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Assay Detail

CHEMBL659425

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Functional
In vitro inhibitory activity against replication of HIV type-1 virus in CEM cells
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Intermediate

Target

CCRF-CEM (CHEMBL382)
Type CELL-LINE
Organism Homo sapiens

Publication

Potent human immunodeficiency virus type 1 protease inhibitors that utilize noncoded D-amino acids as P2/P3 ligands.
Jungheim LN, Shepherd TA, Baxter AJ, Burgess J, Hatch SD, Lubbehusen P, Wiskerchen M, Muesing MA.
J Med Chem (1996) 39 : 96 -108
PubMed 8568831 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.04 9.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL11116 1 9.10
CHEMBL273368 1 8.17
CHEMBL262714 1 7.92
CHEMBL274186 1 7.80
CHEMBL276656 1 7.50
CHEMBL11143 1 7.31
CHEMBL275237 1 7.23
CHEMBL267092 1 7.08
CHEMBL266398 1 6.97
CHEMBL406991 1 6.49
CHEMBL273827 1 6.32
CHEMBL274569 1 6.19
CHEMBL276833 1 5.30
CHEMBL275592 1 5.24

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL11116 IC50 = 0.8 nM 9.10
CHEMBL273368 IC50 = 6.7 nM 8.17
CHEMBL262714 IC50 = 12.0 nM 7.92
CHEMBL274186 IC50 = 16.0 nM 7.80
CHEMBL276656 IC50 = 32.0 nM 7.50
CHEMBL11143 IC50 = 49.0 nM 7.31
CHEMBL275237 IC50 = 59.0 nM 7.23
CHEMBL267092 IC50 = 83.0 nM 7.08
CHEMBL266398 IC50 = 107.0 nM 6.97
CHEMBL406991 IC50 = 323.0 nM 6.49
CHEMBL273827 IC50 = 474.0 nM 6.32
CHEMBL274569 IC50 = 646.0 nM 6.19
CHEMBL276833 IC50 = 5010.0 nM 5.30
CHEMBL275592 IC50 = 5780.0 nM 5.24