BDBM50234661 CHEBI:76227::CHEMBL1619630

SMILES OC(=O)[C@@H]1CCn2c1ccc2C(=O)c1ccccc1

InChI Key InChIKey=OZWKMVRBQXNZKK-LLVKDONJSA-N

Data  3 IC50

PDB links: 2 PDB IDs match this monomer.

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50234661   

TargetCell division control protein 42 homolog/Ras-related C3 botulinum toxin substrate 1(Homo sapiens (Human))
Kagoshima University

Curated by ChEMBL

LigandBDBM50234661(CHEBI:76227 | CHEMBL1619630)Copy SMILESCopy InChI

Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of RAC1/CDC42 in human ovarian cancer cellsMore data for this Ligand-Target Pair

Target InfoPDBMMDBReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaantibodypediaGoogleScholar

Ligand InfoPurchaseCHEMBLMCE
KEGGPC cidPC sidPDBSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI

TargetProstaglandin G/H synthase 1(Homo sapiens (Human))TBA

LigandBDBM50234661(CHEBI:76227 | CHEMBL1619630)Copy SMILESCopy InChI

Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human COX1More data for this Ligand-Target Pair

Target InfoPDBReactome pathway
UniProtKB/SwissProt
antibodypediaGoogleScholar

Ligand InfoPurchaseCHEMBLMCE
KEGGPC cidPC sidPDBSimilars

In DepthDetails PubMed
Copy BDB DOI

TargetProstaglandin G/H synthase 2(Homo sapiens (Human))TBA

LigandBDBM50234661(CHEBI:76227 | CHEMBL1619630)Copy SMILESCopy InChI

Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human COX2More data for this Ligand-Target Pair

Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar

Ligand InfoPurchaseCHEMBLMCE
KEGGPC cidPC sidPDBSimilars

In DepthDetails PubMed
Copy BDB DOI