Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Duc Dung Pham"'
Publikováno v:
Vietnam Journal of Science, Technology and Engineering, Vol 64, Iss 2 (2022)
Five new derivatives of N-(4-oxo-2-thioxothiazolidin-3-yl)-2-((3-aryl-4-oxo-3,4-dihydroquinazolin-2-yl)thio) acetamides have been synthesized successfully through a four-step process from anthranilic acid and aryl isothiocyanates as starting material
Externí odkaz:
https://doaj.org/article/8ee8cdad6dc141b6901d78f639ab01f5
Autor:
Nguyen-Kim-Tuyen Pham, Nguyen-Minh-An Tran, Huy Truong Nguyen, Duc-Dung Pham, Thi-Quynh-Trang Nguyen, Thi-Hong-Anh Nguyen, Huu-Tri Nguyen, Thanh-Hung Do, Ngoc-Hong Nguyen, Thuc-Huy Duong
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 1, Pp 103535- (2022)
Data on synthesized derivatives of salazinic acid are scarce, with existing reports addressing only derivative hexaacetyl salazinic acid. This study investigated a set of novel potential antidiabetic agents. Analogs of salazinic acid were designed an
Externí odkaz:
https://doaj.org/article/fb74b27e54f54a419bbf36b29bbda4e8
Autor:
Thi-Anh-Tuyet Nguyen, Thuc-Huy Duong, Duc Dung Pham, Jirapast Sichaem, Dinh-Long Huynh, Thi-Thanh-Van Le, Ngoc-Hong Nguyen
Publikováno v:
Chemistry of Natural Compounds. 57:1038-1041
Seven synthetic derivatives of ursolic acid, lupeol, and betulinic acid (1a–1b, 2a–2b, and 3a–3c) were synthesized to study their α-glucosidase inhibitory activity. Three of them (2b, 3b, and 3c) are new compounds. Among the synthetic derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec21527f66f6d32964527a7e89e7d4d4
https://doi.org/10.1007/s10600-021-03545-1
https://doi.org/10.1007/s10600-021-03545-1
Autor:
Huu-Hung Nguyen, Thuc-Huy Duong, Tran-Van-Anh Nguyen, Thanh-Hung Do, Duc-Dung Pham, Ngoc-Hong Nguyen, Huy Truong Nguyen
Lichen-derived depsidones have been a successful source for alpha-glucosidase inhibitory agents with numerous advantages. In this article, derivatives of protocetraric acids were designed and synthesised. Diels-Alder reaction, esterification, and Fri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d48df81409fba558366d9cb91e0fc07
Akademický článek
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Autor:
Xuan Hieu Nguyen, Warinthorn Chavasiri, Thi-Phuong Nguyen, Thi-Thu-Loi Huynh, Kim-Phi-Phung Nguyen, Thuc-Huy Duong, Nakorn Niamnont, Jirapast Sichaem, Dinh Hung Mac, Van-Kieu Nguyen, Huu-Hung Nguyen, Duc-Dung Pham
Publikováno v:
Natural Product Research. 35:1097-1106
A series of usnic acid benzylidene derivatives (groups I-V) were designed, synthesized and evaluated for their anticancer activity in the search for potentially new anticancer agents. Compounds 1a, 5b, 2b, 2e and 2f exhibited the most potent cytotoxc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67ce3cf68fc4bc52e8e5ce69358c8383
https://doi.org/10.1080/14786419.2019.1639176
https://doi.org/10.1080/14786419.2019.1639176
Autor:
Thuc-Huy Duong, Van-Kieu Nguyen, Bui-Linh-Chi Huynh, Asshaima Paramita Devi, Ngoc-Hong Nguyen, Huy Truong Nguyen, Jirapast Sichaem, Warinthorn Chavasiri, Tran-Van-Anh Nguyen, Duc-Dung Pham
Publikováno v:
Chemistrybiodiversity. 18(4)
This study investigated a set of new potential antidiabetes agents. Derivatives of usnic acid were designed and synthesized. These analogs and nineteen benzylidene analogs from a previous study were evaluated for enzyme inhibition of α-glucosidase.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e05f80dd26890a323f0110e226b3f71
https://pubmed.ncbi.nlm.nih.gov/33538053
https://pubmed.ncbi.nlm.nih.gov/33538053
Autor:
Hoang-Vinh-Truong, Phan, Thuc-Huy, Duong, Duc-Dung, Pham, Hoang-Anh, Pham, Van-Kieu, Nguyen, Thi-Phuong, Nguyen, Huu-Hung, Nguyen, Ngoc-Hong, Nguyen, Pornpat, Sam-Ang, Kiettipum, Phontree, Jirapast, Sichaem
Publikováno v:
Natural product research. 36(1)
A series of lupeol derivatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d38809b4066cbc7bc19e6dfc282c60b
https://pubmed.ncbi.nlm.nih.gov/32378438
https://pubmed.ncbi.nlm.nih.gov/32378438
Autor:
Huu-Hung Nguyen, Thi-Phuong Nguyen, Hoang-Vinh-Truong Phan, Hoang-Anh Pham, Ngoc-Hong Nguyen, Pornpat Sam-ang, Kiettipum Phontree, Van-Kieu Nguyen, Jirapast Sichaem, Duc-Dung Pham, Thuc-Huy Duong
A series of lupeol derivatives 2, 2a-2f, 2a-2h, 3a-3e, and 4a-4b were designed, synthesised and evaluated for their α-glucosidase inhibitory and cytotoxic activities. Among synthetic derivatives, lupeol analogues 2b and 2e containing a benzylidene c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6df98b25acb241a26959d5d15a490cbe
Autor:
Thanh-The Ngo, Thi-Phuong Nguyen, Jirapast Sichaem, Thuc-Huy Duong, Hoang-Vinh-Truong Phan, Van-Giau Vo, Tien-Cong Nguyen, Van-Kieu Nguyen, Duc-Dung Pham, Ngoc-Hong Nguyen, Huu-Hung Nguyen
Twelve benzylidene derivatives, one Baeyer-Villiger oxidative, six imine derivatives were successfully designed and synthesised from phyllanthone. In the search for potential new anti-diabetic agents, phyllanthone along with its benzylidene and oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c71b12c49aaba2af8425612253a7c07c