Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Anupong Joompang"'
Autor:
Ruedeemars Yubolphan, Anupong Joompang, Sittiruk Roytrakul, Chantana Boonyarat, Kiattawee Choowongkomon, Sakda Daduang, Sompong Klaynongsruang, Nisachon Jangpromma
Publikováno v:
Journal of Functional Foods, Vol 119, Iss , Pp 106354- (2024)
Amyloid-β (Aβ) aggregation is central to Alzheimer’s disease (AD), causing oxidative and synaptic damage. We developed IL15.5, a peptide-base inhibitor derived from IL15, a natural peptide from Siamese crocodile hemoglobin. Computational and mole
Externí odkaz:
https://doaj.org/article/15ddc8af03e44bb1b547d078082eb7b5
Autor:
Boonyarit Kukaew, Wanna Sirisangtragul, Sittiruk Roytrakul, Anupong Joompang, Napaporn Roamcharern, Anupong Tankrathok, Pattralak Songserm, Sakda Daduang, Sompong Klaynongsruang, Nisachon Jangpromma
Publikováno v:
Journal of King Saud University: Science, Vol 36, Iss 6, Pp 103229- (2024)
Methomyl, an extremely hazardous substance, is widely used for controlling insects and pests in agricultural production. This compound can cause several illnesses in humans. In this research, we determined the alleviation potential of Yanang water ex
Externí odkaz:
https://doaj.org/article/3c5291d54bed48ac910ba179c064d29b
Autor:
La-or Somsakeesit, Anupong Joompang, Santi Phosr, Pattaravadee Srikoon, Pakit Kumboonma, Thanaset Senawong, Chanokbhorn Phaosiri
Publikováno v:
Songklanakarin Journal of Science and Technology (SJST), Vol 44, Iss 6, Pp 1481-1488 (2022)
Piperine (1) was obtained from the seeds of Piper nigrum L. It could act as a pan-histone deacetylase (HDAC) inhibitor. This lead compound was structurally modified to six derivatives that exhibited improved HDAC inhibitory activity. Based on the p
Externí odkaz:
https://doaj.org/article/fb0291b4a4874c05b059ffa285edfd17
Autor:
Anupong Joompang, Preeyanan Anwised, Sompong Klaynongsruang, Lapatrada Taemaitree, Anuwat Wanthong, Kiattawee Choowongkomon, Sakda Daduang, Somporn Katekaew, Nisachon Jangpromma
Publikováno v:
Current Research in Food Science, Vol 7, Iss , Pp 100598- (2023)
There has been a resurgence of interest in bioactive peptides as therapeutic agents. This is particularly interesting for tyrosinase, which can be inhibited by thiol-containing peptides. This work demonstrates that an N-terminal cysteine-containing t
Externí odkaz:
https://doaj.org/article/464a7fa26da740f3a90ecad19706623b
Autor:
Anupong Joompang, Preeyanan Anwised, Sompong Klaynongsruang, Sittiruk Roytrakul, Lapatrada Taemaitree, Nisachon Jangpromma
Publikováno v:
Molecules, Vol 27, Iss 10, p 3228 (2022)
There is a desire to develop new molecules that can combat hyperpigmentation. To this end, the N-terminal cysteine-containing heptapeptide TILI-2 has shown promising preliminary results. In this work, the mechanism by which it works was evaluated usi
Externí odkaz:
https://doaj.org/article/0a2e70779e7c46dfb26798e6fdc73422
Autor:
Anupong Joompang, Preeyanan Anwised, Kunlathida Luangpraditkun, Nisachon Jangpromma, Jarupa Viyoch, Céline Viennet, Sompong Klaynongsruang
Publikováno v:
Journal of Medicinal Food. 25:818-827
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffd16347ecdc32236eabdc629b3bcda6
https://doi.org/10.1089/jmf.2021.k.0130
https://doi.org/10.1089/jmf.2021.k.0130
Autor:
Kiattawee Choowongkomon, Kunlathida Luangpraditkun, Anupong Joompang, Wisarut Payoungkiattikun, Anupong Tankrathok, Jarupa Viyoch, Nisachon Jangpromma, Sompong Klaynongsruang
Publikováno v:
Journal of Bioscience and Bioengineering. 130:239-246
This research first reports the tyrosinase inhibition and mechanism of Leucrocin I and its modified peptides (TILI-1 and TILI-2). Docking simulation showed that these peptides were predicted to bind and interact to active site of tyrosinase and exhib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e00c2b1914396d387b31ae4531203c7
https://doi.org/10.1016/j.jbiosc.2020.04.002
https://doi.org/10.1016/j.jbiosc.2020.04.002
Publikováno v:
Journal of Food Science and Technology. 57:3157-3163
This research screened for α-amylase inhibitory activity of twenties-five varieties Thai indigenous rice seeds. Based on specific inhibition, crude protein of var. Gai Ngaw (Gs. No. 13719) was selected for purification. The unbound proteins of the Q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::948410674468c24012aeaf3919dc5c72
https://doi.org/10.1007/s13197-020-04560-w
https://doi.org/10.1007/s13197-020-04560-w
Autor:
Francois Grandmottet, Céline Viennet, Kunlathida Luangpraditkun, Marion Tissot, Jarupa Viyoch, Pensri Charoensit, Anupong Joompang
Publikováno v:
Oxidative Medicine and Cellular Longevity, Vol 2021 (2021)
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity
Natural substances have gained considerable attention for skin protection against UV light reactions. Artocarpus altilis plant’s heartwood extract is comprised of artocarpin as a major substance, already known for its interesting biological attribu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40660204fc155eac6fc393d2dcedf231
Publikováno v:
J Food Sci Technol
This research screened for α-amylase inhibitory activity of twenties-five varieties Thai indigenous rice seeds. Based on specific inhibition, crude protein of var. Gai Ngaw (Gs. No. 13719) was selected for purification. The unbound proteins of the Q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71a6374470ac88f26591dc5ef60acde5
https://pubmed.ncbi.nlm.nih.gov/32624617
https://pubmed.ncbi.nlm.nih.gov/32624617