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Details

Stereochemistry ACHIRAL
Molecular Formula C20H26NO3.Cl
Molecular Weight 363.878
Optical Activity NONE
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LACHESINE CHLORIDE

SMILES

[Cl-].CC[N+](C)(C)CCOC(=O)C(O)(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=TVCAZGSWNBZVJN-UHFFFAOYSA-M
InChI=1S/C20H26NO3.ClH/c1-4-21(2,3)15-16-24-19(22)20(23,17-11-7-5-8-12-17)18-13-9-6-10-14-18;/h5-14,23H,4,15-16H2,1-3H3;1H/q+1;/p-1

HIDE SMILES / InChI
Molecular Formula C20H25NO3
Molecular Weight 327.4174
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity NONE
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Allosteric modulators of class B G-protein-coupled receptors.
2007-09
Development of cricket mushroom bodies.
2002-10-21
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:17:55 GMT 2025
Edited
by admin
on Mon Mar 31 18:17:55 GMT 2025
Record UNII
720J8565ZF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LACHESINE [MI]
Preferred Name English
LACHESINE CHLORIDE
MART.  
Common Name English
LACHESINE CHLORIDE [MART.]
Common Name English
(2-BENZILOYLOXYETHYL)ETHYLDIMETHYLAMMONIUM CHLORIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
Code System Code Type Description
MESH
C005089
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
NCI_THESAURUS
C81456
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-610-1
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
RXCUI
103231
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY RxNorm
EPA CompTox
DTXSID60922037
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
MERCK INDEX
m791
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY Merck Index
FDA UNII
720J8565ZF
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
CAS
1164-38-1
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
PUBCHEM
14415
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
ChEMBL
CHEMBL2110848
Created by admin on Mon Mar 31 18:17:55 GMT 2025 , Edited by admin on Mon Mar 31 18:17:55 GMT 2025
PRIMARY
Related Record Type Details
Structure of LACHESINE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of LACHESINE
ACTIVE MOIETY
NIH
NCATS
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