Compile Data Set for Download or QSAR
Report error Found 65 Enz. Inhib. hit(s) with all data for entry = 50011769
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110291((7-Chloro-quinolin-4-yl)-[4-(3-piperidin-1-yl-prop...)
Affinity DataKi:  0.0860nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110288([4-(3-Piperidin-1-yl-propoxy)-phenyl]-quinolin-4-y...)
Affinity DataKi:  0.0910nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110300(N-(4-(3-(piperidin-1-yl)propoxy)phenethyl)-5,6,7,8...)
Affinity DataKi:  0.330nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110311({2-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-ethyl}-qu...)
Affinity DataKi:  0.530nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110285({3-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-propyl}-q...)
Affinity DataKi:  0.75nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110299({3-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-propyl}-(...)
Affinity DataKi:  1.40nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110290({4-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-butyl}-qu...)
Affinity DataKi:  1.5nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110306((6-Piperidin-1-yl-hexyl)-(1,2,3,4-tetrahydro-acrid...)
Affinity DataKi:  1.80nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110310((3-Methyl-quinolin-4-yl)-(6-piperidin-1-yl-hexyl)-...)
Affinity DataKi:  3.60nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110297((6-Piperidin-1-yl-hexyl)-quinolin-4-yl-amine; Oxal...)
Affinity DataKi:  7.60nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110312((7-Chloro-quinolin-4-yl)-(8-piperidin-1-yl-octyl)-...)
Affinity DataKi:  7.80nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110282((7-Chloro-quinolin-4-yl)-(7-piperidin-1-yl-heptyl)...)
Affinity DataKi:  9.90nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110289((7-Chloro-quinolin-4-yl)-(10-piperidin-1-yl-decyl)...)
Affinity DataKi:  12nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110294((5-Piperidin-1-yl-pentyl)-quinolin-4-yl-amine; Oxa...)
Affinity DataKi:  15nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110309(Methyl-(3-piperidin-1-yl-propyl)-quinolin-4-yl-ami...)
Affinity DataIC50: 16nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110295((7-Chloro-quinolin-4-yl)-(6-piperidin-1-yl-hexyl)-...)
Affinity DataKi:  18nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110303((2-Piperidin-1-yl-ethyl)-(1,2,3,4-tetrahydro-acrid...)
Affinity DataKi:  19nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110306((6-Piperidin-1-yl-hexyl)-(1,2,3,4-tetrahydro-acrid...)
Affinity DataIC50: 21nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110304((7-Chloro-quinolin-4-yl)-(5-piperidin-1-yl-pentyl)...)
Affinity DataKi:  26nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110285({3-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-propyl}-q...)
Affinity DataIC50: 31nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110301((7-Chloro-quinolin-4-yl)-(12-piperidin-1-yl-dodecy...)
Affinity DataKi:  32nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110303((2-Piperidin-1-yl-ethyl)-(1,2,3,4-tetrahydro-acrid...)
Affinity DataIC50: 34nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110286((3-Piperidin-1-yl-propyl)-(1,2,3,4-tetrahydro-acri...)
Affinity DataKi:  34nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110286((3-Piperidin-1-yl-propyl)-(1,2,3,4-tetrahydro-acri...)
Affinity DataIC50: 45nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110296({4-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-butyl}-(1...)
Affinity DataIC50: 48nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110300(N-(4-(3-(piperidin-1-yl)propoxy)phenethyl)-5,6,7,8...)
Affinity DataIC50: 48nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110298(Ethyl-(3-piperidin-1-yl-propyl)-quinolin-4-yl-amin...)
Affinity DataIC50: 49nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110281(Methyl-(3-piperidin-1-yl-propyl)-(1,2,3,4-tetrahyd...)
Affinity DataKi:  50nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110288([4-(3-Piperidin-1-yl-propoxy)-phenyl]-quinolin-4-y...)
Affinity DataIC50: 51nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110294((5-Piperidin-1-yl-pentyl)-quinolin-4-yl-amine; Oxa...)
Affinity DataIC50: 53nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110287((3-Piperidin-1-yl-propyl)-quinolin-4-yl-amine; Oxa...)
Affinity DataIC50: 64nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110284((4-Piperidin-1-yl-butyl)-quinolin-4-yl-amine; Oxal...)
Affinity DataIC50: 64nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110307((3-Methyl-quinolin-4-yl)-(3-piperidin-1-yl-propyl)...)
Affinity DataKi:  70nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110290({4-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-butyl}-qu...)
Affinity DataIC50: 73nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110292(Methyl-(2-piperidin-1-yl-ethyl)-(1,2,3,4-tetrahydr...)
Affinity DataKi:  78nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110283((7-Chloro-quinolin-4-yl)-(4-piperidin-1-yl-butyl)-...)
Affinity DataKi:  82nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110297((6-Piperidin-1-yl-hexyl)-quinolin-4-yl-amine; Oxal...)
Affinity DataIC50: 84nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110287((3-Piperidin-1-yl-propyl)-quinolin-4-yl-amine; Oxa...)
Affinity DataKi:  85nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110284((4-Piperidin-1-yl-butyl)-quinolin-4-yl-amine; Oxal...)
Affinity DataKi:  90nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110299({3-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-propyl}-(...)
Affinity DataIC50: 95nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM8961(CHEMBL95 | Cognex | cid_1935 | CHEMBL1337960 | 1,2...)
Affinity DataIC50: 110nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110302(Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...)
Affinity DataIC50: 110nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110293(Methyl-(2-piperidin-1-yl-ethyl)-quinolin-4-yl-amin...)
Affinity DataIC50: 120nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110311({2-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-ethyl}-qu...)
Affinity DataIC50: 120nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110282((7-Chloro-quinolin-4-yl)-(7-piperidin-1-yl-heptyl)...)
Affinity DataIC50: 120nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110304((7-Chloro-quinolin-4-yl)-(5-piperidin-1-yl-pentyl)...)
Affinity DataIC50: 140nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110283((7-Chloro-quinolin-4-yl)-(4-piperidin-1-yl-butyl)-...)
Affinity DataIC50: 160nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine N-methyltransferase(Rat)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110295((7-Chloro-quinolin-4-yl)-(6-piperidin-1-yl-hexyl)-...)
Affinity DataIC50: 180nMAssay Description:Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methyl-histamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110302(Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...)
Affinity DataKi:  188nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50110313((2-Piperidin-1-yl-ethyl)-quinolin-4-yl-amine; Oxal...)
Affinity DataKi:  191nMAssay Description:Affinity for displacement of [125I]iodoproxyfan from human histamine H3 receptors stably expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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