Azapetine

Azapetine
Clinical data
ATC code	C04AX30 (WHO) ;
Identifiers
	IUPAC name 6-prop-2-enyl-5,7-dihydrobenzo[d][2]benzazepine;
CAS Number	146-36-1 ;
PubChem CID	8966;
ChemSpider	8620 ;
UNII	9TTR0UA2KC;
ChEMBL	ChEMBL2110596;
CompTox Dashboard (EPA)	DTXSID50163250 ;
ECHA InfoCard	100.005.153
Chemical and physical data
Formula	C17H17N
Molar mass	235.330 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES c3cc2c(c1c(cccc1)CN(C2)C\C=C)cc3;
	InChI InChI=1S/C17H17N/c1-2-11-18-12-14-7-3-5-9-16(14)17-10-6-4-8-15(17)13-18/h2-10H,1,11-13H2 ; Key:NYGHGTMKALXFIA-UHFFFAOYSA-N ;
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Azapetine is a vasodilator.^[1]^[2]

References

^ Stallworth JM, Jeffords JV (June 1956). "Clinical effects of azapetine (ilidar) on peripheral arterial disease". Journal of the American Medical Association. 161 (9): 840–3. doi:10.1001/jama.1956.02970090066013. PMID 13319017.
^ Youmans PL, Green HD, Denison AB (March 1955). "Nature of the vasodilator and vasoconstrictor receptors in skeletal muscle of the dog". Circulation Research. 3 (2): 171–80. doi:10.1161/01.res.3.2.171. PMID 14352400.

This drug article relating to the cardiovascular system is a stub. You can help Wikipedia by expanding it.

v t e Peripheral vasodilators (C04)
Phenylethanolamine derivatives	Isoxsuprine Buphenine Bamethan
Alpha blockers	Non-selective Buflomedil Phentolamine Phenoxybenzamine Tolazoline Selective α₁-blockers Alfuzosin Doxazosin Prazosin Silodosin Tamsulosin Terazosin
Niacin and derivatives	Niacin Nicotinyl alcohol Inositol nicotinate Ciclonicate
Purine derivatives	Pentifylline Xantinol nicotinate Pentoxifylline Etofylline nicotinate
Ergot alkaloids	Ergoloid Nicergoline Dihydroergocristine
Other peripheral vasodilators	Cyclandelate Vincamine Moxisylyte Bencyclane Vinburnine Sulcotidil Naftidrofuryl Butalamine Visnadine Cetiedil Cinepazide Ifenprodil Azapetine Fasudil