BDBM50358245 CHEMBL1922225

SMILES CC(C)C(=C)CC[C@@H](C)[C@H]1CC[C@H]2[C@H](CCc3cc(O)ccc3C)C(=O)CC[C@]12C

InChI Key InChIKey=HEUHMWCGNUTYFR-SOVKOMHZSA-N

Data  16 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 16 hits for monomerid = 50358245   

TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human Aurora-B using tetra(LRRWLSG) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  4.85E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  4.36E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNUAK family SNF1-like kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human ARK5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  2.02E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  1.07E+4nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of wild type human MEK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  2.75E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Nek2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human NEK2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Nek6(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human NEK6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human PIM1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase PLK1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of recombinant human PLK1 using casein as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase N1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human PRK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  1.48E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human AKT1 using GSK3 (amino acids 14 to 27) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed