- Product Details
Keywords
- Z-FA-FMK
- Purity: >98%
- Z-FA-FMK, Z-Phe-Ala-fluoromethyl ketone
Quick Details
- ProName: Z-FA-FMK
- CasNo: 197855-65-5
- Molecular Formula: C21H23N2O4F
- Application: Z-FA-FMK is an irreversible inhibitor ...
- ProductionCapacity: 10 Milligram /Day
- Purity: 98%
- LimitNum: 1 Milligram
Superiority
Product name:Z-FA-FMK
Purity:98%
Discription:Z-FA-FMK is an irreversible inhibitor of cysteine protease.
General tips:For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
Shipping Condition:Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
Background:Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) A peptidyl fluoromethyl ketone (cathepsin B) was found to be an effective compound in a time dependent inactivation of cathepsin B isozymes from a number of tissues including human tumors The inhibitor of cathepsins B and L Z-FA-fmk blocks the induction of DEVDase activity, DNA fragmentation, and externalization of phosphatidylserine by selective RRMs. Z-FA-FMK can inhibit caspase activity in vitro and selectively inhibits recombinant effector caspases 2, -3, -6, and -7. In contrast, purified initiator caspases 8 and 10 are not affected, whereas the apoptosome-associated caspase 9 is only partially inhibited by Z-FA-FMK in vitro. It is an inhibitor of cysteine proteases, such as cathepsin B, which do not require a P1 Asp residue. It may be used as a negative control inhibitor for FMK P1 Asp caspase inhibitors.