BDBM13015 2-amino-1-phenylethan-1-ol::phenylethanolamine

SMILES NCC(O)c1ccccc1

InChI Key InChIKey=ULSIYEODSMZIPX-UHFFFAOYSA-N

Data  2 KI  1 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 13015   

TargetAlpha-1A adrenergic receptor(Rat)
TBA

Curated by PDSP K_i Database

LigandBDBM13015(2-amino-1-phenylethan-1-ol | phenylethanolamine)Copy SMILESCopy InChI

Affinity DataKi:  1.10E+3nMMore data for this Ligand-Target Pair

Target InfoPDBReactome pathwayKEGG
UniProtKB/SwissProt
GoogleScholar

Ligand InfoPurchaseChEBI
KEGGPC cidPC sidSimilars

In DepthDetails PubMed
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TargetAlpha-1A adrenergic receptor(Rat)
TBA

Curated by PDSP K_i Database

LigandBDBM13015(2-amino-1-phenylethan-1-ol | phenylethanolamine)Copy SMILESCopy InChI

Affinity DataKi:  2.30E+4nMMore data for this Ligand-Target Pair

Target InfoPDBReactome pathwayKEGG
UniProtKB/SwissProt
GoogleScholar

Ligand InfoPurchaseChEBI
KEGGPC cidPC sidSimilars

In DepthDetails PubMed
Copy BDB DOI
Copy reaction URL

TargetNeuraminidase(Influenza A virus)
Shanghai Institute of Technology

Curated by ChEMBL

LigandBDBM13015(2-amino-1-phenylethan-1-ol | phenylethanolamine)Copy SMILESCopy InChI

Affinity DataIC50:  8.70E+5nMAssay Description:Inhibition of Influenza A H1N1 virus neuraminidase activity preincubated for 2 mins followed by MUNANA substrate addition measured after 30 mins by f...More data for this Ligand-Target Pair

Target InfoPDBMMDB
UniProtKB/SwissProt
B.MOADGoogleScholar

Ligand InfoPurchaseChEBI
KEGGPC cidPC sidSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI
Copy reaction URL