| CAS NO: | 61281-38-7 |
| 包装: | 20mg |
| 市场价: | 1113元 |
| Cas No. | 61281-38-7 |
| 别名 | 五味子甲素; Schizandrin-A; Wuweizisu-A; Deoxyschizandrin |
| 化学名 | 1,2,3,10,11,12-hexamethoxy-6,7-dimethyl-5,6,7,8-tetrahydrodibenzo[a,c][8]annulen-6-ol |
| Canonical SMILES | [H]C(C([H])([H])C(C1=C2OC([H])([H])[H])=C([H])C(OC([H])([H])[H])=C2OC([H])([H])[H])(C([H])([H])[H])C(C([H])([H])C(C1=C3OC([H])([H])[H])=C([H])C(OC([H])([H])[H])=C3OC([H])([H])[H])(C([H])([H])[H])O[H] |
| 分子式 | C24H32O7 |
| 分子量 | 432.51 |
| 溶解度 | ≥ 43.3mg/mL in DMSO |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
| Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
| 产品描述 | Schisandrin has various therapeutic effects on a range of medical conditions such as anti-asthmatic, anti-cancer, and anti-inflammatory effects.IC50 value:Target:in vitro: Sch inhibited the pro-fibrotic activity of TGF-β1 in AML12 cells; thus, it suppressed the accumulation of ECM proteins. Also, Sch inhibited the EMT as assessed by reduced expression of vimentin and fibronectin, and increased E-cadherin and ZO-1 in TGF-β1 induced AML12 cells. Sch reduced TGF-β1-mediated phosphorylation of Smad2/3 and Smad3/4 DNA binding activity. On the other hand, Sch reduced TGF-β1-induced ERK1/2 and PI3K/Akt phosphorylation in the non-Smad pathway [1]. the anti-inflammatory properties of schisandrin result from the inhibition of nitric oxide (NO) production, prostaglandin E(2) (PGE(2)) release, cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, which in turn results from the inhibition of nuclear factor-kappaB (NF-kappaB), c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) activities in a RAW 264.7 macrophage cell line [2]. References: |
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