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Assay Detail

CHEMBL695249

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

Functional
Inhibition of herpes simplex virus (HSV-1) in plaque reduction assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism herpes simplex virus
Confidence 1 — Organism
Curated By Expert

Target

Human alphaherpesvirus 1 (CHEMBL377)
Type ORGANISM
Organism Human alphaherpesvirus 1

Publication

Synthesis, antiproliferative, and antiviral activity of certain 4-substituted and 4,5-disubstituted 7-[(1,3-dihydroxy-2-propoxy)methyl]pyrrolo[2,3-d]pyrimidines.
Pudlo JS, Nassiri MR, Kern ER, Wotring LL, Drach JC, Townsend LB.
J Med Chem (1990) 33 : 1984 -1992
PubMed 2163454 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.24 5.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL60469 1 5.70
CHEMBL61716 1 5.54
CHEMBL61003 1 5.40
CHEMBL184 ACYCLOVIR 4.0 1 5.40
CHEMBL182 GANCICLOVIR 4.0 1 5.35
CHEMBL60950 1 4.80
CHEMBL418640 1 4.52
CHEMBL61676 1 -
CHEMBL303055 1 -
CHEMBL291874 1 -
CHEMBL59959 1 -
CHEMBL62215 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL60469 IC50 = 2000.0 nM 5.70
CHEMBL61716 IC50 = 2900.0 nM 5.54
CHEMBL61003 IC50 = 4000.0 nM 5.40
CHEMBL184 ACYCLOVIR IC50 = 4000.0 nM 5.40
CHEMBL182 GANCICLOVIR IC50 = 4500.0 nM 5.35
CHEMBL60950 IC50 = 16000.0 nM 4.80
CHEMBL418640 IC50 = 30000.0 nM 4.52
CHEMBL61676 IC50 > 100000.0 nM -
CHEMBL303055 IC50 > 100000.0 nM -
CHEMBL291874 IC50 > 100000.0 nM -
CHEMBL59959 IC50 > 100000.0 nM -
CHEMBL62215 IC50 > 100000.0 nM -