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Found 23 with Last Name = 'zygmunt' and Initial = 'pm'
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50148573((E,E)-1-piperoylpiperidine | 1-[(2E,4E)-5-(1,3-ben...)
Affinity DataEC50:  3.16E+3nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50562522(CHEMBL4778235)
Affinity DataEC50:  158nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contraction in presence of TRPV1 an...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415870(PIPERANINE)
Affinity DataEC50:  3.98E+3nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50381233(CHEMBL332479)
Affinity DataEC50:  6.31E+3nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415871(ANTIEPILEPSIRINE | ILEPCIMIDE)
Affinity DataEC50:  2.00E+4nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM20461((6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methy...)
Affinity DataEC50:  2.51nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415872(CHEMBL1094074)
Affinity DataEC50:  10nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415873(PIPERLONGUMININE)
Affinity DataEC50:  6.31nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415874(CHEMBL1095331)
Affinity DataEC50:  2nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415875(CHEMBL1097704)
Affinity DataEC50:  2.51nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415876(CHEMBL1096703)
Affinity DataEC50:  2.51nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415877(CHEMBL1096704)
Affinity DataEC50:  6.31nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM20284(CHEMBL391997 | CPZ | Capsazepine | N-[2-(4-chlorop...)
Affinity DataEC50:  2.51E+3nMAssay Description:Antagonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as inhibition of capsaicin-induced intracellular calciu...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50054471((5Z,8Z)-Icosa-5,8,11,14-tetraenoic acid (4-hydroxy...)
Affinity DataEC50:  50nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50473844(CHEMBL123254)
Affinity DataEC50:  0.501nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50246639(CHEMBL472898 | N-(4-hydroxy-3-methoxyphenyl)icosa-...)
Affinity DataEC50:  1.30nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50562521(CHEMBL4747170)
Affinity DataEC50:  3.20nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50246638(CHEMBL472897 | N-(1H-indazol-5-yl)icosa-5,8,11,14-...)
Affinity DataEC50:  13nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50562522(CHEMBL4778235)
Affinity DataEC50:  4nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contractionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50246639(CHEMBL472898 | N-(4-hydroxy-3-methoxyphenyl)icosa-...)
Affinity DataEC50:  16nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contraction in presence of TRPV1 an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50562521(CHEMBL4747170)
Affinity DataEC50:  63nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contraction in presence of TRPV1 an...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Lund University

Curated by ChEMBL
LigandPNGBDBM50246638(CHEMBL472897 | N-(1H-indazol-5-yl)icosa-5,8,11,14-...)
Affinity DataEC50:  398nMAssay Description:Agonist activity at TRPV1 in rat isolated mesenteric arteries assessed as vasorelaxation of phenylephrine-induced contraction in presence of TRPV1 an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universidad De Antioquia

Curated by ChEMBL
LigandPNGBDBM50415869(CHEMBL120919)
Affinity DataEC50:  2.51E+3nMAssay Description:Agonist activity at human TRPV1 expressed in tetracycline-stimulated HEK293 cells assessed as increase in intracellular calcium levels by fluorimetri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed