-
1
-
-
0020284631
-
Pharmacological and Biochemical Aspects of S-Adenosylhomocysteine and S-Adenosylhomocysteine Hydrolase
-
Ueland, P. M. Pharmacological and Biochemical Aspects of S-Adenosylhomocysteine and S-Adenosylhomocysteine Hydrolase. Pharmacol. Rev. 1982, 34, 223-253.
-
(1982)
Pharmacol. Rev.
, vol.34
, pp. 223-253
-
-
Ueland, P.M.1
-
2
-
-
0023235758
-
S-Adenosylhomocysteine Hydrolase Inhibitors as Broad-Spectrum Antiviral Agents
-
(a) De Clercq, E. S-Adenosylhomocysteine Hydrolase Inhibitors as Broad-Spectrum Antiviral Agents. Biochem. Pharmacol. 1987, 36, 2567-2575.
-
(1987)
Biochem. Pharmacol.
, vol.36
, pp. 2567-2575
-
-
De Clercq, E.1
-
3
-
-
77956844792
-
Design and Synthesis of S-Adenosylhomocysteine Hydrolase Inhibitors as Broad-Spectrum Antiviral Agents
-
DeClercq, E., Ed.; JAI Press: Greenwich, CT
-
(b) Yuan, C.-S.; Liu, S.; Wnuk, S. F.; Robins, M. J.; Borchardt, R. T. Design and Synthesis of S-Adenosylhomocysteine Hydrolase Inhibitors as Broad-Spectrum Antiviral Agents. In Advances in Antiviral Drug Design; DeClercq, E., Ed.; JAI Press: Greenwich, CT, 1996; Vol. 2, pp 41-88.
-
(1996)
Advances in Antiviral Drug Design
, vol.2
, pp. 41-88
-
-
Yuan, C.-S.1
Liu, S.2
Wnuk, S.F.3
Robins, M.J.4
Borchardt, R.T.5
-
4
-
-
0025866175
-
S-Adenosyl-L-homocysteine Hydrolase as a Target for Antiviral Chemotherapy
-
(a) Wolfe, M. S.; Borchardt, R. T. S-Adenosyl-L-homocysteine Hydrolase as a Target for Antiviral Chemotherapy. J. Med. Chem. 1991, 34, 1521-1529.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1521-1529
-
-
Wolfe, M.S.1
Borchardt, R.T.2
-
5
-
-
0026739034
-
Rational Approaches to the Design of Antiviral Agents Based on S-Adenosyl-L-homocysteine Hydrolase as a Molecular Target
-
(b) Liu, S.; Wolfe, M. S.; Borchardt, R. T. Rational Approaches to the Design of Antiviral Agents Based on S-Adenosyl-L-homocysteine Hydrolase as a Molecular Target. Antiviral Res. 1992, 19, 247-265.
-
(1992)
Antiviral Res.
, vol.19
, pp. 247-265
-
-
Liu, S.1
Wolfe, M.S.2
Borchardt, R.T.3
-
6
-
-
0001315328
-
Metabolism and Mechanism of Action of Neplanocin A-A Potent Inhibitor of S-Adenosylhomocysteine Hydrolase
-
Borchardt, R. T., Creveling, C. R., Ueland, P. M., Eds.; Humana Press: Clifton, NJ
-
(a) Keller, B. T.; Borchardt, R. T. Metabolism and Mechanism of Action of Neplanocin A-A Potent Inhibitor of S-Adenosylhomocysteine Hydrolase. In Biological Methylatlon and Drug Design; Borchardt, R. T., Creveling, C. R., Ueland, P. M., Eds.; Humana Press: Clifton, NJ, 1986; pp 385-396.
-
(1986)
Biological Methylatlon and Drug Design
, pp. 385-396
-
-
Keller, B.T.1
Borchardt, R.T.2
-
7
-
-
0011880363
-
Inhibition of S-Adenosylmethionine-dependent Transmethylation as an Approach to the Development of Antiviral Agents
-
DeClercq, E., Walker, R. T., Eds.; Plenum: New York
-
(b) Keller, B. T.; Borchardt, R. T. Inhibition of S-Adenosylmethionine-dependent Transmethylation as an Approach to the Development of Antiviral Agents. In Antiviral Drug Development: A Multidisciplinary Approach; DeClercq, E., Walker, R. T., Eds.; Plenum: New York, 1988; pp 123-138.
