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T4498Stiripentol斯利潘托；Diacomit；BCX2600
Stiripentol (STP) is an anticonvulsant agent, which can inhibit N-demethylation of CLB to NCLB mediated by CYP3A4 (noncompetitively) and CYP2C19 (competitively) with Ki of 1.59/0.516 μM and IC50 of 1.58/3.29 μM, respectively.
价 格：￥电议型 号：T4498产 地：中国大陆
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T17225Vercirnon维塞诺；GSK-1605786；Traficet-EN；CCX282-B
Vercirnon is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.
价 格：￥电议型 号：T17225产 地：中国大陆
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T4498Stiripentol斯利潘托斯利潘托|||BCX2600|||Diacomit
Stiripentol (BCX2600) (STP) is an anticonvulsant agent, which can inhibit N-demethylation of CLB to NCLB mediated by CYP3A4 (noncompetitively) and CYP2C19 (competitively) with Ki of 1.59/0.516 μM and IC50 of 1.58/3.29 μM, respectively.
价 格：￥电议型 号：T4498产 地：中国大陆
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T41016Vercirnon sodium维塞诺钠盐GSK-1605786 sodium|||CCX282-Bsodium|||维塞诺钠盐|||Traficet-ENsodium
Vercirnon (GSK1605786A) sodium is an orally bioavailable, selective, and potent CCR9 antagonist. It effectively inhibits CCR9-mediated calcium mobilization and chemotaxis in Molt-4 cells, exhibiting IC50 values of 5.4 nM and 3.4 nM, respectively. Demonstrating high selectivity, Vercirnon sodium does not significantly affect CCR1-12 or CX3CR1-7, with IC50 values exceeding 10 ?M for these receptors. Additionally, it inhibits CCL25-directed chemotaxis equally well in both CCR9 splice variants, CCR9
价 格：￥电议型 号：T41016产 地：中国大陆
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T25011AK-295；化合物 T25011CX295|||CX 295|||AK295|||CX-295；CX295|||CX 295|||AK295|||CX-295
AK 295, also known as CX 295, is a dipeptide inhibitor of alpha-ketoamide calpain.
价 格：￥电议型 号：T25011产 地：中国大陆
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T17225Vercirnon；维塞诺CCX282-B|||GSK-1605786|||Traficet-EN；CCX282-B|||维塞诺|||GSK-1605786|||Traficet-EN
Vercirnon (Traficet-EN) is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.
价 格：￥电议型 号：T17225产 地：中国大陆
