Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Tran Khac Vu"'
Publikováno v:
Journal of Applied Science and Engineering, Vol 27, Iss 1, Pp 1867-1876 (2023)
In the present research, fountain solution without isopropyl alcohol (IPA) for Ultraviolet offset curing ink (UV ink) was prepared by using Ethylene Glycol Mono-butyl Ether (EGME) as a substitute for IPA. The effect of EGME concentration on the wate
Externí odkaz:
https://doaj.org/article/fd36de0eb9d340959301326a2cc6ed29
Akademický článek
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Akademický článek
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Autor:
Dao Viet Hung, Tran Khac Vu
Publikováno v:
Journal of Chemistry, Vol 2021 (2021)
The protein kinase Pkc1 of Candida albicans (CaPkc1), one of the key proteins involved in MAPK pathway, is described as a regulator of cell wall integrity during growth, morphogenesis, and response to cell wall stress. The (–)-cercosporamide is an
Externí odkaz:
https://doaj.org/article/caaf39a6b2ff46cea2523de3e764498b
Autor:
Luu Van Chinh, Truong Ngoc Hung, Luu Xuan Hieu, Tran Thi Hong Ha, Hoang Kim Chi, Tran Khac Vu, Pham Van Chung
Publikováno v:
Letters in Organic Chemistry. 19:1062-1069
Abstract: A two-step procedure was applied to couple zerumbone, a natural sesquiterpene, with thiols 8a-k to obtain a small library of ten novel zerumbone derivatives 9a-k with full-length library data of spectra including 1H-, 13C-NMR, and HRMS. The
Autor:
Do Thi Mai Dung, Phan Thi Phuong Dung, Dao Thi Kim Oanh, Tran Khac Vu, Hyunggu Hahn, Byung Woo Han, Minji Pyo, Young Guk Kim, Sang-Bae Han, Nguyen-Hai Nam
Publikováno v:
Arabian Journal of Chemistry, Vol 10, Iss 4, Pp 465-472 (2017)
A series of novel 5′(7′)-substituted-2′-oxospiro[1,3]dioxolane-2,3′-indoline-based N-hydroxypropenamides were designed, synthesized and evaluated for histone deacetylase (HDAC) inhibition and cytotoxicity. It was found that the compounds in t
Externí odkaz:
https://doaj.org/article/e0efe2b3750d47eeb1373e91ec7b10c9
Autor:
Anh Tuan Phung, Linh Nguyen Pham Duy, Bach Xuan Nguyen, Thuc Bao Nguyen Truong, Tran Thi Hai Van, Nguyen Thi Bich Phuong, Tran Khac Vu, Thi Xuan Vu
Publikováno v:
Letters in Organic Chemistry. 19:558-569
Background: In this study, two novel hybrid series of artemisinin and quinazolinones were synthesized and evaluated in vitro cytotoxicity against two human cancer cell lines, including SKLu-1 (lung cancer), MCF- 7 (breast cancer). The bio-assay resul
Publikováno v:
Indian Journal of Chemistry (0019-5103); 2023, Vol. 62 Issue 3, p244-250, 7p
Autor:
Vu Van Vu, Trinh Thi Nhung, Nguyen Thi Thanh, Luu Van Chinh, Vu Dinh Tien, Vu Thu Thuy, Do Thi Thao, Nguyen Hai Nam, Angela Koeckritz, Tran Khac Vu
Publikováno v:
Journal of Chemistry, Vol 2017 (2017)
A series of 14 new (-)-gossypol Schiff bases and hydrazones have been synthesized via an in situ procedure in high yields. Structural data showed that all target compounds exist as the enamine tautomer. Bioassays showed that several compounds exhibit
Externí odkaz:
https://doaj.org/article/2b39cd247f874222b32549bcc59600c9
Autor:
Hoang T Lien, Ho D Cuong, Luu V Chinh, Pham T Hai, Le Minh-Ngoc, Nguyen Hai Nam, Nguyen Viet Minh, Dinh Thi Phuong Anh, Huong Le-Thi-Thu, Tran Khac Vu, Nguyen Thi Viet Thanh
Publikováno v:
Anti-Cancer Agents in Medicinal Chemistry. 19:1543-1557
Background: Target-based approach to drug discovery currently attracts a great deal of interest from medicinal chemists in anticancer drug discovery and development worldwide, and Histone Deacetylase (HDAC) inhibitors represent an extensive class of