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Assay Detail

CHEMBL654971

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

Functional
Concentration required to protect CEM-SS cells from HIV-1 mediated cytopathicity by 50% relative to drug-free controls was determined
15
Total Activities
14
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 Expert

Target

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

Publication

Structural analogues of the calanolide anti-HIV agents. Modification of the trans-10,11-dimethyldihydropyran-12-ol ring (ring C).
Zembower DE, Liao S, Flavin MT, Xu ZQ, Stup TL, Buckheit RW, Khilevich A, Mar AA, Sheinkman AK.
J Med Chem (1997) 40 : 1005 -1017
PubMed 9083491 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 15 5.70 6.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL267447 CALANOLIDE A 1.0 2 6.57
CHEMBL269090 1 5.92
CHEMBL267693 1 5.77
CHEMBL7840 1 5.70
CHEMBL7211 1 5.64
CHEMBL267679 1 5.62
CHEMBL7378 1 5.55
CHEMBL266552 1 5.24
CHEMBL7242 1 5.21
CHEMBL266091 1 5.14
CHEMBL269063 1 -
CHEMBL266050 1 -
CHEMBL7633 1 -
CHEMBL7270 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL267447 CALANOLIDE A EC50 = 270.0 nM 6.57
CHEMBL267447 CALANOLIDE A EC50 = 490.0 nM 6.31
CHEMBL269090 EC50 = 1200.0 nM 5.92
CHEMBL267693 EC50 = 1700.0 nM 5.77
CHEMBL7840 EC50 = 2000.0 nM 5.70
CHEMBL7211 EC50 = 2300.0 nM 5.64
CHEMBL267679 EC50 = 2400.0 nM 5.62
CHEMBL7378 EC50 = 2800.0 nM 5.55
CHEMBL266552 EC50 = 5700.0 nM 5.24
CHEMBL7242 EC50 = 6200.0 nM 5.21
CHEMBL266091 EC50 = 7200.0 nM 5.14
CHEMBL269063 EC50 > 100000.0 nM -
CHEMBL266050 EC50 > 100000.0 nM -
CHEMBL7633 EC50 > 100000.0 nM -
CHEMBL7270 EC50 > 100000.0 nM -