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Assay Detail

CHEMBL655545

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

Functional
Using the XTT assay for cell viability, inhibitory concentration to protect human lymphoblastoid CEM-SS cells from the cytopathic effects of HIV-1 (RF strain) was determined
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

CEM-SS (CHEMBL614548)
Type CELL-LINE
Organism Homo sapiens

Publication

Structure-activity modifications of the HIV-1 inhibitors (+)-calanolide A and (-)-calanolide B.
Galinis DL, Fuller RW, McKee TC, Cardellina JH, Gulakowski RJ, McMahon JB, Boyd MR.
J Med Chem (1996) 39 : 4507 -4510
PubMed 8893846 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.16 5.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL344417 1 5.28
CHEMBL448418 1 5.24
CHEMBL138199 1 5.23
CHEMBL7187 COSTATOLIDE 1 5.23
CHEMBL267447 CALANOLIDE A 1.0 1 5.14
CHEMBL337344 1 5.10
CHEMBL138469 7,8-DIHYDROCALANOLIDE B 1 5.09
CHEMBL139026 1 5.07
CHEMBL269090 1 5.03
CHEMBL345100 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL344417 IC50 = 5200.0 nM 5.28
CHEMBL448418 IC50 = 5800.0 nM 5.24
CHEMBL138199 IC50 = 5900.0 nM 5.23
CHEMBL7187 COSTATOLIDE IC50 = 5900.0 nM 5.23
CHEMBL267447 CALANOLIDE A IC50 = 7300.0 nM 5.14
CHEMBL337344 IC50 = 7900.0 nM 5.10
CHEMBL138469 7,8-DIHYDROCALANOLIDE B IC50 = 8200.0 nM 5.09
CHEMBL139026 IC50 = 8500.0 nM 5.07
CHEMBL269090 IC50 = 9300.0 nM 5.03
CHEMBL345100 IC50 > 150000.0 nM -