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 |
| 5MG | ¥1150 | 有现货 |
|
| 10MG | ¥1701 | 有现货 |
|
| 25MG | ¥2669 | 有现货 |
|
| 50MG | ¥3618 | 有现货 |
|
| 100MG | ¥4725 | 有现货 |
|
| 200MG | ¥6210 | 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
-
CC214-1
CC214-1 是一种潜在有效的 mTOR抑制剂,可诱导自噬 (autophagy),IC50 为 0.002 μM。 CC214-1 被证明可作为体外工具化合物用于探索 mTOR 激酶生物学。 CC214-1 可用于胶质母细胞瘤研究。
-
Insecticidal agent 3...
Insecticidal agent 364 is a selective small molecule inhibitor of rapamycin kinase target protein. Insecticidal agent 364 has antitumor activity, and by inhibiting mTOR, Insecticidal agent 364 aims to disrupt signaling pathways involved in cancer cell growth and survival, thereby potentially inhibiting tumor growth.
-
Autogramin-2
Autogramin-2 有效抑制饥饿诱导的自噬,IC50 为 0.27 μM,并抑制 mTORC1(雷帕霉素;IC50:0.14 μM)
021-51111890
购物车()
sales@molnova.cn

