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TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2379(S-DABO | 6-[(2,6-dichlorophenyl)methyl]-5-methyl-2...)
Affinity DataAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21222(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21223(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]prop...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21224(N-[2-(methylsulfanyl)-6-propoxypyrimidin-4-yl]acet...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21225(N-[2-(methylsulfanyl)-6-propoxypyrimidin-4-yl]prop...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21226(N-[6-methoxy-2-(propylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21230(N-[2-(benzylsulfanyl)-6-propoxypyrimidin-4-yl]acet...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21234(N-{6-[(4-chlorophenyl)methoxy]-2-(propylsulfanyl)p...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21235(N-{6-[(2,4-dichlorophenyl)methoxy]-2-(propylsulfan...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21238(N-[6-(cyclohexylmethoxy)-2-(propylsulfanyl)pyrimid...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A1(Human)
Universita Di Napoli

LigandPNGBDBM21240(N-[2-(tert-butylsulfanyl)-6-[(4-chlorophenyl)metho...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21222(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21223(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]prop...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21226(N-[6-methoxy-2-(propylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21227(N-[6-methoxy-2-(propylsulfanyl)pyrimidin-4-yl]prop...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21228(N-[6-propoxy-2-(propylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21230(N-[2-(benzylsulfanyl)-6-propoxypyrimidin-4-yl]acet...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21231(N-[6-(benzyloxy)-2-(propylsulfanyl)pyrimidin-4-yl]...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21233(N-{6-[(3-chlorophenyl)methoxy]-2-(propylsulfanyl)p...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21234(N-{6-[(4-chlorophenyl)methoxy]-2-(propylsulfanyl)p...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21235(N-{6-[(2,4-dichlorophenyl)methoxy]-2-(propylsulfan...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21236(N-{6-[(4-methoxyphenyl)methoxy]-2-(propylsulfanyl)...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21237(N-[6-(2-phenylethoxy)-2-(propylsulfanyl)pyrimidin-...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21238(N-[6-(cyclohexylmethoxy)-2-(propylsulfanyl)pyrimid...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21239(N-{6-[(4-chlorophenyl)methoxy]-2-(ethylsulfanyl)py...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A2a(Human)
Universita Di Napoli

LigandPNGBDBM21240(N-[2-(tert-butylsulfanyl)-6-[(4-chlorophenyl)metho...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A3(Human)
Universita Di Napoli

LigandPNGBDBM21222(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]acet...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine receptor A3(Human)
Universita Di Napoli

LigandPNGBDBM21223(N-[6-methoxy-2-(methylsulfanyl)pyrimidin-4-yl]prop...)
Affinity DataAssay Description:The membranes prepared from CHO cells transfected with human adenosine A1 receptors were used in binding assays. Nonspecific binding was determined i...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25460(2-[(4-oxo-4H-triphenylene-11-)sulfinyl]acetic acid...)
Affinity DataKd:  1.80E+5nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25462(2,3-dinitro-9H-fluoren-9-one | NSC133896)
Affinity DataKd:  3.71E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25463(2-(1,2,4-triazatriphenylen-3-ylsulfanyl)acetic aci...)
Affinity DataKd:  4.69E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25464(6-[(7-nitro-2,1,3-benzoxadiazol-4-yl)sulfanyl]-9H-...)
Affinity DataKd:  1.52E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25465((1R,2R,5S,6S,10S,13S,15R)-5-acetyl-13-hydroxy-6,10...)
Affinity DataKd:  1.27E+5nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25466(N-(3-nitro-9-oxo-9H-fluoren-2-yl)acetamide | NSC60...)
Affinity DataKd:  3.18E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25467(2,4-dinitro-9H-fluoren-9-one | NSC55545)
Affinity DataKd:  4.81E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25468(3,7-difluoro-2-nitro-9H-fluoren-9-one | NSC57476)
Affinity DataKd:  4.46E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM22858(2-nitro-9,10-dihydrophenanthrene-9,10-dione | NSC2...)
Affinity DataKd:  6.81E+3nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine 5'-phosphosulfate reductase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
The Scripps Research Institute

LigandPNGBDBM25469(2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)sulfanyl]-1-o...)
Affinity DataKd:  1.95E+4nMpH: 7.5 T: 2°CAssay Description:Values of Ki were determined from the dependence of the observed rate constant (kobs) on inhibitor concentration. With subsaturing APS, the inhibit...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine deaminase(Bovine)
Universita Di Pisa

LigandPNGBDBM28377(2-nonyl-2H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one | ...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of ADA was determined spectrophotometrically by monitoring the change in absorbance at 262 nm, due to the deamination of adenosine catal...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine deaminase(Bovine)
Universita Di Pisa

LigandPNGBDBM28378(2-decyl-2H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one | ...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of ADA was determined spectrophotometrically by monitoring the change in absorbance at 262 nm, due to the deamination of adenosine catal...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAdenosine deaminase(Bovine)
Universita Di Pisa

LigandPNGBDBM28379(2-undecyl-2H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one ...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of ADA was determined spectrophotometrically by monitoring the change in absorbance at 262 nm, due to the deamination of adenosine catal...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28759(CHEMBL191275 | (2S)-3-phenyl-2-(4-phenylphenoxy)pr...)
Affinity DataEC50:  480nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28760((2R)-3-phenyl-2-(4-phenylphenoxy)propanoic acid | ...)
Affinity DataEC50:  5.93E+3nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28681(cid_5281055 | [3H]rosiglitazone | CHEMBL121 | ROSI...)
Affinity DataEC50:  40nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28759(CHEMBL191275 | (2S)-3-phenyl-2-(4-phenylphenoxy)pr...)
Affinity DataEC50:  220nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM24566(JMC515449 Compound 1 | Wyeth 14,643 | 2-({4-chloro...)
Affinity DataEC50:  1.62E+3nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetPeroxisome proliferator-activated receptor alpha(Mouse)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28759(CHEMBL191275 | (2S)-3-phenyl-2-(4-phenylphenoxy)pr...)
Affinity DataEC50:  260nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Mouse)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM24566(JMC515449 Compound 1 | Wyeth 14,643 | 2-({4-chloro...)
Affinity DataEC50:  40nMAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetPeroxisome proliferator-activated receptor alpha(Human)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28760((2R)-3-phenyl-2-(4-phenylphenoxy)propanoic acid | ...)
Affinity DataAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Mouse)
Consiglio Nazionale Delle Ricerche

LigandPNGBDBM28760((2R)-3-phenyl-2-(4-phenylphenoxy)propanoic acid | ...)
Affinity DataAssay Description:The HepG2 cells were co-transfected with DNA construct containing PPAR-Gal4 chimeric receptor and Gal4-luciferase reporter. The luciferase activity w...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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