Dooku1
CAS No. 2253744-54-4
Dooku1 ( —— )
产品货号. M26169 CAS No. 2253744-54-4
Dooku1 是 Yoda1 的类似物,也是内源性 Piezo1 通道的选择性拮抗剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥437 | 有现货 |
|
| 5MG | ¥721 | 有现货 |
|
| 10MG | ¥1158 | 有现货 |
|
| 25MG | ¥2333 | 有现货 |
|
| 50MG | ¥4342 | 有现货 |
|
| 100MG | ¥6261 | 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Dooku1
-
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Dooku1 是 Yoda1 的类似物,也是内源性 Piezo1 通道的选择性拮抗剂。
-
产品描述Dooku1 is an analog of Yoda1 and a selective antagonist of endogenous Piezo1 channels. Dooku1 inhibits Ca2+ entry induced by 2μMYoda1 with IC50 values of 1.3μM (in HEK 293 cells) and 1.5μM (in HUVEC). Dooku1 inhibits Yoda1-induced aortic relaxation.
-
体外实验Cell Viability Assay Cell Line:HUVECs, Piezo1 T-REx cells Concentration:10 μM Incubation Time:40-60 s Result:Had a concentration-dependent inhibitory effect against Yoda1-induced Ca2+ entry in HUVECs, acting with an IC50 of 1.49 μM.Increased potency in HUVECs with an EC50 of 0.23 μM, compared with 2.51 μM in Piezo1 T-REx cells.
-
体内实验Animal Model:wild-type male C57BL/6 mice’s aortic rings Dosage:10 μM Administration:20 min Result:Suppressed the Yoda1-induced relaxation.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Bacterial
-
研究领域——
-
适应症——
化学信息
-
CAS Number2253744-54-4
-
分子量326.2
-
分子式C13H9Cl2N3OS
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (306.56 mM)
-
SMILESClc1cccc(Cl)c1CSc1nnc(o1)-c1ccc[nH]1
-
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.Alois Pískala, et al. Synthesis, molecular conformation and biological activity of 6-amino-5-azacytidine. Collect. Czech. Chem. Commun. 1989, 54, 2502-2512.
产品手册
关联产品
-
Amylin (8-37), rat
Amylin (8-37), rat is a truncated analog of native Amylin that selectively inhibits insulin-related glucose uptake and glycogen deposition in muscle tissue. Amylin is also known as islet amyloid precursor peptide (IAPP) and is co-secreted with insulin from pancreatic β-cells.
-
JNK-IN-7
JNK-IN-7 是一种选择性 JNK1/2/3 抑制剂 (IC50: 1.54/1.99/0.75 nM)。它还可以抑制 c-Jun 的磷酸化,c-Jun 是 JNK 激酶的底物。
-
(Tyr27)-pTH (27-48) ...
(Tyr27)-pTH (27-48) (human)
021-51111890
购物车()
sales@molnova.cn

