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1190-53-0

中文名稱 鹽酸丁雙胍
英文名稱 BuforMin Hydrochloride
CAS 1190-53-0
分子式 C6H16ClN5
分子量 193.68
MOL 文件 1190-53-0.mol
更新日期 2024/12/25 20:56:18
1190-53-0 結(jié)構(gòu)式 1190-53-0 結(jié)構(gòu)式

基本信息

中文別名
鹽酸丁福明
鹽酸丁二胍
鹽酸丁雙胍
丁福明鹽酸鹽
丁雙胍鹽酸鹽
鹽酸丁雙胍 標(biāo)準(zhǔn)品
N-丁基雙胍鹽酸鹽
鹽酸丁二胍/鹽酸丁福明
正丁基亞胺基二碳亞胺二酰胺鹽酸鹽
鹽酸丁福明, 鹽酸丁二胍, 鹽酸丁雙胍
英文別名
BUTYL-BIGUANIDE HYDROCHLORIDE
Andere
Adebit
TideMol
Biforon
Sindiatil
PanforMin
Ziavetine
NSC528218
Aids126511
所屬類別
原料藥:胰腺激素及其它調(diào)節(jié)血糖藥

物理化學(xué)性質(zhì)

熔點(diǎn)177-179?C
儲(chǔ)存條件-20°C Freezer, Under Inert Atmosphere
溶解度DMSO(少許)、甲醇(少許)、水(少許)
形態(tài)固體
顏色白色至灰白色
穩(wěn)定性吸濕性
CAS 數(shù)據(jù)庫1190-53-0

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
警示詞危險(xiǎn)
危險(xiǎn)性描述H302-H315-H318-H335
危險(xiǎn)類別碼22-43-36
安全說明36/39-46
海關(guān)編碼29212900
毒性LD50 i.p. in mice: 380 mg/kg (Rikimaru)

常見問題列表

生物活性
Buformin hydrochloride (1-Butylbiguanide hydrochloride) 是一種有效的 AMPK 活化劑,也是具有口服活性的雙胍類降血糖試劑 (antidiabetic agent)。Buformin 降低肝糖異生并降低血糖生成。Buformin 也具有抗癌活性,可以應(yīng)用于癌癥研究,如宮頸癌、乳腺癌等。
體外研究

Buformin hydrochloride (0-10?mM; 5 days) inhibits SKBR3 and BT474 cells growth as a concentration-dependent manner, exhibits IC 50 values of 246.7?μM and ?98.6?μM for erbB-2-overexpressing SKBR3 and BT474 cells, respectively.Buformin hydrochloride (0-3 mM; 48 hours) ?increases the percentage of cells in G0/G1 phase and reduced the percentage of cells in S phase, especially in the SKBR3 cells.Buformin hydrochloride (0-3 mM; 24 hours) suppresses RTK activation, including erbB-2 and IGF1R signaling ?downstream, and Akt activation/phosphorylation is inhibited in both SKBR3 and BT474 cells.

Cell Viability Assay

Cell Line: ErbB-2-overexpressing SKBR3 and BT474 cells
Concentration: 0 μM, 1 μM, 3 μM, 10 μM, 30 μM, 100 μM, 300 μM, 1, 3, or 10 mM
Incubation Time: 5 days
Result: Reduced cell viability in erbB-2-overexpressing breast cells.

Cell Cycle Analysis

Cell Line: ErbB-2-overexpressing SKBR3 and BT474 cells
Concentration: 0.5 mM; 1 mM; 3 mM
Incubation Time: 48 hours
Result: Increased cells arresting in G0/G1 phase.

Western Blot Analysis

Cell Line: ErbB-2-overexpressing SKBR3 and BT474 cells
Concentration: 0 mM, 0.1 mM, 0.3 mM, 1 mM, or 3 mM
Incubation Time: 24 hours
Result: Decreased p-AMPK, p-p706S, p-ERK1/2 expression in a concentration-dependent manner.
體內(nèi)研究

Buformin hydrochloride (oral administation; 7.6?mmol/kg of chow; 7 days) exhibits significantly reduced tumor volumes and weights, and?hinders mammary morphogenesis and proliferation in MMTV-erbB-2 transgenic mice.

Animal Model: Female MMTV-erbB-2 transgenic mice
Dosage: 7.6 mmol/kg
Administration: Oral administation; 7 days
Result: Inhibited mammary syngeneic tumor growth in MMTV-erbB-2 transgenic mice.
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