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Ziprasidone hydrochloride monohydrate

A full antagonist of D2 and 5-HT2A receptors with Ki of 6.8 and 0.6 nM, respectively; also is a partial agonist of 5-HT1A, and a partial antagonist of 5-HT2C and 5-HT1D receptors; exhibits potent antipsychotic activity in vivo.Schizophrenia Approved (In Vitro) :Ziprasidone hydrochloride monohydrate (0-500 nM, 150 seconds) blocks wild-type hERG current. (In Vivo) :Ziprasidone hydrochloride monohydrate (oral gavage; 20 mg/kg; once daily; 7 weeks) results in weight loss, low level physical activity, high resting energy expenditure and greater capacity for thermogenesis when subjected to cold.

Product Specifications

CAS Number

138982-67-9

Product Name Alternative

CP-88059

Field of Research

Pharmacology & Drug Discovery

Purity

>98% (HPLC)

Solubility

10 mM in DMSO

Smiles

O=C1CC2=CC (CCN3CCN (C4=NSC5=C4C=CC=C5) CC3) =C (Cl) C=C2N1.Cl.O

Molecular Formula

C21H24Cl2N4O2S

Molecular Weight

467.4119

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

2H-Indol-2-one, 5-[2-[4- (1,2-benzisothiazol-3-yl) -1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)

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