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    The effect of insulinomimetic agents on protein degradation in H35 hepatoma cells
    Molecular and Cellular Biochemistry (1986)
    Birgit A. HelmJ. Martyn Gunn
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    37
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    10
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    Keywords:
    Proteolysis
    Protein Degradation
    Oxidizing agent
    Mechanism of Action
    Topics:
    Exercise and Physiological Responses
    Adipose Tissue and Metabolism
    Muscle metabolism and nutrition
    Fluorimetric kinetic method for determination of phenylhydrazine based on the inhibitory effect
    Analytical Laboratory (2004)
    Suling Feng
    A simple and sensitive fluorimetric method for determination of phenylhydrazine was described. This method was based on the inhibitory effect of phenylhydrazine on the reaction of pyronine Y with nitrite in sulfuric acid medium. The detection limit for phenylhydrazine was 7.2 ng/mL, the linear range of the determination was 8.0～60 ng/mL. The method was used to determine phenylhydrazine in water samples with satisfactory results.
    Linear range
    Citations (0)
    Intracellular proteolysis: Signals of selective protein degradation
    Russian Journal of Bioorganic Chemistry (2000)
    Natalie N StarkovaEkaterina P. KorolevaТ. В. Ротанова
    Proteolysis
    Degradation
    Protein Degradation
    Citations (3)
    Studies in spiro heterocycles. Part 4(1): Investigation of the reactions of fluorinated 3-aroylmethylene-indol-2-ones with hydrazine and phenylhydrazine and synthesis of spiro [indole-3,3'-pyrazol]-2-ones.
    PubMed (1985)
    Joshi KcR. K. JainS. GARG
    Reactions of various 3-aroylmethylene-indol-2-ones with hydrazine and phenylhydrazine under exactly similar conditions have been carried out. The reaction with phenylhydrazine has not been investigated earlier. It was found that although the reaction with hydrazine hydrate afforded a spiro derivative viz., spiro[3H-indole-3,3'-(3H)pyrazol]-2(1H)-one, that with phenylhydrazine yielded simply a hydrazone derivative. Representative spiro compounds have been screened for antifertility activity but none was found active at a dose of 10 mg/kg in adult female rats.
    Hydrazine (antidepressant)
    Hydrazone
    Derivative (finance)
    Citations (1)
    Syntheses based on norfluorocurarine. 6. Reaction with phenylhydrazine
    Chemistry of Natural Compounds (2012)
    Б. ТашходжаевM.M. MirzaevaP. Kh. Yuldashev
    Citations (1)
    The Use of Nickel Peroxide as Oxidizing Agent of Phenylhydrazine for the Generation of Phenyl Radicals
    Bulletin of the Chemical Society of Japan (1971)
    Hiroyuki OhtaKatsumi Tokumaru
    Oxidizing agent
    Peroxide
    Citations (5)
    Proteolysis: anytime, any place, anywhere?
    Nature Cell Biology (2005)
    Jonathon PinesCatherine Lindon
    Proteolysis
    Protein Degradation
    Degradation
    Citations (75)
    Enzymatic synthesis of β-N-(γ-l(+)-glutamyl)phenylhydrazine with Escherichia coli γ-glutamyltranspeptidase
    Biotechnology Letters (2012)
    Hongjuan ZhangYueping ZhanJunjun ChangJunzhong LiuLisheng Xu
    Citations (19)
    The reaction between phenylhydrazine and ω‐chloroacetophenone. (The reaction between ω‐halogenoketones and phenylhydrazine, V)
    Recueil des Travaux Chimiques des Pays-Bas (1946)
    J. van Alphen
    Abstract The compound obtained by Hess, the condensation product of phenylhydrazine and ω‐chloroacetophenone has been investigated and its properties can be explained by assigning to it the constitution 1: 3‐diphenyl‐(1: 2‐diazacyclobutene‐2). The structure of the compound obtained by Scholtz from phenylhydrazine and ω‐chloroacetophenone, has been elucidated and proved to be the bis‐phenylhydrazone of diphenacyl.
    Citations (3)
    Proteasome inhibitor MG-132 enhances whole-body protein turnover in rat
    Biochemical and Biophysical Research Communications (2006)
    Milan HolečekTomáš MuthnýMiroslav KovaříkLuděk Šišpera
    Proteolysis
    Protein turnover
    Catabolism
    Protein Degradation
    Protein metabolism
    Citations (10)