Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shaoyong Ke"'
Autor:
Shaoyong Ke, Huang Daye, Wei Fang, Liqiao Shi, Zhigang Zhang, Huang Wenbo, Chunxia Cao, Zhongyi Wan, Kaimei Wang
Publikováno v:
Bioorganicmedicinal chemistry letters. 30(13)
Aryl-oxazole alkaloids are an important class of heterocyclic natural products, and which has been demonstrated to exhibit broad biological functions. During the course of our research for highly active compounds from natural products, the natural hi
Publikováno v:
European Journal of Medicinal Chemistry. 44:2985-2993
A series of diacylhydrazine derivatives containing hydrophobic alkyl chains have been designed and synthesized. The target molecules have been identified on the basis of analytical spectral (IR, 1 H NMR, 13 C NMR, and HRMS) data. All synthesized comp
Publikováno v:
European Journal of Medicinal Chemistry. 44:2113-2121
A new series of nitrogen-containing heterocycles 4 H -1,3,4-oxadiazin-5(6 H )-ones derivatives with hydrophobic and long chains were designed and synthesized by direct cyclization reaction of N ′-alkylation substituted aroylhydrazines with chloroac
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:332-335
Two series of 1,3,4-oxadiazoline heterocycle derivatives were designed, synthesized and identified. Bioactivity assays showed that all synthesized compounds inhibited chitin synthesis in yeast, suggesting they might be a novel class of potential inhi
Publikováno v:
Anti-cancer agents in medicinal chemistry. 13(8)
A series of dehydroepiandrosterone derivatives containing dihydrazone unit was synthesized via a convenient condensation procedure, and which were evaluated for their potential anticancer activities. The preliminary assays indicated that some of the
Publikováno v:
European journal of medicinal chemistry. 54
A series of novel anthranilic diamides derivatives containing aryl-isoxazoline moiety were designed and synthesized as a part of our ongoing search for potential anticancer agents. Their structures were confirmed by 1H NMR, 13C NMR and ESI-MS analyse