Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Xiao-kang Zhu"'
Publikováno v:
Jisuanji kexue, Vol 49, Iss 9, Pp 326-332 (2022)
Embedded devices have become visible everywhere,and they are used in a range of security-critical and privacy-sensitive applications.However,recent studies show that many embedded devices have backdoor,of which hard-coded backdoor(password backdoor)
Externí odkaz:
https://doaj.org/article/440dd76827d04329ba0d895ed205f0e0
Publikováno v:
Journal of Analysis and Testing. 6:111-119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fefb8a51a59c49c85d46bc010dcef859
https://doi.org/10.1007/s41664-022-00227-x
https://doi.org/10.1007/s41664-022-00227-x
Autor:
Xiao-kang Zhu, Bin Fu, Ramon Felipe Bicudo Da Silva, Ying-man Guo, Chan-yuan Qin, Ting Feng, Hai-bing Yu, Kuang Xiao
Publikováno v:
Journal of Mountain Science. 19:925-944
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8e16f0b72bc865d4aa0447ae2dd2921
https://doi.org/10.1007/s11629-021-6832-1
https://doi.org/10.1007/s11629-021-6832-1
Publikováno v:
Carbohydrate Polymers. 88:75-83
A hydrogel sheet composed of chitosan, honey and gelatin (HS; 0.5:20:20, w/w) was developed as a burn wound dressing. HS showed powerful antibacterial efficacy up to 100% to Staphylococcus aureus and Escherichia coli, significantly superior to chitos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::667a2efb9f339129ad064a859af4b722
https://doi.org/10.1016/j.carbpol.2011.11.069
https://doi.org/10.1016/j.carbpol.2011.11.069
Publikováno v:
Bioorganic & Medicinal Chemistry. 12:4267-4273
A series of novel podophyllotoxin derivatives containing structural modifications at C-4 (7-14), C-4' (16-17), and the methylenedioxy A-ring (23-28) was synthesized and tested for inhibition of HIV replication. Four of these compounds (25-28) were pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e596cb226bc1939243f45b5b9cfd9cc8
https://doi.org/10.1016/j.bmc.2004.04.048
https://doi.org/10.1016/j.bmc.2004.04.048
Autor:
Yung-Chi Cheng, Kuo Hsiung Lee, Sung Jin Cho, Huey-Hwa Cheng, Yoko Tachibana, Jian Guan, Kenneth F. Bastow, Marc Gurwith, Xiao-Kang Zhu
Publikováno v:
Journal of Medicinal Chemistry. 42:2441-2446
As a continuation of our structure-activity relationship studies, several new 4-beta-substituted 4'-O-demethyl-4-desoxypodophyllotoxins bearing mono-, di-, or trisubstituted anilines have been synthesized and evaluated as inhibitors of DNA topoisomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e69563bc1fa561254c6dc81cd72a2d
https://doi.org/10.1021/jm990055f
https://doi.org/10.1021/jm990055f
Autor:
Xiao Kang Zhu, Arnold Brossi, Andrew T. McPhail, Kenneth F. Bastow, Ernest Hamel, Jian Guan, Yoko Tachibana, Pascal Verdier-Pinard, Kuo Hsiung Lee
Publikováno v:
Collection of Czechoslovak Chemical Communications. 64:217-228
Two allocolchicinoids 6 and 8, prepared from colchicine, together with allo compounds 9-11, made from 6 by reduction and regiodemethylation, were evaluated for antitubulin and antitumor activities. Structures of 6, 8, and 10 were confirmed by X-ray c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbe2e2d1bcbd07914fa3a807ddee286d
https://doi.org/10.1135/cccc19990217
https://doi.org/10.1135/cccc19990217
Autor:
Arnold Brossi, Kuo Hsiung Lee, Xiao Kang Zhu, Kenneth F. Bastow, Ernest Hamel, Yoko Tachibana, Jian Guan
Publikováno v:
Bioorganic & Medicinal Chemistry. 6:2127-2131
Demethylation of colchiceinamide (2) and its analogues (3-10) afforded a novel class of mammalian DNA topoisomerase II inhibitors (2a-10a) without displaying tubulin inhibitory activity. All target compounds inhibited the catalytic activity of topois
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b159f3cc42f5fbffcb3690afdf9e74
https://doi.org/10.1016/s0968-0896(98)00165-5
https://doi.org/10.1016/s0968-0896(98)00165-5
Publikováno v:
Synthetic Communications. 28:1585-1591
An improved, highly selective demethylation of thiocolchicine (1) to the diphenol 5 is described. Oxidation of 2 to para-quinone 6 and of 4 and 5 to ortho-quinones 8 and 10 is first reported. Also, 2-demethylthiocolchicine (3) was oxidized to the qui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0b52d2a02c63073a90a9ee64ab8c092
https://doi.org/10.1080/00397919808006862
https://doi.org/10.1080/00397919808006862
Autor:
Jian Guan, Xiao Kang Zhu, Arnold Brossi, Yoko Tachibana, Ernest Hamel, Kenneth F. Bastow, Kuo Hsiung Lee
Publikováno v:
Journal of Medicinal Chemistry. 41:1956-1961
Several 1,2,3-tridemethyldeacetylthiocolchicine derivatives have been synthesized and evaluated for cytotoxic activity against various human tumor cell lines and for their inhibitory effects on DNA topoisomerases in vitro. Exhaustive demethylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8938cfaebfd21b73d8630660423b439e
https://doi.org/10.1021/jm980007f
https://doi.org/10.1021/jm980007f