MK-0343
CAS No. 233275-76-8
MK-0343( MRK-409 | MK0343 )
Catalog No. M13670 CAS No. 233275-76-8
MK-0343 (MRK-409) is a potent, α2/3 subtype selective, partial GABAA receptor agonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 336 | Get Quote |
|
| 50MG | 1296 | Get Quote |
|
| 100MG | 1962 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMK-0343
-
NoteResearch use only, not for human use.
-
Brief DescriptionMK-0343 (MRK-409) is a potent, α2/3 subtype selective, partial GABAA receptor agonist.
-
DescriptionMK-0343 (MRK-409) is a potent, α2/3 subtype selective, partial GABAA receptor agonist, shows greater agonist efficacy at the α3 over α1 subtypes; readily penetrates the brain in rats and occupies the benzodiazepine site of GABA(A) receptors with an Occ(50) of 2.2 mg/kg p.o. and a corresponding plasma EC50 of 115 ng/mL; produces anxiolytic-like activity in rodent and primate unconditioned and conditioned models of anxiety.
-
In Vitro——
-
In VivoMK0343 readily penetrates the brain in rats and occupies the benzodiazepine site of GABAA receptors, measured using an in vivo [3H]flumazenil binding assay, with an Occ50 of 2.2?mg/kg p.o. and a corresponding plasma EC50 of 115?ng/mL. Animal Model:Male Sprague-Dawley rats (approximately 250–300g) (pharmacokinetics)Dosage:1, 2 or 3?mg/kg Administration:Oral administration Result:Readily penetrated the brain in rats and occupies the benzodiazepine site of GABAA receptors, with an Occ50 of 2.2?mg/kg p.o. and a corresponding plasma EC50 of 115?ng/mL.
-
SynonymsMRK-409 | MK0343
-
PathwayMembrane Transporter/Ion Channel
-
TargetGAT
-
RecptorGAT
-
Research AreaOther Indications
-
Indication——
Chemical Information
-
CAS Number233275-76-8
-
Formula Weight397.39
-
Molecular FormulaC19H17F2N7O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 250 mg/mL (629.12 mM)
-
SMILESCN1N=CN=C1COC2=NN3C(C=C2C4CCC4)=NN=C3C5=C(F)C=CC=C5F
-
Chemical Name7-Cyclobutyl-3-(2,6-difluorophenyl)-6-[(1-methyl-1H-1,2,4-triazol-5-yl)methoxy]-1,2,4-triazolo[4,3-b]pyridazine
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Atack JR, et al. J Psychopharmacol. 2011 Mar;25(3):314-28.
2. de Haas SL, et al. J Psychopharmacol. 2008 Jan;22(1):24-32.
molnova catalog
related products
-
HZ-166
HZ-166 (HZ166) is a GABAA receptor subtype-selective benzodiazepine site ligand with preferential activity at α2- and α3-GABA(A) receptors.
-
SNAP 5114
A GABA transport inhibitor with IC50 of 5, 21, 388 and 140 uM for hGAT-3, rGAT-2, hGAT-1 and BGT-1, respectively.
-
MRK-016
A potent, functionally selective, CNS-penetrating and orally bioavailable inverse agonist of benzodiazepine site of GABAA α5 receptor.
Cart
sales@molnova.com