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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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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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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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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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Amsilarotene
目录号:SY-128793
Amsilarotene (TAC101) 是口服有活性的合成类视黄醇,对视黄酸受体 α (RAR-α) 具有选择性亲和力,对 RAR-α 和 RAR-β 的 Ki=为 2.4 nM 和 400 nM。它可造成人胃癌、卵巢癌细胞及肝细胞癌的凋亡,可用于研究癌症。
¥561.00
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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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PF-06747711
目录号:SY-128538
PF-06747711 is an effective and selective retinoic acid receptor-related orphan C2 inverse agonist (IC50: 4.1 nM). PF-06747711 also has anti-skin inflammatory activity.
¥583.00
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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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AGN 193109
目录号:SY-128794
AGN 193109 是一种类视黄醇类似物,是一种有效的特异性 RAR 拮抗剂,可抑制 RARα、RARβ和 RARγ的活性,Kd 值分别为 2 nM、2 nM 和 3 nM。
¥671.00
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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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