U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C19H23N
Molecular Weight 265.3926
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPHENIDINE

SMILES

C(C(N1CCCCC1)C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=JQWJJJYHVHNXJH-UHFFFAOYSA-N
InChI=1S/C19H23N/c1-4-10-17(11-5-1)16-19(18-12-6-2-7-13-18)20-14-8-3-9-15-20/h1-2,4-7,10-13,19H,3,8-9,14-16H2

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
3.3 µM [IC50]
3.4 µM [IC50]
Target ID: P35348|||B0ZBD9|||Q6RUJ8
Gene ID: 148.0
Gene Symbol: ADRA1A
Target Organism: Homo sapiens (Human)
11.0 µM [Ki]
Target ID: P08913
Gene ID: 150.0
Gene Symbol: ADRA2A
Target Organism: Homo sapiens (Human)
4.4 µM [Ki]
Target ID: P08908
Gene ID: 3350.0
Gene Symbol: HTR1A
Target Organism: Homo sapiens (Human)
11.0 µM [Ki]
Target ID: P28223
Gene ID: 3356.0
Gene Symbol: HTR2A
Target Organism: Homo sapiens (Human)
11.0 µM [Ki]
PubMed

PubMed

TitleDatePubMed
Are unconventional NMDA receptors involved in slowly adapting type I mechanoreceptor responses?
2005
NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds.
2009 May 1
Name Type Language
DIPHENIDINE
Common Name English
1-(1,2-DIPHENYLETHYL)PIPERIDINE
Systematic Name English
PIPERIDINE, 1-(1,2-DIPHENYLETHYL)-
Systematic Name English
J2.366.921H
Code English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Diphenidine
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
Code System Code Type Description
CAS
36794-52-2
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY
SMS_ID
100000175024
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY
FDA UNII
H8Q4VPL82Y
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY
WIKIPEDIA
Diphenidine
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID50724547
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY
PUBCHEM
206666
Created by admin on Sat Dec 16 11:21:42 GMT 2023 , Edited by admin on Sat Dec 16 11:21:42 GMT 2023
PRIMARY