
Aromadendrin
CAS No. 480-20-6
Aromadendrin ( —— )
产品货号. M22807 CAS No. 480-20-6
香薰素是一种天然产品。它诱导细胞凋亡并抑制 Bcl-2 和 Bcl-xL 表达,具有抗炎、抗氧化和抗糖尿病特性,具有抗炎活性。Aromadendrin 是一种黄酮醇,据报道具有多种药理活性,例如- 抗炎、抗氧化和抗糖尿病特性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥988 | 有现货 |
![]() ![]() |
10MG | ¥1588 | 有现货 |
![]() ![]() |
25MG | ¥3013 | 有现货 |
![]() ![]() |
50MG | ¥4447 | 有现货 |
![]() ![]() |
100MG | 获取报价 | 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Aromadendrin
-
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
-
产品简述香薰素是一种天然产品。它诱导细胞凋亡并抑制 Bcl-2 和 Bcl-xL 表达,具有抗炎、抗氧化和抗糖尿病特性,具有抗炎活性。Aromadendrin 是一种黄酮醇,据报道具有多种药理活性,例如- 抗炎、抗氧化和抗糖尿病特性。
-
产品描述Aromadendrin is a natural product.?It induces apoptosis and inhibits Bcl-2 and Bcl-xL expression,?possesses anti-inflammatory, antioxidant, and anti-diabetic properties, it exhibits anti-inflammatory activityAromadendrin, a flavonol, has been reported to possess a variety of pharmacological activities such as anti-inflammatory, antioxidant, and anti-diabetic properties.?Aromadendrin significantly suppressed LPS-induced excessive production of pro-inflammatory mediators such as nitric oxide (NO) and PGE2.?In accordance, aromadendrin attenuated LPSinduced overexpression iNOS and COX-2.?In addition, aromadendrin significantly suppressed LPS-induced degradation of IκB, which sequesters NF-κB in cytoplasm, consequently inhibiting the nuclear translocation of pro-inflammatory transcription factor NF- κB.?Aromadendrin significantly attenuated LPS-induced activation of JNK, but not ERK and p38, in a concentration-dependent manner.?Aromadendrin exhibits anti-inflammatory activity through the suppression of nuclear translocation of NF-κB and phosphorylation of JNK in LPS-stimulated RAW 264.7 macrophage cells.
-
体外实验Cell Proliferation Assay Cell Line:Normal synoviocyte cells; RA-FLS cells Concentration:0.3 μM, 3 μM, 30 μM, 300 μM Incubation Time:48 hours Result:Decreased the proliferation of RA-FLSs.Apoptosis Analysis Cell Line:RA-FLS cells Concentration:3 μM, 30 μM Incubation Time:48 hours Result:Induced apoptosis in RA-FLSs.Western Blot Analysis Cell Line:RA-FLS cells Concentration:3 μM, 30 μM Incubation Time:48 hours Result:Promoted Bax and Bad expression, increased the cleaved fragments of caspase-3, caspase-9 and cleaved PARP and inhibited Bcl-2 and Bcl-xL expression.
-
体内实验——
-
同义词——
-
通路Angiogenesis
-
靶点Bcl-2
-
受体Bcl-2|Bcl-xL
-
研究领域——
-
适应症——
化学信息
-
CAS Number480-20-6
-
分子量288.3
-
分子式C15H12O6
-
纯度>98% (HPLC)
-
溶解度DMSO:120 mg/mL (416.31 mM; Need ultrasonic); H2O:< 0.1 mg/mL (insoluble)
-
SMILESO=C1C2=C(O)C=C(O)C=C2O[C@H](C3=CC=C(O)C=C3)[C@H]1O
-
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
1. Stimulation of glucose uptake and improvement of insulin resistance by aromadendrin.Pharmacology. 2011;88(5-6):266-74.
产品手册




关联产品
-
S55746 hydrochloride
S55746(BCL201,Servier-1)是一种新型有效、选择性、口服生物可利用的 BCL-2 抑制剂,Ki 为 1.3 nM。
-
Desmorpholinyl Navit...
Desmorpholinyl Navitoclax-NH-Me 是一种 Bcl-xL 抑制剂。 Desmorpholinyl Navitoclax-NH-Me 和 E3 泛素连接酶的 CRBN 配体可用于合成 PROTAC BCL-XL 降解剂 XZ739 。
-
BDA-366
一种有效的选择性 Bcl2 BH4 结构域拮抗剂,Ki 为 3.3 nM;对其他 Bcl2 家族成员(包括 Bcl-XL、Mcl-1 或 Bfl-1/A1)没有亲和力。