dencichine
CAS No. 5302-45-4
dencichine ( β-ODAP | Dencichine | BRN-2259036 | Ox-Dapro )
产品货号. M18743 CAS No. 5302-45-4
Dencichine 是一种神经毒剂。 Dencichine是一种止血剂,其止血作用与凝血系统、血小板聚集和纤溶系统的调节有关。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1292 | 有现货 |
|
| 10MG | ¥2081 | 有现货 |
|
| 25MG | ¥3422 | 有现货 |
|
| 50MG | ¥4864 | 有现货 |
|
| 100MG | ¥6471 | 有现货 |
|
| 200MG | ¥8712 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1169 | 有现货 |
|
生物学信息
-
产品名称dencichine
-
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Dencichine 是一种神经毒剂。 Dencichine是一种止血剂,其止血作用与凝血系统、血小板聚集和纤溶系统的调节有关。
-
产品描述Dencichin, also known as β-ODAP, has been shown to alleviate metabolism disorder, improve renal function, relieve pathological alterations in the glomerulus of diabetic neuropathy in rats, decrease extracellular matrix deposition and increase the ratio of matrix metalloproteinase (MMP)-9 to tissue inhibitor of metalloproteinase (TIMP)-1 both in vivo and in vitro.
-
体外实验Dencichin (β-ODAP, 10 μM, 50 μM, 100 μM and 200 μM) increases HRE expression by 1.3±0.09, 2.5±0.07, 4.2±0.15 and 1.3±0.07 fold respectively compared to control. Dencichin has intermolecular interactions with PHD-2. Dencichin (10 μM, 100 μM, 1 mM) significantly inhibits cell proliferation and extracellular matrix (ECM) proteins accumulation of HBZY-1 cells, and reduces the secretion of collagen I (Col I), collagen IV (Col IV), and fibronectin (FN).
-
体内实验Dencichin improves metabolism disorder in diabetic nephropathy (DN) secondary to type II diabetes mellitus (DM) model. Dencichin (80, 160 mg/kg/day, p.o.) significantly prevents the up-regulation of TCH, TG, LDL, and HbAlc and the down-regulation of HDL in DN rats induced by STZ injection. Dencichin also attenuates renal injury induced in the DN secondary to type II DM model. Dencichin alleviates pancreas damage in the STZ-induced DN model. Dencichin regulates protein expression in the TGF-β/Smad signalling pathway in STZ-induced DN models.
-
同义词β-ODAP | Dencichine | BRN-2259036 | Ox-Dapro
-
通路MAPK/ERK Signaling
-
靶点p38 MAPK
-
受体Others
-
研究领域Others-Field
-
适应症——
化学信息
-
CAS Number5302-45-4
-
分子量176.13
-
分子式C5H8N2O5
-
纯度>98% (HPLC)
-
溶解度In Vitro:?H2O : 5 mg/mL (28.39 mM)
-
SMILESC([C@@H](C(=O)O)N)NC(=O)C(=O)O
-
化学全称Oxamic acid, (2-amino-2-carboxyethyl)-, L-
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
1. Xie G X, et al. Journal of Pharmaceutical & Biomedical Analysis, 2007, 43(3):920-925.
产品手册
关联产品
-
SM1-71
SM1-71 是一种有效的 TAK1 抑制剂,Ki 值为 160 nM,同时可以共价抑制 MKNK2、MAP2K1/2/3/4/6/7、GAK、AAK1、BMP2K、MAP3K7、MAPKAPK5、GSK3A/B、MAPK1/3、SRC、YES1、FGFR1、ZAK (MLTK)、MAP3K1、LIMK1 和 RSK2。SM1-71 在体外抑制多种癌细胞系的增殖。
-
SB 203580 hydrochlor...
一种特异性 p38 MAPK 抑制剂,IC50 为 0.6 uM。
-
AZD-7624
AZD-7624 是一种有效的、选择性的吸入式 p38α MAPK 抑制剂,pIC50 为 10.0。
021-51111890
购物车()
sales@molnova.cn

