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X-ray powder diffraction data for olmesartan medoxomil, C29H30N6O6

Published online by Cambridge University Press:  17 February 2016

Xiaochun Chen
Affiliation:
Research Center of Analytical Instrumentation, Key laboratory of Bio-resource and Eco-environment, Ministry of Education, College of Life Science, Sichuan University, Chengdu 610064, China
Peixiao Tang
Affiliation:
College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, China
Shanshan Li
Affiliation:
College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, China
Kailin Xu
Affiliation:
College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, China
Hui Li*
Affiliation:
College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, China
*
a)Author to whom correspondence should be addressed. Electronic mail: [email protected]

Abstract

X-ray powder diffraction data, unit-cell parameters, and space group for olmesartan medoxomil, C29H30N6O6, are reported [a = 12.3969(7) Å, b = 21.2667(3) Å, c = 10.9603(5) Å, α = γ = 90°, β = 101.38(9)°, unit-cell volume V = 2832.72 Å3, Z = 4 and space group P21/c]. All measured lines were indexed and are consistent with the P21/c space group. No detectable impurities were observed.

Type
Data Reports
Copyright
Copyright © International Centre for Diffraction Data 2016 

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References

Engel, G. E., Wilke, S., König, O., Harris, K. D. M., and Leusen, F. J. J. (1999). “Powder solve – a complete package for crystal structure solution from powder diffraction patterns,” J. Appl. Crystallogr. 32, 11691179.CrossRefGoogle Scholar
Hiroaki, Y., Yoshiya, A., Takuro, K., Yasuo, S., Koichi, F., Yoshiko, K., Toshio, S., Makoto, M., Masahiro, I., Shuichi, M., Youji, F., and Hiroyuki, K. (1996). “Nonpeptide angiotensin II receptor antagonists: synthesis, biological activities, and structure-activity relationships of imidazole-5-carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compounds,” J. Med. Chem. 39, 323338.Google Scholar
Makoto, M., Toshio, S., Masahiro, I., Norio, F., Masaaki, M., Hiroaki, Y., and Hiroyuki, K. (1995). “Pharmacology of CS-866, a novel nonpeptide angiotensin II receptor antagonist,” Eur. J. Pharmacol. 285, 181188.Google Scholar
Richard, B., Eric, H., Thomas, G., Alaloor, S. D., Hemmige, S. Y., and Thomas, S. (2013). “Redetermination of the structure of olmesartan medoxomil, (5-methyl-2-oxo-2H-1,3-dioxol-4-yl)-methyl-4-(2-hydroxypropan-2-yl)-2-propyl-1-(-[2-(2H-1,2,3,4-tetrazol-5-yl)-phenyl]phenylmethyl)-1H-imidazole-5-carboxylate, C29H30N6O6 ,” Z. Kristallogr. NCS 228, 141143.Google Scholar
Smith, D. H., Dubiel, R., and Jones, M. (2005). “Use of 24-hour ambulatory blood pressure monitoring to assess antihypertensive efficacy,” Am. J. Cardiovasc. Drug 5, 4150.CrossRefGoogle ScholarPubMed
Xu, K. L., Liang, B., Wu, X. Q., Zhang, L. L., Tang, P. X., and Li, H. (2014). “X-ray powder diffraction data for levetiracetam,” Powder Diffr. 29, 5152.CrossRefGoogle Scholar
Zhang, L. L., Pan, Q. Q., Xiao, D., Wu, X. Q., Wang, Q., and Li, H. (2013). “X-ray powder diffraction data for deoxyschisandrin,” Powder Diffr. 28, 231233.CrossRefGoogle Scholar
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