Reaction Details |
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Target | GTPase HRas |
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Ligand | BDBM50287944 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_143166 |
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IC50 | 10000±n/a nM |
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Citation | Wolin, R; Wang, D; Kelly, J; Afonso, A; James, L; Kirschmeier, P; McPhail, AT Synthesis and evaluation of pyrazolo[3,4-b]quinoline ribofuranosides and their derivatives as inhibitors of oncogenic Ras Bioorg Med Chem Lett6:195-200 (1996) Article |
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More Info.: | Get all data from this article, Assay Method |
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GTPase HRas |
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Name: | GTPase HRas |
Synonyms: | GTPase HRas, N-terminally processed | H-Ras | H-Ras-1 | HRAS | HRAS1 | Ha-Ras | His6-Ha-Ras-CVLS | RASH_HUMAN | Transforming protein p21 | Transforming protein p21/H-Ras-1 | Wild-type Ha-Ras | c-H-ras | p21ras |
Type: | Other Protein Type |
Mol. Mass.: | 21293.37 |
Organism: | Homo sapiens (Human) |
Description: | P01112 |
Residue: | 189 |
Sequence: | MTEYKLVVVGAGGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTAG
QEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHQYREQIKRVKDSDDVPMVLVGNKCDL
AARTVESRQAQDLARSYGIPYIETSAKTRQGVEDAFYTLVREIRQHKLRKLNPPDESGPG
CMSCKCVLS
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BDBM50287944 |
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n/a |
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Name | BDBM50287944 |
Synonyms: | (E)-3-[(2S,3S,4R,5R)-5-(4-Chloro-6-methoxy-3-methyl-pyrazolo[3,4-b]quinolin-1-yl)-3,4-dihydroxy-tetrahydro-furan-2-yloxy]-1-phenyl-propenone | CHEMBL304637 |
Type | Small organic molecule |
Emp. Form. | C25H22ClN3O6 |
Mol. Mass. | 495.912 |
SMILES | COc1ccc2nc3n(nc(C)c3c(Cl)c2c1)[C@@H]1O[C@H](O\C=C\C(=O)c2ccccc2)[C@@H](O)[C@H]1O |
Structure |
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