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Details

Stereochemistry ACHIRAL
Molecular Formula C22H24ClN5O
Molecular Weight 409.912
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RABEXIMOD

SMILES

CN(C)CCNC(=O)CN1C2=CC=C(Cl)C=C2C3=C1N=C4C=C(C)C(C)=CC4=N3

InChI

InChIKey=PDNNUMNEXITLCZ-UHFFFAOYSA-N
InChI=1S/C22H24ClN5O/c1-13-9-17-18(10-14(13)2)26-22-21(25-17)16-11-15(23)5-6-19(16)28(22)12-20(29)24-7-8-27(3)4/h5-6,9-11H,7-8,12H2,1-4H3,(H,24,29)

HIDE SMILES / InChI

Molecular Formula C22H24ClN5O
Molecular Weight 409.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Rabeximod is an indolo[2,3-b]quinoxaline derivative patented by OxyPharma AB as anti-inflammatory agent useful for the treatment of autoimmune disease. Rabeximod impaired monocyte differentiation into monocyte-derived dendritic cells and pro-inflammatory allostimulated macrophages. Monocyte-derived dendritic cells that were treated with Rabeximod resulted in a significant decrease in their ability to pinocytose antigens, while no effect was exerted by the drug on the ability of allostimulated macrophages and anti-inflammatory macrophages to phagocytose. Rabeximod reduces the severity of arthritis in rodent models of rheumatoid arthritis and multiple sclerosis. Rabeximod efficiently prevented arthritis during the time window when TLR2 or TLR4 ligands activate inflammatory macrophages.

Approval Year

PubMed

PubMed

TitleDatePubMed
Rabeximod reduces arthritis severity in mice by decreasing activation of inflammatory cells.
2010 Aug
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:10:22 GMT 2023
Edited
by admin
on Fri Dec 15 18:10:22 GMT 2023
Record UNII
J4D3K58W3Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RABEXIMOD
INN  
INN  
Official Name English
rabeximod [INN]
Common Name English
ROB-803
Code English
6H-INDOLO(2,3-B)QUINOXALINE-6-ACETAMIDE, 9-CHLORO-N-(2-(DIMETHYLAMINO)ETHYL)-2,3-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C308
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
Code System Code Type Description
FDA UNII
J4D3K58W3Z
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
PUBCHEM
56841552
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
CAS
872178-65-9
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID701007428
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
SMS_ID
300000027018
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
INN
8866
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
NCI_THESAURUS
C152136
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
DRUG BANK
DB05772
Created by admin on Fri Dec 15 18:10:22 GMT 2023 , Edited by admin on Fri Dec 15 18:10:22 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY