Reaction Details |
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Target | Target of rapamycin complex 2 subunit MAPKAP1 |
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Ligand | BDBM582478 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2261205 (CHEMBL5216216) |
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IC50 | 11±n/a nM |
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Citation | Oleksak, P; Nepovimova, E; Chrienova, Z; Musilek, K; Patocka, J; Kuca, K Contemporary mTOR inhibitor scaffolds to diseases breakdown: A patent review (2015-2021). Eur J Med Chem238:0 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Target of rapamycin complex 2 subunit MAPKAP1 |
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Name: | Target of rapamycin complex 2 subunit MAPKAP1 |
Synonyms: | MAPKAP1 | MIP1 | Mitogen-activated protein kinase 2-associated protein 1 | SAPK-interacting protein 1 | SIN1 | SIN1_HUMAN | Stress-activated map kinase-interacting protein 1 | TORC2 subunit MAPKAP1 | Target of rapamycin complex 2 subunit MAPKAP1 | mSIN1 |
Type: | PROTEIN |
Mol. Mass.: | 59129.70 |
Organism: | Homo sapiens |
Description: | ChEMBL_119716 |
Residue: | 522 |
Sequence: | MAFLDNPTIILAHIRQSHVTSDDTGMCEMVLIDHDVDLEKIHPPSMPGDSGSEIQGSNGE
TQGYVYAQSVDITSSWDFGIRRRSNTAQRLERLRKERQNQIKCKNIQWKERNSKQSAQEL
KSLFEKKSLKEKPPISGKQSILSVRLEQCPLQLNNPFNEYSKFDGKGHVGTTATKKIDVY
LPLHSSQDRLLPMTVVTMASARVQDLIGLICWQYTSEGREPKLNDNVSAYCLHIAEDDGE
VDTDFPPLDSNEPIHKFGFSTLALVEKYSSPGLTSKESLFVRINAAHGFSLIQVDNTKVT
MKEILLKAVKRRKGSQKVSGPQYRLEKQSEPNVAVDLDSTLESQSAWEFCLVRENSSRAD
GVFEEDSQIDIATVQDMLSSHHYKSFKVSMIHRLRFTTDVQLGISGDKVEIDPVTNQKAS
TKFWIKQKPISIDSDLLCACDLAEEKSPSHAIFKLTYLSNHDYKHLYFESDAATVNEIVL
KVNYILESRASTARADYFAQKQRKLNRRTSFSFQKEKKSGQQ
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BDBM582478 |
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n/a |
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Name | BDBM582478 |
Synonyms: | 5-(2-aminobenzoxazol-5-yl)-7-isobutyl-6, 7-dihydro-5H-pyrrolo[3,2-d]pyrimidin-4-ylamine | US11518767, Example 3 |
Type | Small organic molecule |
Emp. Form. | C17H20N6O |
Mol. Mass. | 324.3803 |
SMILES | CC(C)CC1CN(c2c1ncnc2N)c1ccc2oc(N)nc2c1 |
Structure |
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