Swainsonine
CAS No. 72741-87-8
Swainsonine ( 苦马豆素 )
产品货号. M39478 CAS No. 72741-87-8
Swainsonine (Tridolgosir) 是一种天然的吲哚里西啶生物碱,是一种有效且可逆的 α-甘露糖苷酶 (α-mannosidase) 抑制剂。Swainsonine 诱导细胞凋亡 (apoptosis)和细胞周期停滞在 G2/M 期。Swainsonine 具有抗肿瘤活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | 获取报价 | 有现货 |
|
| 50MG | 获取报价 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Swainsonine
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Swainsonine (Tridolgosir) 是一种天然的吲哚里西啶生物碱,是一种有效且可逆的 α-甘露糖苷酶 (α-mannosidase) 抑制剂。Swainsonine 诱导细胞凋亡 (apoptosis)和细胞周期停滞在 G2/M 期。Swainsonine 具有抗肿瘤活性。
-
产品描述Swainsonine (Tridolgosir) is an natural indolizidine alkaloid, a potent and reversible α-mannosidase inhibitor. Swainsonine induces apoptosis and cell cycle arrest at G2/M phase. Swainsonine shows anti-tumor activity.
-
体外实验Swainsonine (1 mg/kg;腹腔注射;每天两次,持续 10 天) 和顺铂提高了小鼠的抗肿瘤功效。Animal Model:Eighty-seven sixty-day-old male C57BL/6 mice Dosage:1 mg/kg (cisplatin; 0.25 mg/kg, i.p., every other day for 10 days)Administration:I.p.; twice daily for ten days Result:Showed a significant reduction in ascites volume of 63.5% was observed in mice and a significant reduction in the percentage of cells in the G0/G1, S and G2 phases.
-
体内实验Swainsonine (0-40 μM;12 h) 在 U251 和 LN444 细胞中显示抗增殖活性。 Swainsonine (30 μM;12 h) 诱导细胞凋亡和细胞周期停滞在 G2/M 期,并降低 CyclinD1 和 CDK4 蛋白水平的表达,增加 p16 蛋白水平的表达。 Swainsonine (30 μM;12 h) 减少胶质瘤细胞迁移和侵袭。Cell Viability Assay Cell Line:U251, LN444 cells Concentration:0, 10, 20, 30, 40 μM Incubation Time:12 h Result:Inhibited cell viability in a dose-dependent manner, and shows no cytotoxicity in normal brain cells.Cell Cycle Analysis Cell Line:U251 cells Concentration:30 μM Incubation Time:12 h Result:Induced cell cycle arrest at G2/M phase.Apoptosis Analysis Cell Line:U251 cells Concentration:30 μM Incubation Time:12 h Result:Induced apoptosis with the cleaved-Caspase-3 and cleaved-Caspase-9 expression were obviously increased.
-
同义词苦马豆素
-
通路Others
-
靶点Other Targets
-
受体α-mannosidase
-
研究领域———
-
适应症———
化学信息
-
CAS Number72741-87-8
-
分子量173.21
-
分子式C8H15NO3
-
纯度>98% (HPLC)
-
溶解度DMSO : 10 mg/mL (57.73 mM; ultraphonic; ) Ethanol : 10 mg/mL (57.73 mM; ultraphonic)
-
SMILESOC1CN2CCCC(O)C2C1O
-
化学全称OC1CN2CCCC(O)C2C1O
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Dorling PR, et al. Inhibition of lysosomal alpha-mannosidase by swainsonine, an indolizidine alkaloid isolated from Swainsona canescens. Biochem J. 1980 Nov 1;191(2):649-51.?
产品手册
关联产品
-
β-Casomorphin, bovin...
β-Casomorphin, bovine TFA (β-Casomorphin-7 (bovine) TFA) is a opioid peptide with an IC50 of 14 μM in an Opioid receptors binding assay.
-
TAT-amide
TAT-amide is a cell penetrating peptide. Cell-penetrating peptides (CPPs) are short amino acid sequences able to enter different cells.
-
BI-9321 trihydrochlo...
BI-9321 trihydrochloride 是一种有效的,选择性的,具有细胞活性的 NSD3-PWWP1 拮抗剂,Kd 值为 166 nM。BI-9321 对 NSD2-PWWP1 和 NSD3-PWWP2 无效。BI-9321 trihydrochloride 在 U2OS 细胞中特异性破坏 NSD3-PWWP1 与组蛋白相互作用,IC50 为 1.2 μM。
021-51111890
购物车()
sales@molnova.cn

