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
[Additional observations on the treatment of myocardial infarct in old age with Panthesin and Hydergin (PH 203)].
1961 Feb 24
[TREATMENT OF APOPLEXY WITH PANTHESIN-HYDERGIN].
1964 Aug 21
[Comparative studies on prevention of thromboembolism using panthesin-hydergin].
1971 Apr
[Prevention of thromboembolism in meniscus surgery using Panthesin-Hydergin].
1974 Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:58:30 GMT 2023
Edited
by admin
on Sat Dec 16 10:58:30 GMT 2023
Record UNII
72E501K01E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEUCINOCAINE MESYLATE
MI  
Common Name English
P-AMINOBENZOIC ACID N,N-DIETHYLLEUCINOL ESTER METHANESULFONATE
Common Name English
S.P. 147
Code English
LEUCINOCAINE MESILATE
WHO-DD  
Common Name 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 Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY Merck Index
CAS
135-44-4
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
FDA UNII
72E501K01E
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
SMS_ID
100000086666
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
PUBCHEM
101618
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-191-6
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID30928849
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
EVMPD
SUB02898MIG
Created by admin on Sat Dec 16 10:58:30 GMT 2023 , Edited by admin on Sat Dec 16 10:58:30 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY