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BDBM526632

E3L022703
Internal ID: BDB022703
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB022703/BDB022703.sdf
Basic Properties
Compound ID
E3L022703
Internal ID
BDB022703
Molecular formula
C31H40N8O3
Molecular weight
572.714000
Exact mass
572.322337
XLogP
3.8863
TPSA
125.7800
HBA / HBD
8 / 3
Rotatable bonds
10
Heavy atoms / rings
42 / 6
Activity summary
IC50 < 300.00000000 nM
1 activity record(s) imported
InChIKey
VDTCFLVQPCODSU-ZRZAMGCNSA-N
SMILES
C=CC(=O)N[C@H]1CC[C@@H](C(=O)Nc2cccc(CNc3nc(OC4CCN(C)CC4)nc4c(C5CC5)cnn34)c2)CC1
Aliases
BDBM526632 (preferred) BDBM526632 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P51948 MNAT1;CAP35;MAT1;RNF66
CDK-activating kinase assembly factor MAT1		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM526632 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM526632 Open - 10.7270/Q2Z03CCX
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C=CC(=O)N[C@H]1CC[C@@H](C(=O)Nc2cccc(CNc3nc(OC4CCN(C)CC4)nc4c(C5CC5)cnn34)c2)CC1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB022703/BDB022703.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB022703/BDB022703.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB022703/BDB022703.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB022703/BDB022703.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB022703/BDB022703.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM526632 IC50 <300 nM Uncertain DOI: 10.7270/Q2Z03CCX 1