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Results: 1-11 |
Results: 11

Authors: VANDERDONK WA YU GX PEREZ L SANCHEZ RJ STUBBE J SAMANO V ROBINS MJ
Citation: Wa. Vanderdonk et al., DETECTION OF A NEW SUBSTRATE-DERIVED RADICAL DURING INACTIVATION OF RIBONUCLEOTIDE REDUCTASE FROM ESCHERICHIA-COLI BY GEMCITABINE 5'-DIPHOSPHATE, Biochemistry, 37(18), 1998, pp. 6419-6426

Authors: SILVA DJ STUBBE J SAMANO V ROBINS MJ
Citation: Dj. Silva et al., GEMCITABINE 5'-TRIPHOSPHATE IS A STOICHIOMETRIC MECHANISM-BASED INHIBITOR OF LACTOBACILLUS-LEICHMANNII RIBONUCLEOSIDE TRIPHOSPHATE REDUCTASE - EVIDENCE FOR THIYL RADICAL-MEDIATED NUCLEOTIDE RADICAL FORMATION, Biochemistry, 37(16), 1998, pp. 5528-5535

Authors: PEREZ L VANDERDONK WA STUBBE J SAMANO V ROBINS MJ
Citation: L. Perez et al., INACTIVATION OF RIBONUCLEOTIDE REDUCTASE FROM ESCHERICHIA-COLI BY GEMCITABINE 5'-DIPHOSPHATE, The FASEB journal, 11(9), 1997, pp. 1714-1714

Authors: ROBINS MJ SARKER S SAMANO V WNUK SF
Citation: Mj. Robins et al., NUCLEIC-ACID RELATED-COMPOUNDS .94. REMARKABLY HIGH STEREOSELECTIVE REDUCTIONS OF 2'-KETONUCLEOSIDE AND 3'-KETONUCLEOSIDE DERIVATIVES TO GIVE ARABINO, RIBO, AND XYLOFURANOSYL NUCLEOSIDES WITH HYDROGEN ISOTOPESAT C2' AND C3', Tetrahedron, 53(2), 1997, pp. 447-456

Authors: SILVA DJ VANDERDONK W LAWRENCE C GERFEN G LICHT S SAMANO V ROBINS MJ STUBBE J
Citation: Dj. Silva et al., MECHANISM-BASED INHIBITION OF RIBONUCLEOTIDE REDUCTASES, Biochemistry, 35(28), 1996, pp. 87-87

Authors: ROBINS MJ SAMANO MC SAMANO V
Citation: Mj. Robins et al., RIBONUCLEOTIDE REDUCTASE TARGETS FOR CHEMOTHERAPY - MECHANISTIC ASPECTS AND BIOLOGICALLY-ACTIVE AGENTS, Nucleosides & nucleotides, 14(3-5), 1995, pp. 485-493

Authors: MILES RW SAMANO V ROBINS MJ
Citation: Rw. Miles et al., NUCLEIC-ACID RELATED-COMPOUNDS .87. NUCLEOPHILIC FUNCTIONALIZATION OFCYTIDINE AND 2'-DEOXYCYTIDINE DERIVATIVES VIA ELABORATION OF THE 4-AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT, Journal of organic chemistry, 60(21), 1995, pp. 7066-7069

Authors: MILES RW SAMANO V ROBINS MJ
Citation: Rw. Miles et al., NUCLEIC-ACID RELATED-COMPOUNDS .86. NUCLEOPHILIC FUNCTIONALIZATION OFADENINE, ADENOSINE, TUBERCIDIN, AND FORMYCIN DERIVATIVES VIA ELABORATION OF THE HETEROCYCLIC AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT, Journal of the American Chemical Society, 117(22), 1995, pp. 5951-5957

Authors: SAMANO V ROBINS MJ
Citation: V. Samano et Mj. Robins, SYNTHESIS OF 3'-DEOXYADENOSINE-3'-SPIROCYCLOPROPANE, 3'-DEOXYURIDINE-5'-SPIROCYCLOPROPANE, AND 5'-DEOXY-4',5'-METHANOADENOSINE, Tetrahedron letters, 35(21), 1994, pp. 3445-3448

Authors: CORY AH SAMANO V ROBINS MJ CORY JG
Citation: Ah. Cory et al., 2'-DEOXY-2'-METHYLENE DERIVATIVES OF ADENOSINE, GUANOSINE, TUBERCIDIN, CYTIDINE AND URIDINE AS INHIBITORS OF L1210 CELL-GROWTH IN CULTURE, Biochemical pharmacology, 47(2), 1994, pp. 365-371

Authors: SAMANO V MILES RW ROBINS MJ
Citation: V. Samano et al., EFFICIENT CONVERSION OF 6-AMINOPURINES AND NUCLEOSIDES INTO 6-SUBSTITUTED ANALOGS VIA NOVEL 6-(1,2,4-TRIAZOL-4-YL)PURINE DERIVATIVES, Journal of the American Chemical Society, 116(20), 1994, pp. 9331-9332
Risultati: 1-11 |