Reaction Details |
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Target | Fibroblast growth factor 2 |
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Ligand | BDBM50307389 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_610686 (CHEMBL1072347) |
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Kd | 35±n/a nM |
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Citation | Johnstone, KD; Karoli, T; Liu, L; Dredge, K; Copeman, E; Li, CP; Davis, K; Hammond, E; Bytheway, I; Kostewicz, E; Chiu, FC; Shackleford, DM; Charman, SA; Charman, WN; Harenberg, J; Gonda, TJ; Ferro, V Synthesis and biological evaluation of polysulfated oligosaccharide glycosides as inhibitors of angiogenesis and tumor growth. J Med Chem53:1686-99 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Fibroblast growth factor 2 |
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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: | MVGVGGGDVEDVTPRPGGCQISGRGARGCNGIPGAAAWEAALPRRRPRRHPSVNPRSRAA
GSPRTRGRRTEERPSGSRLGDRGRGRALPGGRLGGRGRGRAPERVGGRGRGRGTAAPRAA
PAARGSRPGPAGTMAAGSITTLPALPEDGGSGAFPPGHFKDPKRLYCKNGGFFLRIHPDG
RVDGVREKSDPHIKLQLQAEERGVVSIKGVCANRYLAMKEDGRLLASKCVTDECFFFERL
ESNNYNTYRSRKYTSWYVALKRTGQYKLGSKTGPGQKAILFLPMSAKS
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BDBM50307389 |
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n/a |
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Name | BDBM50307389 |
Synonyms: | 2,3,4,6-Tetra-O-sulfo-alpha-D-mannopyranosyl-(1->3)-2,4,6-tri-O-sulfo-alpha-D-mannopyranosyl-(1->3)-2,4,6-tri-O-sulfo-alpha-D-mannopyranosyl-(1->3)-2,4,6-tri-O-sulfo-alpha-D-mannopyranosyl-(1->2)-3,4,6-tri-O-sulfor-D-mannopyranoside | CHEMBL590011 |
Type | Small organic molecule |
Emp. Form. | C50H59N3O74S16 |
Mol. Mass. | 2399.028 |
SMILES | [O-]S(=O)(=O)OC[C@H]1O[C@H](OCCCCCCCCn2cc(nn2)-c2cccc3ccccc23)[C@@H](O[C@H]2O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](O[C@H]3O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](O[C@H]4O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](O[C@H]5O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@@H]5OS([O-])(=O)=O)[C@@H]4OS([O-])(=O)=O)[C@@H]3OS([O-])(=O)=O)[C@@H]2OS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@@H]1OS([O-])(=O)=O |r| |
Structure |
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