Molecular diversity of phenothiazines: design and synthesis of phenothiazine-dithiocarbamate hybrids as potential cell cycle blockers.

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Molecular diversity of phenothiazines: design and synthesis of phenothiazine-dithiocarbamate hybrids as potential cell cycle blockers.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Molecular diversity of phenoth ...... potential cell cycle blockers.

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Molecular diversity of phenoth ...... potential cell cycle blockers.

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Molecular diversity of phenoth ...... potential cell cycle blockers.

@en

Molecular diversity of phenoth ...... potential cell cycle blockers.

@nl

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Molecular diversity of phenoth ...... potential cell cycle blockers.

@en

Molecular diversity of phenoth ...... potential cell cycle blockers.

@nl

P1476

Molecular diversity of phenoth ...... potential cell cycle blockers.

@en

P2093

Bo-Wen Wu

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Dong-Jun Fu

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Hong-Min Liu

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Hui-Jie Cai

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Jia-Huan Li

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Jia-Jia Yang

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Ping Li

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Qing-Qing Zhang

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Ruo-Han Zhao

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Ruo-Wang Mao

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P2860

Antitumor potential and possible targets of phenothiazine-related compounds.

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Triazole-dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration.

Recent progress in biological activities of synthesized phenothiazines.

Design and synthesis of formononetin-dithiocarbamate hybrids that inhibit growth and migration of PC-3 cells via MAPK/Wnt signaling pathways.

Synthesis of first ever 4-quinolone-3-carboxylic acid-appended spirooxindole-pyrrolidine derivatives and their biological applications.

Synthesis and evaluation of new benzodioxole-based dithiocarbamate derivatives as potential anticancer agents and hCA-I and hCA-II inhibitors.

Fluorescein hydrazones: A series of novel non-intercalative topoisomerase IIα catalytic inhibitors induce G1 arrest and apoptosis in breast and colon cancer cells.

Design, synthesis and antiproliferative activity studies of novel dithiocarbamate-chalcone derivates.

P2888

s11030-017-9773-4

P304

933-942

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P31

scholarly article

P356

10.1007/S11030-017-9773-4

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-08-07T00:00:00Z

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P698

28785928

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P921

molecular design

P932

5975273

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