-
(1988)
Antiviral Drug Development: A Multidisciplinary Approach
, pp. 123-138
-
-
Keller, B.T.1
Borchardt, R.T.2
-
8
-
-
0023264391
-
Priming of Influenza mRNA Transcription Is Inhibited in CHO Cells Treated with the Methylation Inhibitor, Neplanocin a
-
(c) Ransohoff, R. M.; Narayan, P.; Ayers, D. F.; Rottman, F. M.; Nilsen, T. W. Priming of Influenza mRNA Transcription Is Inhibited in CHO Cells Treated with the Methylation Inhibitor, Neplanocin A. Antiviral Res. 1987, 7, 317-327.
-
(1987)
Antiviral Res.
, vol.7
, pp. 317-327
-
-
Ransohoff, R.M.1
Narayan, P.2
Ayers, D.F.3
Rottman, F.M.4
Nilsen, T.W.5
-
9
-
-
0024344550
-
Relationship between Intracellular Concentration of S-Adenosylhomocysteine and Inhibition of Vaccinia Virus Replication and Inhibition of Murine L-929 Cell Growth
-
(a) Hasobe, M.; McKee, J. G.; Borchardt, R. T. Relationship between Intracellular Concentration of S-Adenosylhomocysteine and Inhibition of Vaccinia Virus Replication and Inhibition of Murine L-929 Cell Growth. Antimcrob. Agents Chemother. 1989, 33, 828-834.
-
(1989)
Antimcrob. Agents Chemother.
, vol.33
, pp. 828-834
-
-
Hasobe, M.1
McKee, J.G.2
Borchardt, R.T.3
-
10
-
-
0025147766
-
Influence of S-Adenosylhomocysteine Hydrolase Inhibitors on S-Adenosylhomocysteine and S-Adenosylmethionine Pool Levels in L929 Cells
-
(b) Cools, M.; De Clercq, E. Influence of S-Adenosylhomocysteine Hydrolase Inhibitors on S-Adenosylhomocysteine and S-Adenosylmethionine Pool Levels in L929 Cells. Biochem. Pharmacol. 1990, 40, 2259-2264.
-
(1990)
Biochem. Pharmacol.
, vol.40
, pp. 2259-2264
-
-
Cools, M.1
De Clercq, E.2
-
11
-
-
0024593335
-
Correlation between the Antiviral Activity of Acyclic and Carbocyclic Adenosine Analogues in Murine L929 Cells and Their Inhibitory Effect on L929 Cell S-Adenosylhomocysteine Hydrolase
-
(a) Cools, M.; De Clercq, E. Correlation Between the Antiviral Activity of Acyclic and Carbocyclic Adenosine Analogues in Murine L929 Cells and Their Inhibitory Effect on L929 Cell S-Adenosylhomocysteine Hydrolase. Biochem. Pharmacol. 1989, 38, 1061-1067.
-
(1989)
Biochem. Pharmacol.
, vol.38
, pp. 1061-1067
-
-
Cools, M.1
De Clercq, E.2
-
12
-
-
0028104514
-
Nucleic Acid Related Compounds. 84. Synthesis of 6′(E and Z)-Halohomovinyl Derivatives of Adenosine, Inactivation of S-Adenosyl-L-homocysteine Hydrolase, and Correlation of Anticancer and Antiviral Potencies with Enzyme Inhibition
-
(b) Wnuk, S. F.; Yuan, C.-S.; Borchardt, R. T.; Balzarini, J.; De Clercq, E.; Robins, M. J. Nucleic Acid Related Compounds. 84. Synthesis of 6′(E and Z)-Halohomovinyl Derivatives of Adenosine, Inactivation of S-Adenosyl-L-homocysteine Hydrolase, and Correlation of Anticancer and Antiviral Potencies with Enzyme Inhibition. J. Med. Chem. 1994, 37, 3579-3587.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3579-3587
-
-
Wnuk, S.F.1
Yuan, C.-S.2
Borchardt, R.T.3
Balzarini, J.4
De Clercq, E.5
Robins, M.J.6
-
13
-
-
0346791564
-
Inhibition of Ebola Virus by S-Adenosylhomocysteine Hydrolase Inhibitors
-
Abstracts of the Eighth International Conference on Antiviral Research, Santa Fe, NM
-
Huggins, J. W.; Zhang, Z. X.; Davis, K.; Coulombe, R. A. Inhibition of Ebola Virus by S-Adenosylhomocysteine Hydrolase Inhibitors. Abstracts of the Eighth International Conference on Antiviral Research, Santa Fe, NM; Antiviral Res. 1995, A301.
-
(1995)
Antiviral Res.
-
-
Huggins, J.W.1
Zhang, Z.X.2
Davis, K.3
Coulombe, R.A.4
-
14
-
-
0027460256
-
Adenosine-5′-carboxaldehyde: A Potent Inhibitor of S-AdenosylL-homocysteine Hydrolase
-
Liu, S.; Wnuk, S. F.; Yuan, C.; Robins, M. J.; Borchardt, R. T. Adenosine-5′-carboxaldehyde: A Potent Inhibitor of S-AdenosylL-homocysteine Hydrolase. J. Med. Chem. 1993, 36, 883-887.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 883-887
-
-
Liu, S.1
Wnuk, S.F.2
Yuan, C.3
Robins, M.J.4
Borchardt, R.T.5
-
15
-
-
0024546618
-
4′,5′-Unsaturated 5′-Fluoroadenosine Nucleosides: Potent Mechanism-Based Inhibitors of S-Adenosyl-L-homocysteine Hydrolase
-
McCarthy, J. R.; Jarvi, E. T.; Matthews, D. P.; Edwards, M. L.; Prakash, N. J.; Bowlin, T. L.; Mehdi, S.; Sunkara, P. S.; Bey, P. 4′,5′-Unsaturated 5′-Fluoroadenosine Nucleosides: Potent Mechanism-Based Inhibitors of S-Adenosyl-L-homocysteine Hydrolase. J. Am. Chem. Soc. 1989, 111, 1127-1128.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 1127-1128
-
-
McCarthy, J.R.1
Jarvi, E.T.2
Matthews, D.P.3
Edwards, M.L.4
Prakash, N.J.5
Bowlin, T.L.6
Mehdi, S.7
Sunkara, P.S.8
Bey, P.9
-
16
-
-
0027209984
-
Mechanism of Inactivation of S-Adenosylhomocysteine Hydrolase by (Z)-4′,5′-Didehydro-5′-Deoxy-5′-Fluoroadenosine
-
Yuan, C.-S.; Yeh, J.; Liu, S.; Borchardt, R. T. Mechanism of Inactivation of S-Adenosylhomocysteine Hydrolase by (Z)-4′,5′-Didehydro-5′-Deoxy-5′-Fluoroadenosine. J. Biol. Chem. 1993, 268, 17030-17037.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 17030-17037
-
-
Yuan, C.-S.1
Yeh, J.2
Liu, S.3
Borchardt, R.T.4
-
17
-
-
0023811791
-
Fluorination at C5′ of Nucleosides. Synthesis of the New Class of 5′-Fluoro-5′-S-Aryl (Alkyl) Thionucleosides from Adenosine
-
(a) Robins, M. J.; Wnuk, S. F. Fluorination at C5′ of Nucleosides. Synthesis of the New Class of 5′-Fluoro-5′-S-Aryl (Alkyl) Thionucleosides from Adenosine. Tetrahedron Lett. 1988, 29, 5729-5732.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 5729-5732
-
-
Robins, M.J.1
Wnuk, S.F.2
-
18
-
-
6844235558
-
Adenosine-Derived 5′-α-Halo Thioether, Sulfoxide, Sulfone, and (5′-Halo)methylene Analogues. Inhibition of S-Adenosyl-L-Homocysteine Hydrolase
-
Chu, C. K., Baker, D. C., Eds.; Plenum Press: New York
-
(b) Robins, M. J.; Wnuk, S. F.; Mullah, K. B.; Dalley, N. K.; Borchardt, R. T.; Lee, Y.; Yuan, C.-S. Adenosine-Derived 5′-α-Halo Thioether, Sulfoxide, Sulfone, and (5′-Halo)methylene Analogues. Inhibition of S-Adenosyl-L-Homocysteine Hydrolase. In Nucleosides and Nucleotides as Antitumor and Antiviral Agents; Chu, C. K., Baker, D. C., Eds.; Plenum Press: New York, 1993; pp 115-126.
