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カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
TQ0310 | FMK | S6 Kinase | |
FMK is an irreversible inhibitor of RSK2 kinase. | |||
T7020 | Z-VAD-FMK | Z-VAD(OH)-FMK,Caspase Inhibitor VI,Z-VAD | Caspase |
Z-VAD-FMK (Caspase Inhibitor VI) is a broad-spectrum inhibitor of caspases with irreversible properties. Z-VAD-FMK binds to activated caspases, thereby inhibiting apoptosis. | |||
T6013 | Z-VAD(OMe)-FMK | Z-VAD-FMK,Z-Val-Ala-Asp(OMe)-FMK | Caspase |
Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a broad-spectrum inhibitor of caspases that is cell-permeable and irreversible. Z-VAD(OMe)-FMK binds to activated caspases, thereby inhibiting apoptosis. | |||
T7019 | Z-IETD-FMK | Z-IE(OMe)TD(OMe)-FMK,Caspase-8 Inhibitor | Caspase |
Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) is a selective caspase 8 inhibitor, which has cell permeable. | |||
T15303 | FMK 9a | Cysteine Protease , Autophagy | |
FMK 9a is an irreversible inhibitor of ATG4B with IC50 values of 80 and 73 nM in the TR-FRET and cellular-based LRA assays. | |||
T6005 | Z-DEVD-FMK | Caspase-3 Inhibitor | Caspase |
Z-DEVD-FMK (Caspase-3 Inhibitor) is a selective, irreversible Caspase-3 inhibitor, and also exhibits effective inhibition activity on caspase-6, caspase-7, caspase-8, and caspase-10. | |||
T21835 | Z-LEHD-fmk | Apoptosis , Caspase | |
Z-LEHD-FMK is a selective and potent caspase-9 inhibitor that protects against reperfusion injury and slows apoptosis.Z-LEHD-FMK exhibits antitumor and neuroprotective activity, increases the yield of in vitro-produced p... | |||
TP1466 | Z-YVAD-FMK | Caspase | |
AA-Z-YVAD-FMK is a Irreversible caspase-1 inhibitor,with anti-inflammatory and anti-tumor activities. | |||
T6738 | Z-FA-FMK | SARS-CoV , Cysteine Protease | |
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases. | |||
T10580 | BOC-D-FMK | Apoptosis , Caspase | |
Boc-D-FMK is an irreversible, cell-permeable, and broad-spectrum caspase inhibitor and inhibits apoptosis stimulated by TNF-α (IC50: 39 µM). | |||
T36331 | Z-AEVD-FMK | Z-AEVD-FMK,Z-Ala-Glu-Val-Asp-Fluoromethyl Ketone | |
Z-AEVD-FMK is an irreversible inhibitor of caspase-10 and related caspases.[1] At 10 µM, it can prevent the initiation of Fas signaling by caspase-10 in Jurkat T lymphoma cells, preventing Bid cleavage into its activ... | |||
T11310 | FMK-MEA | Others | |
T39344 | Z-VDVA-(DL-Asp)-FMK | ||
Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2. | |||
T10548 | Biotin-VAD-FMK | Caspase | |
Biotin-VAD-FMK is a cell-permeable, irreversible biotin-labeled inhibitor of caspase. It is used to identify active caspases in cell lysates. | |||
TP2161 | Z-WEHD-FMK | Caspase | |
Z-WEHD-FMK is a cell-permeable and irreversible inhibitor of caspase-1/5. It also shows a robust inhibitory effect on cathepsin B activity (IC50: 6 μM). | |||
T40602 | Z-LEHD-FMK TFA | ||
Z-LEHD-FMK TFA is a specific and irreversible inhibitor of caspase-9, offering protection against detrimental reperfusion injury and moderating apoptosis. Additionally, Z-LEHD-FMK TFA demonstrates its neuroprotective pot... | |||
TP1014 | Z-VRPR-FMK (TFA) | VRPR | |
Z-VRPR-FMK (TFA) (VRPR) is a tetrapeptide and a selective and irreversible inhibitor of lymphoma translocation protein 1 (MALT1) in mucosa-associated lymphoid tissue. | |||
T23555 | Z-VEID-FMK | Others | |
When compared to other caspase inhibitors, Z-DRHD-FMK inhibited caspase 6 activity more effectively than the general caspase inhibitor of Z-Val-Ala-Asp (OMe)-fluoromethy ketone (Z-VAD-FMK) or the caspase 6 inhibitor Z-V... | |||
TP2037 | Z-DQMD-FMK | ||
Caspase-3 inhibitor. Inhibits MG 132-induced small cell lung cancer cell death in vitro. | |||
T38469 | (Rac)-Z-Phe-Phe-FMK | Cathepsin L-IN-2 | Beta Amyloid , Cysteine Protease |
(Rac)-Z-Phe-Phe-FMK (Cathepsin L-IN-2) is a cathepsin L inhibitor that inhibits the tendency of β-amyloid to induce apoptotic changes . | |||
T78186 | Ac-VLPE-FMK | Ac-Val-Leu-Pro-Glu(OMe)-CH2F | |
Ac-VLPE-FMK, a tetrapeptidyl mono-fluoromethyl ketone (m-FMK), functions as an inhibitor of both Cathepsin B (Cat-B) and Cathepsin L (Cat-L), and is utilized in research pertaining to the aggressiveness of cancer [1] [2]... | |||
T78185 | Ac-PLVE-FMK | Ac-Pro-Leu-Val-Glu(OMe)-CH2F | Others |
Ac-PLVE-FMK (Ac-Pro-Leu-Val-Glu(OMe)-CH2F), a tetrapeptidyl fluoromethylketone (FMKs), serves as a cathepsin inhibitor. It is utilized in cancer research [1]. | |||
T39308 | Boc-Asp(OMe)-fluoromethyl ketone | Boc-Asp(OMe)-fluoromethyl ketone,Boc-Asp(OMe)-FMK | Caspase |
Boc-Asp(OMe)-fluoromethyl ketone (Boc-Asp(OMe)-FMK) is a broad range caspase inhibitor. Boc-Asp(OME)-Fluoromethyl Ketone inhibits Fas-mediated phagocytosis and oxidative rupture inhibition, but does not affect the chemot... | |||
TP2101 | Z-VRPR-FMK trifluoroacetate salt | ||
Irreversible MALT1 inhibitor. Suppresses T cell activation-induced cleavage of Bcl-10 in a dose-dependent manor. Reduces Jurkat cell adhesion to fibronectin. Cell permeable. | |||
T71586 | Z-VAE(OMe)-fmk | ||
Z-VAE(OMe)-fmk is a cell-permeable and irreversible UCHL1 inhibitor. The inhibitor approaches the active-site cleft from the opposite side of the crossover loop as compared to the direction of approach of ubiquitin's C-t... | |||
T76665 | Z-LEED-FMK | ||
Z-LEED-FMK is a chemical compound that acts as an inhibitor for caspase-13 and caspase-4. Additionally, it impedes caspase-1 processing in S. typhimurium-infected macrophages [1] [2]. | |||
T80542 | Z-Leu-Leu-Leu-fluoromethyl ketone | Z-LLL-FMK | |
Z-Leu-Leu-Leu-fluoromethyl ketone (Z-LLL-FMK) functions as a cysteine protease inhibitor and has been shown to impede SARS infection. Furthermore, it affords protection to mice when challenged with T. crassiceps [1] [2]. | |||
T73096 | Z-LEVD-FMK | ||
Z-LEVD-FMK, a cell-permeable caspase-4 inhibitor, effectively blocks endoplasmic reticulum (ER) stress-induced apoptosis in cancer cells. | |||
T73093 | Z-VRPR-FMK | ||
Z-VRPR-FMK, an irreversible inhibitor of the MALT1 protein, effectively suppresses the proliferation and invasion of diffuse large B-cell lymphoma. This is achieved through the inhibition of MALT1-induced NF-κB activatio... | |||
T78632 | Z-LLY-FMK | Calpain Inhibitor IV | Proteasome |
Z-LLY-FMK (Calpain Inhibitor IV) serves as an inhibitor of calpain, a family of proteases implicated in the apoptosis of various cell systems. Specifically, this compound suppresses intestinal cell apoptosis following co... | |||
T80551 | Calpain inhibitor V | Mu-Val-HPh-FMK | Antibiotic |
Calpain Inhibitor V (Mu-Val-HPh-FMK) is a cell-permeable, irreversible calpain inhibitor with demonstrated anti-chlamydial activity [1]. | |||
T75938 | Z-VRPR-FMK TFA | ||
Z-VRPR-FMK (TFA), a selective and irreversible inhibitor of Mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1), is a tetrapeptide shown to provide protection against influenza A virus (IAV) infect... | |||
T83963 | Z-DEVD-FMK Caspase-3 Inhibitor | ||
Z-DEVD-FMK, a Caspase-3 Inhibitor, is an irreversible, cell-permeable inhibitor of caspase-3/CPP32 that impedes tumor cell apoptosis. In vivo studies show it offers neuroprotection in rat hippocampi post-seizures and con... | |||
T72435 | Z-LE(OMe)TD(OMe)-FMK | ||
Z-LE(OMe)TD(OMe)-FMK is a selective inhibitor of caspase-8, effectively inhibiting cellular apoptosis. | |||
T71584 | Microtubule Inhibitor 185322 | ||
Microtubule inhibitor 185322 is an inhibitor of microtubule assembly, inducung mitotic arrest and apoptosis of MM cells. | |||
T41345 | AFMK | Formyl-N-acetyl-5-methoxykynurenamine,Acetyl-N-formyl-5-methoxykynurenamine | Apoptosis , Free radical scavengers , Antioxidant , Endogenous Metabolite |
AFMK (Formyl-N-acetyl-5-methoxykynurenamine) is an active metabolite of Melatonin with antioxidant and free radical scavenging activity. AFMK is a modulator of apoptosis and improves the anti-tumor effect of Gemcitabine ... | |||
T10845 | CMK | Others | |
CMK, an RSK2 kinase inhibitor, shows similar potency but less chemical stability compared with FMK. | |||
T69200 | CGP74514A | ||
CGP74514A is a CDK1 inhibitor with potential anticancer activity. In U937 cells, CGP74514A - induced apoptosis (5 microM) became apparent within 4 hr and approached 100% by 24 hr. The pan- caspase inhibitor Boc-fmk and t... |