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Pharmaceutical Research|October 23, 2004
Metabolism and disposition of the HIV-1 protease inhibitor lopinavir (ABT-378) given in combination with ritonavir in rats, dogs, and humansGondi N Kumar, Venkata K Jayanti, Marianne K Johnson, et al.
Frontiers in Genetics|November 1, 2012
AhR activation underlies the CYP1A autoinduction by A-998679 in ratsMichael J Liguori, Chih-Hung Lee, Hong Liu, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 2013
Discovery of pyrido[2,3-d]pyrimidine-based inhibitors of HCV NS5ADavid A DeGoey, David A Betebenner, David J Grampovnik, et al.
Veterinary Journal (London, England : 1997)|June 16, 2010
Liver transcriptomic changes associated with ritonavir-induced hyperlipidemia in sensitive and resistant strains of ratsYi Yang, Annette J Dahly-Vernon, Eric A G Blomme, et al.
Journal of Medicinal Chemistry|January 11, 2008
Identification of (R)-1-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-3-(1H-indazol-4-yl)urea (ABT-102) as a potent TRPV1 antagonist for pain managementArthur Gomtsyan, Erol K Bayburt, Robert G Schmidt, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonistsRobert G Schmidt, Erol K Bayburt, Steven P Latshaw, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strainsChen Zhao, Hing L Sham, Minghua Sun, et al.
Journal of Medicinal Chemistry|August 8, 2008
The alkaloid conessine and analogues as potent histamine H3 receptor antagonistsChen Zhao, Minghua Sun, Youssef L Bennani, et al.
Bioorganic & Medicinal Chemistry|March 1, 2006
Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitorsJohn T Randolph, Peggy P Huang, William J Flosi, et al.
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