-
(1993)
Nucleosides and Nucleotides As Antitumor and Antiviral Agents
, pp. 115-126
-
-
Robins, M.J.1
Wnuk, S.F.2
Mullah, K.B.3
Dalley, N.K.4
Borchardt, R.T.5
Lee, Y.6
Yuan, C.-S.7
-
19
-
-
0028344397
-
Nucleic Acid Related Compounds. 80. Synthesis of 5′-S-(Alkyl and aryl)-5′-fluoro-5′-thioadenosines with Xenon Difluoride or (Diethylamido)sulfur Trifluoride, Hydrolysis in Aqueous Buffer, and Inhibition of S-Adenosyl-L-homocysteine Hydrolase by Derived "Adenosine 5′-Aldehyde" Species
-
(c) Robins, M. J.; Wnuk, S. F.; Mullah, K. B.; Dalley, N. K.; Yuan, C.-S.; Lee, Y.; Borchardt, R. T. Nucleic Acid Related Compounds. 80. Synthesis of 5′-S-(Alkyl and aryl)-5′-fluoro-5′-thioadenosines with Xenon Difluoride or (Diethylamido)sulfur Trifluoride, Hydrolysis in Aqueous Buffer, and Inhibition of S-Adenosyl-L-homocysteine Hydrolase by Derived "Adenosine 5′-Aldehyde" Species. J. Org. Chem. 1994, 59, 544-555.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 544-555
-
-
Robins, M.J.1
Wnuk, S.F.2
Mullah, K.B.3
Dalley, N.K.4
Yuan, C.-S.5
Lee, Y.6
Borchardt, R.T.7
-
20
-
-
0028268586
-
Mechanism of Inactivation of S-Adenosylhomocysteine Hydrolase by (E)-5′,6′-Didehydro-6′-Deoxy-6′-Halohomoadenosines
-
Yuan, C.-S.; Liu, S.; Wnuk, S. F.; Robins, M. J.; Borchardt, R. T. Mechanism of Inactivation of S-Adenosylhomocysteine Hydrolase by (E)-5′,6′-Didehydro-6′-Deoxy-6′-Halohomoadenosines. Biochemistry 1994, 33, 3758-3765.
-
(1994)
Biochemistry
, vol.33
, pp. 3758-3765
-
-
Yuan, C.-S.1
Liu, S.2
Wnuk, S.F.3
Robins, M.J.4
Borchardt, R.T.5
-
21
-
-
0028079891
-
(E)-5′,6′-Didehydro-6′-deoxy-6′- fluorohomoadenosine: A Substrate That Measures the Hydrolytic Activity of S-Adenosylhomocysteine Hydrolase
-
Yuan, C.-S.; Wnuk, S. F.; Liu, S.; Robins, M. J.; Borchardt, R. T. (E)-5′,6′-Didehydro-6′-deoxy-6′-fluorohomoadenosine: A Substrate That Measures the Hydrolytic Activity of S-Adenosylhomocysteine Hydrolase. Biochemistry 1994, 33, 12305-12311.
-
(1994)
Biochemistry
, vol.33
, pp. 12305-12311
-
-
Yuan, C.-S.1
Wnuk, S.F.2
Liu, S.3
Robins, M.J.4
Borchardt, R.T.5
-
22
-
-
0021818667
-
Inactivation of S-Adenosylhomocysteine Hydrolase by Nucleosides
-
Kim, I.-Y.; Zhang, C.-Y.; Cantoni, G. L.; Montgomery, J. A.; Chiang, P. K. Inactivation of S-Adenosylhomocysteine Hydrolase by Nucleosides. Biochim. Biophys. Acta 1985, 829, 150-155.
-
(1985)
Biochim. Biophys. Acta
, vol.829
, pp. 150-155
-
-
Kim, I.-Y.1
Zhang, C.-Y.2
Cantoni, G.L.3
Montgomery, J.A.4
Chiang, P.K.5
-
23
-
-
0025941439
-
9-(5′,6′-Dideoxy-β-D-ribo-hex-5′-ynofuranosyl) adenine, a Novel Irreversible Inhibitor of S-Adenosylhomocysteine Hydrolase
-
Parry, R. J.; Muscate, A.; Askonas, L. J. 9-(5′,6′-Dideoxy-β-D-ribo-hex-5′-ynofuranosyl)adenine, a Novel Irreversible Inhibitor of S-Adenosylhomocysteine Hydrolase. Biochemistry 1991, 30, 9988-9997.
-
(1991)
Biochemistry
, vol.30
, pp. 9988-9997
-
-
Parry, R.J.1
Muscate, A.2
Askonas, L.J.3
-
24
-
-
0017163329
-
Modification of the 5′ Position of Purine Nucleosides. 1. Synthesis and Biological Properties of Alkyl Adenosine-5′-carboxylates
-
Prasad, R. N.; Fung, A.; Tietje, K.; Stein, H. H.; Brondyk, H. D. Modification of the 5′ Position of Purine Nucleosides. 1. Synthesis and Biological Properties of Alkyl Adenosine-5′-carboxylates. J. Med. Chem. 1976, 19, 1180-1186.
-
(1976)
J. Med. Chem.
, vol.19
, pp. 1180-1186
-
-
Prasad, R.N.1
Fung, A.2
Tietje, K.3
Stein, H.H.4
Brondyk, H.D.5
-
25
-
-
0015464405
-
Nucleosid-5′-carbonsäureester als Modelle für die Konformationsanalyse von Nucleosiden und Nucleotiden. (Esters of Nucleoside-5′-carboxylic Acids as Model Compounds for Conformational Analysis of Nucleosides and Nucleotides.)
-
Fritz, H.-J.; Machat, R.; Schmidt, R. R. Nucleosid-5′-carbonsäureester als Modelle für die Konformationsanalyse von Nucleosiden und Nucleotiden. (Esters of Nucleoside-5′-carboxylic Acids as Model Compounds for Conformational Analysis of Nucleosides and Nucleotides.) Chem. Ber. 1972, 105, 642-649.
-
(1972)
Chem. Ber.
, vol.105
, pp. 642-649
-
-
Fritz, H.-J.1
Machat, R.2
Schmidt, R.R.3
-
26
-
-
0018832334
-
Modification of the 5′ Position of Purine Nucleosides. 2. Synthesis and Some Cardiovascular Properties of Adenosine-5′-(N-substituted)carboxamides
-
Prasad, R. N.; Bariana, D. S.; Fung, A.; Savic, M.; Tietje, K.; Stein, H. H.; Brondyk, H.; Egan, R. S. Modification of the 5′ Position of Purine Nucleosides. 2. Synthesis and Some Cardiovascular Properties of Adenosine-5′-(N-substituted)carboxamides. J. Med. Chem. 1980, 23, 313-319.
