Ziprasidone (BioDeep_00000001913)
Secondary id: BioDeep_00000402569
human metabolite blood metabolite Chemicals and Drugs
代谢物信息卡片
化学式: C21H21ClN4OS (412.11245260000004)
中文名称: 齐拉西酮
谱图信息:
最多检出来源 Homo sapiens(blood) 95.96%
Last reviewed on 2024-09-14.
Cite this Page
Ziprasidone. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/ziprasidone (retrieved
2024-11-03) (BioDeep RN: BioDeep_00000001913). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: c1ccc2c(c1)c(ns2)N1CCN(CCc2cc3CC(=O)Nc3cc2Cl)CC1
InChI: InChI=1S/C21H21ClN4OS/c22-17-13-18-15(12-20(27)23-18)11-14(17)5-6-25-7-9-26(10-8-25)21-16-3-1-2-4-19(16)28-24-21/h1-4,11,13H,5-10,12H2,(H,23,27)
描述信息
Ziprasidone (marketed as Geodon, Zeldox) was the fifth atypical antipsychotic to gain FDA approval (February 2001). Ziprasidone is Food and Drug Administration (FDA) approved for the treatment of schizophrenia, and the intramuscular injection form of ziprasidone is approved for acute agitation in schizophrenic patients. Ziprasidone has also received approval for acute treatment of mania associated with bipolar disorder. [Wikipedia]
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents
D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists
D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists
N - Nervous system > N05 - Psycholeptics > N05A - Antipsychotics > N05AE - Indole derivatives
D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants
C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent
Ziprasidone (CP-88059), an orally active antipsychotic agent, is a combined 5-HT and dopamine receptor antagonist[1]. Ziprasidone mesylate trihydrate has affinities for Rat D2 (Ki=4.8 nM), 5-HT2A (Ki=0.42 nM) and 5-HT1A (Ki=3.4 nM)[1].
同义名列表
12 个代谢物同义名
5-{2-[4-(1,2-benzothiazol-3-yl)piperazin-1-yl]ethyl}-6-chloro-2,3-dihydro-1H-indol-2-one; 5-(2-(4-(3-Benzisothiazolyl)piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one; Ziprasidone hydrochloride, monohydrate; Ziprasidone mesylate trihydrate; Ziprasidone hydrochloride; Ziprasidonum; Ziprasidona; Ziprazidone; Ziprasidone; Zipradon; Geodon; CP-88059
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:10119
- KEGG: C07568
- KEGGdrug: D08687
- KEGGdrug: D92803
- PubChem: 60854
- HMDB: HMDB0014391
- Metlin: METLIN66685
- DrugBank: DB00246
- ChEMBL: CHEMBL708
- Wikipedia: Ziprasidone
- chemspider: 54841
- CAS: 146939-27-7
- PMhub: MS000001439
- PubChem: 9771
- NIKKAJI: J553.147K
- RefMet: Ziprasidone
- medchemexpress: HY-14542
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Marco Pozzi, Chiara Vantaggiato, Francesca Brivio, Genny Orso, Maria Teresa Bassi. Olanzapine, risperidone and ziprasidone differently affect lysosomal function and autophagy, reflecting their different metabolic risk in patients.
Translational psychiatry.
2024 Jan; 14(1):13. doi:
10.1038/s41398-023-02686-x
. [PMID: 38191558] - Ankita Sahu, Shaban Ahmad, Khalid Imtiyaz, Ajeeshkumar Kizhakkeppurath Kumaran, Mojahidul Islam, Khalid Raza, Murugesh Easwaran, Asha Kurukkan Kunnath, Moshahid A Rizvi, Saurabh Verma. In-silico and in-vitro study reveals ziprasidone as a potential aromatase inhibitor against breast carcinoma.
Scientific reports.
2023 10; 13(1):16545. doi:
10.1038/s41598-023-43789-1
. [PMID: 37783782] - Hannah M Ficarino, Michael Z Caposole, S Noelle Davis, Mackenzie N Krebsbach, Emily F McGowin, Kaitlin M Alexander, Christopher M Kinnard, Jon D Simmons. Neuroleptic Malignant Syndrome: A Potential Etiology of Multisystem Organ Failure in a Burn Patient.
The American surgeon.
2022 Mar; 88(3):519-520. doi:
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. [PMID: 32988244] - Yub Raj Sedhai, Alok Atreya, Prabin Phuyal, Soney Basnyat, Sagar Pokhrel. Case Report: Ziprasidone induced neuroleptic malignant syndrome.
