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5-(Piperidine-1-carbonyl)-1,3-dihydroindol-2-one

E3L029412
Internal ID: BDB029412
Activity data available Local docking-ready structure
Dock with Q96SW2
Structure
/e3_file/ligand_db/generated/BDB029412/BDB029412.sdf
Basic Properties
Compound ID
E3L029412
Internal ID
BDB029412
Molecular formula
C14H16N2O2
Molecular weight
244.294000
Exact mass
244.121178
XLogP
1.8073
TPSA
49.4100
HBA / HBD
2 / 1
Rotatable bonds
1
Heavy atoms / rings
18 / 3
Activity summary
IC50 unknown 200000.00000000 nM
1 activity record(s) imported
InChIKey
SBACMAPGVTWMEM-UHFFFAOYSA-N
SMILES
O=C1Cc2cc(C(=O)N3CCCCC3)ccc2N1
Aliases
BDBM588341 (preferred) 5-(Piperidine-1-carbonyl)-1,3-dihydroindol-2-one (source_name) BDBM588341 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q96SW2 CRBN;AD-006
Protein cereblon		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM588341 medium
; target=Protein cereblon
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM588341 Open - 10.7270/Q2H41W8C
PubChem CID110700311 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O=C1Cc2cc(C(=O)N3CCCCC3)ccc2N1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB029412/BDB029412.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB029412/BDB029412.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB029412/BDB029412.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB029412/BDB029412.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB029412/BDB029412.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Protein cereblon
Q96SW2
E3 ligase component 		BindingDB:BDBM588341 IC50 200000 nM Low DOI: 10.7270/Q2H41W8C 1