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Dondoni, A.1
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25
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0000012858
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29
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0028846226
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For sulfonamide bearing compounds, see:
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0032534853
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Baker C.T., Salituro F.G., Court J.J., Deininger D.D., Kim E.E., Li B., Novak P.M., Rao B.G., Pazhanisamy S., Schairer W.C., Tung R.D. Bioorg. Med. Chem. Lett. 8:1998;3631.
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32
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0032535314
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Salituro F.G., Baker C.T., Court J.J., Deininger D.D., Kim E.E., Li B., Novak P.M., Rao B.G., Pazhanisamy S., Porter M.D., Schairer W.C., Tung R.D. Bioorg. Med. Chem. Lett. 8:1998;3637.
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33
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0031013195
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For the chemistry of hydroxyethylamine, see: and references cited therein
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Shiabata, N.1
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34
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0028362882
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reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar
-
Kaldor et al. reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar. In this case, the ortho-methyl group might affected the conformation of sulfonamide, see: Kaldor, S. W.; Hammond, M.; Dressmen, B. A.; Fritz, J. E.; Crowell, T. A.; Hermann, R. A. Bioorg. Med. Chem. Lett. 1994, 4, 1385.
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Kaldor1
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35
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0028362882
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In this case, the ortho-methyl group might affected the conformation of sulfonamide, see:
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Kaldor et al. reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar. In this case, the ortho-methyl group might affected the conformation of sulfonamide, see: Kaldor, S. W.; Hammond, M.; Dressmen, B. A.; Fritz, J. E.; Crowell, T. A.; Hermann, R. A. Bioorg. Med. Chem. Lett. 1994, 4, 1385.
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36
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0345231018
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For the conformation of N,N-dialkyl-benzenesulfonamides, see: 29 and references cited therein
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For the conformation of N,N-dialkyl-benzenesulfonamides, see: 29 and references cited therein.
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37
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0028328704
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For acyclic symmetric inhibitors, see:
-
For acyclic symmetric inhibitors, see: Housur, M. V., Bhat, T. N., Kempf, D. J., Baldwin, E. T., Liu, B., Gulnik, S., Wideburg, N. E., Norbeck. D. W., Appelt, K., Erickson, J. W. J. Am. Chem. Soc. 1994, 116, 847.
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Appelt, K.9
Erickson, J.W.10
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39
-
-
15444345286
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For carbohydrate based symmetric inhibitors, see:
-
For carbohydrate based symmetric inhibitors, see: Zuccarello, G.; Bouzide, A.; Kvarnström, I.; Niklasson, G.; Svensson, S. C. T.; Brisander, M.; Danielsson, H.; Nillroth, U.; Karlén, A.; Hallberg, A.; Classon, B.; Samuelsson, B. J Org. Chem. 1998, 63, 4898.
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Zuccarello, G.1
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Hallberg, A.10
Classon, B.11
Samuelsson, B.12
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40
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14444280615
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Alterman M., Björsne M., Mühlman A., Classon B., Kvarnström I., Danielson H., Markgren P-O., Nillroth U., Unge T., Hallberg A., Samuelsson B. J Med. Chem. 41:1998;3782.
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41
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13044290051
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-
2 symmetric structure, see: and references cited therein
-
2 symmetric structure, see: Rodgers, J. D.; Lam, P. Y.-S.; Johnson, B. L.; Wang, H.; Ko, S. S.; Seitz, S. P.; Trainor, G. L.; Anderson, P. S.; Kalbe, R. M.; Bacheler, L. T.; Cordova, B.; Garber, S.; Reid, C.; Wright, M. R.; Chang, C.-H.; Erickson-Viitanen, S. Chemistry & Biology 1998, 5, 597 and references cited therein.
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Rodgers, J.D.1
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Garber, S.12
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Wright, M.R.14
Chang, C.-H.15
Erickson-Viitanen, S.16
-
42
-
-
0345231012
-
-
Compounds 19, 21, 23, 27, 32, 33, 34, 35 and 36 could not be separated by PTLC. They were assayed as diastereomixtures
-
Compounds 19, 21, 23, 27, 32, 33, 34, 35 and 36 could not be separated by PTLC. They were assayed as diastereomixtures.
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-
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