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當(dāng)前位置:杭州昊鑫生物科技股份有限公司>>MCE>> HY-18234A亮肽素
HY-18234A
MCE
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杭州市
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更新時(shí)間:2024-06-27 15:05:11瀏覽次數(shù):299次
聯(lián)系我時(shí),請(qǐng)告知來(lái)自 制藥網(wǎng)| CAS號(hào) | 103476-89-7 | 產(chǎn)地 | 國(guó)產(chǎn) |
|---|---|---|---|
| 規(guī)格 | 5mg | 級(jí)別 | 化工級(jí) |
| 證書(shū) | ISO系列證書(shū) |
Leupeptin hemisulfate 是一種可透過(guò)膜的巰基蛋白酶抑制劑,可抑制 Cathepsin B, Cathepsin H 和 Cathepsin L,并損害兩性溶酶體的融合。Leupeptin hemisulfate 也具有抗yan作用。

生物活性
Leupeptin hemisulfate is a membrane-permeable thiol protease inhibitor that inhibits Cathepsin B, Cathepsin H and Cathepsin L, and also impairs amphisome-lysosome fusion[1]. Leupeptin hemisulfate also exhibits anti-inflammatory effect[2]
IC50 & Target:Cathepsin[1]
體內(nèi)研究(In Vivo)
Leupeptin (0-36 mg/kg; intraperitoneal injection; for 4 hours; C57BL/6NCrl male mice) is well tolerated by the animals and produces a strong, dose-dependent increase in LC3b-II in both the total tissue extracts and the lysosome and autophagosome-enriched pellet fraction
| Animal Model: | C57BL/6NCrl male mice (6-8 weeks old, 20-25 g)[1] |
| Dosage: | 0 mg/kg, 9 mg/kg, 18 mg/kg, 36 mg/kg |
| Administration: | Intraperitoneal injection; for 4 hours |
| Result: | Promoted the accumulation of LC3b-II in mouse liver. |
分子量:475.59
Formula:C20H38N6O4.1/2H2SO4
CAS 號(hào):103476-89-7
equence Shortening:Ac-LLR-CHO
中文名稱(chēng):亮肽素
運(yùn)輸條件:Room temperature in continental US; may vary elsewhere.
儲(chǔ)存方式:
-20°C, sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
溶解性數(shù)據(jù)
H2O : 83.33 mg/mL (175.21 mM; ultrasonic and warming and heat to 60°C)
| 濃度溶劑體積質(zhì)量 | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.1027 mL | 10.5133 mL | 21.0265 mL |
| 5 mM | 0.4205 mL | 2.1027 mL | 4.2053 mL |
| 10 mM | 0.2103 mL | 1.0513 mL | 2.1027 mL |
請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合
參考文獻(xiàn)
[1]. Haspel J, et al. Characterization of macroautophagic flux in vivo using a leupeptin-based assay. Autophagy. 2011 Jun;7(6):629-42.
[2]. Aoyagi T, et al. Biological activities of leupeptins. J Antibiot (Tokyo). 1969 Nov;22(11):558-68.
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