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Assay Detail

CHEMBL712506

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

Binding
In vitro binding ability against Luteinizing hormone-releasing hormone release in rat pituitary cells
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type Pituitary gland cell
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Lutropin-choriogonadotropic hormone receptor (CHEMBL2456)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Nonpeptide luteinizing hormone-releasing hormone antagonists derived from erythromycin A: design, synthesis, and biological activity of cladinose replacement analogues.
Randolph JT, Waid P, Nichols C, Sauer D, Haviv F, Diaz G, Bammert G, Besecke LM, Segreti JA, Mohning KM, Bush EN, Wegner CD, Greer J.
J Med Chem (2004) 47 : 1085 -1097
PubMed 14971889 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 4 9.18 9.87

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL275935 1 9.87
CHEMBL12282 1 9.32
CHEMBL303274 1 8.76
CHEMBL273440 1 8.75

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL275935 Kd = 0.1349 nM 9.87
CHEMBL12282 Kd = 0.4786 nM 9.32
CHEMBL303274 Kd = 1.738 nM 8.76
CHEMBL273440 Kd = 1.778 nM 8.75