Literature DB >> 174008

[Lacrimators as acceptors for NADH].

K Wallenfels, W Ertel, A Höckendorf, J Rieser, K H Uberschär.   

Abstract

Lachrymators of varied structure are reduced either by hydrogen addition or halogen substitution using NADH model compounds as donors. Similar compounds without lachrymatory activity were reduced either very slowly or not at all. CS (o-Chlorobenzalmalonitril) is reduced by NADH, the reaction being catalyzed by an enzyme present in erythrocytes. Thus the lachrymatory action follows a general scheme for the activity of sensory transduction. This scheme consists of a reception in the nerve cell membrane and a fast or simultaneous chemical transformation in an enzymic reaction.

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Year:  1975        PMID: 174008     DOI: 10.1007/bf00600500

Source DB:  PubMed          Journal:  Naturwissenschaften        ISSN: 0028-1042


  13 in total

1.  The inhibition of thiol enzymes by lachrymators.

Authors:  J F Mackworth
Journal:  Biochem J       Date:  1948       Impact factor: 3.857

2.  Survey of chemical and related weapons of war.

Authors:  J B Neilands
Journal:  Naturwissenschaften       Date:  1973-04

3.  A new reaction of glutamate dehydrogenase: the enzyme-catalyzed formation of trinitrobenzene from TNBS in the presence of reduced coenzyme.

Authors:  D J Bates; B R Goldin; C Frieden
Journal:  Biochem Biophys Res Commun       Date:  1970-05-11       Impact factor: 3.575

4.  [Thin-layer chromatographic analysis of radioactively labelled insect pheromones. Metabolites of (3H)bombykol (author's transl)].

Authors:  G Kasang; N Weiss
Journal:  J Chromatogr       Date:  1974-05-22

5.  The absorption of ortho-chlorobenzylidenemalononitrile (CS) by the respiratory tract.

Authors:  L Leadbeater
Journal:  Toxicol Appl Pharmacol       Date:  1973-05       Impact factor: 4.219

6.  The presentation and management of individuals contaminated with solutions of dibenzoxazepine (CR).

Authors:  B Ballantyne; F W Beswick; D P Thomas
Journal:  Med Sci Law       Date:  1973-10       Impact factor: 1.266

7.  Reduction of pyridoxal phosphate (and analogs) by 1,4-dihydropyridine.

Authors:  S Shinkai; T C Bruice
Journal:  J Am Chem Soc       Date:  1972-11-15       Impact factor: 15.419

8.  Reactions of an indolenine salt as a possible model for dehydrogenase enzymes.

Authors:  K A Schellenberg; G W McLean
Journal:  J Am Chem Soc       Date:  1966-03-05       Impact factor: 15.419

9.  Reactions of dihydronicotinamides. I. Evidence for an intermediate in the reduction of trifluoroacetophenone by 1-substituted dihydronicotinamides.

Authors:  J J Steffens; D M Chipman
Journal:  J Am Chem Soc       Date:  1971-12       Impact factor: 15.419

10.  Benzylidenemalononitrile derivatives as substrates and inhibitors of a new NAD(P)H dehydrogenase of erythrocytes. Purification and crystallisation of two forms of the enzyme.

Authors:  K H Ueberschär; S Kille; G Laule; P Maurer; K Wallenfels
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1979-10
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