Name | ziprasidone |
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Synonyms |
5-{2-4-(1,2-benzothiazol-3-yl)piperazin-1-ylethyl}-6-chloro-1,3-dihydro-2H-indol-2-one
5-{2-[4-(1,2-Benzisothiazol-3-yl)piperazin-1-yl]ethyl}-6-chloro-1,3-dihydro-2H-indol-2-one ziprasidonum Ziprasidone UNII-6UKA5VEJ6X 5-{2-[4-(1,2-Benzothiazol-3-yl)piperazin-1-yl]ethyl}-6-chloro-1,3-dihydro-2H-indol-2-one ziprasidona EINECS 203-794-9 5-{2-[4-(1,2-Benzisothiazol-3-yl)piperazin-1-yl]ethyl}-6-chlor-1,3-dihydro-2H-indol-2-on Zipwell MFCD00866661 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro- 2H-indol-2-one, 5-2-4-(1,2-benzisothiazol-3-yl)-1-piperazinylethyl-6-chloro-1,3-dihydro- 5-{2-[4-(1,2-Benzothiazol-3-yl)-1-piperazinyl]ethyl}-6-chloro-1,3-dihydro-2H-indol-2-one ziprazidone Ziprasidone [INN:BAN] Geodon Zeldox 5-[2-[4-(1,2-benzothiazol-3-yl)piperazin-1-yl]ethyl]-6-chloro-1,3-dihydroindol-2-one |
Description | Ziprasidone(CP88059) is a combined 5-HT (serotonin) and dopamine receptor antagonist which exhibits potent effects of antipsychotic activity.IC50 value:Target: 5-HT receptor; Dopamine receptorZiprasidone possesses an in vitro 5-HT2A/dopamine D2 receptor affinity ratio higher than any clinically available antipsychotic agent. In vivo, ziprasidone antagonizes 5-HT2A receptor-induced head twitch with 6-fold higher potency than for blockade of d-amphetamine-induced hyperactivity, a measure of central dopamine D2 receptor antagonism. Ziprasidone also has high affinity for the 5-HT1A, 5-HT1D and 5-HT2C receptor subtypes, which may further enhance its therapeutic potential [1]. Ziprasidone sulfoxide and sulfone were the major metabolites in human serum. The affinities of the sulfoxide and sulfone metabolites for 5-HT2 and D2 receptors are low with respect to ziprasidone, and are thus unlikely to contribute to its antipsychotic effects [2]. Ziprasidone was associated with significant differential adverse effects relative to placebo in BPM, BPD, and schizophrenia with no significant difference in weight gain in all 3 groups. Self-reported somnolence was increased across the 3 conditions. Subjects with BPM were more vulnerable to EPS than those with BPD or schizophrenia [3].Clinical indications: Bipolar I disorder; Bipolar disorder; Mania; SchizophreniaFDA Approved Date: February 2001 |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 554.8±50.0 °C at 760 mmHg |
Melting Point | 213-215°C |
Molecular Formula | C21H21ClN4OS |
Molecular Weight | 412.94 |
Flash Point | 289.3±30.1 °C |
PSA | 76.71000 |
LogP | 4.00 |
Vapour Pressure | 0.0±1.5 mmHg at 25°C |
Index of Refraction | 1.681 |
Storage condition | Refrigerator |
Symbol |
![]() ![]() ![]() GHS02, GHS07, GHS08 |
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Signal Word | Danger |
Hazard Statements | H225-H315-H360FD |
Supplemental HS | May form explosive peroxides. |
Precautionary Statements | P201-P210-P308 + P313-P403 + P235 |
Hazard Codes | C,N |
Risk Phrases | R22:Harmful if swallowed. R34:Causes burns. R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . |
Safety Phrases | S26-S36/37/39-S45-S60-S61 |
RIDADR | UN 3259 8/PG 3 |
WGK Germany | 2 |
RTECS | JR6475000 |
Packaging Group | II |
Hazard Class | 8 |
HS Code | 29211980 |
HS Code | 29211980 |
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