Reaction Details |
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Target | GTPase HRas |
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Ligand | BDBM50287947 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_143166 |
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IC50 | 16000±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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BDBM50287947 |
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n/a |
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Name | BDBM50287947 |
Synonyms: | (E)-4-[(2R,6R)-6-(4-Chloro-6-methoxy-3-methyl-pyrazolo[3,4-b]quinolin-1-yl)-4-(2-nitro-phenylsulfanyl)-morpholin-2-yl]-but-2-enoic acid ethyl ester | CHEMBL299877 |
Type | Small organic molecule |
Emp. Form. | C28H28ClN5O6S |
Mol. Mass. | 598.07 |
SMILES | CCOC(=O)\C=C\C[C@@H]1CN(C[C@@H](O1)n1nc(C)c2c(Cl)c3cc(OC)ccc3nc12)Sc1ccccc1[N+]([O-])=O |
Structure |
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