Linderalactone
CAS No. 728-61-0
Linderalactone ( Linderalactone )
产品货号. M19045 CAS No. 728-61-0
乌药内酯对人中性粒细胞响应 fMLP/CB 产生超氧阴离子显示出显着的抑制作用,IC5 值为 8.48 μg/mL。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥787 | 有现货 |
|
| 10MG | ¥1264 | 有现货 |
|
| 25MG | ¥2074 | 有现货 |
|
| 50MG | ¥3097 | 有现货 |
|
| 100MG | ¥4293 | 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 | ¥1036 | 有现货 |
|
生物学信息
-
产品名称Linderalactone
-
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
-
产品简述乌药内酯对人中性粒细胞响应 fMLP/CB 产生超氧阴离子显示出显着的抑制作用,IC5 值为 8.48 μg/mL。
-
产品描述Linderalactone is an NSAID isolated from Lindera aggregata.
-
体外实验Cell Viability Assay Cell Line:Lung cancer A549 cells Concentration:0 μM, 1.6 μM, 3.2 μM, 6.25 μM, 12.5 μM, 25 μM, 50 μM, 100 μM Incubation Time:24 hours Result:Inhibited the growth of A549 cells concentration-dependently.Apoptosis Analysis Cell Line:Lung cancer A549 cells Concentration:7.5 μM, 15 μM, 30 μM Incubation Time:Result:Induced apoptosis in A549 cells in a dose-dependent manner. Cell Cycle Analysis Cell Line:Lung cancer A549 cells Concentration:7.5 μM, 15 μM, 30 μM Incubation Time:24 hours Result:Induced G2/M cell cycle arrest.Western Blot Analysis Cell Line:Lung cancer A549 cells Concentration:7.5 μM, 15 μM, 30 μM Incubation Time:Result:Inhibited the JAK/STAT pathway in A549 cells.
-
体内实验——
-
同义词Linderalactone
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域Others-Field
-
适应症——
化学信息
-
CAS Number728-61-0
-
分子量244.29
-
分子式C15H16O3
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 33.33 mg/mL (136.44 mM)
-
SMILESCC1=CCCC2=CC(C3=C(C1)OC=C3C)OC2=O
-
化学全称(R,7Z,10E)-3,11-dimethyl-4,8,9,12-tetrahydro-6H-4,7-(metheno)furo[3,2-c][1]oxacycloundecin-6-one
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
-
erythro-Austrobailig...
erythro-Austrobailignan-6 is an orally active anti-cancer agent. erythro-Austrobailignan-6 inhibits DNA topoisomerase I and II activity. erythro-Austrobailignan-6 induces cell apoptosis and increases phosphorylation of p38 and JNK.
-
3-(4-prop-2-en-1-ylp...
3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox 对 2-methyl-5-HT 诱导的豚鼠回肠收缩的拮抗作用
-
TH1217
TH1217 (ZINC1775962367) 是一种有效的、选择性的 dCTPase pyrophosphatase 1 (dCTPase) 抑制剂,IC50 值为 47 nM。TH1217 可增强胞苷类似物在白血病细胞中的细胞毒性作用。TH1217 还可以调节 SARS-Cov-2 相互作用体,因此它具有抗 COVID-19 的活性。
021-51111890
购物车()
sales@molnova.cn

