Reaction Details Report a problem with these data
Target
Fibroblast growth factor 2
Ligand
BDBM167951
Substrate
n/a
Meas. Tech.
VEGFR2 Kinase Assay
pH
7.2±n/a
Temperature
298.15±n/a K
IC50
208.54±0.0 nM
Comments
extracted
Citation
 Yin, Y; Sha, S; Wang, YT; Wu, X; Wang, SF; Qiao, F; Lv, PC; Zhu, HL Discovery of new 4-alkoxyquinazoline-based derivatives as potent VEGFR2 inhibitors. Chem Biol Drug Des 86:1323-9 (2015) [PubMed]  Article 
Target
Name:
Fibroblast growth factor 2
Synonyms:
Basic fibroblast growth factor | FGF-2 | FGF2 | FGF2_HUMAN | FGFB | Fibroblast growth factor 2 (bFGF) | Fibroblast growth factor receptor 2 (FGF-2) | HBGF-2 | Heparin-binding growth factor 2
Type:
Protein
Mol. Mass.:
30803.89
Organism:
Homo sapiens (Human)
Description:
P09038
Residue:
288
Sequence:
MVGVGGGDVEDVTPRPGGCQISGRGARGCNGIPGAAAWEAALPRRRPRRHPSVNPRSRAAGSPRTRGRRTEERPSGSRLGDRGRGRALPGGRLGGRGRGRAPERVGGRGRGRGTAAPRAAPAARGSRPGPAGTMAAGSITTLPALPEDGGSGAFPPGHFKDPKRLYCKNGGFFLRIHPDGRVDGVREKSDPHIKLQLQAEERGVVSIKGVCANRYLAMKEDGRLLASKCVTDECFFFERLESNNYNTYRSRKYTSWYVALKRTGQYKLGSKTGPGQKAILFLPMSAKS
  
Inhibitor
Name:
BDBM167951
Synonyms:
1-(4-(2-Methoxyphenyl)piperazin-1-yl)-3-(quinazolin-4-yloxy)propan-2-ol (3g)
Type:
Small organic molecule
Emp. Form.:
C22H26N4O3
Mol. Mass.:
394.4668
SMILES:
COc1ccccc1N1CCN(CC(O)COc2ncnc3ccccc23)CC1
Structure:
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