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Deltasonamide 2
目录号:SY-128130
Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
¥621.00
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endo CNTinh-03
目录号:SY-128128
Endo CNTinh-03 具有抑制作用,可阻止 cAMP 和 cGMP 通过 G 蛋白偶联受体、腺苷酸环化酶及鸟苷酸环化酶的激动剂而升高(IC50为 4 μM)。此外,该化合物能够抑制霍乱毒素与Escherichia coli(STa) 毒素导致的氯离子电流,有效改善小鼠分泌性腹泻的症状,并在多囊肾病模型中防止囊肿的形成。
¥3450.00
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Metaxalone-D6
目录号:SY-128142
Metaxalone-D6 is intended for use as an internal standard for the quantification of metaxalone by GC-or LC-MS. Metaxalone (T1610) is a skeletal muscle relaxant. It inhibits the proliferation of,and induces apoptosis in,RAW 264.7 cells in vitro when used at concentrations ranging from 1 to 100 µM. Metaxalone (T1610)also reduces LPS-induced increases in COX-1,COX-2,and NF-kB levels and inhibits LPS-induced production of TNF-α,IL-6,and prostaglandin E2 in RAW 264.7 cells. Formulations containing metaxalone have been used in the treatment of lower back pain.
¥1023.00
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Denbufylline
目录号:SY-128098
Denbufylline (BRL 30892) 是一种磷酸二酯酶-4 (PDE4) 抑制剂,通过抑制细胞内 cAMP (环磷酸腺苷) 的降解来升高细胞内 cAMP 水平,从而调节多种细胞功能。Denbufylline 可用于慢性阻塞性肺病 (COPD)、哮喘及其他炎症性疾病的研究。
¥1840.00
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Yonkenafil HCl
目录号:SY-128104
Yonkenafil HCl, a PDE5 inhibitor, is used potentially for the treatment of erectile dysfunction.
¥460.00
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Mitapivat
目录号:SY-128144
Mitapivat (PKR-IN-1) 是口服具有活性的变构丙酮酸激酶 (pyruvate kinase) 激活剂,其AC50=20 nM。它在广泛的 PKLR 基因型中增加酶活性、蛋白质稳定性和 ATP 水平。它有潜在的恢复 PK 缺乏的糖酵解途径活性的作用。
¥2850.00
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Sp-cAMPS triethylamine
目录号:SY-128110
Sp-cAMPS triethylamine,一种 cAMP 类似物,是一种依赖 cAMP 的PKAI 和PKAII 的有效激活剂。Sp-cAMPS triethylamine 还是一种有效的竞争性磷酸二酯酶 (PDE3A) 抑制剂,Ki 为 47.6 µM。Sp-cAMPS triethylamine 以EC50为 40 μM 来结合PDE10GAF 域。
¥3312.00
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PF-8380 hydrochloride
目录号:SY-128116
PF-8380 hydrochloride 是一种有效的autotaxin 抑制剂,体外酶实验和人类全血细胞实验中,IC50分别为 2.8 nM 和 101 nM。
¥8706.00
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PF-04449613
目录号:SY-128132
PF-04449613 is a phosphodiesterase 9A (PDE9A) inhibitor (IC50= 22 nM).1It is selective for PDE9A over PDE1C (IC50= >1,000 nM), as well as over a variety of other PDEs, inhibiting PDE2-8, -10, and -11 activity by less than 30% in a panel of enzymes, ion channels, and transporters at 1 μM but does inhibit the human dopamine transporter (DAT; Ki= 293 nM). PF-04449613 (0.1-100 mg/kg, s.c.) increases cerebrospinal fluid (CSF) levels of cyclic GMP (cGMP) in rats. Subcutaneous administration of PF-04449613 (10 mg/kg) increases the rate of dendritic spine formation and elimination in mouse primary motor cortex pyramidal neuronsin vivo.2It increases the average running speed of mice in an accelerating rotarod task, indicating improved motor learning, at the same dose. 1.Claffey, M.M., Helal, C.J., Verhoest, P.R., et al.Application of structure-based drug design and parallel chemistry to identify selective, brain penetrant, in vivo active phosphodiesterase 9A inhibitorsJ. Med. Chem.55(21)9055-90
¥1955.00
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