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TP1114LLeucokinin VIII acetateLeucokinin VIII acetate
Leucokinin VIII acetate is an diuretic octapeptide isolated form head extracts of the cockroach.
价 格：￥电议型 号：TP1114L产 地：中国大陆
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T15612JH-VIII-157-02CD246,Cluster of differentiation 246,inhibit,Anaplastic lymphoma kinase,Anaplastic lym
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-ALKwt, EML4-ALK C1156Y, EML4-ALK F1174L, and EML4-ALK F1174L.
价 格：￥电议型 号：T15612产 地：中国大陆
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T9568SGC-SMARCA-BRDVIIIEpigenetic Reader Domain,adipogenesis,SMARCA2/4,inhibit,PB1,SGCSMARCABRDVIII,Inhib
SGC-SMARCA-BRDVIII is a potent and selective inhibitor of SMARCA2, SMARCA4, PB1(2), PB1(3) and PB1(5) with Kds of 35 nM, 36 nM, 3.7 μM, 2.0 μM and 13 nM, respectively.
价 格：￥电议型 号：T9568产 地：中国大陆
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T7677JNK Inhibitor VIIIJNK,inhibit,Inhibitor,JNK Inhibitor VIII
JNK Inhibitor VIII is an ATP-competitive selective inhibitor of c-Jun N-terminal kinase (JNK)(IC50 values of 45 nM and 160 nM for JNK-1 and -2, respectively).
价 格：￥电议型 号：T7677产 地：中国大陆
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T3924Astragaloside IIAstrasieversianin VIII；黄芪皂苷 II
Astragaloside II is an effective MDR reversal agent and may be a potential adjunctive agent for hepatic cancer chemotherapy. Astragaloside II also induces osteogenic activities, differentiation, proliferation, and mineralization, through the bone morphoge
价 格：￥电议型 号：T3924产 地：中国大陆
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T3346AKT inhibitor VIIIAKTi-1/2
AKT inhibitor VIII is a highly specific Akt1/2 inhibitor (IC50: 58/210 nM). The selectivity for Akt1 is higher about 36-fold than Akt3.
价 格：￥电议型 号：T3346产 地：中国大陆
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T2878Ginsenoside Rd人参皂苷Rd；人参皂苷 Rd；Sanchinoside Rd；Panaxoside Rd；Gypenoside VIII
Ginsenoside Rd may have properties that inhibit or prevent the growth of tumors.
价 格：￥电议型 号：T2878产 地：中国大陆
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T1881AR-A014418GSK-3beta Inhibitor VIII；AR 014418；AR 0133418；GSK 3β inhibitor VIII
AR-A014418 is an ATP-competitive, and selective GSK3β inhibitor.
价 格：￥电议型 号：T1881产 地：中国大陆
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T10549Bisindolylmaleimide VIII acetateBis VIII acetate；Ro 31-7549 acetate
Bisindolylmaleimide VIII acetate is a potent and selective PKC inhibitor (IC50: 158 nM for rat brain PKC). It has IC50s of 53, 195, 163, 213, and 175 nM for PKC-α, PKC-βI, PKC-βII, PKC-γ, PKC-ε, respectively.
价 格：￥电议型 号：T10549产 地：中国大陆
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T10237ACHP HydrochlorideIKK-2 Inhibitor VIII
ACHP Hydrochloride is a highly potent and selective IKK-β inhibitor with an IC50 of 8.5 nM.
价 格：￥电议型 号：T10237产 地：中国大陆
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T10237ACHP HydrochlorideACHP Hydrochloride,IKK-2 Inhibitor VIII,
ACHP Hydrochloride (IKK-2 Inhibitor VIII) is a highly potent and selective IKK-β inhibitor (IC50: 8.5 nM).
价 格：￥电议型 号：T10237产 地：美洲
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T15612JH-VIII-157-02JH-VIII-157-02
JH-VIII-157-02 is a structural analogue of alectinib. This acts as an ALK inhibitor and displays an IC50 of 2 nM for echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) G1202R in cells.
价 格：￥电议型 号：T15612产 地：美洲
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T1881AR-A014418AR-A014418,AR 014418,GSK 3β inhibitor VIII
AR-A014418 is an ATP-competitive, and selective GSK3β inhibitor.
价 格：￥电议型 号：T1881产 地：美洲
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T83852EGFRvIII Peptide TFA；化合物 EGFRvIII Peptide TFAPEGFRvIII (9-mer)|||Epidermal Growth Factor Receptor Va
EGFRvIII peptide, a synthetic peptide mirroring the EGFRvIII fusion junction—a tumor-specific, perpetually active EGFR variant missing amino acids 6-273 of the wild-type—binds to HLA-A*0201-positive T2 cells under MHC class I at 25 ?g/ml. It enables antigen presentation in dendritic cells from human peripheral blood mononuclear cells (PBMCs), thus activating CD8+ cytotoxic T lymphocytes and prompting IFN-γ production. Administered at 15 ?g/animal with the TLR5 agonist flagellin B, EGFRvIII pepti
价 格：￥电议型 号：T83852产 地：中国大陆
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T7677JNK Inhibitor VIII；化合物JNK Inhibitor VIIITCS JNK 6o；TCS JNK 6o
JNK Inhibitor VIII (TCS JNK 6o) is an ATP-competitive selective inhibitor of c-Jun N-terminal kinase (JNK)(IC50 values of 45 nM and 160 nM for JNK-1 and -2, respectively).
价 格：￥电议型 号：T7677产 地：中国大陆
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T75696Ilexoside XLVIII；化合物 Ilexoside XLVIIIIlexoside XLVIII
Ilexoside XLVIII, a triterpene saponin isolated from the aqueous extract of Ilex kudincha leaves [1], functions as an acyl CoA cholesteryl acyl transferase (ACAT) inhibitor.
价 格：￥电议型 号：T75696产 地：中国大陆
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T3924Astragaloside II；黄芪皂苷 IIAstrasieversianin VIII；黄芪皂苷 II|||Astrasieversianin VIII
Astragaloside II (Astrasieversianin VIII) is an effective MDR reversal agent and may be a potential adjunctive agent for hepatic cancer chemotherapy. Astragaloside II also induces osteogenic activities, differentiation, proliferation, and mineralization, through the bone morphogenetic protein-2/MAPK and Smad1/5/8 pathways.
价 格：￥电议型 号：T3924产 地：中国大陆
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T35556GSK-3β inhibitor 8；GSK-3β抑制剂8GSK3β Inhibitor XVIII；GSK3β Inhibitor XVIII
GSK-3β inhibitor 8 (GSK3β Inhibitor XVIII) is a potent and selective GSK-3β inhibitor with an IC50 value of 64 nM.GSK-3β inhibitor 8 is a thienopyrimidine derivative that negatively regulates the Wnt signaling pathway and stimulates β-cell proliferation.
价 格：￥电议型 号：T35556产 地：中国大陆
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T35537Hedgehog Antagonist VIII；Hedgehog Antagonist VIIIHedgehog Antagonist VIII
Hedgehog (Hh) proteins, important regulators of development, bind the cell-surface protein Patched, allowing activation of Smoothened. In vertebrates, this ultimately leads to the activation of the zinc-finger transcription factors of the Gli family. Overactivation of this pathway contributes to certain cancers, including glioblastoma, for which the Gli proteins are named. Hh antagonist VIII is a cell-permeable quinazolinyl-urea compound that has been shown to inhibit Gli transcription activity
价 格：￥电议型 号：T35537产 地：中国大陆
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T34562Scammonin viii；化合物 T34562Scammonin viii
Scammonin viii is a resin glycoside from Convolvulus scammonia.
价 格：￥电议型 号：T34562产 地：中国大陆
