SN 35210

SN 35210

File:SN 35210.svg
Clinical data
ATC code	none
Legal status
Legal status	Investigational new drug
Identifiers
IUPAC name Methyl 4-{[1-(2-chlorophenyl)-2-oxocyclohexyl]amino}pentanoate
CAS Number	1450615-41-4
PubChem CID	71769517
UNII	DS5KFJ4488
E number	{{#property:P628}}
CompTox Dashboard (EPA)	{{#property:P3117}}
ECHA InfoCard	{{#property:P2566}}
Chemical and physical data
Formula	C18H24ClNO3
Molar mass	337.84 g·mol−1
3D model (JSmol)	Interactive image
SMILES Clc1ccccc1C2(NCCCCC(=O)OC)CCCCC2=O
InChI InChI=1S/C18H24ClNO3/c1-23-17(22)11-5-7-13-20-18(12-6-4-10-16(18)21)14-8-2-3-9-15(14)19/h2-3,8-9,20H,4-7,10-13H2,1H3 Key:QFFBIIVCZDWTKZ-UHFFFAOYSA-N

SN 35210 is an arylcyclohexylamine dissociative anesthetic drug. It was derived from ketamine with the intention of producing a shorter acting agent more suitable to be used as a stand-alone drug, whereas ketamine itself generally has to be used in combination with other drugs such as midazolam to minimise the occurrence of emergence reactions due to its hallucinogenic side effects. In common with other short-acting anaesthetic drugs such as remifentanil and remimazolam, SN 35210 has had the chemical structure modified to incorporate a methyl ester group which is rapidly metabolised to a carboxylic acid, producing an inactive compound and thus rapidly terminating the effects of the drug. It was selected for development from a series of structurally related alkyl esters due to having the shortest duration of action and the most similar pharmacological profile to ketamine itself.

See also

• A-NK