Phenothiazines
Phenothiazines are a class of heterocyclic organic compounds characterized by the presence of a phenothiazine ring system, which consists of a benzene ring fused to a thiazine ring. These compounds exhibit diverse biological activities and have been widely studied for their therapeutic potential in various fields of medicine. Commonly used as antipsychotics due to their antagonistic activity at serotonin 2A (5-HT2A) receptors, phenothiazines also display significant effects on other neurotransmitter systems such as dopamine, histamine, muscarinic cholinergic, and adrenergic receptors. Additionally, they are employed in the treatment of nausea and vomiting, especially those caused by cancer chemotherapy or radiation therapy. Beyond their medical applications, certain phenothiazine derivatives have been explored for their potential use as insecticides and fungicides due to their broad-spectrum antimicrobial properties. The structural diversity within this class allows for the development of compounds with tailored pharmacological profiles, making phenothiazines a valuable tool in both academic research and pharmaceutical industries.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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7H-Benzo[c]phenothiazine, 9-chloro- | 6314-37-0 | C16H10ClNS |
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Oxomemazine | 3689-50-7 | C18H22N2O2S |
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Piperacetazine | 3819-00-9 | C24H30N2O2S |
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10H-Phenothiazine, 8-chloro-1,4-dimethoxy- | 72418-78-1 | C14H12ClNO2S |
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10H-Phenothiazine, 10-ethenyl- | 19210-66-3 | C14H11NS |
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Chlorpromazine | 50-53-3 | C17H19ClN2S |
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Promazine Hydrochloride | 53-60-1 | C17H21ClN2S |
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Promethazine hydrochloride | 58-33-3 | C17H21ClN2S |
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Aminopromazine | 58-37-7 | C19H25N3S |
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Alimemazine | 84-96-8 | C18H22N2S |
Related Literature
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
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