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Details

Stereochemistry ACHIRAL
Molecular Formula C15H21N3O6
Molecular Weight 339.3437
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LM22A-4

SMILES

OCCNC(=O)C1=CC(=CC(=C1)C(=O)NCCO)C(=O)NCCO

InChI

InChIKey=RGWJKANXFYJKHN-UHFFFAOYSA-N
InChI=1S/C15H21N3O6/c19-4-1-16-13(22)10-7-11(14(23)17-2-5-20)9-12(8-10)15(24)18-3-6-21/h7-9,19-21H,1-6H2,(H,16,22)(H,17,23)(H,18,24)

HIDE SMILES / InChI

Molecular Formula C15H21N3O6
Molecular Weight 339.3437
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q16620
Gene ID: 4915.0
Gene Symbol: NTRK2
Target Organism: Homo sapiens (Human)
47.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:36:10 GMT 2023
Edited
by admin
on Sat Dec 16 17:36:10 GMT 2023
Record UNII
5GCL3P6AF5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LM22A-4
Code English
LM22A4
Code English
N1,N3,N5-Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide
Systematic Name English
LM-22A4
Code English
1,3,5-Benzenetricarboxamide, N,N′,N′′-tris(2-hydroxyethyl)-
Systematic Name English
1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)-
Systematic Name English
1-N,3-N,5-N-Tris(2-hydroxyethyl)benzene-1,3,5-tricarboxamide
Systematic Name English
Code System Code Type Description
PUBCHEM
2054170
Created by admin on Sat Dec 16 17:36:10 GMT 2023 , Edited by admin on Sat Dec 16 17:36:10 GMT 2023
PRIMARY
CAS
37988-18-4
Created by admin on Sat Dec 16 17:36:10 GMT 2023 , Edited by admin on Sat Dec 16 17:36:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID201045819
Created by admin on Sat Dec 16 17:36:10 GMT 2023 , Edited by admin on Sat Dec 16 17:36:10 GMT 2023
PRIMARY
FDA UNII
5GCL3P6AF5
Created by admin on Sat Dec 16 17:36:10 GMT 2023 , Edited by admin on Sat Dec 16 17:36:10 GMT 2023
PRIMARY
WIKIPEDIA
LM22A-4
Created by admin on Sat Dec 16 17:36:10 GMT 2023 , Edited by admin on Sat Dec 16 17:36:10 GMT 2023
PRIMARY
Related Record Type Details
TARGET->PARTIAL AGONIST