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BDBM50158885 CHEMBL3787118

SMILES: CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](C(C)C)C(N)=O

InChI Key: InChIKey=ATVWNFORRVGXLR-NGJKBPNDNA-N

Data: 1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50158885   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50158885
PNG
(CHEMBL3787118)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](C(C)C)C(N)=O
Show InChI InChI=1/C34H56N10O7/c1-19(2)16-24(32(50)44-27(20(3)4)28(35)46)41-31(49)25(17-21-10-6-5-7-11-21)42-33(51)26(18-45)43-30(48)23(13-9-15-39-34(36)37)40-29(47)22-12-8-14-38-22/h5-7,10-11,19-20,22-27,38,45H,8-9,12-18H2,1-4H3,(H2,35,46)(H,40,47)(H,41,49)(H,42,51)(H,43,48)(H,44,50)(H4,36,37,39)/t22-,23-,24-,25-,26-,27-/s2
PDB
MMDB

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PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
2.84E+4n/an/an/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant His-tagged KDM1A (171 to 836 residues) using H3K4me2 as substrate by peroxidase coupled enzyme assay


J Med Chem 59: 1308-29 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01758
BindingDB Entry DOI: 10.7270/Q2MP5559
More data for this
Ligand-Target Pair