Reaction Details |
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Target | Phosphoenolpyruvate carboxykinase, cytosolic [GTP] |
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Ligand | BDBM50214002 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_438956 (CHEMBL889299) |
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IC50 | 1250±n/a nM |
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Citation | Pietranico, SL; Foley, LH; Huby, N; Yun, W; Dunten, P; Vermeulen, J; Wang, P; Toth, K; Ramsey, G; Gubler, ML; Wertheimer, SJ C-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase. Bioorg Med Chem Lett17:3835-9 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phosphoenolpyruvate carboxykinase, cytosolic [GTP] |
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Name: | Phosphoenolpyruvate carboxykinase, cytosolic [GTP] |
Synonyms: | PCK1 | PCKGC_HUMAN | PEPCK1 | Phosphoenolpyruvate carboxykinase cytosolic |
Type: | PROTEIN |
Mol. Mass.: | 69189.74 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_438956 |
Residue: | 622 |
Sequence: | MPPQLQNGLNLSAKVVQGSLDSLPQAVREFLENNAELCQPDHIHICDGSEEENGRLLGQM
EEEGILRRLKKYDNCWLALTDPRDVARIESKTVIVTQEQRDTVPIPKTGLSQLGRWMSEE
DFEKAFNARFPGCMKGRTMYVIPFSMGPLGSPLSKIGIELTDSPYVVASMRIMTRMGTPV
LEAVGDGEFVKCLHSVGCPLPLQKPLVNNWPCNPELTLIAHLPDRREIISFGSGYGGNSL
LGKKCFALRMASRLAKEEGWLAEHMLILGITNPEGEKKYLAAAFPSACGKTNLAMMNPSL
PGWKVECVGDDIAWMKFDAQGHLRAINPENGFFGVAPGTSVKTNPNAIKTIQKNTIFTNV
AETSDGGVYWEGIDEPLASGVTITSWKNKEWSSEDGEPCAHPNSRFCTPASQCPIIDAAW
ESPEGVPIEGIIFGGRRPAGVPLVYEALSWQHGVFVGAAMRSEATAAAEHKGKIIMHDPF
AMRPFFGYNFGKYLAHWLSMAQHPAAKLPKIFHVNWFRKDKEGKFLWPGFGENSRVLEWM
FNRIDGKASTKLTPIGYIPKEDALNLKGLGHINMMELFSISKEFWEKEVEDIEKYLEDQV
NADLPCEIEREILALKQRISQM
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BDBM50214002 |
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n/a |
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Name | BDBM50214002 |
Synonyms: | CHEMBL244590 | N-(4-((1-(2-fluorobenzyl)-3-(cyclopropylmethyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl)methyl)phenyl)methanesulfonamide |
Type | Small organic molecule |
Emp. Form. | C24H24FN5O4S |
Mol. Mass. | 497.542 |
SMILES | CS(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 |
Structure |
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