Compile Data Set for Download or QSAR
Report error Found 50 Enz. Inhib. hit(s) with all data for entry = 50015030
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582143BDBM50582143(CHEMBL4095682)
Affinity DataIC50: 110nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582148BDBM50582148(CHEMBL5077959)
Affinity DataIC50: 135nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582142BDBM50582142(CHEMBL5088013)
Affinity DataIC50: 140nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582146BDBM50582146(CHEMBL5085478)
Affinity DataIC50: 204nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582150BDBM50582150(CHEMBL5091513)
Affinity DataIC50: 250nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582147BDBM50582147(CHEMBL5083349)
Affinity DataIC50: 268nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582144BDBM50582144(CHEMBL5090566)
Affinity DataIC50: 389nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582143BDBM50582143(CHEMBL4095682)
Affinity DataIC50: 400nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582145BDBM50582145(CHEMBL5084070)
Affinity DataIC50: 449nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582142BDBM50582142(CHEMBL5088013)
Affinity DataIC50: 460nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280100BDBM50280100(CHEMBL4172184)
Affinity DataIC50: 800nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582141BDBM50582141(CHEMBL5075056)
Affinity DataIC50: 800nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280100BDBM50280100(CHEMBL4172184)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582139BDBM50582139(CHEMBL5069932)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582150BDBM50582150(CHEMBL5091513)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582150BDBM50582150(CHEMBL5091513)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582142BDBM50582142(CHEMBL5088013)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582139BDBM50582139(CHEMBL5069932)
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280101BDBM50280101(CHEMBL4061296)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582153BDBM50582153(CHEMBL5071698)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582155BDBM50582155(CHEMBL5079189)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582143BDBM50582143(CHEMBL4095682)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582141BDBM50582141(CHEMBL5075056)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582149BDBM50582149(CHEMBL5077113)
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280100BDBM50280100(CHEMBL4172184)
Affinity DataIC50: 4.50E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582154BDBM50582154(CHEMBL5081679)
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582141BDBM50582141(CHEMBL5075056)
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582157BDBM50582157(CHEMBL5088461)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582158BDBM50582158(CHEMBL5090033)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582139BDBM50582139(CHEMBL5069932)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582140BDBM50582140(CHEMBL5093593)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 4(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582143BDBM50582143(CHEMBL4095682)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR4 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582151BDBM50582151(CHEMBL5084072)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582152BDBM50582152(CHEMBL5083827)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582140BDBM50582140(CHEMBL5093593)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582140BDBM50582140(CHEMBL5093593)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582156BDBM50582156(CHEMBL5094067)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280101BDBM50280101(CHEMBL4061296)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of FGFR1 (unknown origin) (458 to 765 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582144BDBM50582144(CHEMBL5090566)
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50280101BDBM50280101(CHEMBL4061296)
Affinity DataIC50: 5.10E+4nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582148BDBM50582148(CHEMBL5077959)
Affinity DataIC50: 7.70E+4nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582146BDBM50582146(CHEMBL5085478)
Affinity DataIC50: 7.70E+4nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582145BDBM50582145(CHEMBL5084070)
Affinity DataIC50: 9.60E+4nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582149BDBM50582149(CHEMBL5077113)
Affinity DataIC50: 1.98E+5nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 2(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582147BDBM50582147(CHEMBL5083349)
Affinity DataIC50: 2.58E+5nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) (461 to 763 residues) transfected in Escherichia coli BL21(DE3) cells using Tyr04 peptide as substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582148BDBM50582148(CHEMBL5077959)
Affinity DataIC50: 5.01E+5nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582147BDBM50582147(CHEMBL5083349)
Affinity DataIC50: 7.53E+5nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582144BDBM50582144(CHEMBL5090566)
Affinity DataIC50: 7.58E+5nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582146BDBM50582146(CHEMBL5085478)
Affinity DataIC50: 9.15E+5nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 3(Human)
University of Leeds

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50582149BDBM50582149(CHEMBL5077113)
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Tyr04 peptide as substrate incubated for 1 hr by FRET based Z'-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed