E3Docker 2.0

BDBM259340

E3L012094

Internal ID: BDB012094

Activity data available Local docking-ready structure

Structure

/e3_file/ligand_db/generated/BDB012094/BDB012094.sdf

Basic Properties

Compound ID

E3L012094

Internal ID

BDB012094

Molecular formula

C24H33F3N4O2S

Molecular weight

498.615000

Exact mass

498.227632

XLogP

4.7011

TPSA

68.4400

HBA / HBD

5 / 2

Rotatable bonds

Heavy atoms / rings

34 / 3

Activity summary

IC50 unknown 316.00000000 nM
8 activity record(s) imported

InChIKey

SMXOJCJHWCTJOO-QAQDUYKDSA-N

SMILES

CCN(c1scc(C(=O)NCc2c(C)cc(C(F)(F)F)[nH]c2=O)c1C)[C@H]1CC[C@H](N(C)C)CC1

Aliases

BDBM259340 (preferred) BDBM259340 (source_id)

E3 Relation

E3 UniProt	Gene / protein	Relation type	Ligand role	Direct	Functional	Docking	Source	Evidence
O75530	EED Polycomb protein EED	reported_binder	bindingdb_reported	Yes	No	low	BindingDB:BDBM259340	medium ; target=Histone-lysine N-methyltransferase EZH2
Q09028	RBBP4;RBAP48 Histone-binding protein RBBP4	reported_binder	bindingdb_reported	Yes	No	low	BindingDB:BDBM259340	medium ; target=Histone-lysine N-methyltransferase EZH2

Sources and Literature

Source	Source ID	Source URL	Download URL	DOI / PMID
BindingDB	BDBM259340	Open	-	10.7270/Q23B5Z3T; 10.7270/Q2PZ5BZ2

Structure Files

Kind	Format	Status	Docking use	File / link	Preparation note
canonical_2d	SMILES	raw	Docking-ready	CCN(c1scc(C(=O)NCc2c(C)cc(C(F)(F)F)[nH]c2=O)c1C)[C@H]1CC[C@H](N(C)C)CC1	keep_bindingdb_unique
generated_3d	SDF	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB012094/BDB012094.sdf	Generated from canonical SMILES
generated_3d	MOL2	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB012094/BDB012094.mol2	Generated from canonical SMILES
docking_ready	PDBQT	prepared	Docking-ready	public/e3_file/ligand_db/generated/BDB012094/BDB012094.pdbqt	Generated from canonical SMILES
image	PNG	prepared	Reference	public/e3_file/ligand_db/generated/BDB012094/BDB012094.png	Generated from canonical SMILES
image	SVG	prepared	Reference	public/e3_file/ligand_db/generated/BDB012094/BDB012094.svg	Generated from canonical SMILES

Activity

Target	Source	Assay	Result	Potency	Literature	Records
Histone-lysine N-methyltransferase EZH2 O75530 E3 ligase component	BindingDB:BDBM259340	IC50	316 nM	Moderate	DOI: 10.7270/Q2PZ5BZ2	1
Histone-lysine N-methyltransferase EZH2 Q09028 E3 ligase component	BindingDB:BDBM259340	IC50	316 nM	Moderate	DOI: 10.7270/Q23B5Z3T	1
Histone-lysine N-methyltransferase EZH2 O75530 E3 ligase component	BindingDB:BDBM259340	IC50	630 nM	Moderate	DOI: 10.7270/Q23B5Z3T	1
Histone-lysine N-methyltransferase EZH2 O75530 E3 ligase component	BindingDB:BDBM259340	IC50	630 nM	Moderate	DOI: 10.7270/Q2PZ5BZ2	1
Histone-lysine N-methyltransferase EZH2 Q09028 E3 ligase component	BindingDB:BDBM259340	IC50	316 nM	Moderate	DOI: 10.7270/Q2PZ5BZ2	1
Histone-lysine N-methyltransferase EZH2 Q09028 E3 ligase component	BindingDB:BDBM259340	IC50	630 nM	Moderate	DOI: 10.7270/Q2PZ5BZ2	1
Histone-lysine N-methyltransferase EZH2 Q09028 E3 ligase component	BindingDB:BDBM259340	IC50	630 nM	Moderate	DOI: 10.7270/Q23B5Z3T	1
Histone-lysine N-methyltransferase EZH2 O75530 E3 ligase component	BindingDB:BDBM259340	IC50	316 nM	Moderate	DOI: 10.7270/Q23B5Z3T	1