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Robert A Fecik

Showing results (11-20 of 19) with videos related to

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Journal of Medicinal Chemistry|February 18, 2005
Chiral DNA gyrase inhibitors. 3. Probing the chiral preference of the active site of DNA gyrase. Synthesis of 10-fluoro-6-methyl-6,7-dihydro-9-piperazinyl- 2H-benzo[a]quinolizin-20-one-3-carboxylic acid analoguesRobert A Fecik, Pratik Devasthale, Segaran Pillai, et al.
Journal of the American Chemical Society|October 9, 2003
Substrate recognition and channeling of monomodules from the pikromycin polyketide synthaseBrian J Beck, Courtney C Aldrich, Robert A Fecik, et al.
Journal of the American Chemical Society|April 17, 2003
Iterative chain elongation by a pikromycin monomodular polyketide synthaseBrian J Beck, Courtney C Aldrich, Robert A Fecik, et al.
Journal of the American Chemical Society|June 2, 2015
Functional Characterization of a Dehydratase Domain from the Pikromycin Polyketide SynthaseYang Li, Greg J Dodge, William D Fiers, et al.
Chemical Science|September 15, 2015
Tylosin polyketide synthase module 3: stereospecificity, stereoselectivity and steady-state kinetic analysis of β-processing domains <i>via</i> diffusible, synthetic substratesWilliam D Fiers, Greg J Dodge, Yang Li, et al.
ACS Chemical Biology|October 10, 2014
Polyketide intermediate mimics as probes for revealing cryptic stereochemistry of ketoreductase domainsYang Li, William D Fiers, Steffen M Bernard, et al.
Nature Chemical Biology|September 14, 2006
Structural basis for macrolactonization by the pikromycin thioesteraseDavid L Akey, Jeffrey D Kittendorf, John W Giraldes, et al.
Nature Chemical Biology|September 14, 2006
Structural and mechanistic insights into polyketide macrolactonization from polyketide-based affinity labelsJohn W Giraldes, David L Akey, Jeffrey D Kittendorf, et al.
Journal of Medicinal Chemistry|March 18, 2005
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesicsDale L Boger, Hiroshi Miyauchi, Wu Du, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of Medicinal Chemistry|February 18, 2005
Chiral DNA gyrase inhibitors. 3. Probing the chiral preference of the active site of DNA gyrase. Synthesis of 10-fluoro-6-methyl-6,7-dihydro-9-piperazinyl- 2H-benzo[a]quinolizin-20-one-3-carboxylic acid analoguesRobert A Fecik, Pratik Devasthale, Segaran Pillai, et al.
Journal of the American Chemical Society|October 9, 2003
Substrate recognition and channeling of monomodules from the pikromycin polyketide synthaseBrian J Beck, Courtney C Aldrich, Robert A Fecik, et al.
Journal of the American Chemical Society|April 17, 2003
Iterative chain elongation by a pikromycin monomodular polyketide synthaseBrian J Beck, Courtney C Aldrich, Robert A Fecik, et al.
Journal of the American Chemical Society|June 2, 2015
Functional Characterization of a Dehydratase Domain from the Pikromycin Polyketide SynthaseYang Li, Greg J Dodge, William D Fiers, et al.
Chemical Science|September 15, 2015
Tylosin polyketide synthase module 3: stereospecificity, stereoselectivity and steady-state kinetic analysis of β-processing domains <i>via</i> diffusible, synthetic substratesWilliam D Fiers, Greg J Dodge, Yang Li, et al.
ACS Chemical Biology|October 10, 2014
Polyketide intermediate mimics as probes for revealing cryptic stereochemistry of ketoreductase domainsYang Li, William D Fiers, Steffen M Bernard, et al.
Nature Chemical Biology|September 14, 2006
Structural basis for macrolactonization by the pikromycin thioesteraseDavid L Akey, Jeffrey D Kittendorf, John W Giraldes, et al.
Nature Chemical Biology|September 14, 2006
Structural and mechanistic insights into polyketide macrolactonization from polyketide-based affinity labelsJohn W Giraldes, David L Akey, Jeffrey D Kittendorf, et al.
Journal of Medicinal Chemistry|March 18, 2005
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesicsDale L Boger, Hiroshi Miyauchi, Wu Du, et al.
Pageof 2