Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hematopoietic prostaglandin D synthase (Homo sapiens (Human)) | BDBM50576322 (CHEMBL4859922) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description Inhibition of human HPGDS assessed as reduction in PGD2 formation using PGH2 as substrate by mass spectrometry | Citation and Details Article DOI: 10.1016/j.bmcl.2021.128113 BindingDB Entry DOI: 10.7270/Q2B28047 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Hematopoietic prostaglandin D synthase (Rattus norvegicus) | BDBM50576322 (CHEMBL4859922) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description Inhibition of HPGDS in rat RBL cells assessed as reduction in PGD2 formation using PGH2 as substrate by mass spectrometry | Citation and Details Article DOI: 10.1016/j.bmcl.2021.128113 BindingDB Entry DOI: 10.7270/Q2B28047 | |||||||||||
More data for this Ligand-Target Pair |