Report error Found 327 with Last Name = 'chowdhury' and Initial = 'r'
Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.80nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 4nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 5.70nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 7.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 47nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 48nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 61nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 64nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 83nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 128nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 340nMAssay Description:Inhibition of cathepsin B (unknown origin) using Z-Arg-Arg-AMC as substrate after 5 mins by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKi: 398nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 590nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 720nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-Phe-Arg-AMC as substrate after 5 mins by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKi: 763nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+3nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-Phe-Arg-AMC as substrate after 5 mins by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.09E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.36E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.97E+3nMAssay Description:Competitive inhibition of human KDM2A expressed in Escherichia coli using 2-oxoglutarate by enzyme kinetic assayMore data for this Ligand-Target Pair
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.10E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using Z-Arg-Arg-AMC as substrate after 5 mins by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKi: 5.90E+4nMAssay Description:Competitive inhibition of human liver cathepsin L using Z-FR-AMC as substrate measured at 1 min interval for 20 mins followed by every 15 mins for 2 ...More data for this Ligand-Target Pair
Affinity DataKi: 8.50E+4nMAssay Description:Mixed type inhibition of human KDM2A expressed in Escherichia coli assessed inhibition constant for compound-enzyme-substrate complex using methyl ly...More data for this Ligand-Target Pair
Affinity DataKi: 1.46E+5nMAssay Description:Inhibition of human liver cathepsin L using Z-FR-AMC as substrate measured at 1 min interval for 20 mins followed by every 15 mins for 2 hrs by fluor...More data for this Ligand-Target Pair
Affinity DataKi: 2.00E+5nMAssay Description:Inhibition of KRAS G12C mutant (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant human AChE using acetylthiocholine iodide as substrate measured after 7 mins by Ellman's methodMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 14nMAssay Description:Inhibition of recombinant human TCPTP using pNPP as substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 18nMAssay Description:Inhibition of TCPTP (unknown origin) using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 46nMAssay Description:Inhibition of recombinant human PTP1B using pNPP as substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 62nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 11(Human)
Shanghai Jiao Tong University (Sjtu)
Curated by ChEMBL
Shanghai Jiao Tong University (Sjtu)
Curated by ChEMBL
Affinity DataIC50: 81nMAssay Description:Inhibition of SHP2 (unknown origin) using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: 117nMAssay Description:Inhibition of recombinant human BuChe using S-butyrylthiocholine iodide as substrate measured after 7 mins by Ellman's methodMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:Inhibition of human KDM4E expressed in Escherichia coli using methyl lysine peptide substrate by AlphaScreen assayMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shanghai Jiao Tong University
Curated by ChEMBL
Shanghai Jiao Tong University
Curated by ChEMBL
Affinity DataIC50: 230nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair