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174634-09-4

中文名稱(chēng) 6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽
英文名稱(chēng) TAS 103
CAS 174634-09-4
分子式 C20H21Cl2N3O2
分子量 406.306
MOL 文件 174634-09-4.mol
更新日期 2024/06/17 17:25:40
174634-09-4 結(jié)構(gòu)式 174634-09-4 結(jié)構(gòu)式

基本信息

中文別名
TAS-103雙鹽酸鹽
TAS-103(BMS-247615)鹽
拓?fù)洚悩?gòu)酶I和II抑制劑(TAS-103雙鹽酸鹽)
6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽
英文別名
CS-1342
TAS-103(2HCl)
BMS-247615-2HCl
TAS-103(BMS-247615)
TAS 103 (hydrochloride)
BMS247615 dihydrochloride
BMS-247615 dihydrochloride
BMS 247615 dihydrochloride
TAS-103 (dihydrochloride)
TAS 103 dihydrochloride, BMS 247615 dihydrochloride
所屬類(lèi)別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

儲(chǔ)存條件Inert atmosphere,2-8°C
溶解度PBS (pH 7.2):1.0(Max Conc. mg/mL);2.46(Max Conc. mM)
形態(tài)結(jié)晶固體
顏色Brown to orange

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
防范說(shuō)明P261-P305+P351+P338
6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2025/02/08HY-13758A6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽
TAS-103 dihydrochloride
174634-09-41 mg500元
2025/02/08HY-13758A6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽
TAS-103 dihydrochloride
174634-09-45mg1100元
2025/02/08HY-13758A6-[[2-(二甲基氨基)乙基]氨基]-3-羥基-7H-茚并[2,1-C]喹啉-7-酮二鹽酸鹽
TAS-103 dihydrochloride
174634-09-410mM * 1mLin Water1210元

常見(jiàn)問(wèn)題列表

生物活性
TAS-103 dihydrochloride 是一種 DNA 拓?fù)洚悩?gòu)酶 I/II (topoisomerase I/II) 雙重抑制劑,可用于癌癥研究。
靶點(diǎn)

Topoisomerase I

Topoisomerase II

體外研究

TAS-103 is a dual inhibitor of DNA topoisomerase I/II. TAS-103 (0.1-10 μM) is active on CCRF-CEM cells, with an IC 50 value of 5 nM. TAS-103 (0.1 μM) significantly increases levels of topo IIα FITC immunofluorescence in individual CCRF-CEM cells. TAS-103 (0.01-1 μM) is highly cytotoxic to Lewis lung carcinoma (LLC) cells, and Liposomal TAS-103 is almost as active as free TAS-103. TAS-103 inhibits the viability of HeLa cells, with an IC 50 of 40 nM. TAS-103 (10 μM) disrupts signal recognition particle (SRP) complex formation, and induces destabilization of SRP14 and SRP19 and its eventual degradation.

體內(nèi)研究

TAS-103 (30 mg/kg, i.v.) causes significant tumor growth suppression in mice bearing Lewis lung carcinoma (LLC) cells, without obvious body weight loss, and the liposomal TAS-103 is more active than free TAS-103.

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