Reaction Details |
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Target | Cell division cycle 7-related protein kinase |
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Ligand | BDBM50279143 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_546026 (CHEMBL1034201) |
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IC50 | 30±n/a nM |
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Citation | Ermoli, A; Bargiotti, A; Brasca, MG; Ciavolella, A; Colombo, N; Fachin, G; Isacchi, A; Menichincheri, M; Molinari, A; Montagnoli, A; Pillan, A; Rainoldi, S; Sirtori, FR; Sola, F; Thieffine, S; Tibolla, M; Valsasina, B; Volpi, D; Santocanale, C; Vanotti, E Cell division cycle 7 kinase inhibitors: 1H-pyrrolo[2,3-b]pyridines, synthesis and structure-activity relationships. J Med Chem52:4380-90 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cell division cycle 7-related protein kinase |
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Name: | Cell division cycle 7-related protein kinase |
Synonyms: | CDC7 | CDC7-related kinase | CDC7L1 | CDC7_HUMAN | Cell division cycle 7-related protein kinase (CDC7) | HsCdc7 | huCdc7 |
Type: | Protein |
Mol. Mass.: | 63908.16 |
Organism: | Homo sapiens (Human) |
Description: | O00311 |
Residue: | 574 |
Sequence: | MEASLGIQMDEPMAFSPQRDRFQAEGSLKKNEQNFKLAGVKKDIEKLYEAVPQLSNVFKI
EDKIGEGTFSSVYLATAQLQVGPEEKIALKHLIPTSHPIRIAAELQCLTVAGGQDNVMGV
KYCFRKNDHVVIAMPYLEHESFLDILNSLSFQEVREYMLNLFKALKRIHQFGIVHRDVKP
SNFLYNRRLKKYALVDFGLAQGTHDTKIELLKFVQSEAQQERCSQNKSHIITGNKIPLSG
PVPKELDQQSTTKASVKRPYTNAQIQIKQGKDGKEGSVGLSVQRSVFGERNFNIHSSISH
ESPAVKLMKQSKTVDVLSRKLATKKKAISTKVMNSAVMRKTASSCPASLTCDCYATDKVC
SICLSRRQQVAPRAGTPGFRAPEVLTKCPNQTTAIDMWSAGVIFLSLLSGRYPFYKASDD
LTALAQIMTIRGSRETIQAAKTFGKSILCSKEVPAQDLRKLCERLRGMDSSTPKLTSDIQ
GHASHQPAISEKTDHKASCLVQTPPGQYSGNSFKKGDSNSCEHCFDEYNTNLEGWNEVPD
EAYDLLDKLLDLNPASRITAEEALLHPFFKDMSL
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BDBM50279143 |
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n/a |
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Name | BDBM50279143 |
Synonyms: | (Z)-2-(3-Methylphenyl)-5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethylene)-3,5-dihydro-4H-imidazol-4-one | CHEMBL523244 |
Type | Small organic molecule |
Emp. Form. | C18H14N4O |
Mol. Mass. | 302.33 |
SMILES | Cc1cccc(c1)C1=NC(=Cc2c[nH]c3ncccc23)C(=O)N1 |w:10.11,t:8| |
Structure |
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