Azapetine
Chemical compound
- C04AX30 (WHO)
- 6-prop-2-enyl-5,7-dihydrobenzo[d][2]benzazepine
- 146-36-1
N
- 8966
- 8620
Y
- 9TTR0UA2KC
- ChEMBL2110596
- DTXSID50163250
![Edit this at Wikidata](http://upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png)
- Interactive image
- 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
Y
- Key:NYGHGTMKALXFIA-UHFFFAOYSA-N
Y
![☒](http://upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png)
![check](http://upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png)
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.
- v
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Peripheral vasodilators (C04)
- Isoxsuprine
- Buphenine
- Bamethan
- Non-selective
- Selective α1-blockers
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