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Found 48 with Last Name = 'deodato' and Initial = 'd'
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254171(CHEMBL4069120)
Affinity DataKi:  220nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254176(CHEMBL3040884)
Affinity DataKi:  1.41E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254177(CHEMBL3040820)
Affinity DataKi:  1.78E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50015298(CHEMBL3263104)
Affinity DataKi:  2.50E+4nMAssay Description:Inhibition of human neprilysin by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254178(CHEMBL3558827)
Affinity DataKi:  3.13E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254180(CHEMBL3558806)
Affinity DataKi:  3.48E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254181(CHEMBL3558803)
Affinity DataKi:  3.58E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50015297(CHEMBL3263103)
Affinity DataKi:  3.70E+4nMAssay Description:Inhibition of human neprilysin by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254182(CHEMBL3040830)
Affinity DataKi:  4.20E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254179(CHEMBL3558802)
Affinity DataKi:  4.53E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254183(CHEMBL575667)
Affinity DataKi:  5.08E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Universit£

Curated by ChEMBL
LigandPNGBDBM50500854(CHEMBL3786553)
Affinity DataIC50:  5nMAssay Description:Inhibition of recombinant HIV1 His-tagged p66/p51 reverse transcriptase expressed in Escherichia coli assessed as reduction in [3H]dTTP incorporation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Universit£

Curated by ChEMBL
LigandPNGBDBM50500855(CHEMBL3786368)
Affinity DataIC50:  7.90nMAssay Description:Inhibition of recombinant HIV1 His-tagged p66/p51 reverse transcriptase expressed in Escherichia coli assessed as reduction in [3H]dTTP incorporation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Universit£

Curated by ChEMBL
LigandPNGBDBM50500853(CHEMBL3786696)
Affinity DataIC50:  17nMAssay Description:Inhibition of recombinant HIV1 His-tagged p66/p51 reverse transcriptase expressed in Escherichia coli assessed as reduction in [3H]dTTP incorporation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Universit£

Curated by ChEMBL
LigandPNGBDBM50500852(CHEMBL3787239)
Affinity DataIC50:  90nMAssay Description:Inhibition of recombinant HIV1 His-tagged p66/p51 reverse transcriptase expressed in Escherichia coli assessed as reduction in [3H]dTTP incorporation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Universit£

Curated by ChEMBL
LigandPNGBDBM1434(11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3...)
Affinity DataIC50:  125nMAssay Description:Inhibition of recombinant HIV1 His-tagged p66/p51 reverse transcriptase expressed in Escherichia coli assessed as reduction in [3H]dTTP incorporation...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254171(CHEMBL4069120)
Affinity DataIC50:  680nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM12311((1R,5S)-N-[3-Amino-1-(cyclobutylmethyl)-2,3-dioxop...)
Affinity DataIC50:  1.21E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592436(CHEMBL5179857)
Affinity DataIC50:  1.49E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592428(CHEMBL5194970)
Affinity DataIC50:  2.42E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592428(CHEMBL5194970)
Affinity DataIC50:  2.42E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592433(CHEMBL5191524)
Affinity DataIC50:  2.67E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592444(CHEMBL5201497)
Affinity DataIC50:  2.77E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592440(CHEMBL5179950)
Affinity DataIC50:  2.95E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592435(CHEMBL5186585)
Affinity DataIC50:  2.95E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592431(CHEMBL5184754)
Affinity DataIC50:  2.99E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592443(CHEMBL5189428)
Affinity DataIC50:  3.08E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592432(CHEMBL5194113)
Affinity DataIC50:  3.24E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592430(CHEMBL5170254)
Affinity DataIC50:  3.51E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254176(CHEMBL3040884)
Affinity DataIC50:  3.55E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592442(CHEMBL5202164)
Affinity DataIC50:  3.58E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592434(CHEMBL5182801)
Affinity DataIC50:  3.65E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592445(CHEMBL5205913)
Affinity DataIC50:  4.61E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592441(CHEMBL5172920)
Affinity DataIC50:  5.25E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592437(CHEMBL5205104)
Affinity DataIC50:  5.29E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592438(CHEMBL5196969)
Affinity DataIC50:  5.39E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592446(CHEMBL5171142)
Affinity DataIC50:  5.40E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254177(CHEMBL3040820)
Affinity DataIC50:  5.50E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592439(CHEMBL5202324)
Affinity DataIC50:  5.58E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50592429(CHEMBL5177181)
Affinity DataIC50:  6.22E+4nMAssay Description:Inhibition of His6-tagged SARS-CoV-2 main protease expressed in Escherichia coli BL21 (DE3) using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 as substrate pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254178(CHEMBL3558827)
Affinity DataIC50:  9.70E+4nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254180(CHEMBL3558806)
Affinity DataIC50:  1.08E+5nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254181(CHEMBL3558803)
Affinity DataIC50:  1.11E+5nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254182(CHEMBL3040830)
Affinity DataIC50:  1.30E+5nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254179(CHEMBL3558802)
Affinity DataIC50:  1.40E+5nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase(Hypocrea rufa)
University of Siena

Curated by ChEMBL
LigandPNGBDBM50254183(CHEMBL575667)
Affinity DataIC50:  1.57E+5nMAssay Description:Inhibition of Trichoderma viride chitinase incubated for 10 mins to 3 hrs using 4-nitrophenyl N-acetyl-beta-D-glucosaminide substrate by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlbumin(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50503397(CHEMBL4438023)
Affinity DataKd:  2.33E+4nMAssay Description:Binding affinity to human serum albumin assessed as dissociation constant after 30 mins by fluorescence-based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlbumin(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50036568(CHEMBL3353611)
Affinity DataKd:  2.65E+4nMAssay Description:Binding affinity to human serum albumin after 30 mins by fluorescence spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed