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T80538Lib2-1；化合物 Lib2-1Lib2-1
Lib2-1, a macrocyclic peptide, inhibits the interaction between IL-17C and IL-17RE and is applicable in the study of autoimmune and inflammatory diseases [1].
价 格：￥电议型 号：T80538产 地：中国大陆
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T79600Zharp2-1；化合物 Zharp2-1Zharp2-1
Zharp2-1, a RIPK2 inhibitor, inhibits the transcription of inflammatory cytokines induced by MDP-induced or Listeria monocytogenes infection and alleviates MDP-induced peritonitis symptoms in mice, which can be used for the study of inflammatory bowel disease (IBD).
价 格：￥电议型 号：T79600产 地：中国大陆
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T72015iST2-1；化合物 iST2-1iST2-1
iST2-1 is a first-in-class ST2 inhibitor active in vivo.
价 格：￥电议型 号：T72015产 地：中国大陆
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T40131SGC-CK2-1；SGC-CK2-1SGC-CK2-1；SGC-CK2-1
SGC-CK2-1 is an ATP-competitive chemical compound that acts as a highly potent and cell-active CK2 inhibitor. It demonstrates excellent selectivity towards both isoforms of human CK2, with IC50 values of 36 nM for CK2α and 16 nM for CK2α′ in the nanoBRET assay. Given its properties, SGC-CK2-1 is a suitable tool for the investigation of neurodegenerative diseases.
价 格：￥电议型 号：T40131产 地：中国大陆
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T39586Cantrixil；CantrixilTRX-E-002-1；TRX-E-002-1
Cantrixil (TRX-E-002-1) is a second-generation super-benzopyran (SBP) compound, derived from TRX-E-002. It elicits an increase in phosphorylated c-Jun levels, leading to caspase-mediated apoptosis in ovarian cancer cells. Cantrixil exhibits potent pan anti-cancer activity against various cancer phenotypes.
价 格：￥电议型 号：T39586产 地：中国大陆
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T37151NVS-CECR2-1NVS-CECR2-1NVS-CECR2-1
NVS-CECR2-1 is a potent inhibitor of CECR2 (cat eye syndrome chromosome region, candidate 2), a component of chromatin complexes that regulate gene expression controlling development. It binds CECR2 with high affinity (IC50 = 0.047 μM by Alpha screen, Kd = 0.80 μM by ITC). NVS-CECR2-1 demonstrates no crossreactivity in a panel of 48 bromodomains and has no major activity in kinase, protease, and receptor panels. It shows robust activity in cells by FRAP assay, due to its slow off-rate, and has n
价 格：￥电议型 号：T37151产 地：中国大陆
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T21964KP372-1；化合物 T21964KP372-1
KP372-1 is an Akt inhibitor which block signalling through the PI3K pathway. KP372-1 inhibit cell proliferation while inducing apoptosis and anoikis in squamous cell carcinoma of the head and neck.
价 格：￥电议型 号：T21964产 地：中国大陆
