BDBM26142 (2-phenylethyl)boranediol::Alkylboronic Acid, 21

SMILES OB(O)CCc1ccccc1

InChI Key InChIKey=VPRUMANMDWQMNF-UHFFFAOYSA-N

Data  9 KI  1 IC50

PDB links: 1 PDB ID matches this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 26142   

TargetSubtilisin BL(Bacillus lentus)
TBA

Curated by ChEMBL
LigandPNGBDBM26142((2-phenylethyl)boranediol | Alkylboronic Acid, 21)
Affinity DataKi:  9.50E+4nMAssay Description:Competitive inhibition of Subtilisin BL M222S-mutated enzyme from B. lentusMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSubtilisin BL(Bacillus lentus)
TBA

Curated by ChEMBL
LigandPNGBDBM26142((2-phenylethyl)boranediol | Alkylboronic Acid, 21)
Affinity DataKi:  2.41E+5nMAssay Description:Competitive inhibition of Subtilisin BL M222C-mutated enzyme from B. lentusMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSubtilisin Carlsberg(Bacillus licheniformis)
TBA

Curated by ChEMBL
LigandPNGBDBM26142((2-phenylethyl)boranediol | Alkylboronic Acid, 21)
Affinity DataKi:  2.57E+5nMAssay Description:Competitive inhibition of Subtilisin Carlsberg enzyme from B. lentusMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSubtilisin BL(Bacillus lentus)
TBA

Curated by ChEMBL
LigandPNGBDBM26142((2-phenylethyl)boranediol | Alkylboronic Acid, 21)
Affinity DataKi:  8.01E+5nMAssay Description:Competitive inhibition of Subtilisin BL wild type enzyme from B. lentusMore data for this Ligand-Target Pair
In DepthDetails Article