021-51111890
购物车（0）
sales@molnova.cn
2,2-Dihydroxy chalcone
CAS No. 15131-80-3
2,2-Dihydroxy chalcone ( —— )
产品货号. M37837 CAS No. 15131-80-3
2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ￥2519 | 有现货 |
|
| 5MG | ￥3472 | 有现货 |
|
| 10MG | ￥5136 | 有现货 |
|
| 25MG | ￥7718 | 有现货 |
|
| 50MG | ￥10635 | 有现货 |
|
| 100MG | ￥14000 | 有现货 |
|
| 500MG | ￥28152 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称2,2-Dihydroxy chalcone
-
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2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
-
产品描述2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Autophagy
-
靶点Autophagy
-
受体Autophagy | Antibacterial
-
研究领域——
-
适应症——
化学信息
-
CAS Number15131-80-3
-
分子量240.25
-
分子式C15H12O3
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESOC1=C(\C=C\C(=O)C2=C(O)C=CC=C2)C=CC=C1
-
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
-
HADA Hydrochloride
HADA hydrochloride (HCC-Amino-D-alanine hydrochloride) 是一种蓝色荧光 FDAA (λem~450 nm)。FDAAs 在肽聚糖 (PG) 合成位点有效地与多种细菌的 PGs 结合，允许在最小干扰下特异性和共价探测细菌的生长。
-
Pennogenin 3-O-beta-...
Pennogenin 3-O-beta-chacotrioside 是从重楼中分离出来的活性成分，具有抗结直肠癌活性。它通过增加自噬相关蛋白 LC3 和 Beclin-1 的表达来调节自噬。
-
Glycycoumarin
Glycycoumarin 是一种雌激素激动剂，对 CYP1A2 和 CYP2B6 有中等程度的抑制作用。
