Compile Data Set for Download or QSAR
maximum 50k data
Found 16 of ic50 for monomerid = 50131046
TargetCytochrome P450 1A2(Homo sapiens (Human))
National Research Institute Of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  22nMAssay Description:Inhibition of Cytochrome P450 1A2 enzyme in bacterial membrane expressing human P450sMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1B1(Homo sapiens (Human))
National Research Institute Of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  55nMAssay Description:Inhibition of Cytochrome P450 1B1 enzyme in bacterial membrane expressing human P450sMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1B1(Homo sapiens (Human))
National Research Institute Of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  55nMAssay Description:Inhibition of human CYP1B1 expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A1(Homo sapiens (Human))
National Research Institute Of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  260nMAssay Description:Inhibition of Cytochrome P450 1A1 enzyme in bacterial membrane expressing human P450sMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Devi Ahilya Vishwavidyalaya

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  280nMAssay Description:Inhibition of COX2 in BMMC cells assessed as PGD2 generationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Devi Ahilya Vishwavidyalaya

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  300nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Homo sapiens (Human))
Changzhou University

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  1.23E+3nMAssay Description:Inhibition of PDE5A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Devi Ahilya Vishwavidyalaya

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  8.70E+3nMAssay Description:Inhibition of COX1 in BMMC cells assessed as PGD2 generationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Devi Ahilya Vishwavidyalaya

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  8.70E+3nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  2.78E+4nMAssay Description:Inhibition of human MMP9 by quenched fluorescense assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  6.76E+4nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center Affiliation: UT Southwestern Assay Provider: David Mangelsdorf,...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetNuclear hormone receptor family member daf-12(Caenorhabditis elegans)
The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50:  6.76E+4nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center Affiliation: UT Southwestern Assay Provider: David Mangelsdorf,...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50: >1.00E+5nMAssay Description:inhibition of electic eel AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Anhui Medical University

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Anhui Medical University

Curated by ChEMBL
LigandPNGBDBM50131046(8,13-Dihydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quin...)
Affinity DataIC50: >1.00E+5nMAssay Description:inhibition of equine serum BuChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed