欢迎访问ProbeChem中文网站,英文网站请访问www.probechem.com

首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Potassium Channel-A1899
A1899

Chemical Structure : A1899

CAS No.: 498577-46-1

A1899 (A-1899)

货号: PC-20697Not For Human Use, Lab Use Only.

A1899 (A-1899) is a potent and highly selective blocker of the K(2P) channel TASK-1, selectively blocks human TASK-1 channels expressed in Xenopus oocytes with IC50 of 35.1 nM.

规格 价格 库存 数量
50 mg Get quote
100 mg Get quote
200 mg Get quote
1 g Get quote

大包装,大折扣!

E-mail: sales@probechem.com

Tech Support: tech@probechem.com

纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

A1899 (A-1899) is a potent and highly selective blocker of the K(2P) channel TASK-1, selectively blocks human TASK-1 channels expressed in Xenopus oocytes with IC50 of 35.1 nM.
A1899 has IC50 of 7 nM for TASK-1 channels expressed in CHO cells, 10-fold selectivity over TASK-3 channel.
A1899 also displays high selectivity over different potassium channels in Xenopus oocytes.
A1899 interacts with the M2 and M4 transmembrane segments of TASK-1 channels.
A1899 inhibits TASK-1 channels expressed in human and rodent alpha-cells.

物理化学性质&存储条件

分子量 500.55
分子式 C30H26F2N2O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

O=C(C1=CC=CC=C1C2=CC=CC=C2CNC(CC3=CC=C(OC)C=C3)=O)NCC4=CC=C(F)C=C4F

参考文献

1. Streit AK, et al. J Biol Chem. 2011;286:13977.

2. Schiekel J, et al. Cardiovasc Res. 2013 Jan 1;97(1):97-105.

备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright

联系我们 sales@probechem.com

Bulk Inquiry

* Indicates a Required FieldYour information is safe with us.

  • *Product name:
  • *Applicant name:
  • *Email address:
  • *Organization name:
  • *Requested quantity:
  • *Country:
  • *Additional Information:

询单

  • *产品名称:
  • *姓名:
  • *邮箱:
  • *公司名称:
  • *询单数量:
  • *国籍:
  • 询单信息: