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SMILES: [#6]-[#16]-[#6]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6]=[#6]P([#8])(=O)[#6]-[#6]-[#6](-[#6])-[#6]-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](\[#6])-[#6])-[#6](-[#6])-[#6])-[#6](-[#6])-[#6])-[#6](-[#8])=O

InChI Key: InChIKey=XJHAVUJMGHEIKM-RRLLAZLHSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50407720   
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))		BDBM50407720
PNG
(CHEMBL5279958)
Show SMILES [#6]-[#16]-[#6]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6]=[#6]P([#8])(=O)[#6]-[#6]-[#6](-[#6])-[#6]-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](\[#6])-[#6])-[#6](-[#6])-[#6])-[#6](-[#6])-[#6])-[#6](-[#8])=O |w:17.17|
Show InChI InChI=1S/C33H58N3O7PS/c1-22(2)12-10-13-25(7)14-11-15-26(8)16-19-44(42,43)20-17-28(37)35-29(23(3)4)32(39)36-30(24(5)6)31(38)34-27(33(40)41)18-21-45-9/h12,14,17,20,23-24,26-27,29-30H,10-11,13,15-16,18-19,21H2,1-9H3,(H,34,38)(H,35,37)(H,36,39)(H,40,41)(H,42,43)/b20-17?,25-14+/t26?,27-,29-,30-/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
n/an/a 5.27E+3n/an/an/an/an/an/a


TBA

Assay Description
Blocking activity was assessed by antagonism of (-)-noradrenaline induced contraction of rat prostatic vas deferens (alpha1A adrenoceptor)

Citation and Details
More data for this
Ligand-Target Pair