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Details

Stereochemistry RACEMIC
Molecular Formula C23H28N2O3
Molecular Weight 380.48
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACOXATRINE

SMILES

CC(=O)NCC1(CCN(CC2COC3=C(O2)C=CC=C3)CC1)C4=CC=CC=C4

InChI

InChIKey=WSWPNPUMDWOKAR-UHFFFAOYSA-N
InChI=1S/C23H28N2O3/c1-18(26)24-17-23(19-7-3-2-4-8-19)11-13-25(14-12-23)15-20-16-27-21-9-5-6-10-22(21)28-20/h2-10,20H,11-17H2,1H3,(H,24,26)

HIDE SMILES / InChI

Molecular Formula C23H28N2O3
Molecular Weight 380.48
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:40:09 GMT 2023
Edited
by admin
on Fri Dec 15 15:40:09 GMT 2023
Record UNII
7IGS0KX75Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACOXATRINE
INN  
INN  
Official Name English
acoxatrine [INN]
Common Name English
(±)-N-((1-(1,4-BENZODIOXAN-2-YLMETHYL)-4-PHENYL-4-PIPERIDYL)METHYL)ACETAMIDE
Systematic Name English
R-5385
Code English
R 5385
Code English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
Code System Code Type Description
FDA UNII
7IGS0KX75Q
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
NCI_THESAURUS
C74418
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
PUBCHEM
68938
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
CAS
748-44-7
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID10862398
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
EVMPD
SUB05247MIG
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL1974113
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
SMS_ID
100000087673
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
INN
1552
Created by admin on Fri Dec 15 15:40:09 GMT 2023 , Edited by admin on Fri Dec 15 15:40:09 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY