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A 85380 hydrochloride
目录号:SY-129469
A 85380 hydrochloride 是一种新型、高亲和力神经元烟碱乙酰胆碱受体 (nAChR) 激动剂。A 85380 hydrochloride 对 nAChR 亚型的 α4β2 表现出选择性。A 85380 hydrochloride 具有广谱镇痛作用。
¥847.00
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Pozanicline dihydrochloride
目录号:SY-129438
Pozanicline dihydrochloride (ABT-089 dihydrochloride) 是一种具有口服活性的烟碱型乙酰胆碱受体 (nAChR) 激动剂,与 [3H] 胱氨酸位点结合,Ki 为 16.7 nM。Pozanicline dihydrochloride 是一种 α4β2 选择性 nAChR 激动剂,与大鼠脑 α4β2 nAChR 结合,Ki 为 17 nM,而与 α7nAChR 的结合力很弱。
¥440.00
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Propanidid
目录号:SY-129831
Propanidid (Sombrevin; Fabantol) 是一种 γ-氨基丁酸 A 型受体 (GABAA receptor) 激动剂,也是一种短效的非巴比妥类全身活性剂,可抑制或缓解疼痛。Propanidid 可以降低动脉血压。
¥425.00
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Pivagabine
目录号:SY-129749
Pivagabine (CXB 722) 是具有神经调节活性的疏水性4-氨基丁酸衍生物。Pivagabine 能穿透大鼠的血脑屏障。Pivagabine 拮抗足部休克对大鼠脑内 GABAA 受体功能和促肾上腺皮质激素释放因子 (CRF) 浓度的影响。
¥616.00
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CGP 54626 hydrochloride
目录号:SY-129661
CGP 54626 hydrochloride 是一种选择性 GABAB 受体激动剂。CGP 54626 hydrochloride 可阻断 Baclofen (HY-B0007) 对支配褐家鼠结肠的牵张敏感性盆神经传入纤维的抑制作用。CGP 54626 hydrochloride 可用于内脏伤害感受的相关研究。
¥517.00
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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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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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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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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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