EAAT2 activator 1
CAS No. 892415-28-0
EAAT2 activator 1( F2005-0304 | 3-[(2-Chloro-6-fluorobenzyl)thio]-6-pyridin-2-ylpyridazine )
Catalog No. M28620 CAS No. 892415-28-0
F2005-0304 is a thiopyridazine derivative that has been found to increase EAAT2 protein levels in astrocytes.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
|
| 5MG | 31 | In Stock |
|
| 10MG | 55 | In Stock |
|
| 25MG | 113 | In Stock |
|
| 50MG | 205 | In Stock |
|
| 100MG | 305 | In Stock |
|
| 200MG | 434 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameEAAT2 activator 1
-
NoteResearch use only, not for human use.
-
Brief DescriptionF2005-0304 is a thiopyridazine derivative that has been found to increase EAAT2 protein levels in astrocytes.
-
DescriptionF2005-0304 is a thiopyridazine derivative that has been found to increase EAAT2 protein levels in astrocytes.
-
In Vitro——
-
In Vivo——
-
SynonymsF2005-0304 | 3-[(2-Chloro-6-fluorobenzyl)thio]-6-pyridin-2-ylpyridazine
-
PathwayOthers
-
TargetOther Targets
-
RecptorBD1-BRD4|BRD4-BD2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number892415-28-0
-
Formula Weight331.8
-
Molecular FormulaC16H11ClFN3S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 25 mg/mL (75.35 mM)
-
SMILESFc1cccc(Cl)c1CSc(cc1)nnc1-c1ncccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Kharenko OA, et al. Design and Characterization of Novel Covalent Bromodomain and Extra-Terminal Domain (BET) Inhibitors Targeting a Methionine. J Med Chem. 2018 Sep 27;61(18):8202-8211.
molnova catalog
related products
-
Rezatomidine
Rezatomidine (AGN-203818) is an effective and selective alpha2-adrenergic receptor antagonist for the treatment of chronic pain, including neuropathic pain.
-
Axinysone A
Axinysone A is a natural product.
-
MRS 2578
MRS2578, an effective P2Y6 receptor antagonist with IC50 of 37 nM, shows insignificant inhibition at P2Y1, P2Y2, P2Y4, and P2Y11 receptors.
Cart
sales@molnova.com