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D L Boger

Showing results (71-80 of 85) with videos related to

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Science (New York, N.Y.)|June 9, 1995
Chemical characterization of a family of brain lipids that induce sleepB F Cravatt, O Prospero-Garcia, G Siuzdak, et al.
Bioorganic & Medicinal Chemistry Letters|February 18, 1999
Trifluoromethyl ketone inhibitors of fatty acid amide hydrolase: a probe of structural and conformational features contributing to inhibitionD L Boger, H Sato, A E Lerner, et al.
Bioorganic & Medicinal Chemistry|May 1, 1996
A solution-phase strategy for the synthesis of chemical libraries containing small organic molecules: a universal and dipeptide mimetic templateS Cheng, C M Tarby, D D Comer, et al.
The Journal of Cell Biology|February 7, 1998
The sleep-inducing lipid oleamide deconvolutes gap junction communication and calcium wave transmission in glial cellsX Guan, B F Cravatt, G R Ehring, et al.
Bioorganic & Medicinal Chemistry|November 14, 1997
10-Formyl-5,8,10-trideazafolic acid (10-formyl-TDAF): a potent inhibitor of glycinamide ribonucleotide transformylaseD L Boger, N E Haynes, P A Kitos, et al.
Bioorganic & Medicinal Chemistry|November 14, 1997
Functionalized analogues of 5,8,10-trideazafolate as potential inhibitors of GAR Tfase or AICAR TfaseD L Boger, N E Haynes, M S Warren, et al.
Journal of Medicinal Chemistry|January 21, 1994
Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunitsF Mohamadi, M M Spees, G S Staten, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 19, 2001
Behavioral evidence for the interaction of oleamide with multiple neurotransmitter systemsI Fedorova, A Hashimoto, R A Fecik, et al.
Chemico-Biological Interactions|January 1, 1990
A demonstration of the intrinsic importance of stabilizing hydrophobic binding and non-covalent van der Waals contacts dominant in the non-covalent CC-1065/B-DNA bindingD L Boger, B J Invergo, R S Coleman, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2000
Design, synthesis, and biological evaluation of fluoronitrophenyl substituted folate analogues as potential inhibitors of GAR transformylase and AICAR transformylaseD L Boger, T H Marsilje, R A Castro, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Science (New York, N.Y.)|June 9, 1995
Chemical characterization of a family of brain lipids that induce sleepB F Cravatt, O Prospero-Garcia, G Siuzdak, et al.
Bioorganic & Medicinal Chemistry Letters|February 18, 1999
Trifluoromethyl ketone inhibitors of fatty acid amide hydrolase: a probe of structural and conformational features contributing to inhibitionD L Boger, H Sato, A E Lerner, et al.
Bioorganic & Medicinal Chemistry|May 1, 1996
A solution-phase strategy for the synthesis of chemical libraries containing small organic molecules: a universal and dipeptide mimetic templateS Cheng, C M Tarby, D D Comer, et al.
The Journal of Cell Biology|February 7, 1998
The sleep-inducing lipid oleamide deconvolutes gap junction communication and calcium wave transmission in glial cellsX Guan, B F Cravatt, G R Ehring, et al.
Bioorganic & Medicinal Chemistry|November 14, 1997
10-Formyl-5,8,10-trideazafolic acid (10-formyl-TDAF): a potent inhibitor of glycinamide ribonucleotide transformylaseD L Boger, N E Haynes, P A Kitos, et al.
Bioorganic & Medicinal Chemistry|November 14, 1997
Functionalized analogues of 5,8,10-trideazafolate as potential inhibitors of GAR Tfase or AICAR TfaseD L Boger, N E Haynes, M S Warren, et al.
Journal of Medicinal Chemistry|January 21, 1994
Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunitsF Mohamadi, M M Spees, G S Staten, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 19, 2001
Behavioral evidence for the interaction of oleamide with multiple neurotransmitter systemsI Fedorova, A Hashimoto, R A Fecik, et al.
Chemico-Biological Interactions|January 1, 1990
A demonstration of the intrinsic importance of stabilizing hydrophobic binding and non-covalent van der Waals contacts dominant in the non-covalent CC-1065/B-DNA bindingD L Boger, B J Invergo, R S Coleman, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2000
Design, synthesis, and biological evaluation of fluoronitrophenyl substituted folate analogues as potential inhibitors of GAR transformylase and AICAR transformylaseD L Boger, T H Marsilje, R A Castro, et al.
Pageof 9