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Details

Stereochemistry RACEMIC
Molecular Formula C18H23N
Molecular Weight 253.3819
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIMETHYLDIPHENYLPROPYLAMINE

SMILES

CC(CC(C1=CC=CC=C1)C2=CC=CC=C2)N(C)C

InChI

InChIKey=NSHMKXVHJBBKTN-UHFFFAOYSA-N
InChI=1S/C18H23N/c1-15(19(2)3)14-18(16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-13,15,18H,14H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C18H23N
Molecular Weight 253.3819
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Trimethyldiphenylpropylamine (Recipavrin) is a methadon analog with antispasmodic properties. It exerts both musculotropic (antibarium) and anticholinergic action, relieves smooth muscle spasms, e.g. dysmenorrhea and pains associated with gallstones. It was marketed in Sweden in the 1960s as a spasmolytic drug under tradename Recipavrin.

Approval Year

PubMed

PubMed

TitleDatePubMed
Central and peripheral monoaminergic membrane-pump blockade by some addictive analgesics and antihistamines.
1969-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:55:44 GMT 2025
Edited
by admin
on Mon Mar 31 21:55:44 GMT 2025
Record UNII
P4X899446U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIMETHYLDIPHENYLPROPYLAMINE
Systematic Name English
N,N-1-TRIMETHYL-3,3-DIPHENYLPROPYLAMINE [MI]
Preferred Name English
BENZENEPROPANAMINE, N,N,.ALPHA.-TRIMETHYL-.GAMMA.-PHENYL-
Systematic Name English
N,N,1-TRIMETHYL-3,3-DIPHENYLPROPYLAMINE
Systematic Name English
Classification Tree Code System Code
WHO-ATC A03AX30
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
WHO-VATC QA03AX30
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
Code System Code Type Description
CAS
13957-55-6
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
DRUG BANK
DB13361
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
ChEMBL
CHEMBL3707363
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
PUBCHEM
30966
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
DRUG CENTRAL
4737
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
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EPA CompTox
DTXSID801043073
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
FDA UNII
P4X899446U
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
MERCK INDEX
m507
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
TRIMETHYLDIPHENYLPROPYLAMINE
Created by admin on Mon Mar 31 21:55:44 GMT 2025 , Edited by admin on Mon Mar 31 21:55:44 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY