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Leupeptin hemisulfate (Synonyms: 亮肽素)
Leupeptin hemisulfate 是一種可透過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：103476-89-7
equence Shortening：Ac-LLR-CHO
中文名稱：亮肽素
運輸條件：Room temperature in continental US; may vary elsewhere.
儲存方式：
-20°C, sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
溶解性數據
H2O : 83.33 mg/mL (175.21 mM; ultrasonic and warming and heat to 60°C)
| 濃度溶劑體積質量 | 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 |
請根據產品在不同溶劑中的溶解度選擇合
參考文獻
[2]. Aoyagi T, et al. Biological activities of leupeptins. J Antibiot (Tokyo). 1969 Nov;22(11):558-68.
Leupeptin hemisulfate (Synonyms: 亮肽素)
Leupeptin hemisulfate 是一種可透過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：103476-89-7
equence Shortening：Ac-LLR-CHO
中文名稱：亮肽素
運輸條件：Room temperature in continental US; may vary elsewhere.
儲存方式：
-20°C, sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
溶解性數據
H2O : 83.33 mg/mL (175.21 mM; ultrasonic and warming and heat to 60°C)
| 濃度溶劑體積質量 | 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 |
請根據產品在不同溶劑中的溶解度選擇合
參考文獻
[2]. Aoyagi T, et al. Biological activities of leupeptins. J Antibiot (Tokyo). 1969 Nov;22(11):558-68.
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