MK-0249
CAS No. 1167574-41-5
MK-0249 ( MK0249 )
Catalog No. M10571 CAS No. 1167574-41-5
MK-0249 is a novel potent, selective histamine H3 inverse agonist for the treatment of cognitive impairment with schizophrenia.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
100MG | Get Quote | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMK-0249
-
NoteResearch use only, not for human use.
-
Brief DescriptionMK-0249 is a novel potent, selective histamine H3 inverse agonist for the treatment of cognitive impairment with schizophrenia.
-
DescriptionMK-0249 is a novel potent, selective histamine H3 inverse agonist for the treatment of cognitive impairment with schizophrenia.Sleep Disorder Phase 1 Discontinued
-
SynonymsMK0249
-
PathwayGPCR/G Protein
-
TargetHistamine Receptor
-
RecptorHistamine Receptor
-
Research AreaNeurological Disease
-
IndicationSleep Disorder
Chemical Information
-
CAS Number1167574-41-5
-
Formula Weight431.46
-
Molecular FormulaC23H24F3N3O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1N(C2=CC=C(OCCCN3CCCC3)C=C2)C(C)=NC4=C1C(C(F)(F)F)=CC=C4
-
Chemical Name2-methyl-3-(4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-5-(trifluoromethyl)quinazolin-4(3H)-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Brioni JD, et al. J Pharmacol Exp Ther. 2011 Jan;336(1):38-46.
2. James LM, et al. Psychopharmacology (Berl). 2011 Jun;215(4):643-53.
3. Zoethout RW, et al. J Psychopharmacol. 2012 Feb;26(2):292-302.
2. James LM, et al. Psychopharmacology (Berl). 2011 Jun;215(4):643-53.
3. Zoethout RW, et al. J Psychopharmacol. 2012 Feb;26(2):292-302.
molnova catalog
related products
-
H4 Receptor antagoni...
H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist with an IC50?of 19 nM.
-
Hydroxyzine dihydroc...
Hydroxyzine Dihydrochloride is a histamine H1-receptor antagonist.
-
Pitolisant oxalate
A potent and selective antagonist of H3 receptor with Ki/EC50 of 0.16/1.5 nM; no effect on H1, H2, H4 receptors (IC50>10 uM).