-
1
-
-
77956159941
-
Chiral drugs
-
Stinson SC. Chiral drugs. Chem Eng News 2000;43:55-78.
-
(2000)
Chem Eng News
, vol.43
, pp. 55-78
-
-
Stinson, S.C.1
-
3
-
-
51949113857
-
Interaction yields
-
Thayer AM. Interaction yields. Chem Eng News 2008;12-20.
-
(2008)
Chem Eng News
, pp. 12-20
-
-
Thayer, A.M.1
-
4
-
-
0027264444
-
Biological signi.cance of the enantiomeric purity of drugs
-
Waldeck B. Biological signi.cance of the enantiomeric purity of drugs. Chirality 1993;5:350-355.
-
(1993)
Chirality
, vol.5
, pp. 350-355
-
-
Waldeck, B.1
-
5
-
-
0026437190
-
FDA's policy statement on the development of new stereoisomeric drugs
-
Anonymous.
-
Anonymous. FDA's policy statement on the development of new stereoisomeric drugs. Chirality 1992;43:338-340.
-
(1992)
Chirality
, vol.43
, pp. 338-340
-
-
-
6
-
-
11744286228
-
Considerations of chiral recognition relevant to the liquid chromatographic separation of enantiomers
-
Pirkle WH, Pochapsky TC. Considerations of chiral recognition relevant to the liquid chromatographic separation of enantiomers. Chem Rev 1989;89:347-362.
-
(1989)
Chem Rev
, vol.89
, pp. 347-362
-
-
Pirkle, W.H.1
Pochapsky, T.C.2
-
8
-
-
0032482102
-
Polysaccharide derivatives for chromatographic separation of enantiomers
-
Okamoto Y, Yashima E. Polysaccharide derivatives for chromatographic separation of enantiomers. Angew Chem Int Ed 1998;37:1020-1043.
-
(1998)
Angew Chem Int Ed
, vol.37
, pp. 1020-1043
-
-
Okamoto, Y.1
Yashima, E.2
-
10
-
-
0035847277
-
Polysaccharide-based chiral stationary phases for highperformance liquid chromatographic enantioseparation
-
Yashima E. Polysaccharide-based chiral stationary phases for highperformance liquid chromatographic enantioseparation. J Chromatogr A 2001;906:105-125.
-
(2001)
J Chromatogr a
, vol.906
, pp. 105-125
-
-
Yashima, E.1
-
11
-
-
1542350269
-
Optically active polymers for chiral separation
-
Yamamoto C, Okamoto Y. Optically active polymers for chiral separation. Bull Chem Soc Jpn 2004;77:227-257.
-
(2004)
Bull Chem Soc Jpn
, vol.77
, pp. 227-257
-
-
Yamamoto, C.1
Okamoto, Y.2
-
13
-
-
0031664974
-
Proton pump inhibitors: Pharmacology and rationale for use in gastrointestinal disorders
-
Richardson P, Hawkey CJ, Stack WA. Proton pump inhibitors: pharmacology and rationale for use in gastrointestinal disorders. Drugs 1998;56:307-335.
-
(1998)
Drugs
, vol.56
, pp. 307-335
-
-
Richardson, P.1
Hawkey, C.J.2
Stack, W.A.3
-
14
-
-
42049085520
-
Stereoselective disposition of proton pump inhibitors
-
Andersson T, Weidolf L. Stereoselective disposition of proton pump inhibitors. Clin Drug Invest 2008;28:263-279.
-
(2008)
Clin Drug Invest
, vol.28
, pp. 263-279
-
-
Andersson, T.1
Weidolf, L.2
-
15
-
-
0033581794
-
Significance of angiotensin type I receptor blockade: Why are angiotensin II receptor blockers different?
-
Unger T. Significance of angiotensin type I receptor blockade: why are angiotensin II receptor blockers different? Am J Cardiol A 1999;84: 9S-15S.
-
(1999)
Am J Cardiol a
, vol.84
-
-
Unger, T.1
-
16
-
-
34250839461
-
Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process
-
Zou B, Yuan Q, Ma D. Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process. Angew Chem Int Ed 2007;46:2598-2601.
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 2598-2601
-
-
Zou, B.1
Yuan, Q.2
Ma, D.3
-
17
-
-
35048814533
-
A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles
-
Zheng N, Anderson KW, Huang X, Nguyen HN, Buchwald SL. A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles. Angew Chem Int Ed 2007;46:7509-7512.
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 7509-7512
-
-
Zheng, N.1
Anderson, K.W.2
Huang, X.3
Nguyen, H.N.4
Buchwald, S.L.5
-
18
-
-
0021796711
-
Structure activity relationships of substituted benzimidazoles
-
Brändström A, Lindberg P, Junggren U. Structure activity relationships of substituted benzimidazoles. Scand J Gastroenterol 1985; 20(Suppl 108):15-22.
