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Hormone and Antihormone Induce Distinct Conformational Changes Which Are Central to Steroid Receptor Activation
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0027521287
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Transcriptional Activation by the Estrogen Receptor Requires a Conformational Change in the Ligand Binding Domain
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0028237201
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37049100918
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24
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8944233388
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BIOSYM Technologies, Inc., 9685 Scranton Rd., San Diego, CA 92121-3752
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BIOSYM Technologies, Inc., 9685 Scranton Rd., San Diego, CA 92121-3752.
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25
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8944224039
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TRIPOS Inc., 1699 South Hanley, Suite 303, St. Louis, MO 63144-2913
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TRIPOS Inc., 1699 South Hanley, Suite 303, St. Louis, MO 63144-2913.
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-
-
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26
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8944246811
-
-
note
-
MMX (an enhanced version of MM2) was calculated by using software PCMODEL (Serena Software, Bloomington).
-
-
-
-
27
-
-
8944240863
-
-
note
-
3OCO, R′ = H, and 15, R = R′ = H) and with butyl group in the place of the methyl at C(22)] gave single crystals. However all these crystals contained four molecules in their unit cells. Solution of the crystal structure of compounds with these high formula weights (about 2000) is nearly impossible.
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28
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0026460066
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Highly Diastereo-selective Conjugate Addition of Organocuprate to Acyclic E- and Z-Enones: Reversal Stereoselectivity under Kinetic and Thermodynamic Conditions
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Yamamoto, K.; Yamada, S.; Yamaguchi, K. Highly Diastereo-selective Conjugate Addition of Organocuprate to Acyclic E- and Z-Enones: Reversal Stereoselectivity under Kinetic and Thermodynamic Conditions. Tetrahedron Lett. 1992, 33, 7521-7524.
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29
-
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8944238502
-
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note
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7a and then that of 14′ to be R. Since the reactivity and the face selectivity under kinetic as well as thermodynamic conditions are parallel in the 20R- and 20S-enones, the configurations at C(22) of 13 and 14 were assigned with high probability to be R and S, respectively (those of 15 and 16 to be S and R, respectively). Equation presented
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-
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30
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0004482369
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Identification of the Porcine Intestinal 1,25-Dihydroxyvitamin DS Receptor on Sodium Dodecyl Sulfate/Polyacrylamide Gels by Renaturation and Immunoblotting
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34
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0026583191
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Vitamin D: Structure-Function Analyses and the Design of Analogs
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Okamura's group has reported a dot map for models of 1 and its analogs to study the structure-activity relationships; see: Okamura, W. H.; Palenzuela, J. A.; Plumet, J.; Midland, M. M. Vitamin D: Structure-Function Analyses and the Design of Analogs. J. Cell. Biochem. 1992, 49, 10-18. Midland, M. M.; Plumet, J.; Okamura, W. H. Effect of C20 Stereochemistry on the Conformational Profile of the Side Chains of Vitamin D Analogs. BioMed. Chem. Lett. 1993, 3, 1799-1804.
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35
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0027370857
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Effect of C20 Stereochemistry on the Conformational Profile of the Side Chains of Vitamin D Analogs
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Okamura's group has reported a dot map for models of 1 and its analogs to study the structure-activity relationships; see: Okamura, W. H.; Palenzuela, J. A.; Plumet, J.; Midland, M. M. Vitamin D: Structure-Function Analyses and the Design of Analogs. J. Cell. Biochem. 1992, 49, 10-18. Midland, M. M.; Plumet, J.; Okamura, W. H. Effect of C20 Stereochemistry on the Conformational Profile of the Side Chains of Vitamin D Analogs. BioMed. Chem. Lett. 1993, 3, 1799-1804.
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0029102106
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Conformational Effects on Retinoid Receptor Selectivity. 2. Effects of Retinoid Bridging Group on Retinoid X Receptor Activity and Selectivity
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Synthesis and Structure-Activity Relationships of Novel Retinoid X Receptor-Selective Retinoids
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0025797354
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Synthesis of Four Diastereomeric L-2-(Carboxycyclopropyl)glycines. Conformationally Constrained L-Glutamate Analogues
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39
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8944238501
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note
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7a
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|