3,3-Diphenylpropylamine

3,3-Diphenylpropylamine
Names
	Preferred IUPAC name 3,3-Diphenylpropan-1-amine
Identifiers
CAS Number	5586-73-2 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL609579 ;
ChemSpider	71998 ;
ECHA InfoCard	100.024.532
PubChem CID	79698;
UNII	C31E561S64 ;
CompTox Dashboard (EPA)	DTXSID30204458 ;
	InChI InChI=1S/C15H17N/c16-12-11-15(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,15H,11-12,16H2 Key: KISZTEOELCMZPY-UHFFFAOYSA-N ;
	SMILES C1=CC=C(C=C1)C(CCN)C2=CC=CC=C2;
Properties
Chemical formula	C15H17N
Molar mass	211.308 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

3,3-Diphenylpropylamine is a form of diphenylpropylamine.

It is commonly conjugated to another agent giving a "bifunctional" molecule. Such agents are not infrequently used to treat Cardiovascular disease (CVD).

Further embellishment of the molecular structure can lead to an agent that is called Delucemine.

3,3-Diphenylpropylamine derivatives list table
Name	Identifier	Picture
BIIA 0388	CID:9958467 [337359-07-6]
BZP derivative	[1]
Droprenilamine	[57653-27-7]
Fendiline	[13042-18-7]
Lercanidipine	[100427-26-7]
KD-983	[50597-65-4]
Mepramidil	[23891-60-3]
Milverine	[75437-14-8]
PF 244	Fb: [52017-07-9]
Prenylamine	[390-64-7]
SoRI-20041	now SRI-20041
Tiopropamine	[39516-21-7]

[117-34-0] [5586-73-2] amide:[2]

References

Tadayuki Suzuki & Toshiharu Megumi, U.S. Patent 3,957,790 (1976 to Tokyo Tanabe Co Ltd).
Urbani, P., Cascio, M. G., Ramunno, A., Bisogno, T., Saturnino, C., Marzo, V. D. (August 2008). "Novel sterically hindered cannabinoid CB1 receptor ligands". Bioorganic & Medicinal Chemistry. 16 (15): 7510–7515. doi:10.1016/j.bmc.2008.06.001.

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[1] Tadayuki Suzuki & Toshiharu Megumi, U.S. Patent 3,957,790 (1976 to Tokyo Tanabe Co Ltd).

[2] Urbani, P., Cascio, M. G., Ramunno, A., Bisogno, T., Saturnino, C., Marzo, V. D. (August 2008). "Novel sterically hindered cannabinoid CB1 receptor ligands". Bioorganic & Medicinal Chemistry. 16 (15): 7510–7515. doi:10.1016/j.bmc.2008.06.001.