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Details

Stereochemistry RACEMIC
Molecular Formula C14H14N4O3
Molecular Weight 286.286
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AVADOMIDE

SMILES

CC1=NC2=C(C(N)=CC=C2)C(=O)N1C3CCC(=O)NC3=O

InChI

InChIKey=RSNPAKAFCAAMBH-UHFFFAOYSA-N
InChI=1S/C14H14N4O3/c1-7-16-9-4-2-3-8(15)12(9)14(21)18(7)10-5-6-11(19)17-13(10)20/h2-4,10H,5-6,15H2,1H3,(H,17,19,20)

HIDE SMILES / InChI

Molecular Formula C14H14N4O3
Molecular Weight 286.286
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

CC-122 is the first-in-class pleiotropic pathway modifiers that may work by binding cereblon and promoting the ubiquitination and the resulting degradation of the transcription factors Aiolos and Ikaros. It has been shown to have potent anti-proliferative, anti-angiogenic and immunomodulatory activities in B cell lymphoma, perhaps though its T and NK-cell activation and B-cell inhibition. CC-122 inhibits proliferation and induces apoptosis in a broad panel of diffuse large B-cell lymphoma cell lines, reduces tumor growth in xenograft models established from activated B-cell (ABC) and germinal center B-cell DLBCL cell lines, and stimulates IL-2 production in primary T cells. These activities are dependent on the binding of CC-122 to Cereblon and subsequent ubiquitination and proteasomal degradation of Aiolos and Ikaros, resulting in direct derepression of interferon (IFN)–stimulated gene (ISG) transcription and induction of IFN-inducible proteins, ultimately leading to apoptosis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q96SW2
Gene ID: 51185.0
Gene Symbol: CRBN
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
CC-122 immunomodulatory effects in refractory patients with diffuse large B-cell lymphoma.
2016
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:05:38 GMT 2023
Edited
by admin
on Sat Dec 16 08:05:38 GMT 2023
Record UNII
28DZS29F59
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AVADOMIDE
USAN  
USAN   INN  
Official Name English
AVADOMIDE [USAN]
Common Name English
3-(5-Amino-2-methyl-4-oxo-4H-quinazolin-3-yl)piperidine-2,6-dione
Systematic Name English
CC-122
WHO-DD  
Code English
CC122
Code English
avadomide [INN]
Common Name English
Avadomide [WHO-DD]
Common Name English
2,6-PIPERIDINEDIONE, 3-(5-AMINO-2-METHYL-4-OXO-3(4H)-QUINAZOLINYL)-
Systematic Name English
RAC-(3R)-3-(5-AMINO-2-METHYL-4-OXOQUINAZOLIN-3(4H)-YL)PIPERIDINE-2,6-DIONE
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C160786
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
FDA UNII
28DZS29F59
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
DRUG BANK
DB14857
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
INN
10599
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
SMS_ID
100000175107
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
CAS
1015474-32-4
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
PUBCHEM
24967599
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
USAN
DE-01
Created by admin on Sat Dec 16 08:05:38 GMT 2023 , Edited by admin on Sat Dec 16 08:05:38 GMT 2023
PRIMARY
Related Record Type Details
TARGET->MODULATOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY