نتایج جستجو برای: tyrosinase inhibitor

تعداد نتایج: 214578  

2017
Md Badrul Alam Vivek K. Bajpai JungIn Lee Peijun Zhao Jung-Hee Byeon Jeong-Sic Ra Rajib Majumder Jong Sung Lee Jung-In Yoon Irfan A. Rather Yong-Ha Park Kangmin Kim MinKyun Na Sang-Han Lee

In this study, the authors investigated the anti-melanogenic effects of 3,8-dihydroxyquinoline (jineol) isolated from Scolopendra subspinipes mutilans, the mechanisms responsible for its inhibition of melanogenesis in melan-a cells, and its antioxidant efficacy. Mushroom tyrosinase activities and melanin contents were determined in melan-a cells, and the protein and mRNA levels of MITF, tyrosin...

Journal: :African journal of traditional, complementary, and alternative medicines : AJTCAM 2014
Muhammad Helmi Nadri Yushatika Salim Norazah Basar Azli Yahya Razauden Mohamed Zulkifli

BACKGROUND The ethyl acetate and chloroform extracts of stems, leaves and fruits of Phaleria macrocarpa were screened for their antioxidant capacity and tyrosinase inhibition properties. MATERIAL AND METHOD The total phenolic content (TPC), 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging and ferric-ion reducing power (FRAP) were used to evaluate their antioxidant capacity. Tyrosi...

Journal: :The Biochemical journal 2005
C E Pugh

The blood and tissues of most insects contain tyrosinase, together with a suitable substrate. When blood is shed or the tissues damaged, enzyme and substrate react and eventually produce melanin; why do they not react in the intact animal? The oldest theory was that they were held apart by some structural organization of the cytoplasm and that they only came together when this was destroyed. Th...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
R Halaban E Cheng Y Zhang G Moellmann D Hanlon M Michalak V Setaluri D 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...

2013
Myeong-Jin Goh Hae-Kwang Lee Liang Cheng De-Yun Kong Jae-Ho Yeon Quan-Quan He Jun-Cheol Cho Yong Joo Na

The development of melanogenic inhibitors is important for the prevention of hyperpigmentation, and, recently, consideration has been given to natural materials or traditionally used ingredients such as Chinese medicine. The aim of this study is the evaluation of a new anti-melanogenic candidate, kadsuralignan F, from the natural plant Kadsura coccinea, as well as the determination of mechanism...

2012
Hong-Jian Liu Sunyoung Ji Yong-Qiang Fan Li Yan Jun-Mo Yang Hai-Meng Zhou Jinhyuk Lee Yu-Long Wang

Tyrosinase is a ubiquitous enzyme with diverse physiologic roles related to pigment production. Tyrosinase inhibition has been well studied for cosmetic, medicinal, and agricultural purposes. We simulated the docking of tyrosinase and D-(-)-arabinose and found a binding energy of -4.5 kcal/mol for theup-formof D-(-)-arabinose and -4.4 kcal/mol for thedown-form of D-(-)-arabinose. The results of...

2014
Florence Wing-Ki Cheung Albert Wing-Nang Leung Wing Keung Liu Chun-Tao Che

2,3,5,4'-Tetrahydroxystilbene-2-O-β-D-glucopyranoside (1), isolated from Polygonum multiflorum, is a noncompetitive inhibitor of tyrosinase in cell-free kinetics; it reduced the Vmax values in a dose-dependent manner. Compound 1 inhibited PKA-induced melanogenesis, reduced the protein expression of tyrosinase and its transcription factor, the microphthalmia-associated transcription factor, and ...

Since melanocytes are the origin of melanoma and some skin disorders such as melasma, they are important cells from the perspective of medicinal chemistry. Therefore, a medication that can simultaneously overcome these diseases will be a successful potential therapeutic agent. Arbutin with phenolic structure is a powerful natural anti-tyrosinase agent. Hence, the phenolic structure of this drug...

Journal: :Journal of Food Science and Technology 2014

2017
Zaman Ashraf Muhammad Rafiq Humaira Nadeem Mubashir Hassan Samina Afzal Muhammad Waseem Khurram Afzal Jalifah Latip

The present work describesthe development of highly potent mushroom tyrosinase inhibitor better than the standard kojic acid. Carvacrol derivatives 4a-f and 6a-d having substituted benzoic acid and cinnamic acidresidues were synthesized with the aim to possess potent tyrosinase inhibitory activity.The structures of the synthesized compounds were ascertained by their spectroscopic data (FTIR, 1H...

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