ETYBENZATROPINE

Etybenzatropine
Clinical data
Routes of; administration	Oral, IM, IV
ATC code	N04AC30 ( WHO) ;
Identifiers
	IUPAC name (3-endo)-3-(Diphenylmethoxy)-8-ethyl-8-azabicyclo[3.2.1]octane;
CAS Number	524-83-4 ;
PubChem CID	71637;
ChemSpider	16736129 ;
UNII	G1X2X9N95N;
KEGG	D04087 ;
CompTox Dashboard ( EPA)	DTXSID50905096 ;
Chemical and physical data
Formula	C22H27NO
Molar mass	321.464 g·mol−1
3D model ( JSmol)	Interactive image;
	SMILES CCN1[C@@H]2CC[C@H]1C[C@H](C2)OC(c3ccccc3)c4ccccc4;
	InChI InChI=1S/C22H27NO/c1-2-23-19-13-14-20(23)16-21(15-19)24-22(17-9-5-3-6-10-17)18-11-7-4-8-12-18/h3-12,19-22H,2,13-16H2,1H3/t19-,20+,21+ ; Key:PHTMLLGDZBZXMW-AERCQKQUSA-N ;
	(verify)

Etybenzatropine ( INN), also known as ethybenztropine ( USAN, BAN) and tropethydrylin, is an anticholinergic/ antihistamine marketed under the trade names Panolid, Ponalid, and Ponalide, which is used as an antiparkinsonian agent.^[1] Like its analogue benzatropine, it may act as a dopamine reuptake inhibitor.^{[
citation needed]}

References

^ Pourcher E, Bonnet AM, Kefalos J, Dubois B, Agid Y (1989). "Effects of etybenzatropine and diazepam on levodopa-induced diphasic dyskinesias in Parkinson's disease". Movement Disorders. 4 (3): 195–201. doi: 10.1002/mds.870040301. PMID 2779590. S2CID 1826853.

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Clinical data

Routes of administration	Oral, IM, IV
ATC code	N04AC30 ( WHO)
Identifiers
IUPAC name (3-endo)-3-(Diphenylmethoxy)-8-ethyl-8-azabicyclo[3.2.1]octane
CAS Number	524-83-4^Y
PubChem CID	71637
ChemSpider	16736129^Y
UNII	G1X2X9N95N
KEGG	D04087^Y
CompTox Dashboard ( EPA)	DTXSID50905096
Chemical and physical data
Formula	C₂₂H₂₇NO
Molar mass	321.464 g·mol⁻¹
3D model ( JSmol)	Interactive image
SMILES CCN1[C@@H]2CC[C@H]1C[C@H](C2)OC(c3ccccc3)c4ccccc4
InChI InChI=1S/C22H27NO/c1-2-23-19-13-14-20(23)16-21(15-19)24-22(17-9-5-3-6-10-17)18-11-7-4-8-12-18/h3-12,19-22H,2,13-16H2,1H3/t19-,20+,21+^Y Key:PHTMLLGDZBZXMW-AERCQKQUSA-N^Y
(verify)