Found 92 with Last Name = 'de ceballos' and Initial = 'ml' TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 5nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the Dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 6.5nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 21nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 25nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 74nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Santiago De Compostela
Curated by ChEMBL
University Of Santiago De Compostela
Curated by ChEMBL
Affinity DataKi: 78nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]spiperone binding to the dopamine receptor D2Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 98nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the Dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 324nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 380nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 741nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 912nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 1.35E+3nMAssay Description:Compound was evaluated for its affinity (pKi) to inhibit [3H]SCH-23390 binding to the dopamine receptor D1Checked by AuthorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0700nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.150nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.260nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.5nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
3D Structure (crystal)
Affinity DataIC50: 24nMAssay Description:Compound was evaluated for its inhibitory potency against purified membrane bound rat brain aminopeptidaseMore data for this Ligand-Target Pair
Affinity DataIC50: 70nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 80nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 230nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 290nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 300nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 330nMAssay Description:Compound was evaluated for its inhibitory potency against purified membrane bound rat brain aminopeptidaseMore data for this Ligand-Target Pair
Affinity DataIC50: 390nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 800nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.54E+3nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.01E+3nMAssay Description:Compound was evaluated for its inhibitory potency against purified membrane bound rat brain AminopeptidaseMore data for this Ligand-Target Pair
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+3nMAssay Description:Compound was evaluated for its inhibitory potency against purified membrane bound rat brain Aminopeptidase B using L-lysine-beta napthylamide as subs...More data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+3nMAssay Description:Compound was evaluated for its inhibitory potency against purified membrane bound rat brain Aminopeptidase M (AP-M) using [3H]Leu-enkephalin as subst...More data for this Ligand-Target Pair
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.40E+3nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.40E+3nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.70E+3nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.70E+3nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine as substrate by Ellman's assayMore data for this Ligand-Target Pair
