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Assay Detail

CHEMBL1120184

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

Binding
Inhibition of HIV integrase strand transfer activity
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Scaffold rearrangement of dihydroxypyrimidine inhibitors of HIV integrase: Docking model revisited.
Tang J, Maddali K, Pommier Y, Sham YY, Wang Z.
Bioorg Med Chem Lett (2010) 20 : 3275 -3279
PubMed 20457521 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.58 5.58

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL217285 1 5.58
CHEMBL1084171 1 -
CHEMBL1082495 1 -
CHEMBL1086318 1 -
CHEMBL1085363 1 -
CHEMBL1085364 1 -
CHEMBL1085365 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL217285 IC50 = 2600.0 nM 5.58
CHEMBL1084171 IC50 = 111000.0 nM -
CHEMBL1082495 IC50 = 169000.0 nM -
CHEMBL1086318 IC50 = 206000.0 nM -
CHEMBL1085363 IC50 > 333000.0 nM -
CHEMBL1085364 IC50 = 243000.0 nM -
CHEMBL1085365 IC50 = 241000.0 nM -