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ADTL-EI1712
目录号:SY-121023
ADTL-EI1712 is a dual inhibitor of ERK1 and ERK5 (IC50s = 40.43 and 64.5 nM, respectively).1It reduces ERK1 and ERK5 activity by 93.5% and 89.4%, respectively, but also inhibits ERK2 activity by 92.7%, in a panel of 100 kinases at 1 μM. ADTL-EI1712 inhibits proliferation of HL-60 and MKN74, but not HeLa, cancer cells (IC50s = 1.26, 2.55, and >50 μM, respectively). It reduces tumor growth and intratumor phosphorylation of ERK1/2 and ERK5 in an MKN74 mouse xenograft model when administered at a dose of 50 mg/kg per day. 1.Wang, G., Zhao, Y., Liu, Y., et al.Discovery of a novel dual-target inhibitor of ERK1 and ERK5 that induces regulated cell death to overcome compensatory mechanism in specific tumor typesJ. Med. Chem.63(8)3976-3995(2020)
¥2156.00
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Hypothemycin
目录号:SY-121024
Hypothemycin is a fungal polyketide and is a multikinase inhibitor (Kis: 10/70 nM, 17/38 nM, 90 nM, 900 nM/1.5 μM, and 8.4/2.4 μM for VEGFR2/VEGFR1, MEK1/MEK2, FLT-3, PDGFRβ/PDGFRα, and ERK1/ERK2, respectively).
¥1859.00
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MAP855
目录号:SY-121025
MAP855 是一种高效的、选择性的、口服具有活力的具、 ATP 竞争性的 MEK1/2 激酶抑制剂,对 MEK1 ERK2 cascade 的 IC50 值为 3 nM,pERKEC50 值为 5 nM。MAP855 对野生型和突变型 MEK1/2 表现出同等的抑制效果。
¥2651.00
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(rel)-AR234960
目录号:SY-121026
(rel)-AR234960 is an active relative configuration of AR234960. AR234960 is a non-peptide agonist of MAS.
¥1694.00
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Lidocaine-D10 (N,N-diethyl-D10)
目录号:SY-121027
Lidocaine-D10 (N,N-diethyl-D10)是Lidocaine (T0468)的氘代化合物。Lidocaine的CAS号为137-58-6。Lidocaine是一种酰胺衍生物,抑制涉及复杂电压和依赖性的钠通道,可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制MEK/ERK和NF-κB信号通路来减少胃癌细胞的生长,迁移和侵袭。
¥770.00
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Dodoviscin I
目录号:SY-121028
Dodoviscin I can promote adipocyte differentiation as characterized by increased triglyceride levels in 3T3L1 cells.
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(-)-Sesamin
目录号:SY-121029
(-)-Sesamin是一种具有神经保护作用的天然产物,通过激活ERK1/2-BadSer112和抑制ERK-p38MAPK-JNK1/2-caspase-3,对6-OHDA诱导的神经毒性起到保护作用,可用于研究帕金森病。
¥276.00
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15-Methoxypinusolidic acid
目录号:SY-121030
15-Methoxypinusolidic acid has anti-inflammatory effects, it inhibits LPS-induced iNOS expression and NO production, independent on MAPK and NF-kappaB. 15-Methoxypinusolidic acid suppresses adipocyte differentiation through the inhibition of PPARgamma-dep
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Lup-20(29)-en-28-oic acid
目录号:SY-121031
Lup-20(29)-en-28-oic acid exhibits anticancer activities in various cancer types, inhibiting autophagic flux and synergistically enhancing the anticancer activity of chemotherapeutic agents against HeLa cells. Pulsatilla saponin D has strong haemolytic activity.
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