Nexeridine

Nexeridine
Clinical data
ATC code	None;
Identifiers
	IUPAC name 1-[1-(Dimethylamino)-2-propanyl]-2-phenylcyclohexyl acetate;
CAS Number	53716-48-6 ; 53716-47-5 (HCl);
PubChem CID	10447719;
ChemSpider	8623136;
UNII	8CM77ZQ65K;
CompTox Dashboard (EPA)	DTXSID001023865 ;
Chemical and physical data
Formula	C19H29NO2
Molar mass	303.446 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CN(C)C[C@@H](C)[C@@]1(OC(=O)C)CCCC[C@H]1c1ccccc1;
	InChI InChI=1S/C19H29NO2/c1-15(14-20(3)4)19(22-16(2)21)13-9-8-12-18(19)17-10-6-5-7-11-17/h5-7,10-11,15,18H,8-9,12-14H2,1-4H3; Key:TVQPXLMQOZWEBA-UHFFFAOYSA-N;

Nexeridine (INN; USAN: nexeridine hydrochloride; code name Compound 673-082) is an opioid analgesic with a similar structure to those of pethidine and tramadol.^[1]^[2]^[3]^[4] It was synthesized and assayed in 1975 but was never marketed.^[2] The active isomer is (1R,2S)-1-[(2R)-1-(dimethylamino)-2-propanyl]-2-phenylcyclohexyl acetate.^[5]

References

↑ US 3974157, "1-(Amino-alkyl)-2-aryl-cyclohexane alcohols and esters"
1 2 Ganellin CR, Triggle DJ (21 November 1996). Dictionary of Pharmacological Agents. CRC Press. pp. 1417–. ISBN 978-0-412-46630-4.
↑ Kar A (1 January 2005). Medicinal Chemistry. New Age International. pp. 268–269. ISBN 978-81-224-1565-0.
↑ Unlisted Drugs, Volumes 27-28. Pharmaceutical Section, Special Libraries Association. 1975.
↑ "(1R,2S)-1-[(2R)-1-(Dimethylamino)-2-propanyl]-2-phenylcyclohexyl acetate hydrochloride (1:1)". ChemSpider.

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[1] US 3974157, "1-(Amino-alkyl)-2-aryl-cyclohexane alcohols and esters"

[GanellinTriggle1996-2] 1 2 Ganellin CR, Triggle DJ (21 November 1996). Dictionary of Pharmacological Agents. CRC Press. pp. 1417–. ISBN 978-0-412-46630-4.

[Kar2005-3] Kar A (1 January 2005). Medicinal Chemistry. New Age International. pp. 268–269. ISBN 978-81-224-1565-0.

[Special_Libraries_Association1975-4] Unlisted Drugs, Volumes 27-28. Pharmaceutical Section, Special Libraries Association. 1975.

[5] "(1R,2S)-1-[(2R)-1-(Dimethylamino)-2-propanyl]-2-phenylcyclohexyl acetate hydrochloride (1:1)". ChemSpider.

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References