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

Details

Stereochemistry RACEMIC
Molecular Formula C17H28N2O2.CH4O3S
Molecular Weight 388.522
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEUCINOCAINE MESYLATE

SMILES

CS(O)(=O)=O.CCN(CC)C(COC(=O)C1=CC=C(N)C=C1)CC(C)C

InChI

InChIKey=RFPVXZWXDPIKSD-UHFFFAOYSA-N
InChI=1S/C17H28N2O2.CH4O3S/c1-5-19(6-2)16(11-13(3)4)12-21-17(20)14-7-9-15(18)10-8-14;1-5(2,3)4/h7-10,13,16H,5-6,11-12,18H2,1-4H3;1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula C17H28N2O2
Molecular Weight 292.4164
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Leucinocaine is the local anaesthetic with actions similar to lignocaine. It has been used by topical application for local pain relief.

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of limiting ionic mobilities and dissociation constants of some local anaesthetics.
1992-04-10
[Prevention of thromboembolism in meniscus surgery using Panthesin-Hydergin].
1974-12
[Comparative studies on prevention of thromboembolism using panthesin-hydergin].
1971-04
[TREATMENT OF APOPLEXY WITH PANTHESIN-HYDERGIN].
1964-08-21
[Treatment of thrombophlebitis of the lower extremity with panthesin and hydergine (PH-203)].
1962-04-30
[Panthesin--hydergine therapy in ophthalmology].
1961-12-09
[Results of alternating thromboembolism prophylaxis with panthesin-hydergine].
1961-04-01
[Treatment of postthrombotic edema with panthesin and hydergine].
1961-03-04
[Additional observations on the treatment of myocardial infarct in old age with Panthesin and Hydergin (PH 203)].
1961-02-24
[Experiences with panthesin-hydergine (PH 203) and exacthin (ACTH) in disorders of retinal circulation].
1960-12
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:32:53 GMT 2025
Edited
by admin
on Mon Mar 31 23:32:53 GMT 2025
Record UNII
72E501K01E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEUCINOCAINE MESILATE
WHO-DD  
Preferred Name English
LEUCINOCAINE MESYLATE
MI  
Common Name English
P-AMINOBENZOIC ACID N,N-DIETHYLLEUCINOL ESTER METHANESULFONATE
Common Name English
S.P. 147
Code English
1-PENTANOL, 2-(DIETHYLAMINO)-4-METHYL-, 4-AMINOBENZOATE (ESTER), MONOMETHANESULFONATE (SALT)
Common Name English
LEUCINOCAINE METHANESULFONATE
Common Name English
LEUCINOCAINE MESYLATE [MI]
Common Name English
BENZOIC ACID, P-AMINO-, 2-DIETHYLAMINO-4-METHYLPENTYL ESTER METHANESULFONATE
Common Name English
Leucinocaine mesilate [WHO-DD]
Common Name English
SP-147
Code English
1-PENTANOL, 2-(DIETHYLAMINO)-4-METHYL-, 1-(4-AMINOBENZOATE), METHANESULFONATE (1:1)
Systematic Name English
PANTHESIN
Common Name English
PANTHESINE
Brand Name English
Code System Code Type Description
MERCK INDEX
m272
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY Merck Index
CAS
135-44-4
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
FDA UNII
72E501K01E
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
SMS_ID
100000086666
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
PUBCHEM
101618
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-191-6
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID30928849
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
EVMPD
SUB02898MIG
Created by admin on Mon Mar 31 23:32:53 GMT 2025 , Edited by admin on Mon Mar 31 23:32:53 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY