Reaction Details |
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Target | Interleukin-5 |
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Ligand | BDBM50354850 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_642275 (CHEMBL1177155) |
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IC50 | 26800±n/a nM |
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Citation | Thanigaimalai, P; Lee, KC; Sharma, VK; Yun, JH; Kim, Y; Jung, SH Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity. Bioorg Med Chem18:4625-9 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Interleukin-5 |
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Name: | Interleukin-5 |
Synonyms: | IL5 | IL5_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 15240.67 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_642275 |
Residue: | 134 |
Sequence: | MRMLLHLSLLALGAAYVYAIPTEIPTSALVKETLALLSTHRTLLIANETLRIPVPVHKNH
QLCTEEIFQGIGTLESQTVQGGTVERLFKNLSLIKKYIDGQKKKCGEERRRVNQFLDYLQ
EFLGVMNTEWIIES
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BDBM50354850 |
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n/a |
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Name | BDBM50354850 |
Synonyms: | BUDESONIDE | US10869929, Compound Budesonide | US11554172, Compound Budesonide | US11760775, Compound Budesonide |
Type | Small organic molecule |
Emp. Form. | C25H34O6 |
Mol. Mass. | 430.5339 |
SMILES | CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CO |r,c:15,t:11| |
Structure |
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