A-1899

A-1899
NEW
Item number Size Datasheet Manual SDS Delivery time Quantity Price
Cay43018-5 5 mg -

6 - 10 business days*

48.00€
Cay43018-10 10 mg -

6 - 10 business days*

73.00€
Cay43018-25 25 mg -

6 - 10 business days*

121.00€
Cay43018-50 50 mg -

6 - 10 business days*

169.00€
 
A-1899 is an inhibitor of the two-pore domain potassium channel 3. (K2P3.1/TASK1, IC50 = 0. µM in... more
Product information "A-1899"
A-1899 is an inhibitor of the two-pore domain potassium channel 3. (K2P3.1/TASK1, IC50 = 0. µM in Xenopus oocytes expressing the human channel). It is selective for K2P3.1/TASK1 over K2P5.1/TASK2, K2P9.1/TASK3, and K2P17.1/TASK4 (IC50s = 12, 0. and 8. µM, respectively) and a panel of 16 additional potassium channels at 0. µM. A-1899 (3 mg/kg) selectively increases the effective refractory period (ERP) in the left atrium over the right atrium and does not affect ventricular repolarization in anesthetized pigs. It stimulates breathing and induces respiratory alkalosis in spontaneously breathing anesthetized rats when administered at a dose of 25 mg/kg.. Solulibility: DMSO: Soluble: =10 mg/ml: .
Keywords: S-20951, N-[(2,4-difluorophenyl)methyl]-2'-[[[2-(4-methoxyphenyl)acetyl]amino]methyl]-[1,1'-biphenyl]-2-carboxamide
Supplier: Cayman Chemical
Supplier-Nr: 43018

Properties

Application: K2P3.1/TASK1/KCNK3 inhibitor
MW: 500.55 D
Formula: C30H26F2N2O3
Purity: >95%
Format: Solid

Database Information

CAS : 498577-46-1| Matching products
KEGG ID : K04914 | Matching products

Handling & Safety

Storage: -20°C
Shipping: +20°C (International: -20°C)
Caution
Our products are for laboratory research use only: Not for administration to humans!
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