F1000Research.
2021; 10(?):124. doi:
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European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology.
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Drug design, development and therapy.
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Chemico-biological interactions.
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Schizophrenia research.
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Journal of psychiatric research.
2017 02; 85(?):59-65. doi:
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. [PMID: 27837658] - Tahnee J Dening, Shasha Rao, Nicky Thomas, Clive A Prestidge. Silica encapsulated lipid-based drug delivery systems for reducing the fed/fasted variations of ziprasidone in vitro.
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2016 Apr; 101(?):33-42. doi:
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. [PMID: 27644343] - Hriday Bera, Shashank Boddupalli, Amit Kumar Nayak. Mucoadhesive-floating zinc-pectinate-sterculia gum interpenetrating polymer network beads encapsulating ziprasidone HCl.
Carbohydrate polymers.
2015 Oct; 131(?):108-18. doi:
10.1016/j.carbpol.2015.05.042
. [PMID: 26256166] - Joseph W Iskandar, John Eric Vance, Anita Kablinger, Bush Kavuru. Transient agranulocytosis associated with ziprasidone in a 45-year-old man on hemodialysis.
Journal of clinical psychopharmacology.
2015 Jun; 35(3):347-8. doi:
10.1097/jcp.0000000000000324
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Psychiatry research.
2014 Oct; 219(2):261-7. doi:
10.1016/j.psychres.2014.05.039
. [PMID: 24930580] - Rocio Pérez-Iglesias, Victor Ortiz-Garcia de la Foz, Obdulia Martínez García, Jose Antonio Amado, M Teresa Garcia-Unzueta, Rosa Ayesa-Arriola, Paula Suarez-Pinilla, Rafael Tabares-Seisdedos, Benedicto Crespo-Facorro. Comparison of metabolic effects of aripiprazole, quetiapine and ziprasidone after 12 weeks of treatment in first treated episode of psychosis.
Schizophrenia research.
2014 Oct; 159(1):90-4. doi:
10.1016/j.schres.2014.07.045
. [PMID: 25151200] - Mona Darwish, Mary Bond, Ronghua Yang, Edward T Hellriegel, Philmore Robertson. Evaluation of the potential for a pharmacokinetic drug-drug interaction between armodafinil and ziprasidone in healthy adults.
Clinical drug investigation.
2014 Oct; 34(10):691-9. doi:
10.1007/s40261-014-0220-3
. [PMID: 25047407] - Pierre Chue, Francine S Mandel, François Therrien. The effect of ziprasidone on metabolic syndrome risk factors in subjects with schizophrenia: a 1 year, open-label, prospective study.
Current medical research and opinion.
2014 Jun; 30(6):997-1005. doi:
10.1185/03007995.2014.898139
. [PMID: 24568177] - Laura Mercolini, Roberto Mandrioli, Michele Protti, Andreas Conca, Lawrence J Albers, Maria Augusta Raggi. Dried blood spot testing: a novel approach for the therapeutic drug monitoring of ziprasidone-treated patients.
Bioanalysis.
2014 Jun; 6(11):1487-95. doi:
10.4155/bio.14.3
. [PMID: 25046049] - Laura Mercolini, Michele Protti, Giulia Fulgenzi, Roberto Mandrioli, Nadia Ghedini, Andreas Conca, Maria Augusta Raggi. A fast and feasible microextraction by packed sorbent (MEPS) procedure for HPLC analysis of the atypical antipsychotic ziprasidone in human plasma.
Journal of pharmaceutical and biomedical analysis.
2014 Jan; 88(?):467-71. doi:
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Clinical drug investigation.
2013 Oct; 33(10):743-53. doi:
10.1007/s40261-013-0120-y
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2013 Oct; 33(5):682-5. doi:
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Journal of clinical psychopharmacology.
2013 Aug; 33(4):485-90. doi:
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Pharmacopsychiatry.
2013 Jul; 46(5):175-80. doi:
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. [PMID: 23737243] - Anna Dietrich-Muszalska, Justyna Kopka, Anna Kwiatkowska. The effects of ziprasidone, clozapine and haloperidol on lipid peroxidation in human plasma (in vitro): comparison.
Neurochemical research.
2013 Jul; 38(7):1490-5. doi:
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2013 Apr; 38(4):365-9. doi:
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PloS one.
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Human psychopharmacology.
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Chinese medical journal.
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Psychopharmacology.
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Schizophrenia bulletin.
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Xenobiotica; the fate of foreign compounds in biological systems.
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Biomedical chromatography : BMC.
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