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Assay Detail

CHEMBL821346

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

Binding
Displacement of [3H]AVP from human V2 receptor expressed in murine fibroblast cell line (LV2) membranes
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Fibroblast
Confidence 9 — Direct single protein target
Curated By Expert

Target

Vasopressin V2 receptor (CHEMBL1790)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

5-Fluoro-2-methyl-N-[4-(5H-pyrrolo[2,1-c]-[1, 4]benzodiazepin-10(11H)-ylcarbonyl)-3-chlorophenyl]benzamide (VPA-985): an orally active arginine vasopressin antagonist with selectivity for V2 receptors.
Albright JD, Reich MF, Delos Santos EG, Dusza JP, Sum FW, Venkatesan AM, Coupet J, Chan PS, Ru X, Mazandarani H, Bailey T.
J Med Chem (1998) 41 : 2442 -2444
PubMed 9651149 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.70 9.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL311931 1 9.30
CHEMBL420031 1 9.15
CHEMBL310416 1 9.00
CHEMBL49429 LIXIVAPTAN 3.0 1 8.92
CHEMBL68085 1 8.82
CHEMBL81269 1 8.72
CHEMBL80029 1 8.72
CHEMBL311230 1 8.70
CHEMBL312036 1 8.70
CHEMBL81133 1 8.68
CHEMBL418890 1 8.49
CHEMBL306970 1 8.40
CHEMBL81755 1 8.40
CHEMBL420216 1 8.38
CHEMBL314344 1 8.08

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL311931 IC50 = 0.5 nM 9.30
CHEMBL420031 IC50 = 0.7 nM 9.15
CHEMBL310416 IC50 = 1.0 nM 9.00
CHEMBL49429 LIXIVAPTAN IC50 = 1.2 nM 8.92
CHEMBL68085 IC50 = 1.5 nM 8.82
CHEMBL81269 IC50 = 1.9 nM 8.72
CHEMBL80029 IC50 = 1.9 nM 8.72
CHEMBL311230 IC50 = 2.0 nM 8.70
CHEMBL312036 IC50 = 2.0 nM 8.70
CHEMBL81133 IC50 = 2.1 nM 8.68
CHEMBL418890 IC50 = 3.2 nM 8.49
CHEMBL306970 IC50 = 4.0 nM 8.40
CHEMBL81755 IC50 = 4.0 nM 8.40
CHEMBL420216 IC50 = 4.2 nM 8.38
CHEMBL314344 IC50 = 8.3 nM 8.08