17094-01-8
中文名称
L-墨蝶呤
英文名称
L-SEPIAPTERIN
CAS
17094-01-8
分子式
C9H11N5O3
分子量
237.22
MOL 文件
17094-01-8.mol
更新日期
2024/08/16 10:16:13
![17094-01-8 结构式](/CAS/GIF/17094-01-8.gif)
基本信息
中文别名
墨蝶呤L-墨蝶呤
S-(-)-2-氨基-7,8-二氢-6-(2-羟基-1-氧代丙基)-4(1H)-蝶啶酮
英文别名
SEPIAPTERINL-SEPIAPTERIN
L-Sepiapterin,98%
Sepiapterin solid
L-SEPIAPTERIN DIHYDRATE
L -SEPIAPTERIN DIHYDRATE 99+%
SEPIAPTERIN (L-SEPIAPTERIN) COFACTOR OF NITRIC OX
2-amino-6-(2-hydroxypropanoyl)-7,8-dihydro-1H-pty oeridin-4-one
(S)-2-aMino-6-(2-hydroxypropanoyl)-7,8-dihydropteridin-4(1H)-one
2-AMINO-7,8-DIHYDRO-6-(2S-HYDROXY-1-OXOPROPYL)-4(1H)-PTERIDINONE
物理化学性质
熔点>270 °C (dec.)
沸点448.1±55.0 °C(Predicted)
密度1.86±0.1 g/cm3(Predicted)
储存条件−20°C
溶解度DMSO: 27 mg/mL
酸度系数(pKa)12.33±0.20(Predicted)
形态solid
颜色yellow
稳定性感光
CAS 数据库17094-01-8
常见问题列表
生物活性
L-Sepiapterin (Sepiapterin) 是内皮型一氧化氮合酶 (eNOS) 辅因子四氢生物喋呤 (BH4) 的前体。L-Sepiapterin 改善 db/db 小鼠肠系膜小动脉内皮功能障碍,诱导血管生成。L-Sepiapterin 通过下调 p70S6K 依赖性 VEGFR-2 表达抑制卵巢癌细胞增殖和迁移。靶点
Human Endogenous Metabolite
|
体外研究
L-Sepiapterin (Sepiapterin) (0.1-10 μM; 24 hpurs) Iinduces cell proliferation in a dose-dependent manner.
L-Sepiapterin (1-50 μM; 20 minutes) significantly inhibits the phosphorylation of VEGF-A-induced (50 ng/ml) p70
S6K
.
L-Sepiapterin inhibits VEGF-A-induced cell proliferation and migration through NO-independent mechanism.
Cell Proliferation Assay
Cell Line: | SKOV-3 cells |
Concentration: | 0.1, 1, 10 μM |
Incubation Time: | 24 hours |
Result: | Induced cell proliferation in a dose-dependent manner. |
体内研究
Sepiapterin (10 mg/kg; p.o. (powder chow); daily for or 8 weeks) significantly improves the relaxation to Ach in small mesenteric arteries (SMA) from db/db mice.
Animal Model: | Male C57BL/KsJ diabetic mice (db/db) |
Dosage: | 10 mg/kg |
Administration: | P.o. (powder chow); daily for or 8 weeks |
Result: | Significantly improved the relaxation to Ach in SMA from db/db mice. |