Ziprasidone

SKU: orb1226219

Description

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.

Research Area

Pharmacology & Drug Discovery

Images & Validation

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Key Properties

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CAS Number	146939-27-7
MW	412.9356
Purity	>98% (HPLC)
Formula	C₂₁H₂₁ClN₄OS
SMILES	ClC1=C(CCN2CCN(CC2)C2=NSC3=CC=CC=C23)C=C2CC(=O)NC2=C1
Target	5-HT Receptor
Solubility	10 mM in DMSO

Bioactivity

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In Vivo

Ziprasidone (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. Animal model: Eight-week-old female Sprague-Dawleyrats weighing 200 to 250 g. Dosage: 20 mg/kg. Administration: Oral gavage; 20 mg/kg; once daily; 7 weeks. Result: Gained significantly less weight (P = 0.031), had a lower level of physical activity (P = 0.016), showed a higher resting energy expenditure (P < 0.001), and displayed a greater capacity for thermogenesis when subjected to cold (P < 0.001).

In Vitro

Ziprasidone (0-500 nM, 150 seconds) blocks wild-type hERG current. Cell Viability Assay Cell line: HEK-293 cells. Concentration: 0-500 nM. Incubation time: 150 seconds. Result: Blocked wild-type hERG current in a voltage- and concentration-dependent manner (IC50 = 120 nm).

Storage & Handling

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Storage	Storage temperature: -20°C. Stability: ≥ 2 years
Expiration Date	12 months from date of receipt.
Disclaimer	For research use only

Alternative Names

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CP 88059 | CP-88059 | CP88059

Quality Guarantee

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Gene Symbol

5-HT Receptor

Protocol Information

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MW:	509.04
Formula:	C₂₂H₂₅ClN₄O₄S₂

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MW:	563.08
Formula:	C₂₂H₃₁ClN₄O₇S₂

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Ziprasidone

Description

Research Area

Images & Validation

Key Properties

Bioactivity

Storage & Handling

Alternative Names

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