3,3-Diphenylpropylamine

3,3-Diphenylpropylamine
Names
Preferred IUPAC name
3,3-Diphenylpropan-1-amine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.024.532
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 checkY
    Key: KISZTEOELCMZPY-UHFFFAOYSA-N checkY
  • 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).
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Infobox references

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 0388CID:9958467 [337359-07-6]
BZP derivative[1]
Droprenilamine[57653-27-7]
Delucemine[186495-49-8 ]
Fendiline[13042-18-7]
Lercanidipine[100427-26-7]
KD-983[50597-65-4]
Mepramidil[23891-60-3]
Milverine[75437-14-8]
PF 244Fb: [52017-07-9]
Prenylamine[390-64-7]
SoRI-20041now SRI-20041
Tiopropamine[39516-21-7]
CB1 receptor ligand[117-34-0] [5586-73-2][2]
5-APDI[3]
SRI-29213PC121377378[4]


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): 7510–5. doi:10.1016/j.bmc.2008.06.001. hdl:11563/122572. PMID 18579386.
  3. ↑ Frank Troxler & Albert Hofman, OA01894 (1970 to Sandoz KK).
  4. ↑ Rothman RB, Ananthan S, Partilla JS, Saini SK, Moukha-Chafiq O, Pathak V, Baumann MH (June 2015). "Studies of the biogenic amine transporters 15. Identification of novel allosteric dopamine transporter ligands with nanomolar potency". J Pharmacol Exp Ther. 353 (3): 529–38. doi:10.1124/jpet.114.222299. PMC 4429677. PMID 25788711.


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