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Candesartan Methyl Ester N2-Trityl Methoxy Analog

SZ CAT No SZ-C011034
CAS No 1797136-91-4
Mol.F. 1797136-91-4 
Mol.Wt. 682.8
Inv. Status Custom Synthesis


Chemical Name: 2-Methoxy-1-[[2'-[2-(triphenyl methyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carboxylic acid methyl ester ;

Synonym: N2-Trityl Candesartan Methyl Ester Methoxy Analog ; 

Smiles: O=C(OC)C1=CC=CC(N=C2OC)=C1N2CC(C=C3)=CC=C3C4=CC=CC=C4C5=NN(C(C6=CC=CC=C6)(C7=CC=CC=C7)C8=CC=CC=C8)N=N5

Inchi: InChI=1S/C44H36N6O3/c1-3-53-43-45-39-25-15-24-38(42(51)52-2)40(39)49(43)30-31-26-28-32(29-27-31)36-22-13-14-23-37(36)41-46-48-50(47-41)44(33-16-7-4-8-17-33,34-18-9-5-10-19-34)35-20-11-6-12-21-35/h4-29H,3,30H2,1-2H3

Investigation and structural elucidation of a process related impurity in candesartan cilexetil by LC/ESI-ITMS and NMR
Bhanu Ramana,∗, Brajesh A. Sharmaa,b, Ganesh Mahale b, Dharmendra Singhb, Ashok Kumar
Journal of Pharmaceutical and Biomedical Analysis 56 (2011) 256–263
 
Synergistic suppression of tumor angiogenesis by codelivering of VEGF targeted siRNA and candesartan mediated by functionalized carbon nanovectors
Xuefang Ding, Yujie Su, Cheng Wang, Fangrong Zhang, Kerong Chen, Yu Wang, Min Li, and Wei Wang
ACS Appl. Mater. Interfaces 2017, 9, 28, 23353–23369
 
Identification, Isolation, and Characterization of Five Potential Degradation Impurities in Candesartan Cilexetil Tablets
Arivozhi Mohan1,&, S. Shanmugavel1 , Ajay Goyal1 , B. R. Venkataraman2 , D. Saravanan
Chromatographia volume 69, pages1211–1220(2009)