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Assay Detail

CHEMBL687989

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

Functional
Antiviral activity of the compound was evaluated against the Human cytomegalo virus (HCMV)
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human betaherpesvirus 5
Confidence 1 — Organism
Curated By Intermediate

Target

Human betaherpesvirus 5 (CHEMBL371)
Type ORGANISM
Organism Human betaherpesvirus 5

Publication

Synthesis, cytotoxicity, and antiviral activity of some acyclic analogues of the pyrrolo[2,3-d]pyrimidine nucleoside antibiotics tubercidin, toyocamycin, and sangivamycin.
Gupta PK, Daunert S, Nassiri MR, Wotring LL, Drach JC, Townsend LB.
J Med Chem (1989) 32 : 402 -408
PubMed 2913300 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.56 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL101892 SANGIVAMYCIN 1 7.52
CHEMBL99668 TOYOCAMYCIN 1 7.30
CHEMBL267099 TUBERCIDIN 1 6.30
CHEMBL300485 1 5.10
CHEMBL336797 1 -
CHEMBL133217 1 -
CHEMBL334382 1 -
CHEMBL334634 1 -
CHEMBL303055 1 -
CHEMBL50879 1 -
CHEMBL51484 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL101892 SANGIVAMYCIN IC50 = 30.0 nM 7.52
CHEMBL99668 TOYOCAMYCIN IC50 = 50.0 nM 7.30
CHEMBL267099 TUBERCIDIN IC50 = 500.0 nM 6.30
CHEMBL300485 IC50 = 8000.0 nM 5.10
CHEMBL336797 IC50 > 100000.0 nM -
CHEMBL133217 IC50 > 100000.0 nM -
CHEMBL334382 IC50 > 100000.0 nM -
CHEMBL334634 IC50 > 100000.0 nM -
CHEMBL303055 IC50 > 100000.0 nM -
CHEMBL50879 IC50 > 320000.0 nM -
CHEMBL51484 IC50 = 144000.0 nM -