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Details

Stereochemistry RACEMIC
Molecular Formula C18H29NO2
Molecular Weight 291.4284
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOTUCAINE

SMILES

CC1=CC=CC=C1OCC(O)CN2C(C)(C)CCC2(C)C

InChI

InChIKey=ALJMIOMYHUNJQX-UHFFFAOYSA-N
InChI=1S/C18H29NO2/c1-14-8-6-7-9-16(14)21-13-15(20)12-19-17(2,3)10-11-18(19,4)5/h6-9,15,20H,10-13H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C18H29NO2
Molecular Weight 291.4284
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Lotucaine is a local anesthetic.

Approval Year

PubMed

PubMed

TitleDatePubMed
Derivatives of tetramethylated cyclic amines. 3. Optical isomers of lotucaine: physico-chemical characteristics and pharmacological activities.
1973 Nov
[Experimental comparison of 2 anesthetics, carbocaine and lotucaine, in dentistry].
1985 Jun 30
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:49:28 GMT 2023
Edited
by admin
on Sat Dec 16 17:49:28 GMT 2023
Record UNII
QCA39I2AP7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LOTUCAINE
INN  
INN  
Official Name English
2,2,5,5-TETRAMETHYL-.ALPHA.-((O-TOLYLOXY)METHYL)-1-PYRROLIDINEETHANOL
Systematic Name English
lotucaine [INN]
Common Name English
MY-33-7 FREE BASE
Code English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
Code System Code Type Description
EVMPD
SUB08603MIG
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
MESH
C003612
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
NCI_THESAURUS
C81414
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
SMS_ID
100000082060
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
FDA UNII
QCA39I2AP7
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID10866250
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
CAS
52304-85-5
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105177
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
INN
3211
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
PUBCHEM
212077
Created by admin on Sat Dec 16 17:49:28 GMT 2023 , Edited by admin on Sat Dec 16 17:49:28 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY