| [1] Criscione L, Bradley WA, Buhlmayer P, et al. Valsartan: Preclinical and clinical profile of an antihypertensive angiotensin-II antagonist[J]. Cardiovasc Drug Rev, 1995, 13(3): 230-250. [2] Zoumpoulakis P, Daliani I, Zervou M, et al. Losartan's molecular basis of interaction with membranes and AT(1) receptor[J]. Chem Phys Lipids, 2003, 125(1): 13-25. [3] Mavromoustakos T, Zoumpoulakis P, Kyrikou I, et al. Efforts to understand the molecular basis of hypertension through drug: membrane interactions[J]. Curr Top Med Chem, 2004, 4(4): 445-459. [4] Mcdonnell P A, Opella S J. Effect of detergent concentration on multidimensional solution nmr-spectra of membrane-proteins in micelles[J]. J Magn Reson Series B, 1993, 102(1): 120-125. [5] Parker W, Song P S. Protein structures in SDS micelle-protein complexes[J]. Biophys J, 1992, 61(5): 1 435-1 439. [6] Li F, Wang L Y, Xiao N, et al. Dominant conformation of valsartan in sodium dodecyl sulfate micelles environment[J]. J Phys Chem B, 2010, 114: 2 719-2 727. [7] Potamitis C, Zervou M, Katsiaras V, et al. Antihypertensive drug valsartan in solution and at the AT(1) receptor: conformational analysis, dynamic NMR spectroscopy, in silico docking, and molecular dynamics simulations[J]. J Chem Inf Model, 2009, 49(3): 726-739. [8] Zhang Hui-ting (张会婷), Wang Lin（王琳），Wei Jia （危佳），et al. Quantum chemical investigation of the structure and chemical shifts of AT1 antagonists V8, V12 and BZI8 (AT1受体拮抗剂V8、V12和BZI8机构的量子化学研究)［J］．Chinese J Magn Reson（波谱学杂志）， 2007, 24(4): 519-525. [9] Su Yong-chao（苏永超），Zheng An-min（郑安民），Li Shenhui（李申慧），et al. Quantum chemical calculation on 13C NMR shifts of small drug molecules （药物小分子化学位移的量子化学计算研究）［J］．Chinese J Magn Reson（波谱学杂志），2006, 23(3): 293-301. [10] Frisch M J, Trucks G W, Schlegel H B, Scuseria G E, Robb M A, Cheeseman J R, Montgomery J A, Jr.; Vreven T, Kudin K N, Burant J C, Millam J M, Iyengar S S, Tomasi J, Barone V, Mennucci B, Cossi M, Scalmani G, Rega N, Petersson G A, Nakatsuji H, Hada M, Ehara M, Toyota K, Fukuda R, Hasegawa J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Klene M, Li X, Knox J E, Hratchian H P, Cross J B, Bakken V, Adamo C, Jaramillo J, Gomperts R, Stratmann RE, Yazyev O, Austin A J, Cammi R, Pomelli C, Ochterski J W, Ayala P Y, Morokuma K, Voth G A, Salvador P, Dannenberg J J, Zakrzewski V G, Dapprich S, Daniels A D, Strain M C, Farkas O, Malick D K, Rabuck A D, Raghavachari K, Foresman J B, Ortiz J V, Cui Q, Baboul A G, Clifford S, Cioslowski J, Stefanov B B, Liu G, Liashenko A, Piskorz P, Komaromi I, Martin R L, Fox D J, Keith T, AlLaham M A, Peng C Y, Nanayakkara A, Challacombe M, Gill P M W, Johnson B, Chen W, Wong M W, Gonzalez C, Pople J A. Gaussian 03. B.05[CP]. Pittsburgh, PA: Gaussian, Inc.; 2003. [11] Zheng A M, Chen L, Yang J, et al. Prediction of the 13C NMR chemical shifts of organic species adsorbed on H-ZSM-5 zeolite by the ONIOM-GIAO method[J]. Chem Commun, 2005, 19: 2 474-2 476. |
