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  • T76251Ac-FEID-CMK；化合物 Ac-FEID-CMKAc-FEID-CMK

    Ac-FEID-CMK, a potent peptide inhibitor derived from zebrafish-specific GSDMEb, effectively reduces mortality and kidney injury during septic shock by inhibiting pyroptosis and mitigating acute kidney injury (AKI) in vivo. Additionally, it suppresses the caspy2-mediated noncanonical inflammasome pathway [1].

    价 格：￥电议型 号：T76251产 地：中国大陆

  • T76201LEESGGGLVQPGGSMK TFA；化合物 LEESGGGLVQPGGSMK TFALEESGGGLVQPGGSMK TFA

    LEESGGGLVQPGGSMK TFA, a proteolysis peptide component of Infliximab, serves for the quantitative analysis of the latter. Infliximab is a chimeric monoclonal IgG1 antibody, binding specifically to TNF-α [1].

    价 格：￥电议型 号：T76201产 地：中国大陆

  • T75938Z-VRPR-FMK TFA；化合物 Z-VRPR-FMK TFAZ-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) infection [1].

    价 格：￥电议型 号：T75938产 地：中国大陆

  • T7591Coluracetam；考拉西坦MKC-231；MKC-231|||考拉西坦

    Coluracetam (MKC-231)(MKC-231) is a Choline Uptake Enhancer.

    价 格：￥电议型 号：T7591产 地：中国大陆

  • T75812MMK1 TFA；化合物 MMK1 TFAMMK1 TFA

    MMK1 TFA is a potent, selective agonist for the human formyl peptide receptor like-1 (FPRL-1/FPR2), exhibiting EC50 values of <2 nM for FPRL-1 and >10,000 nM for FPR1. This compound acts as a powerful chemotactic and calcium-mobilizing agent, effectively activating phagocytic leukocytes. It significantly enhances the Pertussis Toxin-sensitive production of proinflammatory cytokines IL-1b and IL-6 by human monocytes. Additionally, MMK1 TFA has been demonstrated to exhibit anxiolytic-like activity

    价 格：￥电议型 号：T75812产 地：中国大陆

  • T75706Ac-DEVD-CMK TFA；化合物 Ac-DEVD-CMK TFAAc-DEVD-CMK TFA

    Ac-DEVD-CMK (Caspase-3 Inhibitor III) TFA is a selective and irreversible inhibitor of caspase-3, effectively preventing apoptosis triggered by elevated glucose levels or 3,20-dibenzoate (IDB). It is applicable in diverse experimental settings to impede apoptosis, as supported by references [1] [2] [3].

    价 格：￥电议型 号：T75706产 地：中国大陆

  • T75629Ganoderic acid Mk；化合物 Ganoderic acid MkGanoderic acid Mk

    Ganoderic acid Mk (GA-Mk), a triterpenoid acid derived from Ganoderma lucidum mycelia, exhibits potent anti-proliferative properties and can induce apoptosis in HeLa cells through a mitochondria-mediated pathway, making it significant for cervical cancer research [1] [2].

    价 格：￥电议型 号：T75629产 地：中国大陆

  • T73462MK-8189；化合物 MK-8189MK-8189

    MK-8189 is a potent, orally active, and selective inhibitor of Phosphodiesterase 10A (PDE10A), exhibiting a K i value of 29 pM. It has potential applications in the research of schizophrenia.

    价 格：￥电议型 号：T73462产 地：中国大陆

  • T73438MK-3402；化合物 MK-3402MK-3402

    MK-3402 is a metallo-beta-lactamase inhibitor. MK-3402can be used in the research of bacteria .

    价 格：￥电议型 号：T73438产 地：中国大陆

  • T73412AAF-CMK；化合物 AAF-CMKAAF-CMK

    AAF-CMK, a tripeptidylpeptidase II (TPPII) inhibitor, exhibits anti-tumor activity and induces apoptosis, making it applicable in leukemia research.

    价 格：￥电议型 号：T73412产 地：中国大陆

  • T73410MK-4541；化合物 MK-4541MK-4541

    MK-4541 is an orally active, selective androgen receptor (AR) modulator that serves as an antagonist to inhibit 5α-reductase. It effectively inhibits proliferation and induces apoptosis in AR-positive prostate cancer cells, significantly reducing the growth of R3327-G prostate tumors in a xenograft mouse model.

    价 格：￥电议型 号：T73410产 地：中国大陆

  • T73096Z-LEVD-FMK；化合物 Z-LEVD-FMKZ-LEVD-FMK

    Z-LEVD-FMK, a cell-permeable caspase-4 inhibitor, effectively blocks endoplasmic reticulum (ER) stress-induced apoptosis in cancer cells.

    价 格：￥电议型 号：T73096产 地：中国大陆

  • T73093Z-VRPR-FMK；化合物 Z-VRPR-FMKZ-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 activation and MMP (matrix metalloproteinase) expression.

    价 格：￥电议型 号：T73093产 地：中国大陆

  • T72745Acipimox sodium；化合物 Acipimox sodiumK-9321 sodium；K-9321 sodium

    Acipimox (K-9321) sodium, a nicotinic acid analogue, functions as an antilipolytic agent by stimulating leptin release, inhibiting lipolysis, and reducing systemic free fatty acids (FFAs) levels, thereby enhancing insulin sensitivity.

    价 格：￥电议型 号：T72745产 地：中国大陆

  • T72435Z-LE(OMe)TD(OMe)-FMK；化合物 Z-LE(OMe)TD(OMe)-FMKZ-LE(OMe)TD(OMe)-FMK

    Z-LE(OMe)TD(OMe)-FMK is a selective inhibitor of caspase-8, effectively inhibiting cellular apoptosis.

    价 格：￥电议型 号：T72435产 地：中国大陆

  • T72399LIMK1 inhibitor BMS-4；化合物 LIMK1 inhibitor BMS-4LIMK1 inhibitor BMS-4

    LIMK1 inhibitor BMS-4 is a compound targeting LIM Kinase (LIMK) 1/2, specifically inhibiting the phosphorylation of its substrate, cofilin, but it remains noncytotoxic on A549 cells.

    价 格：￥电议型 号：T72399产 地：中国大陆

  • T72281Caspase-9 Inhibitor III；化合物 Caspase-9 Inhibitor IIIAc-LEHD-cmk；Ac-LEHD-cmk

    Caspase-9 Inhibitor III (Ac-LEHD-cmk), a caspase-9 inhibitor, exhibits protective effects against ischemia-reperfusion-induced myocardial injury.

    价 格：￥电议型 号：T72281产 地：中国大陆

  • T72145Montelukast dicyclohexylamine；化合物 Montelukast dicyclohexylamineMK0476 dicyclohexylamine；MK0476 dicyc

    Montelukast dicyclohexylamine (MK0476), a potent, selective, and orally active antagonist of the cysteinyl leukotriene receptor 1 (CysLT1), is utilized in the research of asthma, liver injury, and COVID-19. It exhibits antioxidant properties in the context of intestinal ischemia-reperfusion injury and can mitigate cardiac damage. Additionally, it reduces eosinophil infiltration in the airways of asthmatic patients.

    价 格：￥电议型 号：T72145产 地：中国大陆

  • T72111Ala-Ala-Pro-Val-chloromethylketone；化合物 Ala-Ala-Pro-Val-chloromethylketoneAAPV-CMK；AAPV-CMK

    Ala-Ala-Pro-Val-chloromethylketone serves as an irreversible inhibitor of human neutrophil elastase (NE), utilized in researching chronic inflammatory airway diseases.

    价 格：￥电议型 号：T72111产 地：中国大陆

  • T71613MK-8712；化合物 MK-8712MK-8712

    MK-8712 is a monobactam beta-lactamase inhibitor.

    价 格：￥电议型 号：T71613产 地：中国大陆

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