-
1
-
-
0025866175
-
S-Adenosyl-L-homocysteine Hydrolase as a Target for Antiviral Chemotherapy
-
Wolfe, M. S.; Borchardt, R. T. S-Adenosyl-L-homocysteine Hydrolase as a Target for Antiviral Chemotherapy. J. Med. Chem. 1991, 34, 1521-1530.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1521-1530
-
-
Wolfe, M.S.1
Borchardt, R.T.2
-
2
-
-
0023264391
-
Priming of Influenza mRNA Transcription is Inhibited in CHO Cells Treated with the Methylation Inhibitor Neplanocin A
-
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
-
3
-
-
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
-
Keller, B. T.; Borchardt, R. T. Metabolism and Mechanism of Action of Neplanocin A - A Potent Inhibitor of S-Adenosylhomocysteine Hydrolase. In Biological Methylation and Drug Design; Borchardt, R. T., Creveling, C. R., Ueland, P. M., Eds.; Humana Press: Clifton, NJ, 1986; pp 385-396.
-
(1986)
Biological Methylation and Drug Design
, pp. 385-396
-
-
Keller, B.T.1
Borchardt, R.T.2
-
4
-
-
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
-
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
-
5
-
-
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
-
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
-
6
-
-
0024344550
-
Relationship between Intracellular Concentration of S-Adenosylhomocysteine and Inhibition of Vaccinia Virus Replication and Inhibition of Murine L- 29 Cell Growth
-
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- 29 Cell Growth. Antimicrob. Agents Chemother. 1989, 33, 828-834.
-
(1989)
Antimicrob. Agents Chemother.
, vol.33
, pp. 828-834
-
-
Hasobe, M.1
McKee, J.G.2
Borchardt, R.T.3
-
7
-
-
0025147766
-
Influence of S-Adenosylhomocysteine Hydrolase Inhibitors on S- Adenosylhomocysteine and S-Adenosylmethione Pool Levels in L929 Cells
-
Cools, M.; De Clercq, E. Influence of S-Adenosylhomocysteine Hydrolase Inhibitors on S- Adenosylhomocysteine and S-Adenosylmethione 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
-
8
-
-
0346791564
-
Inhibition of Ebola Virus by S- Adenosylhomocysteine Hydrolase Inhibitors
-
Abstracts of the Eighth International Conference on Antiviral Research, Santa Fe, NM
-
Hugging, 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.
-
-
Hugging, J.W.1
Zhang, Z.X.2
Davis, K.3
Coulombe, R.A.4
-
9
-
-
0026739034
-
Rational Approaches to the Design of Antiviral Agents Based on S-Adenosyl-L-homocysteine Hydrolase as a Molecular Target
-
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
-
10
-
-
0027460256
-
Adenosine 5′-Carboxaldehyde: A Potent Inhibitor of S-Adenosyl-L-homocysteine Hydrolase
-
Liu, S.; Wnuk, S. F.; Yuan, C.; Robins, M. J.; Borchardt, R. T. Adenosine 5′-Carboxaldehyde: a Potent Inhibitor of S-Adenosyl-L-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
-
11
-
-
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.; Boelin, T.; 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
Boelin, T.6
Mehdi, S.7
Sunkara, P.S.8
Bey, P.9
-
12
-
-
0024988949
-
The Mechanism of Inhibition of S-Adenosyl-L-homocysteine Hydrolase by Fluorine-containing Adenosine Analogs
-
Mehdi, S.; Jarvi, E. T.; Koehl, J. R.; McCarthy, J. R.; Bey, P. The Mechanism of Inhibition of S-Adenosyl-L-homocysteine Hydrolase by Fluorine-containing Adenosine Analogs. J. Enzyme Inhib. 1990, 4, 1-13.
