Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells

Melanin is a form of pigment that gives colour to human skin, hair and eyes. Whilst it protects against skin damage from the sun, accumulation of excessive amounts of epidermal melanin can lead to various dermatological disorders. This study aimed to evaluate the effects of three selected oxadiazo...

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Main Authors: Mohd Aluwi, Mohd Fadhlizil Fasihi, Rullah, Kamal, Tan, Huan Huan, Chan, Kok Meng, Tan, Si Jie, Leong, Sze Wei, Mansor, Ahmad Hasnan, Yamin, Bohari M., Lam, Kok Wai
Format: Article
Language:English
Published: Royal Society of Chemistry 2016
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Online Access:http://irep.iium.edu.my/73761/
http://irep.iium.edu.my/73761/
http://irep.iium.edu.my/73761/1/Kamal%20Rullah%2010.pdf
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spelling iium-737612019-09-17T08:17:09Z http://irep.iium.edu.my/73761/ Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells Mohd Aluwi, Mohd Fadhlizil Fasihi Rullah, Kamal Tan, Huan Huan Chan, Kok Meng Tan, Si Jie Leong, Sze Wei Mansor, Ahmad Hasnan Yamin, Bohari M. Lam, Kok Wai RS403 Materia Medica-Pharmaceutical Chemistry Melanin is a form of pigment that gives colour to human skin, hair and eyes. Whilst it protects against skin damage from the sun, accumulation of excessive amounts of epidermal melanin can lead to various dermatological disorders. This study aimed to evaluate the effects of three selected oxadiazoles on the o-diphenolase mushroom tyrosinase activity and their cytotoxic effects on SK-MEL-28 malignant melanoma cells. The results showed that compounds 1, 2 and 3 exhibited significant inhibition on the diphenolase activity of mushroom tyrosinase with IC50 values of 40.46 mM, 27.42 mM and 32.51 mM, respectively. Further kinetic studies revealed that compounds 1 (Ki ¼ 3.8 mM) and 3 (Ki ¼ 3.9 mM) exhibited a mixed-type inhibition while compound 2 (Ki ¼ 0.7 mM) displayed a competitive-type inhibition as suggested by the Lineweaver–Burk plots. Molecular docking and dynamics simulations were also performed to understand the binding behaviour of compound 2 in the active site of tyrosinase. Finally, all three compounds displayed relatively low cytotoxicity to SK-MEL-28 cells up to 100 mM treatment via MTT assay. Royal Society of Chemistry 2016 Article PeerReviewed application/pdf en http://irep.iium.edu.my/73761/1/Kamal%20Rullah%2010.pdf Mohd Aluwi, Mohd Fadhlizil Fasihi and Rullah, Kamal and Tan, Huan Huan and Chan, Kok Meng and Tan, Si Jie and Leong, Sze Wei and Mansor, Ahmad Hasnan and Yamin, Bohari M. and Lam, Kok Wai (2016) Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells. RSC Advances, 6 (76). pp. 72177-72184. ISSN 2046-2069 https://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra12754a#!divAbstract
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic RS403 Materia Medica-Pharmaceutical Chemistry
spellingShingle RS403 Materia Medica-Pharmaceutical Chemistry
Mohd Aluwi, Mohd Fadhlizil Fasihi
Rullah, Kamal
Tan, Huan Huan
Chan, Kok Meng
Tan, Si Jie
Leong, Sze Wei
Mansor, Ahmad Hasnan
Yamin, Bohari M.
Lam, Kok Wai
Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
description Melanin is a form of pigment that gives colour to human skin, hair and eyes. Whilst it protects against skin damage from the sun, accumulation of excessive amounts of epidermal melanin can lead to various dermatological disorders. This study aimed to evaluate the effects of three selected oxadiazoles on the o-diphenolase mushroom tyrosinase activity and their cytotoxic effects on SK-MEL-28 malignant melanoma cells. The results showed that compounds 1, 2 and 3 exhibited significant inhibition on the diphenolase activity of mushroom tyrosinase with IC50 values of 40.46 mM, 27.42 mM and 32.51 mM, respectively. Further kinetic studies revealed that compounds 1 (Ki ¼ 3.8 mM) and 3 (Ki ¼ 3.9 mM) exhibited a mixed-type inhibition while compound 2 (Ki ¼ 0.7 mM) displayed a competitive-type inhibition as suggested by the Lineweaver–Burk plots. Molecular docking and dynamics simulations were also performed to understand the binding behaviour of compound 2 in the active site of tyrosinase. Finally, all three compounds displayed relatively low cytotoxicity to SK-MEL-28 cells up to 100 mM treatment via MTT assay.
format Article
author Mohd Aluwi, Mohd Fadhlizil Fasihi
Rullah, Kamal
Tan, Huan Huan
Chan, Kok Meng
Tan, Si Jie
Leong, Sze Wei
Mansor, Ahmad Hasnan
Yamin, Bohari M.
Lam, Kok Wai
author_facet Mohd Aluwi, Mohd Fadhlizil Fasihi
Rullah, Kamal
Tan, Huan Huan
Chan, Kok Meng
Tan, Si Jie
Leong, Sze Wei
Mansor, Ahmad Hasnan
Yamin, Bohari M.
Lam, Kok Wai
author_sort Mohd Aluwi, Mohd Fadhlizil Fasihi
title Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
title_short Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
title_full Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
title_fullStr Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
title_full_unstemmed Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
title_sort synthesis and effects of oxadiazole derivatives on tyrosinase activity and human sk-mel-28 malignant melanoma cells
publisher Royal Society of Chemistry
publishDate 2016
url http://irep.iium.edu.my/73761/
http://irep.iium.edu.my/73761/
http://irep.iium.edu.my/73761/1/Kamal%20Rullah%2010.pdf
first_indexed 2023-09-18T21:44:35Z
last_indexed 2023-09-18T21:44:35Z
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