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1992047-64-9

中文名稱 MS023 二鹽酸鹽
英文名稱 MS023 dihydrochloride
CAS 1992047-64-9
分子式 C??H??Cl?N?O
更新日期 2024/12/20 09:35:51
分子量 323.87
MOL 文件 1992047-64-9.mol
1992047-64-9 結(jié)構(gòu)式 1992047-64-9 結(jié)構(gòu)式

基本信息

中文別名
MS-023 HCL(新增分子)
化合物 MS023 DIHYDROCHLORIDE
英文別名
MS023 dihydrochloride
所屬類別
表面活性劑:胺鹽型

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO: ≥ 150 mg/mL (416.30 mM)
形態(tài)Solid
顏色Gray to gray purple
MS023 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CAS號(hào)包裝價(jià)格
2024/11/08HY-19615BMS023 DIHYDROCHLORIDE
MS023 dihydrochloride
1992047-64-910mM * 1mLin DMSO793元
2024/11/08HY-19615BMS023 DIHYDROCHLORIDE
MS023 dihydrochloride
1992047-64-95mg829元
2024/11/08HY-19615BMS023 DIHYDROCHLORIDE
MS023 dihydrochloride
1992047-64-910mg1303元

常見(jiàn)問(wèn)題列表

生物活性
MS023 dihydrochloride 是一種有效選擇性的,具有細(xì)胞活性的人 I 型蛋白精氨酸甲基轉(zhuǎn)移酶 (PRMTs) 抑制劑,對(duì) PRMT1,PRMT3,PRMT4,PRMT6 和 PRMT8 的 IC50 分別為 30,119,83,4 和 5 nM。
靶點(diǎn)

IC50: 30 nM (PRMT1), 119 nM (PRMT3), 83 nM (PRMT4), 4 nM (PRMT6), 5 nM (PRMT8)

體外研究

MS023 (1-1000 nM; 48 hours) inhibits PRMT1 methyltransferase activity in MCF7 cells.
MS023(1-1000 nM; 20 hours) inhibits PRMT6 methyltransferase activity in HEK293 cells.

Western Blot Analysis

Cell Line: MCF7 and HEK293 cells
Concentration: 1.4, 4, 12, 37, 111, 333, and 1000 nM
Incubation Time: 48 hours for MCF7 cells; 20 hours for HEK293 cells
Result: Treatment potently and concentration-dependently reduced cellular levels of H4R3me2a (IC 50 =9±0.2 nM).
Treatment concentration-dependently reduced the H3R2me2a mark (IC 50 =56±7 nM).
體內(nèi)研究

Administration of MS023 (160 mg/kg, i.p) in combination with PKC412 (100 mg/kg, i.g.) blocks MLL-r acute lymphoblastic leukemia (ALL) propagation by inhibiting maintenance of functional MLL-r ALL-initiating cells.

Animal Model: NOD-scid IL2Rgnull (NSG) mice bearing primary MLL-r ALL cells
Dosage: 160 mg/kg
Administration: Intraperitoneal injection; PKC412 (100 mg/kg, i.g.), MS023 (160 mg/kg, i.p), or a combination for 4 weeks
Result: Combinatorial treatment extended survival of leukemic mice relative to single treatments.
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