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TargetGTPase HRas
LigandBDBM50089978
Substrate/Competitorn/a
Meas. Tech.ChEMBL_82664
IC50 20±n/a nM
Citation Baraldi PGRomagnoli RBeria ICozzi PGeroni CMongelli NBianchi NMischiati CGambari R Synthesis and antitumor activity of new benzoheterocyclic derivatives of distamycin A. J Med Chem 43:2675-84 (2000) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
GTPase HRas
Name:GTPase HRas
Synonyms:GTPase HRas, N-terminally processed | H-Ras | H-Ras-1 | HRAS1 | Ha-Ras | His6-Ha-Ras-CVLS | 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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  Blast E-value cutoff:
BDBM50089978
n/a
NameBDBM50089978
Synonyms:5-[Bis-(2-chloro-ethyl)-amino]-1H-indole-2-carboxylic acid (5-{5-[5-(2-carbamimidoyl-ethylcarbamoyl)-1-methyl-1H-pyrrol-3-ylcarbamoyl]-1-methyl-1H-pyrrol-3-ylcarbamoyl}-1-methyl-1H-pyrrol-3-yl)-amide; hydrochloride | CHEMBL536328
TypeSmall organic molecule
Emp. Form.C34H39Cl2N11O4
Mol. Mass.736.651
SMILESCn1cc(NC(=O)c2cc(NC(=O)c3cc(NC(=O)c4cc5cc(ccc5[nH]4)N(CCCl)CCCl)cn3C)cn2C)cc1C(=O)NCCC(N)=N
Structure
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