-
1
-
-
0343325793
-
Disulfiram and diethyldithiocarbamate as enzyme inhibitors
-
Gessner, P. K., Gessner, T., Eds.; Chapman and Hall: London
-
Gessner, P. K.; Gessner, T. Disulfiram and diethyldithiocarbamate as enzyme inhibitors. In Disulfiram and its Metabolite Diethyldithiacarbamate; Gessner, P. K., Gessner, T., Eds.; Chapman and Hall: London, 1962; pp 167-203.
-
(1962)
Disulfiram and Its Metabolite Diethyldithiacarbamate
, pp. 167-203
-
-
Gessner, P.K.1
Gessner, T.2
-
2
-
-
0017354995
-
The disulfiram-ethanol reaction
-
Kitson, T. M. The disulfiram-ethanol reaction. J. Stud. Alc. 1977, 38, 96-113.
-
(1977)
J. Stud. Alc.
, vol.38
, pp. 96-113
-
-
Kitson, T.M.1
-
3
-
-
0019812327
-
A review of the clinical use of disulfiram and calcium carbimide in alcoholism treatment
-
Peachey, J. E. A review of the clinical use of disulfiram and calcium carbimide in alcoholism treatment. J. Clin. Psychopharmacol. 1981, 1, 368-375.
-
(1981)
J. Clin. Psychopharmacol.
, vol.1
, pp. 368-375
-
-
Peachey, J.E.1
-
4
-
-
0018855449
-
Calcium carbide-ethanol interaction
-
Brien, J. F.; Peachey, J. E.; Loomis, C. W. Calcium carbide-ethanol interaction. Clin, Pharmacol. 1980, 27, 426-433.
-
(1980)
Clin, Pharmacol.
, vol.27
, pp. 426-433
-
-
Brien, J.F.1
Peachey, J.E.2
Loomis, C.W.3
-
5
-
-
0026556655
-
In vitro and in vivo inhibition of rat liver aldehyde dehydrogenase by S-methyl-N,N-diethylthiocarbamate sulfoxide, a new metabolite of diaulfiram
-
Hart, B. W.; Faiman, M. D. In vitro and in vivo inhibition of rat liver aldehyde dehydrogenase by S-methyl-N,N-diethylthiocarbamate sulfoxide, a new metabolite of diaulfiram. Biochem. Pharmacol. 1992, 43, 403-406.
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 403-406
-
-
Hart, B.W.1
Faiman, M.D.2
-
6
-
-
0025200713
-
Evidence for nitroxyl in the catalase-mediated bioactivation of the alcohol deterrent agent, cyanamide
-
Nagasawa, H. T.; DeMaster, E. G.; Redfern, B.; Shirota, F. N.; Goon, D. J. W. Evidence for nitroxyl in the catalase-mediated bioactivation of the alcohol deterrent agent, cyanamide. J. Med. Chem. 1990, 33, 3120-3122.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 3120-3122
-
-
Nagasawa, H.T.1
DeMaster, E.G.2
Redfern, B.3
Shirota, F.N.4
Goon, D.J.W.5
-
7
-
-
0028070184
-
Identification of novel glutathione conjugates of disulfiram and diethyldithiolcarbamate in rat bile by liquid chromatography-tandem mass spectrometry. Evidence for metabolic activation of disulfiram in vivo
-
Jin, L.; Davis, M. R.; Hu, P.; Baille, T. A. Identification of novel glutathione conjugates of disulfiram and diethyldithiolcarbamate in rat bile by liquid chromatography-tandem mass spectrometry. Evidence for metabolic activation of disulfiram in vivo. Chem. Res. Toxicol. 1994, 7, 526-533.
-
(1994)
Chem. Res. Toxicol.
, vol.7
, pp. 526-533
-
-
Jin, L.1
Davis, M.R.2
Hu, P.3
Baille, T.A.4
-
8
-
-
0032554614
-
The reaction between S-nitrosothiols and thiols: Generation of nitroxyl and subsequent chemistry
-
Wong, P. S.; Hyun J.; Fukuto, J. M.; Shirota, F. N.; DeMaster, E. G.; Shoeman, D. W.; Nagasawa, H. T. The reaction between S-nitrosothiols and thiols: generation of nitroxyl and subsequent chemistry. Biochemistry 1998, 37, 5363-5371.
