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Details

Stereochemistry RACEMIC
Molecular Formula C18H28N2O2
Molecular Weight 304.4271
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VADOCAINE

SMILES

COC1=C(NC(=O)CCN2CCCCC2C)C(C)=CC(C)=C1

InChI

InChIKey=UJCARUGFZOJPMI-UHFFFAOYSA-N
InChI=1S/C18H28N2O2/c1-13-11-14(2)18(16(12-13)22-4)19-17(21)8-10-20-9-6-5-7-15(20)3/h11-12,15H,5-10H2,1-4H3,(H,19,21)

HIDE SMILES / InChI

Molecular Formula C18H28N2O2
Molecular Weight 304.4271
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Vadocaine is an anilide derivative with antitussive and local anaesthetic action. Vadocaine is highly distributed to the respiratory tract. In chemical structure vadocaine resembles lidocaine. According to the serum concentrations and pharmacokinetic parameters, no cumulation of vadocaine was observed. The compound had no effect on blood and urinary parameters measured for safety evaluation. Vadocaine is evidently metabolized in the liver and a remarkable part of the drug and its metabolites are excreted into the bile. Accumulation of radioactivity in the kidneys shows that also renal elimination is important.

Approval Year

PubMed

PubMed

TitleDatePubMed
Liquid-chromatographic analysis of a novel antitussive agent, 2',4'-dimethyl-6'-methoxy-3-(2-methyl-piperidyl)propionanilide in human urine.
1986
Patents

Patents

Sample Use Guides

Single dose - 300 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:50 GMT 2023
Edited
by admin
on Fri Dec 15 16:08:50 GMT 2023
Record UNII
OKA45SU1Q4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VADOCAINE
INN   MART.  
INN  
Official Name English
vadocaine [INN]
Common Name English
VADOCAINE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
Code System Code Type Description
MESH
C051410
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
EVMPD
SUB00002MIG
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
SMS_ID
100000079139
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
NCI_THESAURUS
C72163
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
INN
5974
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
PUBCHEM
68912
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
CAS
72005-58-4
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104555
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
FDA UNII
OKA45SU1Q4
Created by admin on Fri Dec 15 16:08:50 GMT 2023 , Edited by admin on Fri Dec 15 16:08:50 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY