Reaction Details |
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Target | Serine/threonine-protein kinase PAK 4 |
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Ligand | BDBM50591934 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2202751 (CHEMBL5115459) |
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IC50 | 96±n/a nM |
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Citation | Sun, Y; Sun, Y; Wang, L; Wu, T; Yin, W; Wang, J; Xue, Y; Qin, Q; Sun, Y; Yang, H; Zhao, D; Cheng, M Design, synthesis, and biological evaluation of novel pyrazolo [3,4-d]pyrimidine derivatives as potent PLK4 inhibitors for the treatment of TRIM37-amplified breast cancer. 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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Serine/threonine-protein kinase PAK 4 |
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Name: | Serine/threonine-protein kinase PAK 4 |
Synonyms: | KIAA1142 | PAK4 | PAK4_HUMAN | p21-Activated kinase 4 (PAK4) |
Type: | Protein |
Mol. Mass.: | 64098.01 |
Organism: | Homo sapiens (Human) |
Description: | O96013 |
Residue: | 591 |
Sequence: | MFGKRKKRVEISAPSNFEHRVHTGFDQHEQKFTGLPRQWQSLIEESARRPKPLVDPACIT
SIQPGAPKTIVRGSKGAKDGALTLLLDEFENMSVTRSNSLRRDSPPPPARARQENGMPEE
PATTARGGPGKAGSRGRFAGHSEAGGGSGDRRRAGPEKRPKSSREGSGGPQESSRDKRPL
SGPDVGTPQPAGLASGAKLAAGRPFNTYPRADTDHPSRGAQGEPHDVAPNGPSAGGLAIP
QSSSSSSRPPTRARGAPSPGVLGPHASEPQLAPPACTPAAPAVPGPPGPRSPQREPQRVS
HEQFRAALQLVVDPGDPRSYLDNFIKIGEGSTGIVCIATVRSSGKLVAVKKMDLRKQQRR
ELLFNEVVIMRDYQHENVVEMYNSYLVGDELWVVMEFLEGGALTDIVTHTRMNEEQIAAV
CLAVLQALSVLHAQGVIHRDIKSDSILLTHDGRVKLSDFGFCAQVSKEVPRRKSLVGTPY
WMAPELISRLPYGPEVDIWSLGIMVIEMVDGEPPYFNEPPLKAMKMIRDNLPPRLKNLHK
VSPSLKGFLDRLLVRDPAQRATAAELLKHPFLAKAGPPASIVPLMRQNRTR
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BDBM50591934 |
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n/a |
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Name | BDBM50591934 |
Synonyms: | CHEMBL5209160 |
Type | Small organic molecule |
Emp. Form. | C16H14F2N8 |
Mol. Mass. | 356.3328 |
SMILES | Cc1cc(Nc2nc(NCc3ccc(F)cc3F)nc3[nH]ncc23)n[nH]1 |
Structure |
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