![](../../files/images/goods/197855-65-5.png)
Z-FA-FMK
CAS No. 197855-65-5
Z-FA-FMK ( —— )
产品货号. M18194 CAS No. 197855-65-5
Z-FA-FMK 可以不可逆地抑制半胱氨酸蛋白酶,还可以抑制效应 caspase。
纯度: >98% (HPLC)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1604 | 有现货 |
![]() ![]() |
10MG | ¥2406 | 有现货 |
![]() ![]() |
25MG | ¥3880 | 有现货 |
![]() ![]() |
50MG | ¥5289 | 有现货 |
![]() ![]() |
100MG | ¥7525 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Z-FA-FMK
-
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Z-FA-FMK 可以不可逆地抑制半胱氨酸蛋白酶,还可以抑制效应 caspase。
-
产品描述Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
-
体外实验Z-FA-FMK ((1S)-Z-FA-FMK; 5-100 μM; 1 h; Jurkat cells) reduces levels of DEVDase activity and DNA fragmentation. Z-FA-FMK inhibits the externalization of phosphatidylserine induced by either MX2870-1 or MX781. Z-FA-FMK (100 μM; 1 h; Jurkat cells) inhibits apoptosis. Z-FA-FMK inhibited the induction of DEVDase activity not only by the RRMs but also by other apoptotic insults, including etoposide-, ceramide-, and CD95/Fas receptor-mediated pathways.Z-FA-FMK (0-100 μM; 1 h; Jurkat cells) inhibits caspases 2, -3, -6, and -7 activity through repressed induction of DEVDase activity in Jurkat cells. Z-FA-FMK (0-20 μM; 48 h; HT1080 and mouse embryonic stem cells) blocks reoviral replication and cures cells of a persistent infection with reovirus in vitro.Z-FA-FMK (20 μM; 48 h; HT1080 cells) induces defects in reoviral maturation.
-
体内实验Z-FA-FMK (1 mg/kg; intratumor injection; every 2 d, for 27 d; SCID mice with HT1080 xenograft) blocks reovirus infection in vivo.Z-FA-FMK (8 mg/kg; i.v.; every 2 d, once; male BALB/c mice) markedly lessens the degree of impairment seen in D-GalN/TNF-α-induced kidney injury. Animal Model:SCID mice with HT1080 xenograft (6-8 weeks)Dosage:1 mg/kg Administration:Intratumor injection; every 2 days, for 27 daysResult:Blocked reovirus replication activity in both tumor and heart tissues.Animal Model:Male BALB/c mice Dosage:8 mg/kg Administration:Intravenous injection; once, 1 hour later, intraperitoneal injection D-GalN (700 mg/kg) and TNF-α (15 μg/kg).Result:Decreased in the D-GalN/TNF-α-induced degenerative changes.Decreased in the number of activated caspase-3-positive tubular epithelial cell.Increased in kidney GSH levels, CAT, SOD and GPx activities and decreased in kidney LPO levels, LDH activity, serum AST and ALT activities, uric acid, and urea levels were determined.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Cysteine protease
-
研究领域Others-Field
-
适应症——
化学信息
-
CAS Number197855-65-5
-
分子量386.42
-
分子式C21H23FN2O4
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 250 mg/mL (646.96 mM)
-
SMILESCC(C(=O)CF)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
-
化学全称——
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. Rasnick D. Anal Biochem. 1985, 149(2), 461-465.
产品手册
![](/themes/theme/en/images/ct.png)
![](/themes/theme/en/images/new12.jpg)
![](/themes/theme/en/images/gift.jpg)
![](/themes/theme/en/images/ct2.png)
关联产品
-
PST2286
PST2286 是罗他福辛代谢物。
-
Uridine 5′-triphosph...
Uridine 5'-tri磷酸三盐是 P2Y 受体的激动剂,已用于研究细胞内 Ca2+ 的浓度,以及体外激酶测定的磷酸盐供体。
-
N3-C3-NHS ester
N3-C3-NHS 酯是一种不可切割的 ADC 连接子,用于合成抗体药物偶联物 (ADC)。