Fantofarone

Fantofarone
Names
	IUPAC name N-[2-(3,4-dimethoxyphenyl)ethyl]-3-[4-[(2-isopropyl-1-indolizinyl)sulfonyl]phenoxy]-N-methylpropan-1-amine
Identifiers
CAS Number	114432-13-2 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL285855 ;
ChemSpider	106600 ;
PubChem CID	119349;
UNII	KU213XYO69 ;
CompTox Dashboard (EPA)	DTXSID30150729 ;
	InChI InChI=1S/C31H38N2O5S/c1-23(2)27-22-33-18-7-6-9-28(33)31(27)39(34,35)26-13-11-25(12-14-26)38-20-8-17-32(3)19-16-24-10-15-29(36-4)30(21-24)37-5/h6-7,9-15,18,21-23H,8,16-17,19-20H2,1-5H3 Key: ITAMRBIZWGDOHW-UHFFFAOYSA-N ; InChI=1/C31H38N2O5S/c1-23(2)27-22-33-18-7-6-9-28(33)31(27)39(34,35)26-13-11-25(12-14-26)38-20-8-17-32(3)19-16-24-10-15-29(36-4)30(21-24)37-5/h6-7,9-15,18,21-23H,8,16-17,19-20H2,1-5H3 Key: ITAMRBIZWGDOHW-UHFFFAOYAL;
	SMILES CC(C)C1=CN2C=CC=CC2=C1S(=O)(=O)C3=CC=C(C=C3)OCCCN(C)CCC4=CC(=C(C=C4)OC)OC;
Properties
Chemical formula	C31H38N2O5S
Molar mass	550.70882
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Fantofarone is a calcium channel blocker.[1]

References

Rosseels, Gilbert; Houben, Christian; Kerckx, Patricia (1995). "Synthesis of a metabolite of fantofarone". Advances in Organobromine Chemistry II. Industrial Chemistry Library. 7. pp. 152–159. doi:10.1016/S0926-9614(05)80016-4. ISBN 9780444821058.

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