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0041565245
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A novel class of nonpeptidic biaryl inhibitors of human cathepsin K
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28144433007
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15
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32344452958
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note
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157).
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16
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32344435562
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note
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See ref 4a for expression and purification procedures. Cyclohexanecarboxamide-based inhibitors were equipotent against humanized-rabbit and human Cat K.
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17
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Angiotensin-converting enzyme inhibitors: Importance of the amide carbonyl of mercaptoacyl amino acids for hydrogen bonding to the enzyme
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18
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0004268506
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University of California, San Francisco
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Case, D. A.; Pearlman, D. A.; Caldwell, J. W.; Cheatham, T. E., III; Ross, W. S.; Simmerling, C. L.; Darden, T. A.; Merz, K. M.; Stanton, R. V.; Cheng, A. L.; Vincent, J. J.; Crowley, M.; Tsui, V.; Radmer, R. J.; Duan, Y.; Pitera, J.; Massova, I.; Seibel, G. L.; Singh, U. C.; Weiner, P. K.; Kollman, P. A. AMBER 6; University of California, San Francisco, 1999. Molecular dynamics calculations were carried out using explicit water in a periodic box under nvt conditions (constant number of molecules, volume, and temperature).
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37049082076
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Dimethyl sulfoxide-trimethylsilyl bromide-amine system as a bromonium ion source containing a potential internal nucleophile; unusual bromolactonization of cyclohex-3-enecarboxylic acid derivatives
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84987351253
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Application of dialkylaminosulfur trifluorides in the synthesis of fluoroorganic compounds
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21
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32344440567
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note
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In general, P3 SAR trends were not influenced by the nature of the P2-P3 linker or the presence of fluorine substituents on the cyclohexyl ring.
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-
-
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22
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0000359812
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Optically active aromatic chromphores. XI. Circular dichroism studies of some 1-substituted 2-phenylcyclohexanes
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32344433125
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note
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This corresponds with the absolute stereochemistry determined for 13e and also with the more potent enantiomer of 12f prepared from (+)-(1R,2R)-9 (purchased from TCI organic chemicals, cat no C1417).
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-
-
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24
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0032714945
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Efficient synthesis of cyclopropylacetylene, a crucial synthetic intermediate for efavirenz (DMP-266)
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2, see: Schmidt, S. E.; Salvatore, R. N.; Jung, K. W.; Kwon, T. Efficient Synthesis of Cyclopropylacetylene, a Crucial Synthetic Intermediate for Efavirenz (DMP-266). Synlett 1999, 1948-50.
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Schmidt, S.E.1
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25
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32344453175
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note
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Coupling constant analysis for the proton attached to the fluorine bearing carbon was used to assign the fluorine orientations on the conformationally biased cyclohexyl ring. The reactions of 36a and 36b with DAST proceeded with inversion at the alcohol bearing stereocenter.
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26
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8844229444
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An activity based probe for the determination of cysteine cathepsin protease activities in whole cells
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Falgueyret, J.-P.; Black, W. C.; Cromlish, W.; Desmarais, S.; Lamontagne, S.; Mellon, C.; Riendeau, D.; Rodan, S.; Tawa, P.; Wesolowski, G.; Bass, K. E.; Venkatraman, S.; Percival, D. An Activity Based Probe for the Determination of Cysteine Cathepsin Protease Activities in Whole Cells. Anal. Biochem. 2004, 335, 218-27.
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Riendeau, D.7
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Tawa, P.9
Wesolowski, G.10
Bass, K.E.11
Venkatraman, S.12
Percival, D.13
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27
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0346333386
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Peptide ketobenzoxazole inhibitors bound to cathepsin K
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McGrath, M. E.; Sprengeler, P. A.; Hill, C. M.; Martichonok, V.; Cheung, H.; Somoza, J. R.; Palmer, J. T.; Jane, J. W. Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K. Biochemistry 2003, 42, 15018-28.
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Jane, J.W.8
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