Crystal and molecular structure of perindopril erbumine salt

Journal of Molecular Structure

Volumn 997, Issue 1-3, 2011, Pages 103-109

  Remko, M ^a   Bojarska, J ^b   Jezko P ^a   Sieron L ^b   Olczak, A ^b   Maniukiewicz, W ^b  

^a Physics and Informatics   (Slovakia)

^b LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

Ab initio calculations; Crystal and molecular structure; Perindopril erbumine; Polymorphs; Solvent effect

Indexed keywords

AB INITIO CALCULATIONS; AMINO GROUP; ANGIOTENSIN-CONVERTING ENZYME; CARBOXYLATE GROUPS; CONFORMATIONAL BEHAVIOR; CRYSTAL AND MOLECULAR STRUCTURE; FULL-MATRIX LEAST-SQUARES METHOD; GAS-PHASE STRUCTURES; GASPHASE; HF/6-31G; IONIZED MOLECULES; ONSAGER MODEL; OXYGEN ATOM; PERINDOPRIL ERBUMINE; POSITIVELY CHARGED; SINGLE CRYSTAL X-RAY DIFFRACTION; SOLVENT EFFECT; SPACE GROUPS; THREE-DIMENSIONAL NETWORKS; TRICLINIC FORMS; UNIT-CELL DIMENSIONS; WATER SOLUTIONS;

CALCULATIONS; CARBOXYLATION; CARBOXYLIC ACIDS; HYDROGEN BONDS; IONIZATION OF GASES; LEAST SQUARES APPROXIMATIONS; MOLECULAR STRUCTURE; PETROLEUM REFINING; X RAY DIFFRACTION;

CRYSTAL STRUCTURE;

EID: 80053643704     PISSN: 00222860     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molstruc.2011.05.005     Document Type: Article

References (37)

1. L.H. Opie Angiotensin Converting Enzyme Inhibitors second ed. 1994 Wiley-Liss New York
2. J. Wong, R.A. Patel, and P.R. Kowey Progr. Cardiovasc. Diseases 47 2004 116
3. M.E. Bertrand Curr. Med. Res. Opin. 20 2004 1559
4. S. Laurent Am. J. Hypertens. 18 2005 155S
5. A. Okrucká, J. Pecháň, and H. Kratochví ľová Platelets 9 1998 63
6. A. Remková, and H. Kratochvíľová Blood Coagul. Fibrinol. 11 2000 641
7. A. Remková, and M. Remko Physiol. Res. 59 2010 13
8. C. Pascard, J. Guilhem, M. Vincent, G. Rémond, B. Portevin, and M. Laubie J. Med. Chem. 34 1991 663
9. M. Remko Eur. J. Med. Chem. 44 2009 101
10. M. Remko Chem. Pap. 61 2007 133
11. E. Telejko Curr. Med. Res. Opinion 23 2007 953
12. Ch. Strassler, V. Lellek, R. Fassler, United States Patent US 7705046 B2.
13. M. Merslavic, J. Smid, Z. Tomsic, United States Patent US 7674814 B2.
14. D. Churchley, A. Amberkhane, Results in WO Patent Application 2008050185.
15. Oxford Diffraction, Crys AlisCCD and CrysAlisRED, ver. 1.172, 2007.
16. G.M. Sheldrick Acta Cryst. A64 2008 112
17. L.J. Faruggia J. Appl. Cryst. 30 1997 565
18. I.J. Bruno, J.C. Cole, P.R. Edgington, M. Kessler, C.F. Macrae, P. McCabe, J. Pearson, and R. Taylor Acta Cryst. B58 2002 389
19. Bruker, 2002. SMART. Version 5.630 for WNT/2000. Bruker AXS Inc., Madison, Wisconsin, USA; Bruker (2003). SAINT-Plus (Version 6.45) and SHELXTL (Version 6.14). Bruker AXS Inc., Madison, Wisconsin, USA.
20. G.M. Sheldrick SADABS. Ver. 2.10 2003 University of Göttingen Germany
21. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, J.A. Montgomery Jr., T. Vreven, T.K.N. Kudin, J.C. Burant, J.M. Millam, S.S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G.A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J.E. Knox, H.P. Hratchian, J.B. Cross, C. Adamo, C. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, P.Y. Ayala, K. Morokuma, G.A. Voth, P. Salvador, J.J. Dannenberg, V.G. Zakrzewski, S. Dapprich, A.D. Daniels, M.C. Strain, O. Farkas, D.K. Malick, A.D. Rabuck, K. Raghavachari, J.B. Foresman, J.V. Ortiz, Q. Cui, A.G. Baboul, S. Clifford, J. Cioslowski, B.B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R.L. Martin, D.J. Fox, T. Keith, M.A. Al-Laham, C.Y. Peng, A. Nanayakkara, M. Challacombe, P.M.W. Gill, B. Johnson, W. Chen, M.W. Wong, C. Gonzalez, and J.A. Pople Gaussian 03, Revision D.01 2004 Gaussian, Inc. Wallingford CT
22. W.J. Hehre, L. Radom, P.v.R. Schleyer, J.A. Pople, Ab Initio Molecular Orbital Theory, Wiley, New York, 1986.
23. W. Kohn, and L.J. Sham Phys. Rev. A 140 1965 1133
24. F.M. Bickelhaupt, and E.J. Baerends K.B. Lipkowitz, D.B. Boyd, Rev. Comput. Chem vol. 15 2000 Wiley-VCH New York 186
25. A.D. Becke Phys. Rev. A 38 1988 3098
26. A.D. Becke J. Chem. Phys. 98 1993 5648
27. C. Lee, W. Yang, and R.G. Parr Phys. Rev. B37 1988 785
28. A. Klamt, and G. Schman J. Chem. Soc., Perkin Trans. 1993 799
29. M. Cossi, N. Rega, G. Scalmani, and V. Barone J. Comp. Chem. 24 2003 669
30. L. Onsager J. Am. Chem. Soc. 58 1936 1486
31. M.W. Wong, M.J. Frisch, and K.B. Wiberg J. Am. Chem. Soc. 113 1991 4776
32. M.W. Wong, M.J. Frisch, and K.B. Wiberg J. Am. Chem. Soc. 114 1992 523
33. E.L. Eliel, and S.H. Wilen The Stereochemistry of Organic Compounds 1994 Wiley Interscience
34. D. Cremer, and J.A. Pople J. Am. Chem. Soc. 97 1975 1354
35. M.C. Etter, J.C. MacDonald, and J. Bernstein Acta Crystallogr. B 46 Pt 2 1990 256
36. J. Bernstein Polymorphism in Molecular Crystals 2002 Clarendon press Oxford
37. M. Akif, D. Georgiadis, A. Mahajan, V. Dive, E.D. Sturrock, R.E. Isaac, and K.R. Acharya J. Mol. Biol. 400 2010 502