Compile Data Set for Download or QSAR
Report error Found 56 Enz. Inhib. hit(s) with all data for entry = 50007702
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211355BDBM211355(US9247759, 12-6)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211356BDBM211356(US9247759, 12-7)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211364BDBM211364(US9247759, 12-15)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211262BDBM211262(US9247759, 10-10)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211264BDBM211264(US9247759, 10-12)
Affinity DataIC50: 40nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211353BDBM211353(US9247759, 12-4)
Affinity DataIC50: 40nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211358BDBM211358(US9247759, 12-9)
Affinity DataIC50: 40nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211350BDBM211350(US9247759, 12-1)
Affinity DataIC50: 60nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211261BDBM211261(US9247759, 10-9)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211273BDBM211273(US9247759, 10-21)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211359BDBM211359(US9247759, 12-10)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211270BDBM211270(US9247759, 10-18)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211272BDBM211272(US9247759, 10-20)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211259BDBM211259(US9247759, 10-7)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211263BDBM211263(US9247759, 10-11)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211244BDBM211244(US9247759, 9-1)
Affinity DataIC50: 200nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211305BDBM211305(US9247759, 10-88 | US9247759, 10-53)
Affinity DataIC50: 200nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210974BDBM210974(US9247759, 4-8)
Affinity DataIC50: 200nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511890BDBM50511890(CHEMBL4514970)
Affinity DataIC50: 200nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511886BDBM50511886(CHEMBL4452065)
Affinity DataIC50: 300nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210975BDBM210975(US9247759, 4-9)
Affinity DataIC50: 300nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211326BDBM211326(US9247759, 10-74)
Affinity DataIC50: 300nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211285BDBM211285(US9247759, 10-33)
Affinity DataIC50: 300nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211020BDBM211020(US9247759, 4-55)
Affinity DataIC50: 400nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211307BDBM211307(US9247759, 10-55)
Affinity DataIC50: 400nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211052BDBM211052(US9247759, 4-88)
Affinity DataIC50: 400nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511892BDBM50511892(CHEMBL4469393)
Affinity DataIC50: 400nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511893BDBM50511893(CHEMBL4567380)
Affinity DataIC50: 500nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211271BDBM211271(US9247759, 10-19)
Affinity DataIC50: 500nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210973BDBM210973(US9247759, compound B | US9247759, 4-7)
Affinity DataIC50: 700nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210983BDBM210983(US9247759, 4-17)
Affinity DataIC50: 700nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511894BDBM50511894(CHEMBL4447100)
Affinity DataIC50: 700nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211021BDBM211021(US9247759, 4-56)
Affinity DataIC50: 800nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210972BDBM210972(US9247759, 4-6)
Affinity DataIC50: 800nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511888BDBM50511888(CHEMBL4456506)
Affinity DataIC50: 800nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211253BDBM211253(US9247759, 10-1)
Affinity DataIC50: 900nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511891BDBM50511891(CHEMBL4530528)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511887BDBM50511887(CHEMBL4588973)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210987BDBM210987(US9247759, 4-21)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211306BDBM211306(US9247759, 10-54)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211325BDBM211325(US9247759, 10-73)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511896BDBM50511896(CHEMBL4526144)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211011BDBM211011(US9247759, 4-46)
Affinity DataIC50: 1.10E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511889BDBM50511889(CHEMBL4579065)
Affinity DataIC50: 1.10E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210989BDBM210989(US9247759, 4-24)
Affinity DataIC50: 1.70E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210985BDBM210985(US9247759, 4-19)
Affinity DataIC50: 1.90E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 211260BDBM211260(US9247759, 10-8)
Affinity DataIC50: 2.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511885BDBM50511885(CHEMBL4443466)
Affinity DataIC50: 2.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50511884BDBM50511884(CHEMBL4471870)
Affinity DataIC50: 2.00E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetTaste receptor type 2 member 8(Human)
Firmenich

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 210967BDBM210967(US9247759, 4-1)
Affinity DataIC50: 2.30E+3nMAssay Description:Antagonist activity at recombinant human TAS2R8 stably expressed in cells co-expressing Galpha16gust44 assessed as inhibition of andrographolide-indu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
Displayed 1 to 50 (of 56 total ) | Next | Last >>
Jump to: