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T80553MeOSuc-AAPA-CMK；化合物 MeOSuc-AAPA-CMKMeOSuc-AAPA-CMK
MeOSuc-AAPA-CMK is a potent inhibitor of human neutrophil elastase (HNE) [1].
价 格：￥电议型 号：T80553产 地：中国大陆
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T80551Calpain inhibitor V；化合物 Calpain inhibitor VMu-Val-HPh-FMK；Mu-Val-HPh-FMK
Calpain Inhibitor V (Mu-Val-HPh-FMK) is a cell-permeable, irreversible calpain inhibitor with demonstrated anti-chlamydial activity [1].
价 格：￥电议型 号：T80551产 地：中国大陆
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T80549Calmodulin Kinase IINtide, Myristoylated；化合物 Calmodulin Kinase IINtide, MyristoylatedMyr-CaMKIINtide
Myristoylated Calmodulin Kinase IINtide (Myr-CaMKIINtide) serves as a selective and noncompetitive inhibitor of CaMKII [1].
价 格：￥电议型 号：T80549产 地：中国大陆
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T80542Z-Leu-Leu-Leu-fluoromethyl ketone；化合物 Z-Leu-Leu-Leu-fluoromethyl ketoneZ-LLL-FMK；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].
价 格：￥电议型 号：T80542产 地：中国大陆
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T80454BmK-M1；化合物 BmK-M1BmK-M1
BmK-M1, a scorpion-derived toxin, consists of a 64-amino acid polypeptide stabilized by four disulfide bridges. This compound functions as an inhibitor of the Na+ channel, classifying it as both a cardiotoxin and a neurotoxin [1].
价 格：￥电议型 号：T80454产 地：中国大陆
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T80101Z-GGF-CMK；化合物 Z-GGF-CMKZ-GGF-CMK
Z-GGF-CMK, a protease inhibitor, impedes ClpP1P2 and proteasome activity and demonstrates cytotoxic effects on HepG2 cells, with a CC50 value of 125 μM [1].
价 格：￥电议型 号：T80101产 地：中国大陆
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T79718CaMKIIα-PHOTAC；化合物 CaMKIIα-PHOTACCaMKIIα-PHOTAC
CaMKIIα-PHOTAC is a photochemically targeted chimera (PHOTAC) that specifically targets Ca2+/calmodulin-dependent protein kinase II α (CaMKIIα). This molecule facilitates the ubiquitination and subsequent proteasome-mediated degradation of CaMKIIα when exposed to certain light wavelengths. Under illumination, CaMKIIα-PHOTAC diminishes synaptic functions and weakens evoked field excitatory postsynaptic potentials in the mouse hippocampus, thus impacting physiological responses. Additionally, it i
价 格：￥电议型 号：T79718产 地：中国大陆
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T79302MK-8768；化合物 MK-8768MK-8768
MK-8768 is a potent, selective, and orally bioavailable negative allosteric modulator of the mGluR2 class, exhibiting an IC50 of 9.6 nM and characterized by excellent brain permeability.
价 格：￥电议型 号：T79302产 地：中国大陆
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T78716MKA031；化合物 MKA031MKA031
MKA031 (compound 6y) is a non-competitive inhibitor of macrophage migration inhibitory factor (MIF), exhibiting an IC50 of 1.7 μM. It disrupts the MIF-aryl hydrocarbon receptor interacting protein (AIF) interaction, impedes MIF nuclear translocation, and mitigates N-methyl-N´-nitro-N-nitrosoguanidine (MNNG)-induced cell death. MKA031 is applicable in research on chronic hepatitis C virus infection [1].
价 格：￥电议型 号：T78716产 地：中国大陆
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T78633MeOSuc-AAPV-CMK；化合物 MeOSuc-AAPV-CMKElastase Inhibitor III；Elastase Inhibitor III
MeOSuc-AAPV-CMK (Elastase Inhibitor III) serves as an inhibitor of elastase, as well as cathepsin G and proteinase 3, and impedes leukocyte elastase-mediated cleavage of adiponectin [1].
价 格：￥电议型 号：T78633产 地：中国大陆
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T78632Z-LLY-FMK；化合物 Z-LLY-FMKCalpain Inhibitor IV；Calpain Inhibitor IV
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 common bile duct ligation [1].
价 格：￥电议型 号：T78632产 地：中国大陆
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T7841MK 571；MK-571钠盐L660711|||L-660711|||MK-571；MK-571钠盐|||L660711|||L-660711|||MK-571
MK 571 (L660711) is an orally active antagonist of CysLT1 receptor.
价 格：￥电议型 号：T7841产 地：中国大陆
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T78186Ac-VLPE-FMK；化合物 Ac-VLPE-FMKAc-Val-Leu-Pro-Glu(OMe)-CH2F；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].
价 格：￥电议型 号：T78186产 地：中国大陆
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T78185Ac-PLVE-FMK；化合物 Ac-PLVE-FMKAc-Pro-Leu-Val-Glu(OMe)-CH2F；Ac-Pro-Leu-Val-Glu(OMe)-CH2F
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].
价 格：￥电议型 号：T78185产 地：中国大陆
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T78011Cyclic MKEY TFA；化合物 Cyclic MKEY TFACyclic MKEY TFA
Cyclic MKEY TFA, a synthetic cyclic peptide, inhibits CXCL4-CCL5 heterodimer formation, thus guarding against atherosclerosis and aortic aneurysm by mitigating inflammation. Additionally, it affords protection against stroke-induced brain injury in mice [1] [2].
价 格：￥电议型 号：T78011产 地：中国大陆
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T77132Clesrovimab；单抗ClesrovimabMK-1654；MK-1654
Clesrovimab (MK1654) is an anti-respiratory syncytial virus protein F human monoclonal antibody for the prevention and treatment of respiratory syncytial virus infections.
价 格：￥电议型 号：T77132产 地：中国大陆
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T76784Tildrakizumab；替瑞奇珠单抗MK 3222|||SCH 900222；MK 3222|||SCH 900222
Tildrakizumab (SCH 900222) is a potent humanized monoclonal antibody against IL-23 (p19 subunit). Tildrakizumab targets single-stranded IL-23 with a Kd value of 136 pM. Tildrakizumab can be used to study psoriasis and psoriasis.
价 格：￥电议型 号：T76784产 地：中国大陆
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T76711Golimumab；戈利木单抗MK-8259|||SCH 900259|||CNTO-148；MK-8259|||SCH 900259|||CNTO-148
Golimumab (CNTO-148) is a potent humanized anti-TNFα IgG1κ monoclonal antibody.Golimumab has anti-inflammatory and anticancer activity, inhibits the production of IL-6 and IL-1β, and induces apoptosis.Golimumab can be used to prevent inflammation and destruction of cartilage or bone, and can be used to study rheumatoid arthritis and cancer. Golimumab can be used to prevent inflammation and cartilage or bone destruction and can be used to study rheumatoid arthritis and cancer.
价 格：￥电议型 号：T76711产 地：中国大陆
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T76665Z-LEED-FMK；化合物 Z-LEED-FMKZ-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].
价 格：￥电议型 号：T76665产 地：中国大陆
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T76251LAc-FEID-CMK TFA；Ac-FEID-CMK 三氟乙酸盐Ac-FEID-CMK TFA
Ac-FEID-CMK TFA is a selective zebrafish GSDMEb-derived peptide inhibitor that reduces mortality and renal injury in infectious shock.Ac-FEID-CMK TFA inhibits pyroptosis in vivo, attenuates septic AKI (acute kidney injury), and inhibits the caspy2-mediated atypical inflammatory vesicle pathway.
价 格：￥电议型 号：T76251L产 地：中国大陆
