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SMILES COc1ccc(cc1C(=O)NCC1CCCN1C)S(N)(=O)=O

InChI Key InChIKey=QCKAYJICSQJJCU-UHFFFAOYSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 10889   

TargetCarbonic anhydrase 5B, mitochondrial(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2902200PubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2902200PubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2TQBPubMed
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  174nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2902200PubMed
TargetCARBONIC ANHYDRASE(Helicobacter pylori J99)
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  204nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2TQBPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2TQBPubMed
TargetBeta-carbonic anhydrase 1(Mycobacterium tuberculosis)
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  2.30E+3nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7SBRPubMed
TargetCarbonic anhydrase(Mycobacterium tuberculosis)
Kochi Medical School

LigandPNGBDBM10889(2-methoxy-N-[(1-methylpyrrolidin-2-yl)methyl]-5-su...)copy SMILEScopy InChI
Affinity DataKi:  7.92E+3nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8J2GPubMed