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

Details

Stereochemistry ACHIRAL
Molecular Formula C24H35ClN2O2
Molecular Weight 419.0
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZD-9056

SMILES

OCCCNCCCC1=CC=C(Cl)C(=C1)C(=O)NCC23CC4CC(CC(C4)C2)C3

InChI

InChIKey=HSQAARMBHJCUOK-UHFFFAOYSA-N
InChI=1S/C24H35ClN2O2/c25-22-5-4-17(3-1-6-26-7-2-8-28)12-21(22)23(29)27-16-24-13-18-9-19(14-24)11-20(10-18)15-24/h4-5,12,18-20,26,28H,1-3,6-11,13-16H2,(H,27,29)

HIDE SMILES / InChI

Molecular Formula C24H35ClN2O2
Molecular Weight 419.0
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

AZD9056 was developed as a selective inhibitor of the purinergic receptor P2X7, a key player in the generation and secretion of several proinflammatory cytokines. AZD 9056 participated is phase II clinical trials for osteoarthritis, inflammatory bowel disease, and chronic obstructive pulmonary disease but these studies were discontinued in 2009 because the drug failed to show significant efficacy in trials. In addition, in 2015 AZD 9056 was studied for the treatment of Crohn's disease (CD), although the drug has shown a beneficial risk profile the lack in the change of inflammatory biomarkers questions its anti-inflammatory potential.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
11.2 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Targeting the P2X7 receptor in rheumatoid arthritis: biological rationale for P2X7 antagonism.
2013-11-07
Clinical evaluation of the efficacy of the P2X7 purinergic receptor antagonist AZD9056 on the signs and symptoms of rheumatoid arthritis in patients with active disease despite treatment with methotrexate or sulphasalazine.
2012-10
Patents

Sample Use Guides

AZD9056 administered daily over 4 weeks
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:34:00 GMT 2025
Edited
by admin
on Mon Mar 31 23:34:00 GMT 2025
Record UNII
F13K378W4L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AZD-9056
Common Name English
AZD9056
Preferred Name English
BENZAMIDE, 2-CHLORO-5-(3-((3-HYDROXYPROPYL)AMINO)PROPYL)-N-(TRICYCLO(3.3.1.13,7)DEC-1-YLMETHYL)-
Systematic Name English
AZD 9056 [WHO-DD]
Common Name English
Code System Code Type Description
ChEMBL
CHEMBL3545108
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
CAS
345304-65-6
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
FDA UNII
F13K378W4L
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
SMS_ID
100000175722
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
PUBCHEM
10161381
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
DRUG BANK
DB12594
Created by admin on Mon Mar 31 23:34:00 GMT 2025 , Edited by admin on Mon Mar 31 23:34:00 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY