BDBM50664150 CHEMBL6149416

SMILES C=CS(=O)(=O)NCCCC(=O)NCCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)C[C@@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CC(C)(CC)NC(=O)CN1C/C=CCCCC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCC(=O)O)C1=O)C(=O)N[C@@H](CCCCN)C(=O)NCCC(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(N)=O

InChI Key InChIKey=RVQBRLKZQGOCSK-UHFFFAOYSA-N

Data  1 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50664150   

TargetGTPase HRas(Human)
Second Military Medical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664150BDBM50664150(CHEMBL6149416)
Affinity DataKd:  4.10E+3nMAssay Description:Binding affinity to wild-type H-Ras (unknown origin) assessed as dissociation constant by fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed