| Reaction Details |
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 | Report a problem with these data |
| Target | Cell division cycle 7-related protein kinase |
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| Ligand | BDBM50443666 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1277971 (CHEMBL3095009) |
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| IC50 | 730±n/a nM |
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| Citation |  Harrington, PE; Bourbeau, MP; Fotsch, C; Frohn, M; Pickrell, AJ; Reichelt, A; Sham, K; Siegmund, AC; Bailis, JM; Bush, T; Escobar, S; Hickman, D; Heller, S; Hsieh, F; Orf, JN; Rong, M; San Miguel, T; Tan, H; Zalameda, L; Allen, JG The optimization of aminooxadiazoles as orally active inhibitors of Cdc7. Bioorg Med Chem Lett23:6396-400 (2013) [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 |
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| Synonyms: | CDC7 | CDC7-related kinase | CDC7L1 | CDC7_HUMAN | Cell division cycle 7-related protein kinase (CDC7) | HsCdc7 | huCdc7 |
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| Type: | Protein |
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| Mol. Mass.: | 63908.16 |
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| Organism: | Homo sapiens (Human) |
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| Description: | O00311 |
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| Residue: | 574 |
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| Sequence: | MEASLGIQMDEPMAFSPQRDRFQAEGSLKKNEQNFKLAGVKKDIEKLYEAVPQLSNVFKI
EDKIGEGTFSSVYLATAQLQVGPEEKIALKHLIPTSHPIRIAAELQCLTVAGGQDNVMGV
KYCFRKNDHVVIAMPYLEHESFLDILNSLSFQEVREYMLNLFKALKRIHQFGIVHRDVKP
SNFLYNRRLKKYALVDFGLAQGTHDTKIELLKFVQSEAQQERCSQNKSHIITGNKIPLSG
PVPKELDQQSTTKASVKRPYTNAQIQIKQGKDGKEGSVGLSVQRSVFGERNFNIHSSISH
ESPAVKLMKQSKTVDVLSRKLATKKKAISTKVMNSAVMRKTASSCPASLTCDCYATDKVC
SICLSRRQQVAPRAGTPGFRAPEVLTKCPNQTTAIDMWSAGVIFLSLLSGRYPFYKASDD
LTALAQIMTIRGSRETIQAAKTFGKSILCSKEVPAQDLRKLCERLRGMDSSTPKLTSDIQ
GHASHQPAISEKTDHKASCLVQTPPGQYSGNSFKKGDSNSCEHCFDEYNTNLEGWNEVPD
EAYDLLDKLLDLNPASRITAEEALLHPFFKDMSL
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| BDBM50443666 |
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| n/a |
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| Name | BDBM50443666 |
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| Synonyms: | CHEMBL3093058 |
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| Type | Small organic molecule |
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| Emp. Form. | C16H13N5O |
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| Mol. Mass. | 291.3073 |
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| SMILES | C(Nc1nnc(o1)-c1ccc2[nH]ncc2c1)c1ccccc1 |
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| Structure | 
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