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BDBM50200445

E3L048383

Internal ID: BDB048383

Activity data available Local docking-ready structure

Dock with Q09472 Dock with Q92793

Structure

/e3_file/ligand_db/generated/BDB048383/BDB048383.sdf

Basic Properties

Compound ID

E3L048383

Internal ID

BDB048383

Molecular formula

C22H25FN6O2

Molecular weight

424.480000

Exact mass

424.202302

XLogP

3.0323

TPSA

77.2100

HBA / HBD

5 / 1

Rotatable bonds

Heavy atoms / rings

31 / 5

Activity summary

IC50 unknown 20.00000000 nM
6 activity record(s) imported

InChIKey

NKOJNOBJGYTLLZ-KRWDZBQOSA-N

SMILES

CC(=O)N1CCc2c(c(Nc3ccc(-c4cnn(C)c4)cc3F)nn2[C@H]2CCOC2)C1

Aliases

BDBM50200445 (preferred) 1-[3-[[2-Fluoranyl-4-(1-Methylpyrazol-4-Yl)phenyl]amino]-1-[(3~{s})-Oxolan-3-Yl]-6,7-Dihydro-4~{h}-Pyrazolo[4,3-C]pyridin-5-Yl]ethanone (source_name) BDBM50200445 (source_id)

E3 Relation

E3 UniProt	Gene / protein	Relation type	Ligand role	Direct	Functional	Docking	Source	Evidence
Q09472	EP300;P300 Histone acetyltransferase p300	reported_binder	bindingdb_reported	Yes	No	low	BindingDB:BDBM50200445	medium ; target=CREB-binding protein
Q92793	CREBBP;CBP CREB-binding protein	reported_binder	bindingdb_reported	Yes	No	low	BindingDB:BDBM50200445	medium ; target=CREB-binding protein

Sources and Literature

Source	Source ID	Source URL	Download URL	DOI / PMID
BindingDB	BDBM50200445	Open	-	10.1021/acs.jmedchem.6b01022; 10.7270/Q23N25G6; 10.1021/acs.jmedchem.7b00796 PMID: 27682507; 28892380
PubChem	CID121372887	Open	-

Structure Files

Kind	Format	Status	Docking use	File / link	Preparation note
canonical_2d	SMILES	raw	Docking-ready	CC(=O)N1CCc2c(c(Nc3ccc(-c4cnn(C)c4)cc3F)nn2[C@H]2CCOC2)C1	keep_bindingdb_unique
generated_3d	SDF	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB048383/BDB048383.sdf	Generated from canonical SMILES
generated_3d	MOL2	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB048383/BDB048383.mol2	Generated from canonical SMILES
docking_ready	PDBQT	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB048383/BDB048383.pdbqt	Generated from canonical SMILES
image	PNG	prepared	Reference	public/e3_file/ligand_db/generated/BDB048383/BDB048383.png	Generated from canonical SMILES
image	SVG	prepared	Reference	public/e3_file/ligand_db/generated/BDB048383/BDB048383.svg	Generated from canonical SMILES

Activity

Target	Source	Assay	Result	Potency	Literature	Records
CREB-binding protein Q92793 E3 ligase component	BindingDB:BDBM50200445	IC50	410 nM	Moderate	DOI: 10.1021/acs.jmedchem.7b00796 PMID: 28892380	1
CREB-binding protein Q92793 E3 ligase component	BindingDB:BDBM50200445	IC50	22 nM	High	DOI: 10.7270/Q23N25G6	1
CREB-binding protein Q92793 E3 ligase component	BindingDB:BDBM50200445	IC50	20 nM	High	DOI: 10.1021/acs.jmedchem.7b00796 PMID: 28892380	1
CREB-binding protein Q09472 E3 ligase component	BindingDB:BDBM50200445	EC50	1900 nM	Low	DOI: 10.1021/acs.jmedchem.6b01022 PMID: 27682507	1
CREB-binding protein Q92793 E3 ligase component	BindingDB:BDBM50200445	EC50	910 nM	Moderate	DOI: 10.1021/acs.jmedchem.7b00796 PMID: 28892380	1
CREB-binding protein Q92793 E3 ligase component	BindingDB:BDBM50200445	EC50	1900 nM	Low	DOI: 10.1021/acs.jmedchem.6b01022 PMID: 27682507	1