نتایج جستجو برای: tyrosinase inhibitors

تعداد نتایج: 192087  

2013
Ying Ying

Tyrosinase is a key enzyme that catalyzes melanogenesis in human skin. It oxidizes tyrosine to L-3,4dihydroxyphenylalanine (L-DOPA) and subsequently to dopachrome, which further polymerizes to melanin pigments. Therefore finding an effective tyrosinase inhibitor, either from synthetic or natural sources, is not only useful as skin whitening agents in cosmetic application, but also beneficial in...

Journal: :The Yale Journal of Biology and Medicine 1973
M. Seiji H. Fukuzawa N. Miyazaki H. Akiba T. Kato

The activity of tyrosinase (EC 1.10.3,1 o-diphenol:02 oxidoreductase) was found to be in melanosomes, smooth-surface membranes, rough-surface membranes , and ribosomes when they are isolated from Harding-Passey mouse mela-noma. In vivo incorporation studies of 14C-dopa into these cell particles were carried out in order to clarify the site of malanin formation in melanocytes. '4C-dopa incorpora...

1997
RUTH HALABAN ELAINE CHENG YUHUA ZHANG GISELA MOELLMANN DOUGLAS HANLON MAREK MICHALAK VIJAYASARADHI SETALURI DANIEL N. HEBERT

The loss of tyrosinase, the key enzyme in melanin synthesis, has been implicated in the dedifferentiation of malignant melanocytes. The presence of tyrosinase transcripts and antigenic peptides in melanoma tumors prompted us to investigate whether the basis for the loss of the enzyme was proteolytic degradation. Toward this aim, we followed the kinetics of synthesis, degradation, processing, ch...

Journal: :Annals of botany 2006
Zsanett Laufer Richard P Beckett Farida V Minibayeva

BACKGROUND AND AIMS Following previous findings of high extracellular redox activity in lichens and the presence of laccases in lichen cell walls, the work presented here additionally demonstrates the presence of tyrosinases. Tests were made for the presence of tyrosinases in 40 species of lichens, and from selected species their cellular location and molecular weights were determined. The effe...

2014
Ni Ai William J. Welsh Uma Santhanam Hong Hu John Lyga

Tyrosinase is the key enzyme involved in the human pigmentation process, as well as the undesired browning of fruits and vegetables. Compounds inhibiting tyrosinase catalytic activity are an important class of cosmetic and dermatological agents which show high potential as depigmentation agents used for skin lightening. The multi-step protocol employed for the identification of novel tyrosinase...

Journal: :Molecules 2018
Jang Hoon Kim Hyo Young Kim Si Yong Kang Jin-Baek Kim Young Ho Kim Chang Hyun Jin

The goal of this study was to identify phytochemicals with inhibitory activity against tyrosinase. Nine compounds 1-9 were isolated from the tubers of Apios americana. This is the first report of aromadendrin 5-methyl ether (1) being isolated from the Apios species. Among them, compounds 2 and 8 showed inhibitory activity toward tyrosinase. Based on a Dixon plot, the potential Ki values of comp...

2010
Mika Tada Masahiro Kohno Shigenobu Kasai Yoshimi Niwano

Alleviated melanin formation in the skin through inhibition of tyrosine-tyrosinase reaction is one of the major targets of cosmetics for whitening ability. Since melanin has a pivotal role for photoprotection, there are pros and cons of inhibition of melanin formation. This study applying electron spin resonance (ESR)-spin trapping method revealed that (•)H and (•)OH are generated through tyros...

Journal: :Molecular bioSystems 2011
Hyang Yeon Lee Seung Bum Park

Small-molecule microarrays are powerful, high-throughput tools for gathering information about direct binding events between proteins of interest and small molecules. However, nonspecific binding on modified glass slides is the major factor reducing the quality of information obtained in proteomic screening with small-molecule microarrays. To improve the signal-to-noise ratio by suppressing the...

Journal: :Chemical & pharmaceutical bulletin 2004
Viqar Uddin Ahmad Farman Ullah Javid Hussain Umar Farooq Muhammad Zubair Mahmud Tareq Hassan Khan Muhammad Iqbal Choudhary

A new coumarinolignoid 8'-epi-cleomiscosin A (1) together with the new glycoside 8-O-beta-D-glucopyranosyl-6-hydroxy-2-methyl-4H-1-benzopyrane-4-one (2) have been isolated from the aerial parts of Rhododendron collettianum and their structures determined on the basis of spectroscopic evidences. Tyrosinase inhibition study of these compounds and their structure-activity relationship (SAR) were a...

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