BDBM50279677 CHEMBL4170654

SMILES Cc1cc(Cl)cc(CNC(=O)Nc2ccc3COB(O)c3c2)c1

InChI Key InChIKey=ZQVWAERNZDQQOS-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50279677   

TargetCarbonic anhydrase(Candida glabrata)
University Of Montpellier

Curated by ChEMBL
LigandPNGBDBM50279677(CHEMBL4170654)
Affinity DataKi:  79nMAssay Description:Inhibition of Candida glabrata Nce103 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Montpellier

Curated by ChEMBL
LigandPNGBDBM50279677(CHEMBL4170654)
Affinity DataKi:  276nMAssay Description:Inhibitory activity against human liver Dihydrodipicolinate reductase (DHPR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Montpellier

Curated by ChEMBL
LigandPNGBDBM50279677(CHEMBL4170654)
Affinity DataKi:  276nMAssay Description:Inhibition of human carbonic anhydrase 2 incubated for 30 mins prior to testing measured for 10 to 100 secs by phenol red-based stopped-flow CO2 hydr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Cryptococcus neoformans var. grubii (Filobasidiell...)
University Of Montpellier

Curated by ChEMBL
LigandPNGBDBM50279677(CHEMBL4170654)
Affinity DataKi:  400nMAssay Description:Inhibition of Cryptococcus neoformans Can2 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
University Of Montpellier

Curated by ChEMBL
LigandPNGBDBM50279677(CHEMBL4170654)
Affinity DataKi:  570nMAssay Description:Inhibitory activity against human liver Dihydrodipicolinate reductase (DHPR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed