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

Details

Stereochemistry RACEMIC
Molecular Formula C14H20N2O2
Molecular Weight 248.3208
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIRIDOCAINE

SMILES

NC1=C(C=CC=C1)C(=O)OCCC2CCCCN2

InChI

InChIKey=BMIJYAZXNZEMLI-UHFFFAOYSA-N
InChI=1S/C14H20N2O2/c15-13-7-2-1-6-12(13)14(17)18-10-8-11-5-3-4-9-16-11/h1-2,6-7,11,16H,3-5,8-10,15H2

HIDE SMILES / InChI

Molecular Formula C14H20N2O2
Molecular Weight 248.3208
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Piridocaine is a piperidyl propanol ester of orthoaminobenzoic acid. The toxicity of this drug resembles that of procaine. It differs from procaine in that the minimum anesthetic dose is smaller, the minimal lethal dose larger, and duration of anesthesia longer. Subarachnoid piridocaine with and without epinephrine or ephedrine offers a simple and dependable means of obtaining any degree or extent of analgesia up to the third thoracic nerves without profound or widespread motor paralysis. The most promising clinical field of usefulness for piridocaine is obstetrics.

Approval Year

PubMed

PubMed

TitleDatePubMed
Lucaine as a spinal anesthetic agent for urological surgery.
1948 Nov
Obstetric saddle block anesthesia with lucaine hydrochloride.
1950 Feb
The use of lucaine in the study of spinal anesthesia.
1950 Nov
Anesthesia for anorectal surgery; discussion of experiences with lucaine hydrochloride.
1952 Dec
Lucaine hydrochloride for obstetrical spinal analgesia; preliminary report.
1952 Feb
Spinal analgesia with piridocaine hydrochloride for cesarean and vaginal deliveries.
1955 Jan
Spinal anesthesia with piridocaine (lucaine) further investigations and refinements of technic.
1955 May
Spinal analgesia with lucaine: a critical appraisal based on 6,000 cases.
1956 Jan
Lucaine for obstetric anesthesia.
1962 May-Jun

Sample Use Guides

Single dose - 30 mg
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:52:58 GMT 2023
Edited
by admin
on Sat Dec 16 17:52:58 GMT 2023
Record UNII
488S0H4SQF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIRIDOCAINE
INN   MI  
INN  
Official Name English
PIRIDOCAINE [MI]
Common Name English
PD-14
Code English
2-PIPERIDINEETHANOL ANTHRANILATE
Systematic Name English
LUCAINE
Common Name English
PIPERIDINEETHANOL ANTHRANILATE
Systematic Name English
2-PIPERIDINEETHANOL, 2-(2-AMINOBENZOATE)
Systematic Name English
PT-14
Code English
.BETA.-(2-PIPERIDYL)ETHYL O-AMINOBENZOATE
Common Name English
piridocaine [INN]
Common Name English
ANTHRANILIC ACID 2-(2-PIPERIDYL)ETHYL ESTER
Systematic Name English
2-PIPERIDINEETHANOL 2-AMINOBENZOATE (ESTER)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID601024704
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
MERCK INDEX
m1228
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C84065
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
RXCUI
1947299
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
WIKIPEDIA
Piridocaine
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
PUBCHEM
6875
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
EVMPD
SUB09910MIG
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
DRUG CENTRAL
3477
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110989
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
FDA UNII
488S0H4SQF
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
INN
21
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
CAS
87-21-8
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
SMS_ID
100000081666
Created by admin on Sat Dec 16 17:52:59 GMT 2023 , Edited by admin on Sat Dec 16 17:52:59 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY