Avadomide hydrochlorideProduct ingredient for Avadomide
- Name
- Avadomide hydrochloride
- Drug Entry
- Avadomide
Avadomide is under investigation in clinical trial NCT02031419 (Novel Combinations of CC-122, CC-223, CC-292, and Rituximab in Diffuse Large B-cell Lymphoma and Follicular Lymphoma).
- Accession Number
- DBSALT003275
- Structure
Structure for Avadomide hydrochloride (DBSALT003275)
- Synonyms
- (3RS)-3-(5-Amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione monohydrochloride / 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl) piperidine-2,6-dione hydrochloride / 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione hydrochloride / CC-122 HCI / CC122 HYDROCHLORIDE
- UNII
- 6CX4AEX3KR
- CAS Number
- 1398053-45-6
- Weight
- Average: 322.75
Monoisotopic: 322.0832681 - Chemical Formula
- C14H15ClN4O3
- InChI Key
- BVJRNKXVSYLNFD-UHFFFAOYSA-N
- InChI
- InChI=1S/C14H14N4O3.ClH/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);1H
- IUPAC Name
- 3-(5-amino-2-methyl-4-oxo-3,4-dihydroquinazolin-3-yl)piperidine-2,6-dione hydrochloride
- SMILES
- Cl.CC1=NC2=C(C(N)=CC=C2)C(=O)N1C1CCC(=O)NC1=O
- External Links
- ChemSpider
- 58825998
- ChEMBL
- CHEMBL3989913
- Predicted Properties
Property Value Source logP -0.083 Chemaxon pKa (Strongest Acidic) 11.61 Chemaxon pKa (Strongest Basic) 5.39 Chemaxon Physiological Charge 0 Chemaxon Hydrogen Acceptor Count 5 Chemaxon Hydrogen Donor Count 2 Chemaxon Polar Surface Area 104.86 Å2 Chemaxon Rotatable Bond Count 1 Chemaxon Refractivity 77.1 m3·mol-1 Chemaxon Polarizability 28.19 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon