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TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM50189842(2-[4-(4-chlorophenyl)piperazin-1-yl)methyl]imidazo...)
Affinity DataEC50:  2.60nMAssay Description:Activity at human D4.4 receptor expressed in CHOK1 cells assessed as stimulation of [35S]GTP-gammaS bindingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM84637(NSC_54562 | CHEMBL240773 | QUINPIROLE | CAS_85760-...)
Affinity DataEC50:  1.40nMAssay Description:Activity at human D4.2 receptor assessed as [3H]thymidine incorporation in CHO 10001 cells by mitogenesis assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM50189842(2-[4-(4-chlorophenyl)piperazin-1-yl)methyl]imidazo...)
Affinity DataEC50:  1.80nMAssay Description:Activity at human D4.2 receptor assessed as [3H]thymidine incorporation in CHO 10001 cells by mitogenesis assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM50189845(2-[4-(2-methoxyphenyl)piperazin-1-ylmethyl]imidazo...)
Affinity DataEC50:  4.5nMAssay Description:Activity at human D4.4 receptor expressed in CHOK1 cells assessed as stimulation of [35S]GTP-gammaS bindingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM50189845(2-[4-(2-methoxyphenyl)piperazin-1-ylmethyl]imidazo...)
Affinity DataEC50:  3nMAssay Description:Activity at human D4.2 receptor assessed as [3H]thymidine incorporation in CHO 10001 cells by mitogenesis assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM50189841(6-iodo-2-[4-(2-methoxyphenyl)piperazin-1-ylmethyl]...)
Affinity DataEC50:  0.520nMAssay Description:Activity at human D4.2 receptor assessed as [3H]thymidine incorporation in CHO 10001 cells by mitogenesis assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetD(4) dopamine receptor(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM84637(NSC_54562 | CHEMBL240773 | QUINPIROLE | CAS_85760-...)
Affinity DataEC50:  49nMAssay Description:Activity at human D4.4 receptor expressed in CHOK1 cells assessed as stimulation of [35S]GTP-gammaS bindingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111905((S)-4-[(S)-2-{(S)-2-[(S)-2-Amino-3-(4-hydroxy-phen...)
Affinity DataIC50: 0.0220nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096716(Enkephalin derivative | CHEMBL100480)
Affinity DataIC50: 0.170nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096716(Enkephalin derivative | CHEMBL100480)
Affinity DataIC50: 0.550nMAssay Description:In vitro inhibitory activity was determined against Opioid receptor mu 1 in guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50001468(deltorphin C | CHEMBL317956 | H-Tyr-D-Ala-Phe-Asp-...)
Affinity DataIC50: 0.582nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111903((S)-1-[(S)-2-{2-[(S)-2-{(S)-2-[(S)-2-Amino-3-(4-hy...)
Affinity DataIC50: 1.20nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in guinea pig ileum (Opioid receptor mu 1); inhibitory concentration ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096719((S)-2-[(R)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-2,6-d...)
Affinity DataIC50: 1.5nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096719((S)-2-[(R)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-2,6-d...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity was determined against Opioid receptor mu 1 in guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50059841(CHEMBL278789 | (S)-1-[(S)-2-[2-((S)-2-{(R)-2-[(S)-...)
Affinity DataIC50: 3.70nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in guinea pig ileum (Opioid receptor mu 1); inhibitory concentration ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111903((S)-1-[(S)-2-{2-[(S)-2-{(S)-2-[(S)-2-Amino-3-(4-hy...)
Affinity DataIC50: 4.60nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096718((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-2,6-d...)
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096717((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)
Affinity DataIC50: 10nMAssay Description:In vitro inhibitory activity was determined against Opioid receptor mu 1 in guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096718((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-2,6-d...)
Affinity DataIC50: 10nMAssay Description:In vitro inhibitory activity was determined against Opioid receptor mu 1 in guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096717((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183824(1-(2-bromobenzyl)-4-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 11nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50001465(2-[2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-propionyl...)
Affinity DataIC50: 22nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPutative alpha-glucosidase(Rice)
Toyama Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration against rice alpha-glucosidaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50059841(CHEMBL278789 | (S)-1-[(S)-2-[2-((S)-2-{(R)-2-[(S)-...)
Affinity DataIC50: 34nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMaltase-glucoamylase(Human)
Toyama Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataIC50: 40nMAssay Description:Inhibitory concentration against human alpha-glucosidaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111906((S)-1-[(S)-2-{2-[(R)-2-{(R)-2-[(S)-2-Amino-3-(4-hy...)
Affinity DataIC50: 44nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in guinea pig ileum (Opioid receptor mu 1); inhibitory concentration ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183823(1-(3-bromobenzyl)-3-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 46nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183817(1-(2-bromobenzyl)-3-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 47nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183813(1-benzyl-4-(4-phenylpiperazin-1-yl)piperidin-3-ol ...)
Affinity DataIC50: 57nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183818(1-(3-bromobenzyl)-4-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 66nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Toyama Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50163440((2R,3S,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration against human alpha-galactosidaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183822(1-(2-methylallyl)-4-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183812(1-(4-bromobenzyl)-3-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183819(1-(2-methylallyl)-3-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183821(1-allyl-3-(4-phenylpiperazin-1-yl)piperidin-4-ol |...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183809(1-allyl-4-(4-phenylpiperazin-1-yl)piperidin-3-ol |...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183829(1-(4-bromobenzyl)-4-(4-phenylpiperazin-1-yl)piperi...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183816(3-(4-phenylpiperazin-1-yl)piperidin-4-ol | CHEMBL2...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183827((E)-1-(3-iodoallyl)-3-(4-phenylpiperazin-1-yl)pipe...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183826((E)-1-(but-2-enyl)-4-(4-phenylpiperazin-1-yl)piper...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183810(1-benzyl-3-(4-phenylpiperazin-1-yl)piperidin-4-ol ...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183825((E)-1-(3-iodoallyl)-4-(4-phenylpiperazin-1-yl)pipe...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183828(4-(4-phenylpiperazin-1-yl)piperidin-3-ol | CHEMBL3...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183820((E)-1-(but-2-enyl)-3-(4-phenylpiperazin-1-yl)piper...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVesicular acetylcholine transporter(Human)
Université

Curated by ChEMBL
LigandPNGBDBM50183814(3-(4-phenylpiperazin-1-yl)-1-(prop-2-ynyl)piperidi...)
Affinity DataIC50: 100nMAssay Description:Displacement of [3H]vesamicol from human VAChT transfected in PC12 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMu-type opioid receptor(Guinea pig)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50001465(2-[2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-propionyl...)
Affinity DataIC50: 103nMAssay Description:In vitro inhibitory activity was determined against Opioid receptor mu 1 in guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111904((S)-4-[(R)-2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phen...)
Affinity DataIC50: 145nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50111906((S)-1-[(S)-2-{2-[(R)-2-{(R)-2-[(S)-2-Amino-3-(4-hy...)
Affinity DataIC50: 358nMAssay Description:In vitro biological activity by electrically induced smooth muscle contractions in mouse vas deferens (Opioid receptor delta 1); inhibitory concentra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDelta-type opioid receptor(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50096720((S)-2-[(R)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)
Affinity DataIC50: 624nMAssay Description:Inhibitory activity against Opioid receptor delta 1 of (endomorphin 2) in mouse vas deferens was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue alpha-L-fucosidase(Bovine)
Toyama Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50163439((2S,3R,4S,5R)-2-Hydroxymethyl-piperidine-3,4,5-tri...)
Affinity DataIC50: 630nMAssay Description:Inhibitory concentration against bovine alpha-L-fucosidaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMed
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