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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H26NO3.Cl
Molecular Weight 363.878
Optical Activity NONE
Defined Stereocenters 0 / 0
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 / 0
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

PubMed

PubMed

TitleDatePubMed
Development of cricket mushroom bodies.
2002 Oct 21
Allosteric modulators of class B G-protein-coupled receptors.
2007 Sep
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:03:53 GMT 2023
Edited
by admin
on Fri Dec 15 16:03:53 GMT 2023
Record UNII
720J8565ZF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LACHESINE CHLORIDE
MART.  
Common Name English
LACHESINE [MI]
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 Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
Code System Code Type Description
MESH
C005089
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
NCI_THESAURUS
C81456
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-610-1
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
RXCUI
103231
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID60922037
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
MERCK INDEX
m791
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY Merck Index
FDA UNII
720J8565ZF
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
CAS
1164-38-1
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
PUBCHEM
14415
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110848
Created by admin on Fri Dec 15 16:03:53 GMT 2023 , Edited by admin on Fri Dec 15 16:03:53 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY