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Elizabeth H Fry

Showing results (1-10 of 15) with videos related to

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Bioorganic & Medicinal Chemistry Letters|February 1, 2006
Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphataseChunqiu Lai, Rebecca J Gum, Melissa Daly, et al.
Bioorganic & Medicinal Chemistry Letters|January 31, 2006
Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding modeThomas W von Geldern, Chunqiu Lai, Rebecca J Gum, et al.
Proteins|March 11, 2009
Crystal structure and thermodynamic analysis of diagnostic mAb 106.3 complexed with BNP 5-13 (C10A)Kenton L Longenecker, Qiaoqiao Ruan, Elizabeth H Fry, et al.
Bioorganic & Medicinal Chemistry Letters|March 11, 2006
Synthesis and SAR of 1,9-dihydro-9-hydroxypyrazolo[3,4-b]quinolin-4-ones as novel, selective c-Jun N-terminal kinase inhibitorsMei Liu, Zhili Xin, Jill E Clampit, et al.
Bioorganic & Medicinal Chemistry Letters|November 17, 2006
Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studiesMei Liu, Sanyi Wang, Jill E Clampit, et al.
Bioorganic & Medicinal Chemistry Letters|June 26, 2009
Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)Julie Miyashiro, Keith W Woods, Chang H Park, et al.
Protein Science : a Publication of the Protein Society|December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closureKenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Biochemistry|June 14, 2006
Crystal structures of DPP-IV (CD26) from rat kidney exhibit flexible accommodation of peptidase-selective inhibitorsKenton L Longenecker, Kent D Stewart, David J Madar, et al.
Chemical Biology & Drug Design|February 24, 2006
Structure-based optimization of MurF inhibitorsGeoffrey F Stamper, Kenton L Longenecker, Elizabeth H Fry, et al.
Journal of Medicinal Chemistry|July 21, 2006
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitorsHongyu Zhao, Michael D Serby, Zhili Xin, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Bioorganic & Medicinal Chemistry Letters|February 1, 2006
Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphataseChunqiu Lai, Rebecca J Gum, Melissa Daly, et al.
Bioorganic & Medicinal Chemistry Letters|January 31, 2006
Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding modeThomas W von Geldern, Chunqiu Lai, Rebecca J Gum, et al.
Proteins|March 11, 2009
Crystal structure and thermodynamic analysis of diagnostic mAb 106.3 complexed with BNP 5-13 (C10A)Kenton L Longenecker, Qiaoqiao Ruan, Elizabeth H Fry, et al.
Bioorganic & Medicinal Chemistry Letters|March 11, 2006
Synthesis and SAR of 1,9-dihydro-9-hydroxypyrazolo[3,4-b]quinolin-4-ones as novel, selective c-Jun N-terminal kinase inhibitorsMei Liu, Zhili Xin, Jill E Clampit, et al.
Bioorganic & Medicinal Chemistry Letters|November 17, 2006
Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studiesMei Liu, Sanyi Wang, Jill E Clampit, et al.
Bioorganic & Medicinal Chemistry Letters|June 26, 2009
Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)Julie Miyashiro, Keith W Woods, Chang H Park, et al.
Protein Science : a Publication of the Protein Society|December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closureKenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Biochemistry|June 14, 2006
Crystal structures of DPP-IV (CD26) from rat kidney exhibit flexible accommodation of peptidase-selective inhibitorsKenton L Longenecker, Kent D Stewart, David J Madar, et al.
Chemical Biology & Drug Design|February 24, 2006
Structure-based optimization of MurF inhibitorsGeoffrey F Stamper, Kenton L Longenecker, Elizabeth H Fry, et al.
Journal of Medicinal Chemistry|July 21, 2006
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitorsHongyu Zhao, Michael D Serby, Zhili Xin, et al.
Pageof 2