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TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111610(US8623903, I-23)
Affinity DataKi:  1.40nM IC50:  1.60nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111612(US8623903, I-31)
Affinity DataKi:  4.30nM IC50:  2.90nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111611(US8623903, I-30)
Affinity DataKi:  5.40nM IC50:  1.20nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111606(US8623903, I-14)
Affinity DataKi:  5.60nM IC50:  2.20nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111597(US8623903, I-1)
Affinity DataKi:  7.70nM IC50:  4.70nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111598(US8623903, I-5)
Affinity DataKi:  22nM IC50:  4.10nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181395(1-benzyl-N-[3-spiro(2,3-dihydro-1H-indene-1,4'-pip...)
Affinity DataIC50:  0.120nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181392((R)-N-(3-(3H-spiro[isobenzofuran-1,4'-piperidine]-...)
Affinity DataIC50:  0.150nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181395(1-benzyl-N-[3-spiro(2,3-dihydro-1H-indene-1,4'-pip...)
Affinity DataIC50:  0.220nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181392((R)-N-(3-(3H-spiro[isobenzofuran-1,4'-piperidine]-...)
Affinity DataIC50:  0.270nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
TargetNicotinamide N-methyltransferase(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50598881(CHEMBL5194905)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of N-terminal 6His-tagged full length human recombinant NNMT (1 to 264 residues) expressed in Escherichia coli BL21 (DE3) cells using S-ad...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111607(US8623903, I-16)
Affinity DataIC50:  1.30nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50083230(1-((3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-pipe...)
Affinity DataIC50:  1.5nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50386816(CHEMBL2047943)
Affinity DataIC50:  1.80nMAssay Description:Inhibition of human MPS1 expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111600(US8623903, I-7)
Affinity DataIC50:  1.80nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111602(US8623903, I-9)
Affinity DataIC50:  2nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50083230(1-((3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-pipe...)
Affinity DataIC50:  2.40nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111609(US8623903, I-21)
Affinity DataIC50:  3nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent

TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433907(CHEMBL2380582)
Affinity DataIC50:  3.10nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433906(CHEMBL2380583)
Affinity DataIC50:  3.70nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111608(US8623903, I-20)
Affinity DataIC50:  3.80nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181374(2-phenoxy-N-[3-spiro(2,3-dihydro-1H-indene-1,4'-pi...)
Affinity DataIC50:  4nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 8(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM15913(2-pyridinecarboxamide deriv. 8c | 4-Amino-5-cyano-...)
Affinity DataIC50:  4.70nMAssay Description:Inhibition of JNK1-mediated ATF2 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111599(US8623903, I-6)
Affinity DataIC50:  4.80nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111604(US8623903, I-11)
Affinity DataIC50:  4.90nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111601(US8623903, I-8)
Affinity DataIC50:  4.90nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

Target40S ribosomal protein S27(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50420401(CHEMBL2089255 | US11208696, Example 31)
Affinity DataIC50:  6.40nMAssay Description:Inhibition of Mps1-mediated p38 MAPK phosphorylation after 90 mins by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111605(US8623903, I-12)
Affinity DataIC50:  6.90nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111603(US8623903, I-10)
Affinity DataIC50:  6.90nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetProstaglandin D2 receptor 2(Human)
Shionogi

US Patent
LigandPNGBDBM111613(US8623903, I-32)
Affinity DataIC50:  7nMAssay Description:A prepared WP was homogenated and a membrane fraction was collected with high-speed centrifugation. A compound of the present invention was added to ...More data for this Ligand-Target Pair
In DepthDetails US Patent

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50605058(CHEMBL5208218)
Affinity DataIC50:  7.10nMAssay Description:Inhibition of wild type HIV1 protease expressed in Escherichia coli BL21 DE3 assessed as cleavage of fluorogenic substrate using EDANS-RESGIFLETSKR-D...More data for this Ligand-Target Pair
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181382(CHEMBL199639 | N-[3-spiro(2,3-dihydro-1H-indene-1,...)
Affinity DataIC50:  7.5nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433904(CHEMBL2380585)
Affinity DataIC50:  7.90nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50349102(CHEMBL1236095 | US11208696, Example 3)
Affinity DataIC50:  8nMAssay Description:Inhibition of MPS1 (unknown origin)More data for this Ligand-Target Pair
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181374(2-phenoxy-N-[3-spiro(2,3-dihydro-1H-indene-1,4'-pi...)
Affinity DataIC50:  8.20nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181380(CHEMBL413571 | N-[3-spiro(2,3-dihydro-1H-indene-1,...)
Affinity DataIC50:  8.30nMAssay Description:Antagonist activity on nociceptin-induced [35S]GTPgammaS binding to ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433908(CHEMBL2380581)
Affinity DataIC50:  9.80nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433903(CHEMBL2380586)
Affinity DataIC50:  10nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181380(CHEMBL413571 | N-[3-spiro(2,3-dihydro-1H-indene-1,...)
Affinity DataIC50:  10nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433902(CHEMBL2380587)
Affinity DataIC50:  12nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181382(CHEMBL199639 | N-[3-spiro(2,3-dihydro-1H-indene-1,...)
Affinity DataIC50:  12nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Shionogi

Curated by ChEMBL
LigandPNGBDBM513874(bioRxiv20220126.477782, S-217622 | bioRxiv20220126...)
Affinity DataIC50:  13nMAssay Description:Inhibition of N-terminal 10-His-tagged SARS-CoV-2 3CL protease (1 to 306 residues) expressed in Escherichia coli BL21(DE3) using Dabcyl-KTSAVLQSGFRKM...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Shionogi

Curated by ChEMBL
LigandPNGBDBM513874(bioRxiv20220126.477782, S-217622 | bioRxiv20220126...)
Affinity DataIC50:  13nMAssay Description:The 3CL protease inhibition assay was conducted in 384-well plates (Corning 3702). The substance solution (10 mM dimethyl sulfoxide [DMSO] solution) ...More data for this Ligand-Target Pair
In DepthDetails
TargetNicotinamide N-methyltransferase(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50598880(CHEMBL5187248)
Affinity DataIC50:  16nMAssay Description:Inhibition of N-terminal 6His-tagged full length human recombinant NNMT (1 to 264 residues) expressed in Escherichia coli BL21 (DE3) cells using S-ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433911(CHEMBL2380578)
Affinity DataIC50:  17nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181366(2-benzyl-N-(3-{2,3-dihydrospiro[indene-1,4'-piperi...)
Affinity DataIC50:  21nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433903(CHEMBL2380586)
Affinity DataIC50:  21nMAssay Description:Inhibition of FLAG-tagged MPS1 phosphorylation in human RERF-LC-AI Tet-off cells after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181378((4R)-3-benzyl-N-(3-{2,3-dihydrospiro[indene-1,4'-p...)
Affinity DataIC50:  24nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase TTK(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50433912(CHEMBL2380577)
Affinity DataIC50:  28nMAssay Description:Inhibition of MPS1 (unknown origin) using biotin-labeled AGAGLARHTDDEMTGYVA as substrate after 90 mins by DELFIAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNociceptin receptor(Human)
Banyu Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50181402((4S,5S)-4-benzyl-N-(3-{2,3-dihydrospiro[indene-1,4...)
Affinity DataIC50:  30nMAssay Description:Displacement of [125I]Tyr-nociceptin from cloned human ORL1 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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