Reaction Details |
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Target | Adenosine kinase |
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Ligand | BDBM50143575 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_31117 |
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IC50 | >1±n/a nM |
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Citation | Bauser, M; Delapierre, G; Hauswald, M; Flessner, T; D'Urso, D; Hermann, A; Beyreuther, B; De Vry, J; Spreyer, P; Reissmüller, E; Meier, H Discovery and optimization of 2-aryl oxazolo-pyrimidines as adenosine kinase inhibitors using liquid phase parallel synthesis. Bioorg Med Chem Lett14:1997-2000 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Adenosine kinase |
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Name: | Adenosine kinase |
Synonyms: | ADK | ADK_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 40545.97 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1467841 |
Residue: | 362 |
Sequence: | MAAAEEEPKPKKLKVEAPQALRENILFGMGNPLLDISAVVDKDFLDKYSLKPNDQILAED
KHKELFDELVKKFKVEYHAGGSTQNSIKVAQWMIQQPHKAATFFGCIGIDKFGEILKRKA
AEAHVDAHYYEQNEQPTGTCAACITGDNRSLIANLAAANCYKKEKHLDLEKNWMLVEKAR
VCYIAGFFLTVSPESVLKVAHHASENNRIFTLNLSAPFISQFYKESLMKVMPYVDILFGN
ETEAATFAREQGFETKDIKEIAKKTQALPKMNSKRQRIVIFTQGRDDTIMATESEVTAFA
VLDQDQKEIIDTNGAGDAFVGGFLSQLVSDKPLTECIRAGHYAASIIIRRTGCTFPEKPD
FH
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BDBM50143575 |
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n/a |
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Name | BDBM50143575 |
Synonyms: | 7-(1-Benzyl-hexahydro-pyrrolo[3,4-b]pyrrol-5-yl)-2-pyridin-4-yl-oxazolo[5,4-d]pyrimidine | CHEMBL369374 |
Type | Small organic molecule |
Emp. Form. | C23H22N6O |
Mol. Mass. | 398.4604 |
SMILES | C(N1CCC2CN(CC12)c1ncnc2oc(nc12)-c1ccncc1)c1ccccc1 |
Structure |
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