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) .
-
In Vitro——
-
In VivoClocapramine 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 (ED50 of 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 Weight572.01
-
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
-
Azelaprag
Azelaprag (AMG 986) is an effective small-molecule apelin receptor agonist. Azelaprag can be used to treat neurological diseases and cardiovascular diseases.
-
4,5-Dimethoxycanthin...
4,5-Dimethoxycanthin-6-one is an alkaloid isolated from Picrasma quassioides BENNET (Simaroubaceae).4,5-Dimethoxycanthin-6-one was isolated from Picrasma quassioides BENNET (Simaroubaceae) with antimicrobial activity.4,5-Dimethoxycanthin-6-one was isolated from Picrasma quassioides BENNET (Simaroubaceae) with antimicrobial activity.
-
CINPA1
CINPA1 is a selective inhibitor of constitutive androstane receptor (CAR) with an IC50 of 70 nM for CAR-mediated transcription. CINPA1 can be used in studies about CAR function.
Cart
sales@molnova.com