-
(1990)
J. Enzyme Inhib.
, vol.4
, pp. 1-13
-
-
Mehdi, S.1
Jarvi, E.T.2
Koehl, J.R.3
McCarthy, J.R.4
Bey, P.5
-
13
-
-
0027209984
-
Mechanism of Inactivation of S-Adenosyl-L- homocysteine Hydrolase by (Z)-4′, 5′-Didehydro-5′-deoxy-5′-fluoroadenosine
-
Yuan, C.; Yeh, J.; Liu, S.; Borchardt, R. T. Mechanism of Inactivation of S-Adenosyl-L- homocysteine 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.1
Yeh, J.2
Liu, S.3
Borchardt, R.T.4
-
14
-
-
0015087735
-
Inhibition of Guanine Metabolism of Mammalian Tumor Cell by the Carbocyclic Analogue of Adenosine
-
Hill, D.; Straight, S.; Allan, P. W.; Bennett, L. L. J. Inhibition of Guanine Metabolism of Mammalian Tumor Cell by the Carbocyclic Analogue of Adenosine. Mol. Pharmacol. 1971, 7, 375-380.
-
(1971)
Mol. Pharmacol.
, vol.7
, pp. 375-380
-
-
Hill, D.1
Straight, S.2
Allan, P.W.3
Bennett, L.L.J.4
-
15
-
-
0019508989
-
Adenosine Analogues as Substrates and Inhibitors of S-Adenosylhomocysteine Hydrolase
-
Guranowski, A.; Montgomery, J. A.; Cantoni, G. L.; Chiang, P. K. Adenosine Analogues as Substrates and Inhibitors of S-Adenosylhomocysteine Hydrolase. Biochemistry 1981, 20, 110-115.
-
(1981)
Biochemistry
, vol.20
, pp. 110-115
-
-
Guranowski, A.1
Montgomery, J.A.2
Cantoni, G.L.3
Chiang, P.K.4
-
16
-
-
0026685862
-
Synthesis and Evaluation of 4′,5′- Dehydro-5′-fluoroaristeromycins as S-Adenosyl-L-homocysteine (AdoHcy) Hydrolase Inhibitors
-
Liu, S.; Wolfe, M. S.; Yuan, C.; Ali, S. M.; Borchardt, R. T. Synthesis and Evaluation of 4′,5′- Dehydro-5′-fluoroaristeromycins as S-Adenosyl-L-homocysteine (AdoHcy) Hydrolase Inhibitors. Bioorg. Med. Chem. Lett. 1992, 2, 1741-1744.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 1741-1744
-
-
Liu, S.1
Wolfe, M.S.2
Yuan, C.3
Ali, S.M.4
Borchardt, R.T.5
-
17
-
-
0023628495
-
Synthesis of Analogues of Neplanocin A: Utilization of Optically Active Dihydroxycyclopentenones Derived from Carbohydrates
-
Borcherding, D. R.; Scholtz, S. A.; Borchardt, R. T. Synthesis of Analogues of Neplanocin A: Utilization of Optically Active Dihydroxycyclopentenones Derived from Carbohydrates. J. Org. Chem. 1987, 52, 5457-5461.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 5457-5461
-
-
Borcherding, D.R.1
Scholtz, S.A.2
Borchardt, R.T.3
-
18
-
-
0026734169
-
4′-Modified Analogues of Aristeromycin and Neplanocin A: Synthesis and Inhibitory Activity toward S-Adenosyl-l-homocysteine Hydrolase
-
Wolfe, M. S.; Lee, Y.; Bartlett, W. J.; Borcherding, D. R.; Borchardt, R. T. 4′-Modified Analogues of Aristeromycin and Neplanocin A: Synthesis and Inhibitory Activity toward S-Adenosyl-l-homocysteine Hydrolase. J. Med. Chem. 1992, 35, 1782-1791.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1782-1791
-
-
Wolfe, M.S.1
Lee, Y.2
Bartlett, W.J.3
Borcherding, D.R.4
Borchardt, R.T.5
-
19
-
-
73649151319
-
Esters of Methanesulfonic Acid as Irreversible Inhibitors of Acetylcholinesterase
-
Kitz, K.; Wilson, Z. B. Esters of Methanesulfonic Acid as Irreversible Inhibitors of Acetylcholinesterase. J. Biol. Chem. 1962, 237, 3245-3249.
-
(1962)
J. Biol. Chem.
, vol.237
, pp. 3245-3249
-
-
Kitz, K.1
Wilson, Z.B.2
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