Fluphenazine dihydrochloride is a phenothiazine-class D1DR and D2DR inhibitor. Fluphenazine 2HCl also inhibits Histamine H1 Receptor.
|Body Surface Area (m2)||0.007||0.025||0.15||0.05||0.02||0.5|
|Animal A (mg/kg) = Animal B (mg/kg) multiplied by||Animal B Km|
|Animal A Km|
For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.
|Solubility||DMSO 100 mg/mL
Water 100 mg/mL
A comparative study of the anticholinesterase activity of several antipsychotic agents.
Nasello AG, et al. Pharmacol Biochem Behav. 2003 Jul;75(4):895-901. PMID: 12957233.
Behavioral effects of withdrawal of fluphenazine after long-term treatment.
Trzeciak HI, et al. Arzneimittelforschung. 1976;26(9):1697-700. PMID: 1036703.
|Related Dopamine Receptor Products|
Sulpiride is a dopamine D2-receptor antagonist. It has been used therapeutically as an antidepressant, antipsychotic, and as a digestive aid.
rac-Rotigotine Hcl is a high potency and selectivity agonist for D-2 receptor with Ki of 0.69 nM.
Promazine (hydrochloride) is a D2 dopamine receptor antagonist, belongs to the phenothiazine class of antipsychotics, used to treat schizophrenia.
|Prochlorperazine dimaleate salt
Prochlorperazine dimaleate is a dopamine (D2) receptor antagonist.
Pramipexole 2Hcl is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.
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