Clocapramine dihydrochloride hydrate
CAS No. 60789-62-0
Clocapramine dihydrochloride hydrate ( —— )
Catalog No. M26121 CAS No. 60789-62-0
Clocapramine hydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 1008 | Get Quote |
|
10MG | 1341 | Get Quote |
|
25MG | 2007 | Get Quote |
|
50MG | 2664 | Get Quote |
|
100MG | 3573 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameClocapramine dihydrochloride hydrate
-
NoteResearch use only, not for human use.
-
Brief DescriptionClocapramine hydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
-
DescriptionClocapramine hydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.(In Vivo):Clocapramine shows the lowest potency for D2-occupancy in vivo . An in vivo receptor binding technique is used to evaluate the binding profiles of typical and atypical antipsychotic drugs to striatal dopamine-D2 and frontal serotonin-5-HT2 receptors in a rat brain using more specific ligands. Clocapramine produces ratios of potency in occupying 5-HT2 versus D2 receptors that fall between these two groups (ED50s: 14.5 mg/kg for D2, 4.9 mg/kg for 5-HT2) .
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorWnt
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number60789-62-0
-
Formula Weight572.0
-
Molecular FormulaC28H41Cl3N4O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO.Cl.Cl.NC(=O)C1(CCN(CCCN2c3ccccc3CCc3ccc(Cl)cc23)CC1)N1CCCCC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Charlene F. Barroga, et al. Diketones and hydroxyketones as catenin signaling pathway activators. WO2012024404A1.
molnova catalog
related products
-
Ciraparantag acetate
Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.?
-
S26131
S26131 behaves as an antagonist on MT1 and MT2 receptors with Ki of 0.5 and 112 nM respectively.
-
L-Methionine-DL-sulf...
L-Methionine-DL-sulfoximine inhibits glutamine synthetase and metabolically and morphologically primarily affects astroglia. L-Methionine-DL-sulfoximine can be used in convulsant studies.