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Results: 1-7 |
Results: 7
Synthesis of 5-alkenylated d4T analogues via the Pd-catalyzed cross-coupling reaction
Authors: Ciurea, A Fossey, C Benzaria, S Gavriliu, D Delbederi, Z Lelong, B Laduree, D Aubertin, AM Kirn, A
Citation: A. Ciurea et al., Synthesis of 5-alkenylated d4T analogues via the Pd-catalyzed cross-coupling reaction, NUCLEOS NUC, 20(9), 2001, pp. 1655-1670
Conformationally constrained analogues of diacylglycerol. 18. The incorporation of a hydroxamate moiety into diacylglycerol-lactones reduces lipophilicity and helps discriminate between sn-1 and sn-2 binding modes to proteinkinase c (PK-C). Implications for isozyme specificity
Authors: Lee, J Han, KC Kang, JH Pearce, LL Lewin, NE Yan, SQ Benzaria, S Nicklaus, MC Blumberg, PM Marquez, VE
Citation: J. Lee et al., Conformationally constrained analogues of diacylglycerol. 18. The incorporation of a hydroxamate moiety into diacylglycerol-lactones reduces lipophilicity and helps discriminate between sn-1 and sn-2 binding modes to proteinkinase c (PK-C). Implications for isozyme specificity, J MED CHEM, 44(25), 2001, pp. 4309-4312
Synthesis and antiviral activity of C-5 substituted beta-D- and beta-L-D4Tanalogues
Authors: Delbederi, Z Fossey, C Fontaine, G Benzaria, S Gavriliu, D Ciurea, A Lelong, B Laduree, D Aubertin, AM Kirn, A
Citation: Z. Delbederi et al., Synthesis and antiviral activity of C-5 substituted beta-D- and beta-L-D4Tanalogues, NUCLEOS NUC, 19(9), 2000, pp. 1441-1461
Synthesis and antiviral activity of C-5 substituted analogues of d4T bearing methylamino- or methyldiamino-linker arms
Authors: Gavriliu, D Fossey, C Fontaine, G Benzaria, S Ciurea, A Delbederi, Z Lelong, B Laduree, D Aubertin, AM Kirn, A
Citation: D. Gavriliu et al., Synthesis and antiviral activity of C-5 substituted analogues of d4T bearing methylamino- or methyldiamino-linker arms, NUCLEOS NUC, 19(5-6), 2000, pp. 1017-1031
Conformationally constrained analogues of diacylglycerol (DAG). 16. How much structural complexity is necessary for recognition and high binding affinity to protein kinase C?
Authors: Nacro, K Bienfait, B Lee, J Han, KC Kang, JH Benzaria, S Lewin, NE Bhattacharyya, DK Blumberg, PM Marquez, VE
Citation: K. Nacro et al., Conformationally constrained analogues of diacylglycerol (DAG). 16. How much structural complexity is necessary for recognition and high binding affinity to protein kinase C?, J MED CHEM, 43(5), 2000, pp. 921-944
The transition from a pharmacophore-guided approach to a receptor-guided approach in the design of potent protein kinase C ligands
Authors: Marquez, VE Nacro, K Benzaria, S Lee, J Sharma, R Teng, K Milne, GWA Bienfait, B Wang, SM Lewin, NE Blumberg, PM
Citation: Ve. Marquez et al., The transition from a pharmacophore-guided approach to a receptor-guided approach in the design of potent protein kinase C ligands, PHARM THERA, 82(2-3), 1999, pp. 251-261
Conformationally constrained analogues of diacylglycerol (DAG). 15. The indispensable role of the sn-1 and sn-2 carbonyls in the binding of DAG-lactones to protein kinase C (PK-C)
Authors: Benzaria, S Bienfait, B Nacro, K Wang, SM Lewin, NE Beheshti, M Blumberg, PM Marquez, VE
Citation: S. Benzaria et al., Conformationally constrained analogues of diacylglycerol (DAG). 15. The indispensable role of the sn-1 and sn-2 carbonyls in the binding of DAG-lactones to protein kinase C (PK-C), BIOORG MED, 8(23), 1998, pp. 3403-3408
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