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Found 42 with Last Name = 'obando' and Initial = 'd'
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50083164((S)-2-[(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-pheny...)
Affinity DataKi:  1.20nMAssay Description:Antagonist activity at DORMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50323341(CHEMBL1209039)
Affinity DataKi:  8nMAssay Description:Inhibition of human CA2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50396058(CHEMBL2170198)
Affinity DataKi:  10nMAssay Description:Inhibition of human CA2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM82104(Investigational agent, 5)
Affinity DataKi:  13nMAssay Description:Inhibition of human CA2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50083164((S)-2-[(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-pheny...)
Affinity DataKi:  86nMAssay Description:Antagonist activity at MORMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-lysosomal glucosylceramidase(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50299749((2R,3R,4R,5S)-1-[5-(Adamantan-1-ylmethoxy)-pentyl]...)
Affinity DataIC50:  0.300nMAssay Description:Inhibition of non-lysosomal glucosylceramidase in cultured melanoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-lysosomal glucosylceramidase(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50299749((2R,3R,4R,5S)-1-[5-(Adamantan-1-ylmethoxy)-pentyl]...)
Affinity DataIC50:  2nMAssay Description:Inhibition of non-lysosomal glucosylceramidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVitamin D3 receptor(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50396056(CHEMBL2170202)
Affinity DataIC50:  3nMAssay Description:Transactivation of VDR expressed in COS7 cells assessed as reduction in 1,25-dihydroxyvitamin D3-induced transcriptional activity by transient transc...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50:  10nMAssay Description:Inhibition of mouse recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Rattus norvegicus)
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50:  11nMAssay Description:Inhibition of rat recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-lysosomal glucosylceramidase(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM18355((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...)
Affinity DataIC50:  300nMAssay Description:Inhibition of non-lysosomal glucosylceramidase in cultured melanoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180984(1,12-Bis(tripentyl ammonium)dodecane dibromide | C...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180993(1,12-Bis(tripropyl ammonium)dodecane dibromide | C...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180985(1,12-Bis(trihexyl ammonium)dodecane dichloride | C...)
Affinity DataIC50:  7.50E+3nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180987(1,12-Bis(triisopentyl ammonium)dodecane dichloride...)
Affinity DataIC50: >7.50E+3nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180986(1,12-Bis(tributyl ammonium)dodecane dichloride | C...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180992(1,12-Bis(tributyl phosphonium)dodecane dibromide |...)
Affinity DataIC50: >2.50E+4nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-lysosomal glucosylceramidase(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of non-lysosomal glucosylceramidase in cultured melanoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304136(1,12-Bis(3',4'-dipentylpyridinium)dodecane dichlor...)
Affinity DataIC50:  5.20E+4nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304137(1,12-Bis(4'-(5''-nonylpyridinium)dodecane dichlori...)
Affinity DataIC50:  5.30E+4nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304129(1,12-Bis[4'-(1''-pentenyl)pyridinium]dodecanedichl...)
Affinity DataIC50:  5.60E+4nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304130(1,12-Bis(4'-isopentylpyridinium)dodecane dichlorid...)
Affinity DataIC50:  6.70E+4nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304133(1,12-Bis[4'-(3' '-phenylpropyl)pyridinium]dodecane...)
Affinity DataIC50:  1.04E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304135(1,12-Bis(3'-methyl-4'-pentylpyridinium)dodecane di...)
Affinity DataIC50:  1.34E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180990(1,12-Bis(N-methylmorpholinium)dodecane dibromide |...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180989(1,12-Bis(trioctyl ammonium)dodecane dichloride | C...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180988(1,12-Bis(N-quinuclidlinium)dodecane dibromide | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50180991(1,12-Bis(N-butylpyrrolidinium)dodecane dichloride ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304134(1,12-Bis(4'-pyridinium propanol)dodecane dichlorid...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304132(1,12-Bis(4'-isohexylpyridinium)dodecane dichloride...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304131(1,12-Bis(4'-hexylpyridinium)dodecane dichloride | ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304126(1,12-Bis(4'-ethylpyridinium)dodecane dibromide | C...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304127(1,12-Bis-(4-tert-butylpyridinium)dodecane dibromid...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304128(1,12-Bis(4'-pentylpyridinium)dodecane dichloride |...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50060582(1,10-Bis(trimethyl ammonium)decane dibromide | 1,1...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50304125(1,1'-(dodecane-1,12-diyl)bis(4-methylpyridinium)br...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase A2, major isoenzyme(Sus scrofa (pig))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50119793(1,1'-(dodecane-1,12-diyl)dipyridinium bromide | 1,...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of porcine pancreatic PLA2 after 1 hr by radiometric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50060533(1,12-Bis(trimethyl ammonium)dodecane dibromide | 1...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50084929(1,12-Bis(triethyl ammonium)dodecane dibromide | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospholipase B(Cryptococcus neoformans)
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50084949(1,12-Bis(N-methylpyrrolidinium)dodecane dibromide ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cryptococccus neoformans H99 PLB1activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMediator of RNA polymerase II transcription subunit 23(Homo sapiens (Human))
University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50396057(CHEMBL2170196)
Affinity DataKd:  1.80E+3nMAssay Description:Binding affinity to Sur2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed