Cart
sales@molnova.com
CHET3
CAS No. 2489231-47-0
CHET3( —— )
Catalog No. M36427 CAS No. 2489231-47-0
CHET3 is a highly selective allosteric activator for TASK-3-containing K2P channels. CHET3 has shown potent in vivo analgesic effects in various acute and chronic pain models in rodents.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 304 | Get Quote |
|
| 5MG | 494 | Get Quote |
|
| 10MG | 715 | Get Quote |
|
| 25MG | 1067 | Get Quote |
|
| 50MG | 1444 | Get Quote |
|
| 100MG | 1908 | Get Quote |
|
| 500MG | 3825 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameCHET3
-
NoteResearch use only, not for human use.
-
Brief DescriptionCHET3 is a highly selective allosteric activator for TASK-3-containing K2P channels. CHET3 has shown potent in vivo analgesic effects in various acute and chronic pain models in rodents.
-
DescriptionCHET3 is a highly selective allosteric activator for TASK-3-containing K2P channels. CHET3 has shown potent in vivo analgesic effects in various acute and chronic pain models in rodents.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
RecptorPotassium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2489231-47-0
-
Formula Weight423.49
-
Molecular FormulaC21H21N5O3S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESN(C(NC=1NC(CSC2=CC=C(C)C=C2)=CC(=O)N1)=N)C=3C=C4C(=CC3)OCCO4
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
OR-1896
OR-1896 is the active metabolite of Levosimendan, a highly specific phosphodiesterase (PDE III) inhibitor, a vasodilator with partial anti-inflammatory properties that produces vasodilation in different types of blood vessels through activation of ATP-sensitive (KATP) and other potassium channels.
-
Charybdotoxin
Specific inhibitor of the big conductance Ca2+-activated K+ channel.
-
TRAM 39
TRAM 39 is a selective blocker of intermediate-conductance Ca2+-activated K+channels.
