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Terrence R Burke

Showing results (71-80 of 169) with videos related to

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Antimicrobial Agents and Chemotherapy|July 1, 2020
HIV-1 Integrase Inhibitors That Are Active against Drug-Resistant Integrase MutantsSteven J Smith, Xue Zhi Zhao, Dario Oliveira Passos, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 24, 2011
Isothiazolidinone (IZD) as a phosphoryl mimetic in inhibitors of the Yersinia pestis protein tyrosine phosphatase YopHSung Eun Kim, Medhanit Bahta, George T Lountos, et al.
The Journal of Biological Chemistry|January 24, 2002
Structural determinants for HIV-1 integrase inhibition by beta-diketo acidsChristophe Marchand, Xuechun Zhang, Godwin C G Pais, et al.
Chembiochem : a European Journal of Chemical Biology|February 19, 2005
Ring-closing metathesis of C-terminal allylglycine residues with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic as an approach to novel Grb2 SH2 domain-binding macrocyclesShinya Oishi, Zhen-Dan Shi, Karen M Worthy, et al.
Journal of Medicinal Chemistry|January 10, 2003
Macrocyclization in the design of Grb2 SH2 domain-binding ligands exhibiting high potency in whole-cell systemsChang-Qing Wei, Yang Gao, Kyeong Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2006
Discovery of a small-molecule HIV-1 integrase inhibitor-binding siteLaith Q Al-Mawsawi, Valery Fikkert, Raveendra Dayam, et al.
Molecular Pharmacology|December 19, 2006
Probing HIV-1 integrase inhibitor binding sites with position-specific integrase-DNA cross-linking assaysAllison A Johnson, Christophe Marchand, Sachindra S Patil, et al.
Frontiers in Chemistry|September 2, 2022
Phosphonic acid-containing inhibitors of tyrosyl-DNA phosphodiesterase 1Xue Zhi Zhao, Wenjie Wang, George T Lountos, et al.
Organic & Biomolecular Chemistry|January 6, 2007
Utilization of achiral alkenyl amines for the preparation of high affinity Grb2 SH2 domain-binding macrocycles by ring-closing metathesisFa Liu, Karen M Worthy, Lakshman Bindu, et al.
Bioorganic & Medicinal Chemistry Letters|April 15, 2009
Examination of halogen substituent effects on HIV-1 integrase inhibitors derived from 2,3-dihydro-6,7-dihydroxy-1H-isoindol-1-ones and 4,5-dihydroxy-1H-isoindole-1,3(2H)-dionesXue Zhi Zhao, Kasthuraiah Maddali, B Christie Vu, et al.
Pageof 17

Showing results (71-80 of 169) with videos related to

Sort By:
Pageof 17
Antimicrobial Agents and Chemotherapy|July 1, 2020
HIV-1 Integrase Inhibitors That Are Active against Drug-Resistant Integrase MutantsSteven J Smith, Xue Zhi Zhao, Dario Oliveira Passos, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 24, 2011
Isothiazolidinone (IZD) as a phosphoryl mimetic in inhibitors of the Yersinia pestis protein tyrosine phosphatase YopHSung Eun Kim, Medhanit Bahta, George T Lountos, et al.
The Journal of Biological Chemistry|January 24, 2002
Structural determinants for HIV-1 integrase inhibition by beta-diketo acidsChristophe Marchand, Xuechun Zhang, Godwin C G Pais, et al.
Chembiochem : a European Journal of Chemical Biology|February 19, 2005
Ring-closing metathesis of C-terminal allylglycine residues with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic as an approach to novel Grb2 SH2 domain-binding macrocyclesShinya Oishi, Zhen-Dan Shi, Karen M Worthy, et al.
Journal of Medicinal Chemistry|January 10, 2003
Macrocyclization in the design of Grb2 SH2 domain-binding ligands exhibiting high potency in whole-cell systemsChang-Qing Wei, Yang Gao, Kyeong Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2006
Discovery of a small-molecule HIV-1 integrase inhibitor-binding siteLaith Q Al-Mawsawi, Valery Fikkert, Raveendra Dayam, et al.
Molecular Pharmacology|December 19, 2006
Probing HIV-1 integrase inhibitor binding sites with position-specific integrase-DNA cross-linking assaysAllison A Johnson, Christophe Marchand, Sachindra S Patil, et al.
Frontiers in Chemistry|September 2, 2022
Phosphonic acid-containing inhibitors of tyrosyl-DNA phosphodiesterase 1Xue Zhi Zhao, Wenjie Wang, George T Lountos, et al.
Organic & Biomolecular Chemistry|January 6, 2007
Utilization of achiral alkenyl amines for the preparation of high affinity Grb2 SH2 domain-binding macrocycles by ring-closing metathesisFa Liu, Karen M Worthy, Lakshman Bindu, et al.
Bioorganic & Medicinal Chemistry Letters|April 15, 2009
Examination of halogen substituent effects on HIV-1 integrase inhibitors derived from 2,3-dihydro-6,7-dihydroxy-1H-isoindol-1-ones and 4,5-dihydroxy-1H-isoindole-1,3(2H)-dionesXue Zhi Zhao, Kasthuraiah Maddali, B Christie Vu, et al.
Pageof 17