3,5-di-tert-butylcatechol

Known as: 3,5-di-t-butyl catechol 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2018
01219772018

Papers overview

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2014
2014
Three diamino, dihetero-phenol ligands were synthesized by sequential Mannich condensations. These ligands were combined with… (More)
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2009
2009
A novel bacterium capable of utilizing 2-sec-butylphenol as the sole carbon and energy source, Pseudomonas sp. strain MS-1, was… (More)
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2007
2007
Mononuclear CuL and Cu(2L) complexes, where L is propyl-thiazol-2-ylmethylene-amine, covalently immobilized onto SiO2, can… (More)
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2005
2005
In the present study, the effects of 3,5-di-t-butylcatechol (DTCAT) on ryanodine receptor Ca(2+) channel (RyRC) of skeletal… (More)
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2004
2004
A group of tyrosinase isoforms with isoelectric points between 4.9 and 5.2 was isolated from gill tissue of Portabella mushrooms… (More)
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2002
2002
[molecular structure: see text] p-tert-Butylcatechol is used as an antioxidant, stabilizer, and polymerization inhibitor for… (More)
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1999
1999
A latent isoform of Agaricus bisporus tyrosinase has been isolated and activated by benzyl alcohol, one of the major volatile… (More)
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1993
1993
Certain mono- and dihydroxybenzene derivatives are selectively cytotoxic for melanocytes in vivo, and can cause depigmentation of… (More)
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1985
1985
Intermediates of pheomelanin in tissue cultured B16 melanoma cells were analyzed by high performance liquid chromatography, and… (More)
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1977
1977
Pure ascorbate oxidase (L-ascorbate:oxygen oxidoreductase, EC 1.10.3.3) isolated from Cucurbita pepo medullosa, which is known to… (More)
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