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三叶新科每月上新,持续为科研人员提供新颖性研究工具,助力科研创新与突破。
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SPR inhibitor 3
目录号:SY-128790
SPR inhibitor 3是一类用于抑制Sepiapterin reductase活性的小分子化合物,可阻断四氢生物蝶呤(BH4)的生物合成途径,影响一氧化氮合酶及单胺类神经递质的生成。
¥1495.00
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Cintirorgon sodium
目录号:SY-128535
Cintirorgon (LYC-55716) is an orally active RORgamma agonist with potential immunomodulatory and antineoplastic activities. LYC-55716 selectively binds to the RORg, and binds to ROR response elements, enhancing the function, proliferation, and survival of
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TMP778
目录号:SY-128532
TMP778 is an effective and selective RORγt inverse agonist (IC50: 7 nM in FRET assay).
¥1584.00
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ALR2-IN-10
目录号:SY-128789
ALR2-IN-10 (Compound 23) 是一种对醛糖还原酶 2 (Aldose Reductase 2) 具有低效抑制作用的化合物,抑制率在 27μM 浓度下为 6%。ALR2-IN-10 可用于糖尿病并发症研究。
¥138.00
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Ilexoside O
目录号:SY-129050
Ilexoside O, a triterpene saponin derived from Ilex pubescens roots, demonstrates modest inhibition of xanthine oxidase (XOD) activity with an IC50 value of 53.05 μM.
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ER 50891
目录号:SY-128791
ER-50891是一种强效的视黄酸受体α(RARα)拮抗剂。ER-50891能减少全价视黄酸的抑制作用并恢复骨形态生成蛋白2诱导的成骨细胞分化。
¥1386.00
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7β,27-dihydroxy Cholesterol
目录号:SY-128534
7β,27-dihydroxy Cholesterol is an oxysterol and agonist of retinoic acid receptor-related orphan receptor γ (RORγ) and RORγt. [1] It activates RORγ- or RORγt-dependent signaling with EC50 values of 691 and 1,045 nM, respectively, in reporter assays using HEK293T cells expressing the recombinant human receptors. 7β,27-dihydroxy Cholesterol is selective for RORγ and RORγt over a panel of eight additional nuclear receptors at 30 µM. It increases IL-17A production in Th17-polarized isolated human na ve CD4+ T cells when used at a concentration of 300 nM. 7β,27-dihydroxy Cholesterol (60 mg/kg) increases IL-17A production in isolated mouse γδ T cells stimulated with 12-myristate 13-acetate and ionomycin .
¥5742.00
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Fluorobexarotene
目录号:SY-128792
Fluorobexarotene 是一种有效的 类视黄醇 X 受体 (RXR) 激动剂。Fluorobexarotene 对 RXRα 受体的 Ki 值为 12 nM,EC50 值为 43 nM。Fluorobexarotene 具有明显的 RXR 结合亲和力,比 Bexarotene 高75%。
¥2134.00
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RORγt Inverse agonist 10
目录号:SY-128533
RORγt Inverse agonist 10 is a highly potent and orally bioavailable compound that acts as an antagonist for the retinoic acid receptor-related orphan nuclear receptor gamma t (RORγt). With an IC50 of 51 nM, it effectively inhibits the activity of RORγt, a prominent transcription factor involved in the regulation of genes associated with the pathogenesis of psoriasis, including IL-17A, IL-22, and IL-23R.
¥1694.00
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