-
1
-
-
0026469464
-
Regulation of GTP biosynthesis
-
Weber, G.; Nakamura, H.; Natsumeda, Y.; Szekeres, T.; Nagai, M. Regulation of GTP biosynthesis. Adv. Enzyme Regu. 1992, 32, 57-69.
-
(1992)
Adv. Enzyme Regu.
, vol.32
, pp. 57-69
-
-
Weber, G.1
Nakamura, H.2
Natsumeda, Y.3
Szekeres, T.4
Nagai, M.5
-
2
-
-
0025232817
-
Two distinct cDNAs for human IMP dehydrogenase
-
Natsumeda, Y.; Ohno, S.; Kawasaki, H.; Konno, Y.; Weber, G.; Suzuki, K. Two distinct cDNAs for human IMP dehydrogenase. J. Biol. Chem. 1990, 265, 5292-5295.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 5292-5295
-
-
Natsumeda, Y.1
Ohno, S.2
Kawasaki, H.3
Konno, Y.4
Weber, G.5
Suzuki, K.6
-
3
-
-
0023697556
-
Cloning and sequence analysis of the human and Chinese hamster inosine-5-monophosphate dehydrogenase cDNAs
-
Collart, F.R.; Huberman, E. Cloning and sequence analysis of the human and Chinese hamster inosine-5-monophosphate dehydrogenase cDNAs. J. Biol. Chem. 1988, 263, 15769-15772.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 15769-15772
-
-
Collart, F.R.1
Huberman, E.2
-
4
-
-
0028343293
-
Tissue-differential expression of two distinct genes for human IMP dehydrogenase (E.C.1.1.1.205
-
Senda, M.; Natsumeda, Y. Tissue-differential expression of two distinct genes for human IMP dehydrogenase (E.C.1.1.1.205). Life Sciences 1994, 54, 1917-1926.
-
(1994)
Life Sciences
, vol.54
, pp. 1917-1926
-
-
Senda, M.1
Natsumeda, Y.2
-
5
-
-
0026378294
-
Selective up-regulation of type II inosine 5-monophosphate dehydrogenase messenger RNA expression in human leukemias
-
Nagai, M.; Natsumeda, Y.; Konno, Y.; Hoffman, R.; Irino, S.; Weber, G. Selective up-regulation of type II inosine 5-monophosphate dehydrogenase messenger RNA expression in human leukemias. Cancer Res. 1991, 51, 3886-3890.
-
(1991)
Cancer Res.
, vol.51
, pp. 3886-3890
-
-
Nagai, M.1
Natsumeda, Y.2
Konno, Y.3
Hoffman, R.4
Irino, S.5
Weber, G.6
-
6
-
-
0030499593
-
Tiazofurin: Molecular and chemical action
-
Weber, G.; Prajda, N.; Abonyi, M.; Look, K.Y.; Tricot, G. Tiazofurin: molecular and chemical action. Anticancer Res. 1996, 16, 3313-3322.
-
(1996)
Anticancer Res.
, vol.16
, pp. 3313-3322
-
-
Weber, G.1
Prajda, N.2
Abonyi, M.3
Look, K.Y.4
Tricot, G.5
-
7
-
-
36849021519
-
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery
-
Nair, V.; Shu, Q. Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery. Antiviral Chem. & Chemother. 2007, 18, 245-258.
-
(2007)
Antiviral Chem. & Chemother.
, vol.18
, pp. 245-258
-
-
Nair, V.1
Shu, Q.2
-
8
-
-
0029982866
-
IMP dehydrogenase as a target of antitumor and antiviral chemotherapy
-
Franchetti, P.; Cappellacci, L.; Grifantini, M. IMP dehydrogenase as a target of antitumor and antiviral chemotherapy. Farmaco 1996, 51, 457-469.
-
(1996)
Farmaco
, vol.51
, pp. 457-469
-
-
Franchetti, P.1
Cappellacci, L.2
Grifantini, M.3
-
9
-
-
33748604738
-
Inosine 5-monophosphate dehydrogenase inhibitors for the treatment of autoimmune diseases
-
Ratcliffe, A.J. Inosine 5-monophosphate dehydrogenase inhibitors for the treatment of autoimmune diseases. Current Opin. Drug Discov. Develop. 2006, 9, 595-605.
-
(2006)
Current Opin. Drug Discov. Develop.
, vol.9
, pp. 595-605
-
-
Ratcliffe, A.J.1
-
10
-
-
39549088916
-
Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery
-
Shu, Q.; Nair, V. Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery. Med. Res. Rev. 2007, 28, 219-232.
-
(2007)
Med. Res. Rev.
, vol.28
, pp. 219-232
-
-
Shu, Q.1
Nair, V.2
-
11
-
-
84890979835
-
IMPDH inhibitors: Discovery of antiviral agents against emerging diseases
-
ed. P. F. Torrence, Wiley & Sons, Hoboken, NJ
-
Nair, V. IMPDH inhibitors: discovery of antiviral agents against emerging diseases, in Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats, ed. P. F. Torrence, Wiley & Sons, Hoboken, NJ, 2005, pp 179-202.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 179-202
-
-
Nair, V.1
-
12
-
-
0034663926
-
Asp338 controls hydride transfer in Escherichia coli IMP dehydrogenase
-
Kerr, K.M.; Hedstrom, L. Asp338 controls hydride transfer in Escherichia coli IMP dehydrogenase. Biochemistry 2000, 39, 9804-9810.
-
(2000)
Biochemistry
, vol.39
, pp. 9804-9810
-
-
Kerr, K.M.1
Hedstrom, L.2
-
13
-
-
0029670363
-
Trapping of an IMP dehydrogenase-substrate covalent intermediate by mycophenolic acid
-
Link, J.O.; Straub, K. Trapping of an IMP dehydrogenase-substrate covalent intermediate by mycophenolic acid. J. Am. Chem. Soc. 1996, 118, 2091-2092.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2091-2092
-
-
Link, J.O.1
Straub, K.2
-
14
-
-
0017309493
-
Synthesis of 3- deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid by a novel ring closure of imidazole precursors
-
Cook, P.D.; Rousseau, R.J.; Mian, A.M.; Dea, P.; Meyer, R.B.; Robins, R.K. Synthesis of 3- deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid by a novel ring closure of imidazole precursors. J. Am. Chem. Soc. 1976, 98, 1492-1498.
-
(1976)
J. Am. Chem. Soc.
, vol.98
, pp. 1492-1498
-
-
Cook, P.D.1
Rousseau, R.J.2
Mian, A.M.3
Dea, P.4
Meyer, R.B.5
Robins, R.K.6
-
15
-
-
0036836965
-
Inhition of inosine monophosphate dehydrogenase (IMPDH) by the antiviral compound, 2-vinylinosine monophosphate
-
Pal, S.; Bera, B.; Nair, V. Inhition of inosine monophosphate dehydrogenase (IMPDH) by the antiviral compound, 2-vinylinosine monophosphate. Bioorg. Med. Chem. 2002, 10, 3615-3618.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 3615-3618
-
-
Pal, S.1
Bera, B.2
Nair, V.3
-
16
-
-
0017396912
-
Antiviral activity of 3-deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid. Antimicrob
-
Allen, L.B.; Huffman, J.H.; Cook, P.D.; Meyer, R.B., Jr.; Robins, R.K.; Sidwell, R.W. Antiviral activity of 3-deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid. Antimicrob. Agents Chemother. 1977, 12, 114-119.
-
(1977)
Agents Chemother.
, vol.12
, pp. 114-119
-
-
Allen, L.B.1
Huffman, J.H.2
Cook, P.D.3
Meyer Jr., R.B.4
Robins, R.K.5
Sidwell, R.W.6
-
17
-
-
0021742976
-
Synthesis and antiviral/antitumor activities of certain 3-deazaguanine nucleosides and nucleotides
-
Revankar, G.R.; Gupta, P.K.; Adams, A.D.; Dalley, N.K.; McKernan, P.A.; Cook, P.D.; Canonico, P.G.; Robins, R.K. Synthesis and antiviral/antitumor activities of certain 3-deazaguanine nucleosides and nucleotides. J. Med. Chem., 1984, 27, 1389-1396.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 1389-1396
-
-
Revankar, G.R.1
Gupta, P.K.2
Adams, A.D.3
Dalley, N.K.4
Mc Kernan, P.A.5
Cook, P.D.6
Canonico, P.G.7
Robins, R.K.8
-
18
-
-
0026687301
-
New hypoxanthine nucleosides with RNA antiviral activity
-
Nair, V.; Ussery, M.A. New hypoxanthine nucleosides with RNA antiviral activity. Antiviral Res. 1992, 19, 173-178.
-
(1992)
Antiviral Res.
, vol.19
, pp. 173-178
-
-
Nair, V.1
Ussery, M.A.2
-
19
-
-
0034670164
-
Phosphorylation of the anti-HIV compound,(S,S)-isodideoxyadenosine by human recombinant deoxycytidine kinase
-
Pal, S.; Nair, V. Phosphorylation of the anti-HIV compound,(S,S)- isodideoxyadenosine by human recombinant deoxycytidine kinase. Biochem. Pharmacol. 2000, 60, 1505-1508.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 1505-1508
-
-
Pal, S.1
Nair, V.2
-
20
-
-
0037027990
-
A thymidine-phosphorylase stable analogue of BVDU with significant antiviral activity
-
Guenther, S.; Balzarini, J.; DeClercq, E.; Nair, V. A thymidine-phosphorylase stable analogue of BVDU with significant antiviral activity. J. Med. Chem. 2002, 45, 5426-5429.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5426-5429
-
-
Guenther, S.1
Balzarini, J.2
De Clercq, E.3
Nair, V.4
-
21
-
-
0017803457
-
Synthesis of carbocyclic aminonucleosides
-
Daluge, S.; Vince, R. Synthesis of carbocyclic aminonucleosides. J. Org. Chem., 1978, 43, 2311-2320.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 2311-2320
-
-
Daluge, S.1
Vince, R.2
-
22
-
-
0002122119
-
Synthesis of carbocyclic NAD containing a methylenebisphosphonate linkage for the investigation of ADP-ribosyl cyclase
-
Hutchinson, E.J.; Taylor, B.F.; Blackburn, G.M. Synthesis of carbocyclic NAD containing a methylenebisphosphonate linkage for the investigation of ADP-ribosyl cyclase. Chem.Commun. 1996, 24, 2765-2766.
-
(1996)
Chem.Commun.
, vol.24
, pp. 2765-2766
-
-
Hutchinson, E.J.1
Taylor, B.F.2
Blackburn, G.M.3
-
23
-
-
0034110180
-
An efficient, scalable synthesis of the HIV reverse transcriptase inhibitor Ziagen
-
Daluge, S.M.; Martin, M.T.; Sickle, B.R.; Livingston, D.A. An efficient, scalable synthesis of the HIV reverse transcriptase inhibitor Ziagen. Nucleosides, Nucleotides Nucleic Acids 2000, 19, 297-327.
-
(2000)
Nucleosides, Nucleotides Nucleic Acids
, vol.19
, pp. 297-327
-
-
Daluge, S.M.1
Martin, M.T.2
Sickle, B.R.3
Livingston, D.A.4
-
24
-
-
0029905691
-
Synthesis of novel bicyclic nucleosides related to griseolic acids
-
Pickering, L.; Nair, V. Synthesis of novel bicyclic nucleosides related to griseolic acids. Nucleosides Nucleotides 1996, 15, 1751-1769.
-
(1996)
Nucleosides Nucleotides
, vol.15
, pp. 1751-1769
-
-
Pickering, L.1
Nair, V.2
-
25
-
-
0019196854
-
Utility of purinyl radicals in the synthesis of base-modified nucleosides and alkylpurines: 6-Amino group replacement by hydrogen, chlorine, bromine, and iodine
-
Nair, V.; Richardson, S.G. Utility of purinyl radicals in the synthesis of base-modified nucleosides and alkylpurines: 6-amino group replacement by hydrogen, chlorine, bromine, and iodine. J. Org. Chem., 1980, 45, 3969-3974.
-
(1980)
J. Org. Chem.
, vol.45
, pp. 3969-3974
-
-
Nair, V.1
Richardson, S.G.2
-
26
-
-
0023233102
-
Novel approaches to functionalized nucleosides via palladium-catalyzed cross-coupling with organostannanes
-
Nair, V.; Turner, G.A.; Chamberlain, S.D. Novel approaches to functionalized nucleosides via palladium-catalyzed cross-coupling with organostannanes. J. Am Chem. Soc. 1987, 109, 7223-7224.
-
(1987)
J. Am Chem. Soc.
, vol.109
, pp. 7223-7224
-
-
Nair, V.1
Turner, G.A.2
Chamberlain, S.D.3
-
27
-
-
0037016581
-
Synthesis stability and conformation of the formamidopyrimidine G DNA lesion
-
Burgdorf, L.T.; Carell, T. Synthesis, stability and conformation of the formamidopyrimidine G DNA lesion. Chem. Eur. J., 2002, 8, 293-301.
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 293-301
-
-
Burgdorf, L.T.1
Carell, T.2
-
29
-
-
0026069463
-
Synthetic approaches to new doubly modified nucleosides: Congeners of cordycepin and related 2-deoxyadenosine
-
Purdy, D.F.; Nair, V. Synthetic approaches to new doubly modified nucleosides: congeners of cordycepin and related 2-deoxyadenosine. Tetrahedron 1991, 47, 365-382.
-
(1991)
Tetrahedron
, vol.47
, pp. 365-382
-
-
Purdy, D.F.1
Nair, V.2
|