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Valiglurax (VU2957),也称为 VU0652957和 VU2957,是一种强效、选择性、中枢神经系统渗透剂,可口服生物利用的 mGlu4正变构调节剂。VU2957具有良好的跨物种的体内外药理学和药代动力学性质。VU2957被评估为治疗帕金森病的临床前开发候选药物。
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Valiglurax (VU2957),也称为 VU0652957和 VU2957,是一种强效、选择性、中枢神经系统渗透剂,可口服生物利用的 mGlu4正变构调节剂。VU2957具有良好的跨物种的体内外药理学和药代动力学性质。VU2957被评估为治疗帕金森病的临床前开发候选药物。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 108 | 现货 | |
5 mg | ¥ 267 | 现货 | |
10 mg | ¥ 443 | 现货 | |
25 mg | ¥ 953 | 现货 | |
50 mg | ¥ 1,420 | 现货 | |
100 mg | ¥ 2,020 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 295 | 现货 |
产品描述 | Valiglurax (VU2957), also known as VU0652957 and VU2957, is a potent, selective, CNS penetrant, and orally bioavailable mGlu4 PAM. VU2957 possessed attractive in vitro and in vivo pharmacological and DMPK properties across species. VU2957 was evaluated as a preclinical development candidate for the treatment of Parkinson’s disease. |
体内活性 | Valiglurax (0.3-30 mg/kg; po) reversed haloperidol-induced catalepsy (HIC) in rats[1]. |
别名 | VU-2957, VU2957, VU-0652957, VU0652957, VU 2957, VU 0652957 |
分子量 | 329.28 |
分子式 | C16H10F3N5 |
CAS No. | 1976050-09-5 |
Smiles | C(F)(F)(F)C=1C2=C(C=C(NC=3C=4C(NN3)=NC=CC4)C=C2)C=CN1 |
密度 | 1.530 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 112.5 mg/mL (341.7 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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