-
(1985)
Scand J Gastroenterol
, vol.20
, Issue.SUPPL. 108
, pp. 15-22
-
-
Brändström, A.1
Lindberg, P.2
Junggren, U.3
-
19
-
-
0024523246
-
Antisecretory and antiulcer activities of a novel proton pump inhibitor AG-1749 in dogs and rats
-
Satoh H, Inatomi N, Nagaya H, Inada I, Nohara A, Nakamura N, Maki Y. Antisecretory and antiulcer activities of a novel proton pump inhibitor AG-1749 in dogs and rats. J Pharmacol Exp Ther 1989;248:806-815.
-
(1989)
J Pharmacol Exp Ther
, vol.248
, pp. 806-815
-
-
Satoh, H.1
Inatomi, N.2
Nagaya, H.3
Inada, I.4
Nohara, A.5
Nakamura, N.6
Maki, Y.7
-
20
-
-
0031757056
-
A review of its use in essential hypertension
-
McClellan KJ, Goa KL. Candesartan Cilexetil: A review of its use in essential hypertension. Drugs 1998;56:847-869.
-
(1998)
Drugs
, vol.56
, pp. 847-869
-
-
McClellan, K.J.1
Goa, K.L.2
Cilexetil, C.3
-
21
-
-
0027431141
-
Pharmacological profile of a highly potent and long acting angiotensin II receptor antagonist, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl] methyl]-1H-benzimid azole-7-carboxylic acid (CV-11974), and its prodrug, (±)-1-(cyclohexyloxycarbonyloxy) ethyl 2-ethoxy-1-[2′-(1H-tetrazol- 5-yl)biphenyl-4-y]methyl-11Hbenzimidazole-7-carboxylate (TCV-116)
-
Shibouta Y, Inada Y, Ojima M, Wada T, Noda M, Sanada T, Kubo K, Kohara Y, Naka T, Nishikawa K. Pharmacological profile of a highly potent and long acting angiotensin II receptor antagonist, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl) biphenyl-4-yl]methyl]-1H-benzimid azole-7-carboxylic acid (CV-11974), and its prodrug, (±)-1-(cyclohexyloxycarbonyloxy) ethyl 2-ethoxy-1-[[2′- (1H-tetrazol-5-yl)biphenyl-4-y]methyl-11Hbenzimidazole-7-carboxylate (TCV-116). J Pharmacol Exp Ther 1993; 266:114-120.
-
(1993)
J Pharmacol Exp Ther
, vol.266
, pp. 114-120
-
-
Shibouta, Y.1
Inada, Y.2
Ojima, M.3
Wada, T.4
Noda, M.5
Sanada, T.6
Kubo, K.7
Kohara, Y.8
Naka, T.9
Nishikawa, K.10
-
23
-
-
0034874986
-
Telmisartan: A review of its use in hypertension
-
Sharpe M, Jarvis B, Goa KL. Telmisartan: a review of its use in hypertension. Drugs 2001;61:1501-1529.
-
(2001)
Drugs
, vol.61
, pp. 1501-1529
-
-
Sharpe, M.1
Jarvis, B.2
Goa, K.L.3
-
24
-
-
0027218706
-
Pharmacological characterization of the novel nonpeptide angiotensin II receptor antagonist, BIBR 277
-
Wienen W, Hauel N, Van Meel JC, Narr B, Ries U, Entzeroth M. Pharmacological characterization of the novel nonpeptide angiotensin II receptor antagonist, BIBR 277. Br J Pharmacol 1993;110:245-252.
-
(1993)
Br J Pharmacol
, vol.110
, pp. 245-252
-
-
Wienen, W.1
Hauel, N.2
Van Meel, J.C.3
Narr, B.4
Ries, U.5
Entzeroth, M.6
-
25
-
-
34548544506
-
A novel practical synthesis of benzothiazoles via Pd-catalyzed thiol cross-coupling
-
Itou T, Mase T. A novel practical synthesis of benzothiazoles via Pd-catalyzed thiol cross-coupling. Org Lett 2007;18:3687-3689.
-
(2007)
Org Lett
, vol.18
, pp. 3687-3689
-
-
Itou, T.1
Mase, T.2
-
26
-
-
0035847188
-
Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases
-
Tachibana K, Ohnishi A. Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases. J Chromatogr A 2001;906:127-154.
-
(2001)
J Chromatogr a
, vol.906
, pp. 127-154
-
-
Tachibana, K.1
Ohnishi, A.2
-
27
-
-
40949091451
-
Comparative study of immobilized α1 acid glycoprotein and ovomucoid protein stationary phases for the enantiomeric separation of pharmaceutical compounds
-
Zhou L, Mao B, Ge Z. Comparative study of immobilized α1 acid glycoprotein and ovomucoid protein stationary phases for the enantiomeric separation of pharmaceutical compounds. J Pharm Bio Anal 2008;46:898-906.
-
(2008)
J Pharm Bio Anal
, vol.46
, pp. 898-906
-
-
Zhou, L.1
Mao, B.2
Ge, Z.3
-
28
-
-
0026599548
-
Effect of super.uous remote polar functionality on chiral recognition
-
Pirkle WH, Welch CJ. Effect of super.uous remote polar functionality on chiral recognition. J Chromatogr A 1992;589:45-51.
-
(1992)
J Chromatogr a
, vol.589
, pp. 45-51
-
-
Pirkle, W.H.1
Welch, C.J.2
|