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SMILES: Cc1n[nH]c2ccc(cc12)-c1cc(NCCO)cnc1-c1cc(F)ccc1O

InChI Key: InChIKey=XBRPPAQWEPQQQL-UHFFFAOYSA-N

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50240795   
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
Fibroblast growth factor receptor 3


(Homo sapiens (Human))
BDBM50240795
PNG
(CHEMBL4100109)
Show SMILES Cc1n[nH]c2ccc(cc12)-c1cc(NCCO)cnc1-c1cc(F)ccc1O
Show InChI InChI=1S/C21H19FN4O2/c1-12-16-8-13(2-4-19(16)26-25-12)17-10-15(23-6-7-27)11-24-21(17)18-9-14(22)3-5-20(18)28/h2-5,8-11,23,27-28H,6-7H2,1H3,(H,25,26)
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n/an/a>1.00E+3n/an/an/an/an/an/a



University of Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of recombinant human FGFR3 using poly (Glu,Tyr) 4:1 as substrate after 60 mins by ELISA


J Med Chem 60: 6018-6035 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00076
BindingDB Entry DOI: 10.7270/Q2K939NC
More data for this
Ligand-Target Pair
Fibroblast growth factor receptor 2


(Homo sapiens (Human))
BDBM50240795
PNG
(CHEMBL4100109)
Show SMILES Cc1n[nH]c2ccc(cc12)-c1cc(NCCO)cnc1-c1cc(F)ccc1O
Show InChI InChI=1S/C21H19FN4O2/c1-12-16-8-13(2-4-19(16)26-25-12)17-10-15(23-6-7-27)11-24-21(17)18-9-14(22)3-5-20(18)28/h2-5,8-11,23,27-28H,6-7H2,1H3,(H,25,26)
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Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



University of Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of recombinant human FGFR2 using poly (Glu,Tyr) 4:1 as substrate after 60 mins by ELISA


J Med Chem 60: 6018-6035 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00076
BindingDB Entry DOI: 10.7270/Q2K939NC
More data for this
Ligand-Target Pair
Fibroblast growth factor receptor 1


(Homo sapiens (Human))
BDBM50240795
PNG
(CHEMBL4100109)
Show SMILES Cc1n[nH]c2ccc(cc12)-c1cc(NCCO)cnc1-c1cc(F)ccc1O
Show InChI InChI=1S/C21H19FN4O2/c1-12-16-8-13(2-4-19(16)26-25-12)17-10-15(23-6-7-27)11-24-21(17)18-9-14(22)3-5-20(18)28/h2-5,8-11,23,27-28H,6-7H2,1H3,(H,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



University of Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of recombinant human FGFR1 using poly (Glu,Tyr) 4:1 as substrate after 60 mins by ELISA


J Med Chem 60: 6018-6035 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00076
BindingDB Entry DOI: 10.7270/Q2K939NC
More data for this
Ligand-Target Pair