-
(1980)
J. Med. Chem.
, vol.23
, pp. 313-319
-
-
Prasad, R.N.1
Bariana, D.S.2
Fung, A.3
Savic, M.4
Tietje, K.5
Stein, H.H.6
Brondyk, H.7
Egan, R.S.8
-
27
-
-
0025296118
-
2 Receptor Ligands
-
2 Receptor Ligands. J. Med. Chem. 1990, 33, 1919-1924.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1919-1924
-
-
Hutchison, A.J.1
Williams, M.2
De Jesus, R.3
Yokoyama, R.4
Oei, H.H.5
Ghai, G.R.6
Webb, R.L.7
Zoganas, H.C.8
Stone, G.A.9
Jarvis, M.F.10
-
28
-
-
0026651404
-
Nucleosides and Nucleotides. 112. 2-(1-Hexyn-1-yl)adenosine-5′-uronamides: A New Entry of Selective A2 Adenosine Receptor Agonists with Potent Antihypertensive Activity
-
(b) Homma, H.; Watanabe, Y.; Abiru, T.; Murayama, T.; Nomura, Y.; Matsuda, A. Nucleosides and Nucleotides. 112. 2-(1-Hexyn-1-yl)adenosine-5′-uronamides: A New Entry of Selective A2 Adenosine Receptor Agonists with Potent Antihypertensive Activity. J. Med. Chem. 1992, 35, 2881-2890.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2881-2890
-
-
Homma, H.1
Watanabe, Y.2
Abiru, T.3
Murayama, T.4
Nomura, Y.5
Matsuda, A.6
-
29
-
-
0028218322
-
3-Selective Adenosine Agonists
-
3-Selective Adenosine Agonists. J. Med. Chem. 1994, 37, 636-646.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 636-646
-
-
Gallo-Rodriguez, C.1
Ji, X.-D.2
Melman, N.3
Siegman, B.D.4
Sanders, L.H.5
Orlina, J.6
Fischer, B.7
Pu, Q.8
Olah, M.E.9
Van Galen, P.J.M.10
Stiles, G.L.11
Jacobson, K.A.12
-
31
-
-
0026527978
-
Ruthenium Tetraoxide: A Mild Reagent for the Oxidation of 2′,3′-Ο-Isopropylidene Purine Nucleosides
-
(a) Singh, A. K.; Varma, R. S. Ruthenium Tetraoxide: A Mild Reagent for the Oxidation of 2′,3′-Ο-Isopropylidene Purine Nucleosides. Tetrahedron Lett. 1992, 33, 2307-2310.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 2307-2310
-
-
Singh, A.K.1
Varma, R.S.2
-
32
-
-
0026676681
-
Ruthenium Tetraoxide Catalyzed Oxidation of Nucleosides: A Facile Synthesis of 5′-Carboxylic Acid Derivatives
-
(b) Varma, R. S.; Hogan, M. E. Ruthenium Tetraoxide Catalyzed Oxidation of Nucleosides: A Facile Synthesis of 5′-Carboxylic Acid Derivatives. Tetrahedron Lett. 1992, 33, 7719-7720.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 7719-7720
-
-
Varma, R.S.1
Hogan, M.E.2
-
33
-
-
0014781245
-
Conversion of 2′,3′-Ο-Isopropylidene Adenosine into Its 5′,5′-Di-C-Methyl Derivative
-
Harper, P. J.; Hampton, A. Conversion of 2′,3′-Ο-Isopropylidene Adenosine into Its 5′,5′-Di-C-Methyl Derivative. J. Org. Chem. 1970, 35, 1688-1689.
-
(1970)
J. Org. Chem.
, vol.35
, pp. 1688-1689
-
-
Harper, P.J.1
Hampton, A.2
-
34
-
-
0024418257
-
Expression of Rat Liver S-Adenosylhomocysteinase cDNA in Escherichia coli and Mutagenesis at the Putative NAD Binding Site
-
Gomi, T.; Date, T.; Ogawa, H.; Fujioka, M.; Aksamit, R. R.; Backlund, P. S., Jr.; Contoni, G. L. Expression of Rat Liver S-Adenosylhomocysteinase cDNA in Escherichia coli and Mutagenesis at the Putative NAD Binding Site. J. Biol. Chem. 1989, 264, 16138-16142.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 16138-16142
-
-
Gomi, T.1
Date, T.2
Ogawa, H.3
Fujioka, M.4
Aksamit, R.R.5
Backlund Jr., P.S.6
Contoni, G.L.7
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