![]() TYROSINASE structure
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Common Name | TYROSINASE | ||
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CAS Number | 9002-10-2 | Molecular Weight | 1031.161 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 1578.2±65.0 °C at 760 mmHg | |
Molecular Formula | C42H66N10O16S2 | Melting Point | N/A | |
MSDS | USA | Flash Point | 908.2±34.3 °C |
Separation of the antioxidant compound quercitrin from Lindera obtusiloba Blume and its antimelanogenic effect on B16F10 melanoma cells.
Biosci. Biotechnol. Biochem. 77(1) , 58-64, (2013) Considering the growing evidence of the presence of antioxidant compounds in plant extracts, the objectives of this study were to identify antioxidant compounds in Lindera obtusiloba Blume (Lauraceae) and to evaluate their antimelanogenic activities on B16F10... |
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The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res. 14 , 2121-7, (2004) The National Institutes of Health's Mammalian Gene Collection (MGC) project was designed to generate and sequence a publicly accessible cDNA resource containing a complete open reading frame (ORF) for every human and mouse gene. The project initially used a r... |
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Standardised herbal extract of chlorogenic acid from leaves of Etlingera elatior (Zingiberaceae).
Pharmacognosy Res. 3 , 178-184, (2011) Chlorogenic acid (CGA) or 5-caffeoylquinic acid, was found to be the dominant phenolic compound in leaves of Etlingera elatior (Zingiberaceae). The CGA content of E. elatior leaves was significantly higher than flowers of Lonicera japonica (honeysuckle), the ... |
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Potent microbial and tyrosinase inhibitors from stem bark of Bauhinia rufescens (Fabaceae).
Nat. Prod. Commun. 8(10) , 1435-7, (2013) The stem bark extracts of Bauhinia rufescens Lam. (Fabaceae) yielded 6-methoxy-7-methyl-8-hydroxydibenz[b,f]oxepin, alpha-amyrin acetate, beta-sitosterol 3-O-beta-D-xylopyranoside, 4-(2'-Hydroxyphenethyl)-5-methoxy-2-methylphenol, menisdaurin and sequoyitol. ... |
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Identification and characterization of the related immune-enhancing proteins in crab Scylla paramamosain stimulated with rhubarb polysaccharides.
Mol. Immunol. 57(2) , 263-73, (2014) Recently, considerable interest has been focused on immunostimulants to reduce diseases in crab aquaculture. However, information regarding to the related immune-enhancing proteins in crabs is not available yet. In this study, rhubarb polysaccharides were tes... |
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The sequence of the human genome.
Science 291(5507) , 1304-51, (2001) A 2.91-billion base pair (bp) consensus sequence of the euchromatic portion of the human genome was generated by the whole-genome shotgun sequencing method. The 14.8-billion bp DNA sequence was generated over 9 months from 27,271,853 high-quality sequence rea... |
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Inhibitory mechanism of red globe amaranth on tyrosinase.
J. Cosmet. Sci. 64(2) , 99-110, (2013) Tyrosinase inhibitors from natural plants are currently attracting great interest. In this study, vanillic acid (VA) from red globe amaranth flower was identified as an effective tyrosinase inhibitor. The 50% inhibitory concentration values of VA were 0.53 an... |
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In vitro melanogenesis inhibitory effects of N-feruloyldopamine.
J. Cosmet. Sci. 64(2) , 133-44, (2013) Tyrosinase is the rate-limiting enzyme in the melanogenesis process. It remains the most efficient way to downregulate melanin production and improve unsightly pigmentary disorders. The aim of our investigations was to find a structurally characterized molecu... |
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Epidermal growth factor and epidermal growth factor signaling attenuate laser-induced melanogenesis.
Dermatol. Surg. 39(12) , 1903-11, (2013) Epidermal growth factor (EGF) is a peptide that promotes cell growth by binding to its receptor (EGFR) on the cell surface. EGF has been used in cosmetics to whiten the skin and for the prevention of postinflammatory hyperpigmentation (PIH), presumably by acc... |
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Inhibition of melanin content by Punicalagins in the super fruit pomegranate (Punica granatum).
J. Cosmet. Sci. 64(6) , 445-53, (2013) Current efforts to develop effective skin lightening products through the inhibition of melanin production have focused on compounds that inhibit the function and activity of tyrosinase, the rate-limiting enzyme in the melanin biosynthesis pathway. Synthetic ... |