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Details

Stereochemistry RACEMIC
Molecular Formula C18H21N
Molecular Weight 251.366
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N,N-DIMETHYL-3,3-DIPHENYL-1-METHYLALLYLAMINE

SMILES

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

InChI

InChIKey=QZWMYBWMOFESDA-UHFFFAOYSA-N
InChI=1S/C18H21N/c1-15(19(2)3)14-18(16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-15H,1-3H3

HIDE SMILES / InChI

Molecular Formula C18H21N
Molecular Weight 251.366
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Analgesic effect and bioavailability of oral ketogan given as tablets or mixture to patients with chronic pain of malignant origin.
1988
Premedication for day-case surgery: double-blind comparison of ketobemidone + dimethylaminodiphenylbuten (A-29) and morphine + scopolamine.
1986-10
5-HT-uptake inhibition potentiates antinociception induced by morphine, pethidine, methadone and ketobemidone in rats.
1985-09
Histamine release from human basophils and isolated rat mast cells induced by ketobemidone, pethidine and the spasmolytic A29.
1982-01
Clinical pharmacokinetics of ketobemidone. Its bioavailability after rectal administration.
1981-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:25:41 GMT 2025
Edited
by admin
on Mon Mar 31 23:25:41 GMT 2025
Record UNII
A6FGC19UYP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N,N-DIMETHYL-3,3-DIPHENYL-1-METHYLALLYLAMINE
Systematic Name English
A-29 LUNDBECK
Preferred Name English
N,N,1-TRIMETHYL-3,3-DIPHENYLALLYLAMINE
Systematic Name English
3-BUTEN-2-AMINE, N,N-DIMETHYL-4,4-DIPHENYL-
Systematic Name English
ALLYLAMINE, N,N,1-TRIMETHYL-3,3-DIPHENYL-
Systematic Name English
Code System Code Type Description
SMS_ID
100000138721
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
FDA UNII
A6FGC19UYP
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
PUBCHEM
122535
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
CAS
29869-90-7
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
ECHA (EC/EINECS)
249-909-6
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
EVMPD
SUB78417
Created by admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
PRIMARY
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