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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase kinase kinase kinase 2 | ||
| Ligand | BDBM51878 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | Dose Response Confirmation via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | ||
| EC50 | 9160±n/a nM | ||
| Citation |  PubChem, PC Dose Response Confirmation via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype PubChem Bioassay(2009)[AID] | ||
| More Info.: | Get all data from this article, Solution Info, Assay Method | ||
| Mitogen-activated protein kinase kinase kinase kinase 2 | |||
| Name: | Mitogen-activated protein kinase kinase kinase kinase 2 | ||
| Synonyms: | 2.7.11.1 | B lymphocyte serine/threonine-protein kinase | GC kinase | GCK | Germinal center kinase | M4K2_HUMAN | MAP4K2 | MAPK/ERK kinase kinase kinase 2 | MEK kinase kinase 2 | MEKKK 2 | RAB8IP | Rab8-interacting protein | ||
| Type: | n/a | ||
| Mol. Mass.: | 91551.35 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | n/a | ||
| Residue: | 820 | ||
| Sequence: |
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| BDBM51878 | |||
| n/a | |||
| Name | BDBM51878 | ||
| Synonyms: | 2,6-bis(iodanyl)-4-[2-(1,3,3-trimethylindol-2-ylidene)ethenyl]phenol | 2,6-diiodo-4-[2-(1,3,3-trimethyl-2-indolylidene)ethenyl]phenol | 2,6-diiodo-4-[2-(1,3,3-trimethylindol-2-ylidene)ethenyl]phenol | 2,6-diiodo-4-[2-(1,3,3-trimethylindolin-2-ylidene)vinyl]phenol | MLS000737639 | SMR000393809 | cid_233331 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C19H17I2NO | ||
| Mol. Mass. | 529.1533 | ||
| SMILES | CN1C(=C=Cc2cc(I)c(O)c(I)c2)C(C)(C)c2ccccc12 |(7.68,-1.39,;7.2,.08,;8.1,1.32,;9.64,1.32,;11.18,1.32,;11.95,-.02,;11.18,-1.35,;11.95,-2.69,;11.18,-4.02,;13.49,-2.69,;14.26,-4.02,;14.26,-1.35,;15.8,-1.35,;13.49,-.02,;7.2,2.55,;8.45,3.46,;6.73,4.02,;5.75,2.09,;4.41,2.86,;3.08,2.09,;3.08,.55,;4.41,-.22,;5.75,.55,)| | ||
| Structure | 
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