Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0310 |
FMK
|
S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
FMK 是一种不可逆的 RSK2 抑制剂,能够共价修饰 RSK 的 C 末端区域。 | |||
T6013 |
Z-VAD(OMe)-FMK
Z-VAD-FMK,Z-Val-Ala-Asp(OMe)-FMK |
Caspase | Apoptosis; Proteases/Proteasome |
Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) 是一种 caspase 的广谱抑制剂,具有细胞渗透性和不可逆性。Z-VAD(OMe)-FMK 与活化的 caspase 结合,从而抑制细胞凋亡。 | |||
T7020 |
Z-VAD-FMK
Z-VAD(OH)-FMK,Caspase Inhibitor VI,Z-VAD |
Caspase | Apoptosis; Proteases/Proteasome |
Z-VAD-FMK (Caspase Inhibitor VI) 是一种 caspase 的广谱抑制剂,具有不可逆性。Z-VAD-FMK 与活化的 caspase 结合,从而抑制细胞凋亡。 | |||
T7019 |
Z-IETD-FMK
Z-IE(OMe)TD(OMe)-FMK,Caspase-8 Inhibitor |
Caspase | Apoptosis; Proteases/Proteasome |
Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) 是一种选择性 caspase 8 抑制剂,具有细胞渗透性。它也是颗粒酶 B 抑制剂。 | |||
TP1466 |
Z-YVAD-FMK
|
Caspase | Apoptosis; Proteases/Proteasome |
Z-YVAD-FMK 是一种不可逆的 caspase-1 抑制剂,具有抗炎和抗肿瘤活性。 | |||
T15303 |
FMK 9a
|
Cysteine Protease; Autophagy | Autophagy; Proteases/Proteasome |
FMK 9a 是一种不可逆的 ATG4B 抑制剂,在 TR-FRET 和基于细胞的 LRA 试验中 IC50 值为 80 和 73 nM。 | |||
T21835 |
Z-LEHD-fmk
|
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Z-LEHD-FMK 是一种具有选择性和有效性的 caspase-9 抑制剂,可防减轻再灌注损伤,减缓细胞凋亡。Z-LEHD-FMK 具有抗肿瘤和神经保护活性,可提高体外生产的水牛 (Bubalus bubalis) 植入前胚胎的产量并改变细胞应激反应。 | |||
T6005 |
Z-DEVD-FMK
Caspase-3 Inhibitor |
Caspase | Apoptosis; Proteases/Proteasome |
Z-DEVD-FMK (Caspase-3 Inhibitor) 是一种选择性、不可逆的 Caspase-3 抑制剂,IC50为 18 μM。 它也抑制 caspase-6、caspase-7、caspase-8 和 caspase-10。 | |||
T6738 |
Z-FA-FMK
|
SARS-CoV; Cysteine Protease | Microbiology/Virology; Proteases/Proteasome |
Z-FA-FMK 是一种广谱的卤代甲基酮抑制剂,可抑制冠状病毒蛋白酶3CL,Ki 为 25.7 μM。它可以不可逆地抑制半胱氨酸蛋白酶,也可以抑制效应半胱天冬酶。 | |||
T10580 |
BOC-D-FMK
|
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Boc-D-FMK 是一种可渗透细胞,不可逆的泛半胱天冬酶抑制剂。它抑制 TNF-α 诱导的细胞凋亡的IC50值为 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 active form, caspase cascade activation, and apoptosis.[2] | |||
T11310 |
FMK-MEA
|
Others | Others |
FMK-MEA is a potent and selective p90 Ribosomal S6 Kinase (RSK) inhibitor. | |||
T39308 |
Boc-Asp(OMe)-fluoromethyl ketone
Boc-Asp(OMe)-fluoromethyl ketone,Boc-Asp(OMe)-FMK |
Caspase | Apoptosis; Proteases/Proteasome |
Boc-Asp(OMe)-fluoromethyl ketone (Boc-Asp(OMe)-FMK) 是广谱的 caspase 抑制剂,可抑制 Fas 介导的吞噬作用和氧化破裂抑制,但对 IL-8 的趋化活性无影响。 | |||
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 potential in a rat model of spinal cord trauma. | |||
T38469 |
(Rac)-Z-Phe-Phe-FMK
Cathepsin L-IN-2 |
Beta Amyloid; Cysteine Protease | Neuroscience; Proteases/Proteasome |
(Rac)-Z-Phe-Phe-FMK (Cathepsin L-IN-2) 是一种 cathepsin L 抑制剂,抑制 β-淀粉样蛋白诱导凋亡变化的倾向 。(Rac)-Z-Phe-Phe-FMK 通过 siRNA 敲低 LC3B 表达可抑制 PI 诱导的 IkappaBalpha 降解。 | |||
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. | |||
T78185 |
Ac-PLVE-FMK
Ac-Pro-Leu-Val-Glu(OMe)-CH2F |
Others | Others |
Ac-PLVE-FMK(Ac-Pro-Leu-Val-Glu(OMe)-CH2F),一种四肽基m-FMK化合物,具有Cats抑制作用,常用于癌症研究。 | |||
T23555 |
Z-VEID-FMK
|
Others | 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-Val-Glu(Ome)-Ile-Asp(OMe)-fluorometh | |||
T10548 |
Biotin-VAD-FMK
|
Caspase | Apoptosis; Proteases/Proteasome |
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 | Apoptosis; Proteases/Proteasome |
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). | |||
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. | |||
TP2037 |
Z-DQMD-FMK
|
||
Caspase-3 inhibitor. Inhibits MG 132-induced small cell lung cancer cell death in vitro. | |||
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-terminal tail, thereby occupying the P1' (leaving group) site, a binding site perhaps used by the unknown C-terminal extension of ubiquitin in the actual in vivo substrate(s) of UCHL1. | |||
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. | |||
T78186 |
Ac-VLPE-FMK
Ac-Val-Leu-Pro-Glu(OMe)-CH2F |
||
Ac-VLPE-FMK为一种四肽基单氟甲基酮(m-FMK),兼作Cat-B及Cat-L抑制剂,适用于癌症侵袭性研究。 | |||
T80551 |
Calpain inhibitor V
Mu-Val-HPh-FMK |
Antibiotic | Microbiology/Virology |
Calpain inhibitor V (Mu-Val-HPh-FMK) 为具抗衣原体活性的细胞渗透性不可逆钙蛋白酶抑制剂。 | |||
T80542 |
Z-Leu-Leu-Leu-fluoromethyl ketone
Z-LLL-FMK |
||
Z-Leu-Leu-Leu-fluoromethyl ketone (Z-LLL-FMK)为半胱氨酸蛋白酶抑制剂,可抑制SARS感染,并能保护小鼠免遭T. crassiceps侵害。 | |||
T73096 |
Z-LEVD-FMK
|
||
Z-LEVD-FMK 是一种细胞渗透性的caspase-4抑制剂。 Z-LEVD-FMK 阻断 ER 应激诱导的癌细胞凋亡。 | |||
T78632 |
Z-LLY-FMK
Calpain Inhibitor IV |
Proteasome | Proteases/Proteasome; Ubiquitination |
Z-LLY-FMK (Calpain Inhibitor IV) 为一种钙蛋白酶抑制剂,涉及调控多个细胞系统的凋亡过程。该化合物能够抑制胆总管结扎所引起的肠细胞凋亡(apoptosis)。 | |||
T76665 |
Z-LEED-FMK
|
||
Z-LEED-FMK 是 caspase-13和 caspase-4抑制剂。Z-LEED-FMK 还能抑制S. typhimurium 感染的巨噬细胞中caspase-1的加工。 | |||
T73093 | Z-VRPR-FMK | ||
Z-VRPR-FMK 是一种不可逆地 MALT1蛋白抑制剂。Z-VRPR-FMK 可通过抑制 MALT1诱导的 NF-κB 活化和 MMP 表达来抑制弥漫性大 B 细胞淋巴瘤的生长和侵袭。 | |||
T75938 |
Z-VRPR-FMK TFA
|
||
Z-VRPR-FMK (TFA) (VRPR) 为一种四肽类选择性及不可逆的粘膜相关淋巴组织淋巴瘤易位蛋白1 (MALT1) 抑制剂,具有抵抗甲型流感病毒 (IAV) 感染的能力。 | |||
T72435 |
Z-LE(OMe)TD(OMe)-FMK
|
||
Z-LE(OMe)TD(OMe)-FMK 是一种选择性的 caspase-8抑制剂,可以抑制细胞凋亡。 | |||
T83963 |
Z-DEVD-FMK Caspase-3 Inhibitor
|
||
Z-DEVD-FMK Caspase-3 Inhibitor 是一种可渗透细胞膜的、不可逆的 caspase-3/CPP32 抑制剂,能够抑制肿瘤细胞的凋亡。在动物体内,它在大鼠发作后的海马区具有神经保护作用,且显著减少创伤后的细胞凋亡,并在诱发的大鼠创伤性脑损伤之前和之后改善神经学恢复情况。 | |||
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 | Apoptosis; Metabolism; oxidation-reduction |
AFMK (Formyl-N-acetyl-5-methoxykynurenamine) 是褪黑激素的活性代谢物,具有抗氧化和自由基清除活性。 AFMK 是一种凋亡调节剂,可提高吉西他滨在 PANC-1 细胞中的抗肿瘤作用。 | |||
T10845 | CMK | Others | 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 the caspase-8 inhibitor lETD-fmk opposed CGP74514A -induced caspase-9 activation and PARP degradation, but not cytochrome c or Smac/DIABLO release. CGP74514A -mediated apoptosis was substantially blocked by ectopic expression of full-length Bel- 2, a loop-deleted mutant Bcl-2, and... |