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Chemical Communications (Cambridge, England)|February 24, 2006
Synthesis and novel structure-activity relationships of potent sansalvamide A derivativesKaterina Otrubova, Thomas J Styers, Po-Shen Pan, et al.
ACS Medicinal Chemistry Letters|August 24, 2010
Mechanistic studies of Sansalvamide A-amide: an allosteric modulator of Hsp90Robert C Vasko, Rodrigo A Rodriguez, Christian N Cunningham, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|September 6, 2019
C-Terminal HSP90 Inhibitors Block the HIF-1 Hypoxic Response by Degrading HIF-1α through the Oxygen-Dependent Degradation PathwayNalin Kataria, Chloe-Anne Martinez, Bernadette Kerr, et al.
Organic Letters|December 22, 2007
Synthesis and cytotoxicity of a new class of potent decapeptide macrocyclesMelinda R Davis, Thomas J Styers, Rodrigo A Rodriguez, et al.
Bioorganic & Medicinal Chemistry Letters|July 19, 2011
Synthesis and evaluation of biotinylated sansalvamide A analogs and their modulation of Hsp90Joseph B Kunicki, Mark N Petersen, Leslie D Alexander, et al.
ACS Medicinal Chemistry Letters|July 23, 2014
Chemically accessible hsp90 inhibitor that does not induce a heat shock responseYen Chin Koay, Jeanette R McConnell, Yao Wang, et al.
Bioorganic & Medicinal Chemistry|April 4, 2006
Novel antibiotics: C-2 symmetrical macrocycles inhibiting Holliday junction DNA binding by E. coli RuvCPo-Shen Pan, Fiona A Curtis, Chris L Carroll, et al.
Journal of Bacteriology|June 22, 2005
Binding of Pseudomonas aeruginosa AlgZ to sites upstream of the algZ promoter leads to repression of transcriptionDeborah M Ramsey, Patricia J Baynham, Daniel J Wozniak
Organic Letters|January 17, 2003
Novel antibiotics: macrocyclic peptides designed to trap Holliday junctionsMegan L Bolla, Enrique V Azevedo, Jason M Smith, et al.
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