Zoran Ham 1 , Rok Grahek 1 , and Uroš Urleb 1
Acta Pharm. 69 (2019) 363–380
 
Development and Validation of method for the determination of related substances of Tacrolimus in Tacrolimus Capsules and Degradation Studies
Qingping Shi*1,2, Jianchun Li2 , Feng Ding
International Journal of ChemTech Research Vol.4, No.4, pp 1543-1552,
 
Reutilization of Tacrolimus Extracted from Expired Prograf Capsules: Physical, Chemical, and Pharmacological Assessment
Ziyad Binkhathlan, Mohamed M. Badran, Abdullah Alomrani, Ibrahim A. Aljuffali, Mohammed Alghonaim, Saleh Al-Muhsen, Rabih Halwani & Aws Alshamsan
AAPS PharmSciTech volume 17, pages978–987(2016)