The in vivo production of carbon disulfide from tetraethylthiuramdisulfide (antabuse)(R)
References (14)
- et al.
Biochim. Biophys. Acta
(1952) - et al.
Science
(1951) - et al.
Am. J. Med. Sci.
(1950) - et al.
Acta Chem. Scand.
(1949) - et al.
Scand. J. Clin. Invest.
(1951) J. Ind. Hyg. and Toxicol.
(1941)J. Ind. Hyg. and Toxicol.
(1940)
There are more references available in the full text version of this article.
Cited by (26)
Poly lactic-co-glycolic acid controlled delivery of disulfiram to target liver cancer stem-like cells
2017, Nanomedicine: Nanotechnology, Biology, and MedicineCitation Excerpt :The degradation of DS in the serum kinetically results from a covalent interaction of this drug with the free sulfhydryl of serum albumin. The half-life of DS pH 7.4 is 1-1.5 minutes.19,34,35,36,37 This may introduce the discrepancy between the anticancer activities in vitro, in vivo and in clinic (ClinicalTrials.gov: NCT00256230, NCT00742911, NCT01118741).
Cyclosporine, FK-506, rapamycin, and other immunomodulators
1996, Rheumatic Disease Clinics of North AmericaThe use of immunomodulators in early rheumatoid arthritis
1994, Seminars in Arthritis and RheumatismEffect of thiocarbonyl compounds on α-naphthylisothiocyanate-induced hepatotoxicity and the urinary excretion of [<sup>35</sup>S]α-naphthylisothiocyanate in the rat
1984, Toxicology and Applied PharmacologyMethyl diethyldithiocarbamate, a metabolite of disulfiram in man
1977, Life Sciences
- ★
Part of this material is from a thesis submitted to the Graduate School of Georgetown University, Washington, D.C., in partial fulfilment of the requirements for the Ph.D. degree.
Copyright © 1953 Published by Elsevier B.V.