-
(1998)
Biochemistry
, vol.37
, pp. 5363-5371
-
-
Wong, P.S.1
Hyun, J.2
Fukuto, J.M.3
Shirota, F.N.4
DeMaster, E.G.5
Shoeman, D.W.6
Nagasawa, H.T.7
-
9
-
-
0010299225
-
Trapping of nitroxyl (HNO), generated in vitro by sulfhydryl reagents
-
Shoeman, D. W.; Nagasawa, H. T.; DeMaster, E. G. Trapping of nitroxyl (HNO), generated in vitro by sulfhydryl reagents. FASEB J. 1996, A177.
-
(1996)
FASEB J.
-
-
Shoeman, D.W.1
Nagasawa, H.T.2
DeMaster, E.G.3
-
10
-
-
0032525919
-
Mechanism of inhibition of aldehyde dehydrogenase by nitroxyl, the active metabolite of the alcohol deterrent agent cyanamide
-
DeMaster, E. G.; Redfern, B.; Nagasawa, H. T. Mechanism of inhibition of aldehyde dehydrogenase by nitroxyl, the active metabolite of the alcohol deterrent agent cyanamide. Biochem. Pharmacol. 1998, 55, 2007-2015.
-
(1998)
Biochem. Pharmacol.
, vol.55
, pp. 2007-2015
-
-
DeMaster, E.G.1
Redfern, B.2
Nagasawa, H.T.3
-
11
-
-
0029061283
-
Carbethoxylating agents as inhibitors of aldehyde dehydrogenase
-
Nagasawa, H. T.; DeMaster, E. G.; Goon, D. J. W.; Kawle, S. P.; Shirota, F. N. Carbethoxylating agents as inhibitors of aldehyde dehydrogenase. J. Med. Chem. 1995, 38, 1872-1876.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1872-1876
-
-
Nagasawa, H.T.1
DeMaster, E.G.2
Goon, D.J.W.3
Kawle, S.P.4
Shirota, F.N.5
-
12
-
-
0025909284
-
Molecular cloning of the mitochondrial aldehyde dehydrogenase gene of Saccharomyces cerevisiae by genetic complementation
-
Saigal D.; Cunningham, S. J.; Farres, J.; Weiner, H. Molecular cloning of the mitochondrial aldehyde dehydrogenase gene of Saccharomyces cerevisiae by genetic complementation. J. Bacteriol. 1991, 173, 3199-3208.
-
(1991)
J. Bacteriol.
, vol.173
, pp. 3199-3208
-
-
Saigal, D.1
Cunningham, S.J.2
Farres, J.3
Weiner, H.4
-
13
-
-
0026616787
-
1-hydroxylated derivatives of chlorpropamide and its analogues as inhibitors of aldehyde dehydrogenase in vivo
-
1-Hydroxylated derivatives of chlorpropamide and its analogues as inhibitors of aldehyde dehydrogenase in vivo. J. Med. Chem. 1992, 35, 3641-3647.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3641-3647
-
-
Lee, M.J.C.1
Elberling, J.A.2
Nagasawa, H.T.3
-
14
-
-
0344834733
-
-
note
-
For example, the N,O-bis(ethoxycarbonyl) derivative of 4-chlorobenzenesulfohydroxamic acid is much more readily hydrolyzed by human plasma than by porcine liver esterase (M. J. C. Lee and H. T. Nagasawa, unpublished).
-
-
-
-
15
-
-
0005729782
-
Synthesis of p-nitrophenyl esters of substituted carbamic acids
-
Nesynov, R. P.; Pelkis, P. S. Synthesis of p-nitrophenyl esters of substituted carbamic acids. Obshch. Khim. 1964, 34, 3467-3469.
-
(1964)
Obshch. Khim.
, vol.34
, pp. 3467-3469
-
-
Nesynov, R.P.1
Pelkis, P.S.2
-
16
-
-
0021983716
-
Catalase mediated conversion of cyanamide to an inhibitor of aldehyde dehydrogenase
-
DeMaster, E. G.; Shirota, F. N.; Nagasawa, H. T. Catalase mediated conversion of cyanamide to an inhibitor of aldehyde dehydrogenase. Alcohol 1985, 2, 117-121.
