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Assay Detail

CHEMBL691805

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

ADMET
Cytotoxicity was evaluated against the Human diploid cells (HFF)
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Cell Type HFF
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

ADMET (CHEMBL612558)
Type ADMET

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 13 7.05 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99668 TOYOCAMYCIN 1 7.52
CHEMBL101892 SANGIVAMYCIN 1 7.10
CHEMBL267099 TUBERCIDIN 1 6.52
CHEMBL336797 1 -
CHEMBL184 ACYCLOVIR 4.0 1 -
CHEMBL133217 1 -
CHEMBL334382 1 -
CHEMBL334634 1 -
CHEMBL300485 1 -
CHEMBL303055 1 -
CHEMBL50879 1 -
CHEMBL182 GANCICLOVIR 4.0 1 -
CHEMBL51484 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99668 TOYOCAMYCIN IC50 = 30.0 nM 7.52
CHEMBL101892 SANGIVAMYCIN IC50 = 80.0 nM 7.10
CHEMBL267099 TUBERCIDIN IC50 = 300.0 nM 6.52
CHEMBL336797 IC50 > 100000.0 nM -
CHEMBL184 ACYCLOVIR IC50 > 100000.0 nM -
CHEMBL133217 IC50 > 100000.0 nM -
CHEMBL334382 IC50 > 100000.0 nM -
CHEMBL334634 IC50 > 100000.0 nM -
CHEMBL300485 IC50 > 100000.0 nM -
CHEMBL303055 IC50 > 100000.0 nM -
CHEMBL50879 IC50 > 320000.0 nM -
CHEMBL182 GANCICLOVIR IC50 > 100000.0 nM -
CHEMBL51484 IC50 > 320000.0 nM -