Compile Data Set for Download or QSAR
maximum 50k data
Found 115 with Last Name = 'karin kusnetzow' and Initial = 'a'
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592188(CHEMBL5176490)
Affinity DataIC50:  90nMAssay Description:Time dependent inhibition of CYP2D6 (unknown origin) preincubated for 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataIC50:  280nMAssay Description:Inhibition of hERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592188(CHEMBL5176490)
Affinity DataIC50:  400nMAssay Description:Time dependent inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of hERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin) preincubated for 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataIC50:  5.30E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50:  7.50E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin) preincubated for 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) preincubated for 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) preincubated for 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP2C19 (unknown origin) by fluorescent assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin) by fluorescent assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592167(CHEMBL5182561)
Affinity DataEC50:  5.60nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592168(CHEMBL5181646)
Affinity DataEC50:  2.30nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592169(CHEMBL5193208)
Affinity DataEC50:  1.20nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592170(CHEMBL5180721)
Affinity DataEC50:  1.70nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592171(CHEMBL5190580)
Affinity DataEC50:  19nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592172(CHEMBL5200958)
Affinity DataEC50:  400nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592173(CHEMBL5195986)
Affinity DataEC50:  12nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592174(CHEMBL5189678)
Affinity DataEC50:  6.10nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592175(CHEMBL5188855)
Affinity DataEC50:  2.20nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592176(CHEMBL5188516)
Affinity DataEC50:  3.40nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592177(CHEMBL5200338)
Affinity DataEC50:  21nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592178(CHEMBL5170249)
Affinity DataEC50:  0.360nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592179(CHEMBL5182636)
Affinity DataEC50:  2.60nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592180(CHEMBL5184298)
Affinity DataEC50:  2.30nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592181(CHEMBL5178891)
Affinity DataEC50:  0.0770nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592182(CHEMBL5180885)
Affinity DataEC50:  0.200nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592183(CHEMBL5192315)
Affinity DataEC50:  0.270nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592184(CHEMBL5186952)
Affinity DataEC50:  0.320nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592185(CHEMBL5169724)
Affinity DataEC50:  0.0880nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592186(CHEMBL5177695)
Affinity DataEC50:  5.40nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592187(CHEMBL5187920)
Affinity DataEC50:  2.90nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592188(CHEMBL5176490)
Affinity DataEC50:  0.270nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592189(CHEMBL5201920)
Affinity DataEC50:  0.970nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592190(CHEMBL5202527)
Affinity DataEC50:  0.550nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592191(CHEMBL5177934)
Affinity DataEC50:  0.620nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592192(CHEMBL5186865)
Affinity DataEC50:  10nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592193(CHEMBL5192571)
Affinity DataEC50:  45nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592194(CHEMBL5195355)
Affinity DataEC50:  0.370nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592195(CHEMBL5184249)
Affinity DataEC50:  0.560nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592196(CHEMBL5174433)
Affinity DataEC50:  0.230nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592197(CHEMBL5204225)
Affinity DataEC50:  2.10nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592198(CHEMBL5200076)
Affinity DataEC50:  0.650nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592199(CHEMBL5208031)
Affinity DataEC50:  4.20nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592200(CHEMBL5184442)
Affinity DataEC50:  17nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592201(CHEMBL5179782)
Affinity DataEC50:  0.0710nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Crinetics Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50592202(CHEMBL5198832)
Affinity DataEC50:  1nMAssay Description:Agonist activity at human SST5 expressed in CHO-K1 cells assessed as reduction in NKH477-induced intracellular cAMP levelMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
Displayed 1 to 50 (of 115 total ) | Next | Last >>
Jump to: