153088-73-4
中文名称
CASPASE-1 INHIBITOR V ;Z-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE
英文名称
Z-ASP-2,6-DICHLOROBENZOYLOXYMETHYLKETONE
CAS
153088-73-4
分子式
C20H17Cl2NO7
分子量
454.26
MOL 文件
153088-73-4.mol
更新日期
2024/05/24 13:17:50
153088-73-4 结构式
基本信息
中文别名
半胱天冬酶-1 抑制剂 VPASE-1 INHIBITOR V
英文别名
Z-D-CH2-DCBZ-ASP-CH2-DCB
ICE INHIBITOR V
ICE INHIBITOR VI
CASPASE-1 INHIBITOR V
CASPASE-1 INHIBITOR III
Z-ASP-[(2,6-DICHLOROBENZOYL)OXY]METHANE
Z-ASP-2,6-DICHLOROBENZOYLOXYMETHYLKETONE
N-CBZ-L-ASPARTIC ACID A-(2 6-DICHLORO- &
Z-L-ASP-ALPHA-[(2,6-DICHLOROBENZOYL)OXY]METHANE
物理化学性质
储存条件−20°C
溶解度溶于 DMSO(高达 25 mg/ml)。
形态白色至类白色粉末。
颜色白色
稳定性自购买之日起 1 年内保持稳定。 DMSO 中的溶液可在 -20° 下保存长达 3 个月。
CASPASE-1 INHIBITOR V ;Z-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE价格(试剂级)
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2024/04/30 | HY-113953 | CASPASE-1 INHIBITOR V ;Z-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE Z-Asp-CH2-DCB | 153088-73-4 | 1mg | 500元 |
2024/04/30 | HY-113953 | CASPASE-1 INHIBITOR V ;Z-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE Z-Asp-CH2-DCB | 153088-73-4 | 5mg | 800元 |
2024/04/30 | HY-113953 | CASPASE-1 INHIBITOR V ;Z-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE Z-Asp-CH2-DCB | 153088-73-4 | 10 mM * 1 mLin DMSO | 880元 |
常见问题列表
生物活性
Z-Asp-CH2-DCB 是一种不可逆的广谱 caspase 抑制剂,Z-Asp-CH2-DCB 也能抑制具有 caspase 样活性的蛋白酶。Z-D-CH2-DCB 并以剂量依赖的方式阻断 PBMC 细胞中的金黄色葡萄球菌肠毒素 B (SEB) 刺激的 IL-1β、TNF-α、IL-6 和 IFN-γ 的产生,和降低 SEB-1 刺激的 T 细胞增殖。Z-Asp-CH2-DCB 可预防 SU5416 诱导的间隔细胞凋亡和肺气肿的发生。体外研究
Z-Asp-CH2-DCB (10-100 μM) blocks the production of IL-1β, TNF-α, IL-6, and IFN-γ in SEB-stimulated (200 ng; 16 hours) PBMC in a dose-dependent manner. The production of the chemokines MCP-1, MIP-1α, and MIP-1β was also suppresses. The inhibitory effect of Z-Asp-CH2-DCB on TSST-1-activated PBMC is similar, reducing IL-1β, IL-6, TNF-α, IFN-γ, MCP-1, MIP-1α, and MIP-1β to 10, 36, 25, 10, 11, 25, and 30%, respectively, of levels in untreated cells.
Z-Asp-CH2-DCB (10-100 μM; 48 hours) inhibits T-cell proliferation in PBMC stimulated with 200 ng of SEB/ml .
Cell Viability Assay
Cell Line: | Human peripheral blood mononuclear cells |
Concentration: | 10, 50, 100 μM |
Incubation Time: | 48 hours |
Result: | Inhibited T-cell proliferation in PBMC stimulated with SEB. |
体内研究
Z-Asp-CH2-DCB (1 mg; i.p.; every day for 3 weeks) prevents SU5416-induced septal cell apoptosis.
Animal Model: | Male Sprague-Dawley rats (SU5416+ Z-Asp-CH2-DCB group) |
Dosage: | 1 mg |
Administration: | Intraperitoneal injection; every day for 3 weeks |
Result: | The caspase 3-like activity in SU5416-treated rat lungs is significantly higher, whereas lungs from rats treated with SU5416+Z-Asp-CH2-DCB showed no increase in apoptotic activity. |