Obtusifolin
CAS No. 477-85-0
Obtusifolin ( —— )
产品货号. M18597 CAS No. 477-85-0
Obtusifolin has antioxidant properties and improves chemically induced diabetes and its complications by modulation of oxidative stress.
纯度: 98%
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1596 | 有现货 |
|
10MG | ¥2373 | 有现货 |
|
25MG | ¥4026 | 有现货 |
|
50MG | ¥5613 | 有现货 |
|
100MG | ¥7954 | 有现货 |
|
200MG | 获取报价 | 有现货 |
|
500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Obtusifolin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Obtusifolin has antioxidant properties and improves chemically induced diabetes and its complications by modulation of oxidative stress.
-
产品描述Obtusifolin has antioxidant properties and improves chemically induced diabetes and its complications by modulation of oxidative stress. Obtusifolin suppresses phthalate esters-mediated bone resorption, thus may be a novel anti-breast-cancer bone metastasis agent. Obtusifolin has beneficial effects on the development of diabetic retinopathy via inhibition of accumulation of oxidatively modified DNA and nitrotyrosine in the retina, can help prevent vision loss in diabetic patients. Obtusifolin and gluco-Obtusifolin produce significant antinociceptive action in rodent behavioral models of inflammatory/neuropathic pain, and that this activity is associated with modulation of neuroinflammation in spinal cord. Gluco-Obtusifolin and its aglycone may be useful for the treatment of cognitive impairment, and that its beneficial effects are mediated, in part, by the enhancement of cholinergic signaling.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Antioxidant
-
研究领域——
-
适应症——
化学信息
-
CAS Number477-85-0
-
分子量284.26
-
分子式C16H12O5
-
纯度98%
-
溶解度——
-
SMILESCC1=C(C(=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)O)OC)O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册
关联产品
-
Methyl nomilinate
Methyl nomilinate from citrus can modulate cell cycle regulators to induce cytotoxicity in human colon cancer (SW480) cells in vitro.
-
Methyl nomilinate
Methyl nomilinate from citrus can modulate cell cycle regulators to induce cytotoxicity in human colon cancer (SW480) cells in vitro.
-
Schizandrin A
Schisandrin A is a main effective components extracted from the oriental medicine Schisandra chinensis, inhibits CYP3A activity with an IC50 of 6.60 μM and Ki of 5.83 μM, respectively.