Compile Data Set for Download or QSAR
Found 693 with Last Name = 'modi' and Initial = 'd'
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12776(2-(5-carbamimidoyl-1H-indol-3-yl)-3-phenyl-N-[4-(2...)copy SMILEScopy InChI
Affinity DataKi:  0.630nM ΔG°:  -52.0kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPoly [ADP-ribose] polymerase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50446130(AG-014699 | AG-14447 | RUCAPARIB CAMSYLATE | Rucap...)copy SMILEScopy InChI
Affinity DataKi:  0.700nMAssay Description:Inhibition of N-terminal GST-tagged human PARP2 (2 to 583 residues) expressed in baculovirus infected Sf9 cells using histone mixture (H2A and H2B) a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21N84R1PubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476859(CHEMBL232938)copy SMILEScopy InChI
Affinity DataKi:  0.900nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476878(CHEMBL399204)copy SMILEScopy InChI
Affinity DataKi:  1.10nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476861(CHEMBL401044)copy SMILEScopy InChI
Affinity DataKi:  1.20nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12778((2R)-N-[4-(1H-1,3-benzodiazol-1-yl)-2-fluorophenyl...)copy SMILEScopy InChI
Affinity DataKi:  1.30nM ΔG°:  -50.2kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476880(CHEMBL450279)copy SMILEScopy InChI
Affinity DataKi:  1.30nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476871(CHEMBL232182)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50446130(AG-014699 | AG-14447 | RUCAPARIB CAMSYLATE | Rucap...)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Inhibition of N-terminal GST-tagged human full length PARP1 (2 to 1041 residues) expressed in baculovirus infected Sf9 cells using histone mixture (H...More data for this Ligand-Target Pair
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12786(3-(2-{[4-(1H-1,3-benzodiazol-1-yl)-2-fluorophenyl]...)copy SMILEScopy InChI
Affinity DataKi:  1.80nM ΔG°:  -49.4kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476864(CHEMBL429438)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476860(CHEMBL232936)copy SMILEScopy InChI
Affinity DataKi:  2.10nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12781(5-amidinoindole 15 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  2.20nM ΔG°:  -48.9kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476870(CHEMBL232346)copy SMILEScopy InChI
Affinity DataKi:  2.20nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12777(5-amidinoindole 13a | N-[4-(1H-1,3-benzodiazol-1-y...)copy SMILEScopy InChI
Affinity DataKi:  2.5nM ΔG°:  -48.6kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12777(5-amidinoindole 13a | N-[4-(1H-1,3-benzodiazol-1-y...)copy SMILEScopy InChI
Affinity DataKi:  2.5nM ΔG°:  -48.6kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K072H3PubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM209909(US9273014, Comparative Compound 45 | US9427442, Co...)copy SMILEScopy InChI
Affinity DataKi:  2.60nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12782(5-amidinoindole 16 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  2.80nM ΔG°:  -48.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476872(CHEMBL401045)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12780(5-amidinoindole 14 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  3nM ΔG°:  -48.2kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476865(CHEMBL392265)copy SMILEScopy InChI
Affinity DataKi:  3.10nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12775(2-(5-carbamimidoyl-1H-indol-3-yl)-N-[4-(2-sulfamoy...)copy SMILEScopy InChI
Affinity DataKi:  3.20nM ΔG°:  -48.0kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476857(CHEMBL449960)copy SMILEScopy InChI
Affinity DataKi:  3.5nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476862(CHEMBL232739)copy SMILEScopy InChI
Affinity DataKi:  3.90nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12787(3-(4-aminophenyl)-N-[4-(1H-1,3-benzodiazol-1-yl)ph...)copy SMILEScopy InChI
Affinity DataKi:  4nM ΔG°:  -47.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K072H3PubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476856(CHEMBL232138)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12787(3-(4-aminophenyl)-N-[4-(1H-1,3-benzodiazol-1-yl)ph...)copy SMILEScopy InChI
Affinity DataKi:  4nM ΔG°:  -47.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476866(CHEMBL231941)copy SMILEScopy InChI
Affinity DataKi:  4.90nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12791(6-amidinoindole 25 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  5.60nM ΔG°:  -46.6kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12784(5-amidinoindole 18 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  6.10nM ΔG°:  -46.4kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476875(CHEMBL232183)copy SMILEScopy InChI
Affinity DataKi:  6.20nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12788(5-amidinoindole 22 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  7nM ΔG°:  -46.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476879(CHEMBL233172)copy SMILEScopy InChI
Affinity DataKi:  9.90nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476873(CHEMBL231984)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476858(CHEMBL231725)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12783(5-amidinoindole 17 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  14nM ΔG°:  -44.4kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476876(CHEMBL399819)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12789(5-amidinoindole 23 | N-[4-(2-{[4-(1H-1,3-benzodiaz...)copy SMILEScopy InChI
Affinity DataKi:  18nM ΔG°:  -43.8kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12828(2,2,2-trifluoroacetic acid; methyl (1R,2S)-2-[2-(5...)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K072H3PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12790(3-(4-benzenesulfonamidophenyl)-N-[4-(1H-1,3-benzod...)copy SMILEScopy InChI
Affinity DataKi:  19nM ΔG°:  -43.6kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor IX(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12778((2R)-N-[4-(1H-1,3-benzodiazol-1-yl)-2-fluorophenyl...)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12806(2,2,2-trifluoroacetic acid; N-[4-(1H-1,3-benzodiaz...)copy SMILEScopy InChI
Affinity DataKi:  22nM ΔG°:  -43.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K072H3PubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476868(CHEMBL232367)copy SMILEScopy InChI
Affinity DataKi:  22nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12779((2S)-N-[4-(1H-1,3-benzodiazol-1-yl)-2-fluorophenyl...)copy SMILEScopy InChI
Affinity DataKi:  26nM ΔG°:  -42.9kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12785(5-amidinoindole 19 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  28nM ΔG°:  -42.7kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476869(CHEMBL232968)copy SMILEScopy InChI
Affinity DataKi:  36nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12794(5-amidinoindole 28 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  36nM ΔG°:  -42.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetPresenilin-1(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50476874(CHEMBL393520)copy SMILEScopy InChI
Affinity DataKi:  41nMAssay Description:Displacement of [3H]succinamide from gamma secretase in THP1 cell membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M90CFPPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12793(5-amidinoindole 27 | N-[4-(1H-1,3-benzodiazol-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  45nM ΔG°:  -41.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7T6PPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM12802(2,2,2-trifluoroacetic acid; 3-(4-aminophenyl)-N-[4...)copy SMILEScopy InChI
Affinity DataKi:  47nM ΔG°:  -41.4kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K072H3PubMed
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