Cyheptamide
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| Other names | Cyheptamine |
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| ECHA InfoCard | 100.027.792 |
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| Formula | C16H15NO |
| Molar mass | 237.302 g·mol−1 |
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Cyheptamide was a investigational new drug that was developed by Ayerst Research Laboratories in the 1960s and was evaluated as an anticonvulsant.[1]
Cyheptamide undergoes significant metabolic transformation in both animals and humans, primarily through hydroxylation pathways.[2]
Cyheptamide exhibits moderate acute toxicity in animal models, with species-specific variations in lethal dose values.[3]
References
[edit]- ^ "Cyheptamide". Inxight: Drugs. NCATS. Retrieved 2025-06-25.
- ^ Kraml M, Sestanj K, Dvornik D (September 1971). "Metabolism of the anticonvulsant 10,11-dihydro-5H-dibenzo(a,d)cycloheptene-5-carboxamide. I. Metabolic fate of (14C)cyheptamide in animals and man". Biochemical Pharmacology. 20 (9): 2327–2338. doi:10.1016/0006-2952(71)90232-2. PMID 5163146.
- ^ van Eeken CJ, Birtwhistle RD, Mulder D (November 1970). "Toxicological study of cyheptamide: 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-carboxamide (BS 7029)". Archives Internationales de Pharmacodynamie et de Therapie. 188 (1): 79–85. PMID 5485105.