Amedalin

Amedalin
Clinical data
ATC code	None;
Identifiers
	IUPAC name 3-Methyl-3-[3-(methylamino)propyl]-1-phenyl-1,3-dihydro-2H-indol-2-one;
CAS Number	22136-26-1 ; 22232-73-1 (HCl);
PubChem CID	31075;
ChemSpider	28832 ;
UNII	2OWK6X9N16;
KEGG	D02891 ;
ChEMBL	ChEMBL2110769 ;
CompTox Dashboard (EPA)	DTXSID40865034 ;
Chemical and physical data
Formula	C19H22N2O
Molar mass	294.398 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC1(C2=CC=CC=C2N(C1=O)C3=CC=CC=C3)CCCNC;
	InChI InChI=1S/C19H22N2O/c1-19(13-8-14-20-2)16-11-6-7-12-17(16)21(18(19)22)15-9-4-3-5-10-15/h3-7,9-12,20H,8,13-14H2,1-2H3 ; Key:HBGWAZBZXJBYQD-UHFFFAOYSA-N ;
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Amedalin (UK-3540-1) is an antidepressant which was synthesized in the early 1970s but was never marketed.^[1]^[2] It is a selective norepinephrine reuptake inhibitor, with no significant effects on the reuptake of serotonin and dopamine, and no antihistamine or anticholinergic properties.^[2]^[3]

References

^ Triggle DJ (1997). Dictionary of pharmacological agents. London: Chapman & Hall. ISBN 978-0-412-46630-4.
^ ^a ^b Cañas-Rodriguez A, Leeming PR (July 1972). "N-Phenyl-2-indolinones and N-phenylindolines. A new class of antidepressant agents". Journal of Medicinal Chemistry. 15 (7): 762–70. doi:10.1021/jm00277a017. PMID 5043876.
^ Koe BK (December 1976). "Molecular geometry of inhibitors of the uptake of catecholamines and serotonin in synaptosomal preparations of rat brain". Journal of Pharmacology and Experimental Therapeutics. 199 (3): 649–661. doi:10.1016/S0022-3565(25)30726-3. PMID 994022.