BDBM50178961 CHEMBL2385268

SMILES CC1(C)CC=C(c2ccccc2)c2cc(\C=C\c3ccc(cc3)C(O)=O)ccc12

InChI Key InChIKey=VUODRPPTYLBGFM-CMDGGOBGSA-N

Data  1 KI  1 EC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50178961   

TargetRetinoic acid receptor RXR-alpha/alpha(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL

LigandBDBM50178961(CHEMBL2385268)Copy SMILESCopy InChI

Affinity DataKi:  7.70nMAssay Description:Displacement of [3H]-TTNPB from RARalpha/RXRalpha (unknown origin) expressed in baculovirus expression system by scintillation proximity assayMore data for this Ligand-Target Pair

Target InfoPDBMMDBReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaantibodypediaGoogleScholar

Ligand InfoPurchaseCHEMBLPC cidPC sidSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI

TargetNuclear receptor subfamily 2 group E member 1(Homo sapiens)TBA

LigandBDBM50178961(CHEMBL2385268)Copy SMILESCopy InChI

Affinity DataEC50:  200nMAssay Description:Inhibitory activity against Dihydrofolate reductase of Escherichia coliMore data for this Ligand-Target Pair

Target InfoPDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
DrugBankGoogleScholar

Ligand InfoPurchaseCHEMBLPC cidPC sidSimilars

In DepthDetails PubMed
Copy BDB DOI