Indexed keywords
4 ( 3,4 DIETHOXYPHENYL) 4 OXO N 1,1':3',1'' TERPHENYL 5' YL BUTANAMIDE;
4 ( 3,4 DIETHOXYPHENYL) N ( 2,6 DIPHENYLPYRIDIN 4 YL) 4 OXOBUTANAMIDE;
4 ( 3,4 DIETHOXYPHENYL) N ( 4,6 DIPHENYLPYRIDIN 2 YL) 4 OXOBUTANAMIDE;
ACYL COENZYME A;
ACYLTRANSFERASE INHIBITOR;
AMIDE;
BENZAMIDE DERIVATIVE;
BENZODIOXAN DERIVATIVE;
DIACYLGLYCEROL ACYLTRANSFERASE 1;
DIACYLGLYCEROL ACYLTRANSFERASE 1 INHIBITOR;
N ( 2,5 DIPHENYL 1,3 THIAZOL 4 YL) 4 ( 3,4 DIETHOXYPHENYL) 4 OXOBUTANAMIDE;
N ( 4,5 DIPHENYL 1,3 THIAZOL 2 YL) 4 ( 3,4 DIETHOXYPHENYL) 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 ( 3 ETHOXYOHENYL) 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 ( 3,4 DIETHOXYPHENYL) 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 ( 4 ETHOXYPHENYL) 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 ( 4,5 DIETHOXY 2 METHYLPHENYL) 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 OXO 4 ( 4 PROPYLPHENYL)BUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL) 4 PHENYL 4 OXOBUTANAMIDE;
N ( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL0 4 ( 2,3 DIHYDRO 1,4 BENZODIOXIN 6 YL)BUTANAMIDE;
N ( 5 BENZYL 4 PHENYLTHIOPHEN 2 YL) 4 ( 3,4 DIETHOXYPHENYL) 4 OXOBUTANAMIDE;
N [ 2 [( 5 BENZYL 4 PHENYL 1,3 THIAZOL 2 YL)AMINO] 2 OXOETHYL] 3,4 DIETHOXYBENZAMIDE;
RECOMBINANT DIACYLGLYCEROL ACYLTRANSFERASE 1;
RECOMBINANT ENZYME;
THIAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ARTICLE;
COMBINATORIAL LIBRARY;
CONTROLLED STUDY;
DIABETES MELLITUS;
DRUG ACTIVITY;
DRUG EFFICACY;
DRUG INHIBITION;
DRUG POTENCY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
FEMALE;
FOOD INTAKE;
HUMAN;
HUMAN CELL;
LIPID DIET;
MOUSE;
NONHUMAN;
OBESITY;
STRUCTURE ACTIVITY RELATION;
SUBSTITUTION REACTION;
WEIGHT GAIN;
WEIGHT REDUCTION;
WHITE ADIPOSE TISSUE;
AMIDES;
ANIMALS;
DIACYLGLYCEROL O-ACYLTRANSFERASE;
DRUG DESIGN;
ENZYME INHIBITORS;
HIGH-THROUGHPUT SCREENING ASSAYS;
HUMANS;
INHIBITORY CONCENTRATION 50;
MICE;
MOLECULAR STRUCTURE;
RECOMBINANT PROTEINS;
SMALL MOLECULE LIBRARIES;
2
13144281703
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Novak, S.7
Collins, C.8
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Lusis, A.J.10
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Farese Jr., R.V.12
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Cases, S.1
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Tow, B.5
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Voelker, T.7
Farese Jr., R.V.8
4
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Sande, E.5
Tow, B.6
Sanan, D.A.7
Raber, J.8
Eckel, R.H.9
Farese Jr., R.V.10
5
0036228339
Chen H. C., Smith S. J., Ladha Z., Jensen D. R., Ferreira L. D., Pulawa L. K., McGuire J. G., Pitas R. E., Eckel R. H., Farese R. V. Jr., J. Clin. Invest., 109, 1049-1055 (2002).
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McGuire, J.G.7
Pitas, R.E.8
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Farese Jr., R.V.5
7
39149122218
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Droz, B.5
Brodjian, S.6
Lau, Y.Y.7
Iyengar, R.R.8
Gao, J.9
Judd, A.S.10
Wagaw, S.H.11
Ravn, M.M.12
Engstrom, K.M.13
Lynch, J.K.14
Mulhern, M.M.15
Freeman, J.16
Dayton, B.D.17
Wang, X.18
Grihalde, N.19
Fry, D.20
Beno, D.W.A.21
Marsh, K.C.22
Su, Z.23
Diaz, G.J.24
Collins, C.A.25
Sham, H.26
Reilly, R.M.27
Brune, M.E.28
Kym, P.R.29
more..
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King, A.J.1
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Kym, P.R.5
9
64349101065
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Birch, A.M.1
Birtles, S.2
Buckett, L.K.3
Kemmitt, P.D.4
Smith, G.J.5
Smith, T.J.D.6
Turnbull, A.V.7
Wang, S.J.Y.8
10
12444292682
12j, 12l
12j, 12l: Park C.-M., Sun C., Olejniczak E. T., Wilson A. E., Meadows R. P., Betz S. F., Elmore S. W., Fesik S. W., Bioorg. Med. Chem. Lett., 15, 771-776 (2005);
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Sun, C.2
Olejniczak, E.T.3
Wilson, A.E.4
Meadows, R.P.5
Betz, S.F.6
Elmore, S.W.7
Fesik, S.W.8
12
57249102966
12m
12m: Buchstaller H.-P., Siebert C. D., Lyssy R. H., Frank I., Duran A., Gottschlich R., Noe C. R., Monatsh. Chem., 132, 279 (2001);
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Siebert, C.D.2
Lyssy, R.H.3
Frank, I.4
Duran, A.5
Gottschlich, R.6
Noe, C.R.7
13
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Zickgraf, A.2
Figler, H.3
Linden, J.4
Olsson, R.A.5
Scammells, P.J.6
14
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Momose, Y.4
15
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Inanaga, J.1
Hirata, K.2
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Katsuki, T.4
Yamaguchi, M.5
16
0025835289
Compound 12k was prepared as described in
Compound 12k was prepared as described in Kerdesky F. A. J., Holms J. H., Moore J. L., Bell R. L., Dyer R. D., Carter G. W., Brooks D. W., J. Med. Chem., 34, 2158-2165 (1991).
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Kerdesky, F.A.J.1
Holms, J.H.2
Moore, J.L.3
Bell, R.L.4
Dyer, R.D.5
Carter, G.W.6
Brooks, D.W.7
17
84987368715
Compound 12o was prepared as described in
Compound 12o was prepared as described in J. A. Van Allan, S. Chie Chang, G. A. Reynolds, J. Hetrocycl. Chem., 11, 195-198 (1974).
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J. Hetrocycl. Chem.
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Van Allan, J.A.1
Chie Chang, S.2
Reynolds, G.A.3
19
85008082485
Compound 12n was prepared as described in
Compound 12n was prepared as described in Ozasa S., Fujioka Y., Kikutake J., Ibuki E., Chem. Pharm. Bull., 31, 1572-1581 (1983).
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Chem. Pharm. Bull.
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Ozasa, S.1
Fujioka, Y.2
Kikutake, J.3
Ibuki, E.4
20
77951734406
in preparation
Yamamoto T., Yamaguchi H., Miki H., Shimada M., Nakada Y., Ogino M., Asano K., Aoki K., Tamura N., Masago M., Kato K. in preparation.
Yamamoto, T.1
Yamaguchi, H.2
Miki, H.3
Shimada, M.4
Nakada, Y.5
Ogino, M.6
Asano, K.7
Aoki, K.8
Tamura, N.9
Masago, M.10
Kato, K.11