-
(1985)
Alcohol
, vol.2
, pp. 117-121
-
-
DeMaster, E.G.1
Shirota, F.N.2
Nagasawa, H.T.3
-
17
-
-
0019214799
-
Metabolic depropargylation and its relationship to aldehyde dehydrogenase inhibition in vivo
-
Shirota, F. N.; DeMaster, E. G.; Elberling, J. A.; Nagasawa, H. T. Metabolic depropargylation and its relationship to aldehyde dehydrogenase inhibition in vivo. J. Med. Chem. 1980, 23, 669-673.
-
(1980)
J. Med. Chem.
, vol.23
, pp. 669-673
-
-
Shirota, F.N.1
DeMaster, E.G.2
Elberling, J.A.3
Nagasawa, H.T.4
-
18
-
-
0344403176
-
-
note
-
For example, N,N-diethylcarbamoyl chloride is considerably less reactive than ethyl chloroformate.
-
-
-
-
19
-
-
0344403177
-
-
note
-
We also addressed the possibility that the positions of the ethoxycarbonyl and diethylcarbamoyl groups might be reversed as in 1f. This is theoretically possible if 7 underwent an O-to-N acyl migration during the carbethoxylation step. However, 1d, prepared unambiguously by carbethoxylation of 6 followed by benzenesulfonylation of the resulting product (structure not shown), had physiochemical properties which were indistinguishable from those of Id prepared via Scheme 2 (see Supporting Information). These data also exclude another possible isomeric structure for 1d, viz., 1g. (equation presented)
-
-
-
-
21
-
-
0028935543
-
m mitochondrial aldehyde dehydrogenase
-
m mitochondrial aldehyde dehydrogenase. Biochem. Pharmacol. 1995, 49, 693-700.
-
(1995)
Biochem. Pharmacol.
, vol.49
, pp. 693-700
-
-
Mays, D.C.1
Nelson, A.N.2
Fauq, A.H.3
Shriver, Z.H.4
Veverka, K.A.5
Naylor, S.6
Lipsky, J.J.7
-
22
-
-
0031852127
-
Prodrugs of nitroxyl and nitrosobenzene as cascade latentiated inhibitors of aldehyde dehydrogenase
-
Conway, T. T.; DeMaster, E. G.; Lee, M. J. C.; Nagasawa, H. T. Prodrugs of nitroxyl and nitrosobenzene as cascade latentiated inhibitors of aldehyde dehydrogenase. J. Med. Chem. 1998, 41, 2903-2909.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2903-2909
-
-
Conway, T.T.1
DeMaster, E.G.2
Lee, M.J.C.3
Nagasawa, H.T.4
-
23
-
-
0029891676
-
Nitrosyl cyanide, a putative metabolic oxidation product of the alcohol-deterrent agent cyanamide
-
Shirota, F. N.; Goon, D. J. W.; DeMaster, E. G.; Nagasawa, H. T. Nitrosyl cyanide, a putative metabolic oxidation product of the alcohol-deterrent agent cyanamide. Biochem. Pharmacol. 1996, 52, 141-147.
-
(1996)
Biochem. Pharmacol.
, vol.52
, pp. 141-147
-
-
Shirota, F.N.1
Goon, D.J.W.2
DeMaster, E.G.3
Nagasawa, H.T.4
-
24
-
-
0347268608
-
Curtius and Lessen rearrangements. I. The benzenesulfonyl system
-
Lwowski, W.; Scheiffele, E. Curtius and Lessen Rearrangements. I. The benzenesulfonyl system. J. Am. Chem. Soc. 1966, 87, 4659-4365.
-
(1966)
J. Am. Chem. Soc.
, vol.87
, pp. 4659-14365
-
-
Lwowski, W.1
Scheiffele, E.2
-
25
-
-
0022445756
-
Acyl, N-protected a-aminoacyl, and peptidyl derivatives as prodrug forms of the alcohol deterrent agent, cyanamide
-
Kwon, C.-H.; Nagasawa, H. T.; DeMaster, E. G.; Shirota, F. N. Acyl, N-protected a-aminoacyl, and peptidyl derivatives as prodrug forms of the alcohol deterrent agent, cyanamide. J. Med. Chem. 1986, 29, 1922-1929.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1922-1929
-
-
Kwon, C.-H.1
Nagasawa, H.T.2
DeMaster, E.G.3
Shirota, F.N.4
|