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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H26ClNO3
Molecular Weight 363.878
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADAFENOXATE

SMILES

ClC1=CC=C(OCC(=O)OCCNC23CC4CC(CC(C4)C2)C3)C=C1

InChI

InChIKey=PLSMXIQMWYSHIV-UHFFFAOYSA-N
InChI=1S/C20H26ClNO3/c21-17-1-3-18(4-2-17)25-13-19(23)24-6-5-22-20-10-14-7-15(11-20)9-16(8-14)12-20/h1-4,14-16,22H,5-13H2

HIDE SMILES / InChI

Molecular Formula C20H26ClNO3
Molecular Weight 363.878
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Adafenoxate exerts nootropic and anxiolytic properties in rodents. Adafenoxate inhibits monoamine oxidase and cAMP phosphodiesterase activity. Adafenoxate inhibits monoamine uptake and regulates the density of the 5-HT1 sites in the brain.

CNS Activity

Approval Year

PubMed

PubMed

TitleDatePubMed
Memory effects of the new derivative of the p-chlorophenoxyacetic acid adafenoxate compared to the effects of some cognition-enhancing drugs in rats.
1989 Sep

Sample Use Guides

mice: i.p. 50 and 100 mg/kg once daily for 7 days rats: p.o. 100 mg/kg for 5 days
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:41:06 GMT 2023
Edited
by admin
on Fri Dec 15 15:41:06 GMT 2023
Record UNII
B8VQU4C05J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ADAFENOXATE
INN  
INN  
Official Name English
2-(1-ADAMANTYLAMINO)ETHYL (P-CHLOROPHENOXY)ACETATE
Common Name English
adafenoxate [INN]
Common Name English
ACETIC ACID, 2-(4-CHLOROPHENOXY)-, 2-(TRICYCLO(3.3.1.13,7)DEC-1-YLAMINO)ETHYL ESTER
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
Code System Code Type Description
CAS
82168-26-1
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
EVMPD
SUB05259MIG
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
INN
5280
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
PUBCHEM
64517
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
FDA UNII
B8VQU4C05J
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
MESH
C054061
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID4046280
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104053
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
NCI_THESAURUS
C72680
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
SMS_ID
100000087679
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
WIKIPEDIA
ADAFENOXATE
Created by admin on Fri Dec 15 15:41:07 GMT 2023 , Edited by admin on Fri Dec 15 15:41:07 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY