Compile Data Set for Download or QSAR
Report error Found 189 Enz. Inhib. hit(s) with all data for entry = 13468
TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795310BDBM795310(N-isoxazol-4-yl-2-[7-[(1-methylindazol-5-yl)amino]...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795309BDBM795309(7-[(1-Methylindazol-5-yl)amino]-2-[2-oxo-2-[(2S)-2...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795309BDBM795309(7-[(1-Methylindazol-5-yl)amino]-2-[2-oxo-2-[(2S)-2...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795308BDBM795308(2-[7-[(1-Methylindazol-5-yl)amino]-1-oxo-isoindoli...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795312BDBM795312(US20260069571, Example 6)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795311BDBM795311(2-{7-[(1-methyl-1H-indazol-5-yl)amino]-1-oxo-2,3-d...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795310BDBM795310(N-isoxazol-4-yl-2-[7-[(1-methylindazol-5-yl)amino]...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795308BDBM795308(2-[7-[(1-Methylindazol-5-yl)amino]-1-oxo-isoindoli...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795307BDBM795307(2-[7-[(1-Methylindazol-5-yl)amino]-1-oxo-isoindoli...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795319BDBM795319(7-[(1-methylindazol-5-yl)amino]-2-[2-oxo-2-[3-(tri...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795318BDBM795318(2-[7-[(7-methyl-1H-indazol-5-yl)amino]-1-oxo-isoin...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795318BDBM795318(2-[7-[(7-methyl-1H-indazol-5-yl)amino]-1-oxo-isoin...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795321BDBM795321(7-[(1-methylindazol-5-yl)amino]-2-[2-oxo-2-[(2S)-(...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795320BDBM795320(N-[4-[(dimethylamino)methyl]-3-(trifluoromethyl)ph...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795398BDBM795398(US20260069571, Example 96)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795398BDBM795398(US20260069571, Example 96)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795312BDBM795312(US20260069571, Example 6)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795317BDBM795317(N-[3-(1-hydroxy-1-methyl-ethyl)phenyl]-2-[7-[(1-me...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795396BDBM795396(US20260069571, Example 93)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795327BDBM795327(N-[3-[(dimethylamino)methyl]-5-(trifluoromethyl)ph...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795328BDBM795328(2-[7-(1H-indazol-5-ylamino)-1-oxo-isoindolin-2-yl]...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795323BDBM795323(2-[2-[(2S)-(difluoromethyl)pyrrolidin-1-yl]-2-oxo-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795321BDBM795321(7-[(1-methylindazol-5-yl)amino]-2-[2-oxo-2-[(2S)-(...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795324BDBM795324(2-[2-[(2S)-(fluoromethyl)pyrrolidin-1-yl]-2-oxo-et...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795324BDBM795324(2-[2-[(2S)-(fluoromethyl)pyrrolidin-1-yl]-2-oxo-et...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795323BDBM795323(2-[2-[(2S)-(difluoromethyl)pyrrolidin-1-yl]-2-oxo-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795335BDBM795335(7-[(3-methyl-1H-indazol-6-yl)amino]-2-[2-oxo-2-[(2...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795334BDBM795334(2-[7-[(3-methyl-1H-indazol-6-yl)amino]-1-oxo-isoin...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795334BDBM795334(2-[7-[(3-methyl-1H-indazol-6-yl)amino]-1-oxo-isoin...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795333BDBM795333(2-[7-[(7-chloro-1-methyl-indazol-5-yl)amino]-1-oxo...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795337BDBM795337(7-[(1-methylindazol-5-yl)amino]-2-[2-oxo-2-[3-(tri...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795336BDBM795336(2-[7-[(3-methyl-1H-pyrazolo[4,3-b]pyridin-6-yl)ami...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795335BDBM795335(7-[(3-methyl-1H-indazol-6-yl)amino]-2-[2-oxo-2-[(2...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795331BDBM795331(N-(2,2-difluorocyclopropyl)-2-[7-[(1-methylindazol...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795333BDBM795333(2-[7-[(7-chloro-1-methyl-indazol-5-yl)amino]-1-oxo...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795343BDBM795343(7-[(3-methyl-1H-indazol-6-yl)amino]-2-[2-oxo-2-[2-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795342BDBM795342(N-[4-[(dimethylamino)methyl]-3-(trifluoromethyl)ph...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795363BDBM795363(7-[(1-methylpyrazolo[3,4-b]pyridin-5-yl)amino]-2-[...)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795341BDBM795341(N-(2,2-difluorocyclopropyl)-2-[7-[(3-methyl-1H-ind...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795345BDBM795345(N-isoxazol-4-yl-2-[7-[(3-methyl-1H-indazol-6-yl)am...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795344BDBM795344(N-[3-[(dimethylamino)methyl]-5-(trifluoromethyl)ph...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795339BDBM795339(2-[2-[(2S)-(fluoromethyl)pyrrolidin-1-yl]-2-oxo-et...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795338BDBM795338(7-[(3-methyl-1H-indazol-6-yl)amino]-2-[2-oxo-2-[3-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795338BDBM795338(7-[(3-methyl-1H-indazol-6-yl)amino]-2-[2-oxo-2-[3-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795341BDBM795341(N-(2,2-difluorocyclopropyl)-2-[7-[(3-methyl-1H-ind...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795339BDBM795339(2-[2-[(2S)-(fluoromethyl)pyrrolidin-1-yl]-2-oxo-et...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795351BDBM795351(N-methyl-2-[7-[(3-methyl-1H-indazol-6-yl)amino]-1-...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetDiscoidin domain-containing receptor 2(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795369BDBM795369(7-[(4-fluoro-3-methyl-1H-indazol-6-yl)amino]-2-[2-...)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795350BDBM795350(7-[(1-methylindazol-5-yl)amino]-2-[2-oxo-2-[(3R)-(...)
Affinity DataIC50: 10nMAssay Description:Cell-based activity under Prompt Conditions. Rat or human NHE3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensiti...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

TargetEpithelial discoidin domain-containing receptor 1(Human)
Redx Pharma

US Patent
LigandChemical structure of BindingDB Monomer ID 795371BDBM795371(2-[7-[(3-methyl-1H-pyrazolo[4,3-b]pyridin-6-yl)ami...)
Affinity DataIC50: 10nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
7/22/2026
Entry Details
US Patent

Displayed 1 to 50 (of 189 total ) | Next | Last >>
Jump to: