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1
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0141446228
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For reviews, see:
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For reviews, see: Drucker D.J. Diabetes Care. 26:2003;2929
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Diabetes Care
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Drucker, D.J.1
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5
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0029907680
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Nauck M.A., Wollschlager D., Werner J., Holst J.J., Orskov C., Creutzfeldt W. Diabetologica. 39:1996;1546
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Diabetologica
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Nauck, M.A.1
Wollschlager, D.2
Werner, J.3
Holst, J.J.4
Orskov, C.5
Creutzfeldt, W.6
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8
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0032969356
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Pauly R.P., Demuth H.U., Rosche F., Schmidt J., White H.A., Lynn F., McIntosh C.H., Pederson R.A. Metab.: Clin. Exp. 48:1999;385
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Pauly, R.P.1
Demuth, H.U.2
Rosche, F.3
Schmidt, J.4
White, H.A.5
Lynn, F.6
McIntosh, C.H.7
Pederson, R.A.8
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10
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1542314925
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Peters J.-U., Weber S., Kritter S., Weiss P., Wallier A., Boehringer M., Hennig M., Kuhn B., Loeffler B.-M. Bioorg. Med. Chem. Lett. 14:2004;1491
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Peters, J.-U.1
Weber, S.2
Kritter, S.3
Weiss, P.4
Wallier, A.5
Boehringer, M.6
Hennig, M.7
Kuhn, B.8
Loeffler, B.-M.9
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11
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2942607200
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note
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Measurements were performed according to an in-house developed method to assess solubility from a 10 mM DMSO stock solution. This method is similar to the classical thermodynamic shake-flask solubility with the only difference that DMSO is removed in the beginning by an additional lyophilization step. Therefore this assay is called lyophilizated solubility assay (LYSA)
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13
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0030799001
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Measurements were performed according to:
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Measurements were performed according to: Obach R.S., Baxter J.G., Liston T.E., Silber B.M., Jones B.C., MacIntyre F., Rance D.J., Wastall P. J. Pharm. Exp. Ther. 283:1997;46
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(1997)
J. Pharm. Exp. Ther.
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, pp. 46
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Obach, R.S.1
Baxter, J.G.2
Liston, T.E.3
Silber, B.M.4
Jones, B.C.5
MacIntyre, F.6
Rance, D.J.7
Wastall, P.8
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14
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0035987896
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Measurements were performed according to: (BFC was used as a substrate)
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Measurements were performed according to: Stresser D.M., Turner S.D., Blanchard A.P., Miller V.P., Crespi C.L. Drug Metab. Dispos. 30:2002;845. (BFC was used as a substrate)
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(2002)
Drug Metab. Dispos.
, vol.30
, pp. 845
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Stresser, D.M.1
Turner, S.D.2
Blanchard, A.P.3
Miller, V.P.4
Crespi, C.L.5
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17
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0021874664
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Mason R.J., Walker S.R., Shields B.A., Henson J.E., Williams M.C. Am. Rev. Respir. Dis. 131:1985;786
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(1985)
Am. Rev. Respir. Dis.
, vol.131
, pp. 786
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Mason, R.J.1
Walker, S.R.2
Shields, B.A.3
Henson, J.E.4
Williams, M.C.5
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20
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2942514250
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note
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Measurements were performed according to an in-house developed miniaturized method to measure the shake flask octanol-water partition coefficient at pH 7.4 ( logD )
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21
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0032146512
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Measurements were performed according to:
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Measurements were performed according to: Allen R.I., Box K.J., Comer J., Peake C., Tam K.Y. J. Pharm. Biomed. Anal. 17:1998;699
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(1998)
J. Pharm. Biomed. Anal.
, vol.17
, pp. 699
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Allen, R.I.1
Box, K.J.2
Comer, J.3
Peake, C.4
Tam, K.Y.5
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22
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2942580533
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note
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An amphiphilic molecule comprises a hydrophobic and a hydrophilic part. Such molecules have an inherent tendency to orient themselves in a suitable environment, for example, a phospholipid bilayer
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24
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0003980770
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R. Mannhold, H. Kubinyi, & H. Timmermann. Weinheim: Wiley-VCH
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Smith A.D., van de Waterbeemd H., Walker D.K. Mannhold R., Kubinyi H., Timmermann H. Pharmacokinetics and Metabolism in Drug Design. 2001;Wiley-VCH, Weinheim
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(2001)
Pharmacokinetics and Metabolism in Drug Design
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Smith, A.D.1
Van De Waterbeemd, H.2
Walker, D.K.3
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25
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2942519077
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Duesseldorf, Germany, Aug 27-Sept 1, 2000; Prous Science: Barcelona, Spain
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Fischer, H.; Kansy, M.; Potthast, M.; Csato, M. In Proceedings of the 13th European Symposium on Quantitative Structure-Activity Relationships, Duesseldorf, Germany, Aug 27-Sept 1, 2000; Prous Science: Barcelona, Spain, 2001
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(2001)
Proceedings of the 13th European Symposium on Quantitative Structure-Activity Relationships
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Fischer, H.1
Kansy, M.2
Potthast, M.3
Csato, M.4
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26
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2942544055
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note
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50 ( x ) measured for NVP-DPP728 in the assay was 11
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30
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0000000497
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Masquelin T., Sprenger D., Baer R., Gerber F., Mercadal Y. Helv. Chim. Acta. 81:1998;646
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(1998)
Helv. Chim. Acta
, vol.81
, pp. 646
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Masquelin, T.1
Sprenger, D.2
Baer, R.3
Gerber, F.4
Mercadal, Y.5
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31
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2942522352
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note
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3): δ 1.61 (2H, br s), 3.01 (3H, s), 3.23 (3H, s), 3.31 (2H, s), 3.45-3.48 (2H, m), 3.61-3.65 (2H, m), 6.70 (2H, br s), 7.38-7.40 (1H, m), 7.46-7.48 (1H, m), 7.67 (1H, s)
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