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Alimemazine
Chemical compound
Chemical compound
| Field | Value | |||
|---|---|---|---|---|
| Watchedfields | changed | |||
| verifiedrevid | 477317349 | |||
| image | Alimemazine.svg | |||
| image_class | skin-invert-image | |||
| image2 | Alimemazine Tartrate 10mg.jpg | |||
| USAN | trimeprazine | |||
| BAN | trimeprazine | |||
| Drugs.com | ||||
| DailyMedID | Trimeprazine | |||
| pregnancy_AU | C | |||
| routes_of_administration | By mouth | |||
| class | Anti-allergic agent | |||
| ATC_prefix | R06 | |||
| ATC_suffix | AD01 | |||
| legal_AU | Schedule 4 | |||
| legal_AU_comment | /Schedule 3; Schedule 2; Appendix K, clause 1 | |||
| legal_UK | POM | |||
| legal_US | Rx-only | |||
| legal_US_comment | ||||
| metabolism | Liver | |||
| elimination_half-life | 4.78 ± 0.59 hours | |||
| IUPHAR_ligand | 7237 | |||
| CAS_number_Ref | ||||
| CAS_number | 84-96-8 | |||
| PubChem | 5574 | |||
| DrugBank_Ref | ||||
| DrugBank | DB01246 | |||
| ChemSpiderID_Ref | ||||
| ChemSpiderID | 5373 | |||
| UNII_Ref | ||||
| UNII | 76H78MJJ52 | |||
| UNII2 | 362NW1LD6Z | |||
| KEGG_Ref | ||||
| KEGG | D07125 | |||
| KEGG2 | D02245 | |||
| ChEMBL_Ref | ||||
| ChEMBL | 829 | |||
| synonyms | ||||
| IUPAC_name | N,N,2-trimethyl-3-phenothiazin-10-yl-propan-1-amine | |||
| C | 18 | H=22 | N=2 | S=1 |
| smiles | S2c1ccccc1N(c3c2cccc3)CC(C)CN(C)C | |||
| StdInChI_Ref | ||||
| StdInChI | 1S/C18H22N2S/c1-14(12-19(2)3)13-20-15-8-4-6-10-17(15)21-18-11-7-5-9-16(18)20/h4-11,14H,12-13H2,1-3H3 | |||
| StdInChIKey_Ref | ||||
| StdInChIKey | ZZHLYYDVIOPZBE-UHFFFAOYSA-N |
| Drugs.com =
| elimination_half-life = 4.78 ± 0.59 hours
Alimemazine (INN), also known as trimeprazine, commonly provided as a tartrate salt, is a phenothiazine derivative that is used as an antipruritic (it prevents itching from causes such as eczema or poison ivy, by acting as an antihistamine). It also acts as a sedative, hypnotic, and antiemetic for prevention of motion sickness.
Despite being structurally related to the molecule chlorpromazine, it is not used as an antipsychotic.
Society and culture
Brand names
Brand names include Nedeltran, Panectyl, Repeltin, Teraligen, Therafene, Theraligene, Theralen, Thegalin, Theralene, Vallergan, Vanectyl, and Temaril.
Use by Country
In the Russian Federation, it is sold under the brand name Teraligen for the treatment of anxiety disorders (including GAD), organic mood disorders, sleep disturbances, personality disorders accompanied by asthenia and depression, somatoform autonomic dysfunction and various neuroses.
Veterinary use
In the United States, the Food and Drug Administration (FDA) has not approved it for human use, and it can only be prescribed by veterinarians.
A novel combination drug that combines alimemazine with prednisolone and sold under the brand name Temaril-P is licensed as an antipruritic and antitussive in dogs (called Vanectyl P in Canada). A generic version of the combination trimeprazine/prednisolone was approved by the US Food and Drug Administration (FDA) in June 2024.
References
References
- (May 2025). "Therapeutic Goods (Poisons Standard— June 2025) Instrument 2025".
- (14 March 2019). "Trimeprazine tartrate powder".
- (March 1986). "Relative bioavailability of trimeprazine tablets investigated in man using HPLC with electrochemical detection". The Journal of Pharmacy and Pharmacology.
- "(3R,4R)-3,4-dihydroxyhexane-2,5-dione;N,N,2-trimethyl-3-phenothiazin-10-ylpropan-1-amine".
- "Alimemazine".
- "Тералиджен — инструкция по применению, дозы, побочные действия, описание препарата: таблетки, покрытые пленочной оболочкой,раствор для внутримышечного введения, 5 мг/мл, 5 мг".
- (12 January 2023). "Temaril-P- trimeprazine tartrate and prednisolone tablet".
- (21 June 2024). "FDA Roundup: June 21, 2024".
- "FOI Summary for the Original Approval of ANADA 200-784". United States Food and Drug Administration.
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