Carmantadine (INN , USAN ; developmental code name SCH-15427) is an antiparkinsonian agent of the adamantane group that was never marketed.[1][2][3][4] It is structurally related to amantadine and shares some of its pharmacological actions.[2] Another related drug is dopamantine.[2][3][4] Carmantadine was first described by 1972 and is said to have reached early clinical trials.[1][2][3][4]
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Other names | SCH-15427; NSC-172618 |
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ECHA InfoCard | 100.048.869 |
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Formula | C14H21NO2 |
Molar mass | 235.327 g·mol−1 |
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References
edit- ^ a b Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 13. ISBN 978-1-4757-2085-3. Retrieved 13 September 2024.
- ^ a b c d Vernier VG, du Pont E (1974). "Chapter 3. Antiparkinsonism Drugs". In Heinzelman RV (ed.). Annual Reports in Medicinal Chemistry. Vol. 9. Elsevier. pp. 19–26. doi:10.1016/s0065-7743(08)61424-4. ISBN 978-0-12-040509-1.
Carmantadine (VII, Sch 151427) is structurally related to amantadine33. It shares some of its pharmacological actions, was effective in a head—turning test34 and is in early clinical trials.
- ^ a b c Barnett A, Goldstein J, Taber R, Fiedler E (January 1974). "Pharmacology of Dopamantine and Carmantadine, 2 Potential Antiparkinson Agents". Pharmacologist. 16 (2): 205–.
- ^ a b c Goldstein J, Barnett A (January 1974). "Antagonism of electrically-induced heart-turning (HT) following intracaudate administration of dopamine (DA), amantadine (AM), apomorphine (APO), dopamantine and carmantadine". Pharmacologist. 16 (2): 206.