3,3-Diphenylpropylamine

Last updated

3,3-Diphenylpropylamine
3,3-diphenylpropylamine.svg
Names
Preferred IUPAC name
3,3-Diphenylpropan-1-amine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.024.532 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • 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 Yes check.svgY
    Key: KISZTEOELCMZPY-UHFFFAOYSA-N Yes check.svgY
  • C1=CC=C(C=C1)C(CCN)C2=CC=CC=C2
Properties
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).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

3,3-Diphenylpropylamine is a form of diphenylpropylamine.

It is commonly conjugated to another agent giving a "bifunctional" molecule. Some such agents are used to treat cardiovascular diseases.

3,3-Diphenylpropylamine derivatives
NameIdentifierChemical structure
BIIA 0388 CID:9958467 [337359-07-6] BIIA 0388.svg
BZP derivative [1] 3,3-Diphenylpropylamine-BZP.svg
Droprenilamine [57653-27-7] Droprenilamine.svg
Delucemine [186495-49-8 ] Delucemine.svg
Fendiline [13042-18-7] Fendiline.png
Lercanidipine [100427-26-7] Lercanidipine.svg
KD-983 [50597-65-4] KD-983.svg
Mepramidil [23891-60-3] Mepramidil.svg
Milverine [75437-14-8] Milverine.svg
PF 244 Fb: [52017-07-9] PF 244.svg
Prenylamine [390-64-7] Prenylamine.svg
SoRI-20041 now SRI-20041 SoRI-20041 Structure.svg
Tiopropamine [39516-21-7] Tiopropamine.svg
CB1 receptor ligand[117-34-0] [5586-73-2] [2] (117-34-0) (5586-73-2) amide.svg


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References

  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. hdl: 11563/122572 . PMID   18579386.