NNC-711
CAS No. 145645-62-1
NNC-711( NNC711 )
Catalog No. M11968 CAS No. 145645-62-1
NNC-711 is a potent and selective inhibitor of GABA uptake by GAT-1 with IC50 of 0.04 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 130 | In Stock |
|
| 10MG | 208 | In Stock |
|
| 25MG | 398 | In Stock |
|
| 50MG | 555 | In Stock |
|
| 100MG | 792 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNNC-711
-
NoteResearch use only, not for human use.
-
Brief DescriptionNNC-711 is a potent and selective inhibitor of GABA uptake by GAT-1 with IC50 of 0.04 uM.
-
DescriptionNNC-711 is a potent and selective inhibitor of GABA uptake by GAT-1 with IC50 of 0.04 uM; displays excellent selectivty over rGAT-2, hGAT-3 and hBGT-1, and other other neurotransmitter receptors; inhibits synaptosomal (IC50=47 nM), neuronal (IC50=1238 nM) and glial (IC50=636 nM) GABA uptake in vitro; demonstrates potent anticonvulsant activity against rodent seizures induced by DMCM.
-
In Vitro——
-
In Vivo——
-
SynonymsNNC711
-
PathwayMembrane Transporter/Ion Channel
-
TargetGAT
-
RecptorGAT
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number145645-62-1
-
Formula Weight386.876
-
Molecular FormulaC21H23ClN2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC1CN(CC(=C1)C(=O)O)CCON=C(C2=CC=CC=C2)C3=CC=CC=C3.Cl
-
Chemical Name1,2,5,6-Tetrahydro-1-[2-[[(diphenylmethylene)amino]oxy]ethyl]-3-pyridinecarboxylic acid hydrochloride
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Suzdak PD, et al. Eur J Pharmacol. 1992 Dec 2;224(2-3):189-98.
2. Oh DJ, et al. Epilepsia. 1994 Mar-Apr;35(2):426-30.
3. Borden LA, et al. Eur J Pharmacol. 1994 Oct 14;269(2):219-24.
molnova catalog
related products
-
Vigabatrin Hydrochlo...
Vigabatrin Hcl(γ-Vinyl-GABA; Sabril) is a structural analog of the inhibitory neurotransmitter γ-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.
-
TPA023
TPA023 is a potent, α2/α3 subtype-selective, and oral GABAA receptor agonist with Kd of 0.92, 1.05 and 0.58 nM for α1-, α2-, α3-, and α5-containing human receptors.
-
(+)-Bicuculline
Bicuculline is a light-sensitive competitive antagonist of GABAA receptors. It was originally identified in 1932 in plant alkaloid extracts and has been isolated from Dicentra cucullaria, Adlumia fungosa, Fumariaceae, and several Corydalis species.
Cart
sales@molnova.com