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Assay Detail

CHEMBL4402289

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Functional
In vivo antagonist activity at HPGDS in po dosed C57BL/6J mouse assessed as inhibition of compound 48/80-induced PGD2 release into peritoneal lavage fluid pretreated for 1 hr followed by compound 48/80 addition and measured after 7 mins by EIA
3
Total Activities
1
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Mus musculus
Confidence 1 — Organism
Curated By Autocuration

Target

Mus musculus (CHEMBL375)
Type ORGANISM
Organism Mus musculus

Publication

The discovery of quinoline-3-carboxamides as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors.
Deaton DN, Do Y, Holt J, Jeune MR, Kramer HF, Larkin AL, Orband-Miller LA, Peckham GE, Poole C, Price DJ, Schaller LT, Shen Y, Shewchuk LM, Stewart EL, Stuart JD, Thomson SA, Ward P, Wilson JW, Xu T, Guss JH, Musetti C, Rendina AR, Affleck K, Anders D, Hancock AP, Hobbs H, Hodgson ST, Hutchinson J, Leveridge MV, Nicholls H, Smith IED, Somers DO, Sneddon HF, Uddin S, Cleasby A, Mortenson PN, Richardson C, Saxty G.
Bioorg Med Chem (2019) 27 : 1456 -1478
PubMed 30858025 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 1 7.68 7.68
ED50 1 - -
Inhibition 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4473072 3 7.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4473072 EC50 = 21.0 nM 7.68
CHEMBL4473072 ED50 = 0.032 mg.kg-1 -
CHEMBL4473072 Inhibition - % -