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Assay Detail

CHEMBL5229753

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

Functional
Cytotoxicity against human HCT-116 cells assessed as inhibition of cell growth incubated for 4 days by CCK-8 assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HCT-116
Confidence 1 — Organism
Curated By Autocuration

Target

HCT-116 (CHEMBL394)
Type CELL-LINE
Organism Homo sapiens

Publication

Transformation of Renieramycin M into Renieramycins T and S by Intramolecular Photoredox Reaction of 7-Methoxy-6-methyl-1,2,3,4-tetrahydroisoquinoline-5,8-dione Derivatives.
Yokoya M, Yamazaki-Nakai M, Nakai K, Sirimangkalakitti N, Chamni S, Suwanborirux K, Saito N.
J Nat Prod (2023) 86 : 222 -231
PubMed 36631738 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 6.96 7.75

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL451147 RENIERAMYCIN M 1 7.75
CHEMBL452709 SAFRAMYCIN A 1 7.70
CHEMBL5273157 1 7.57
CHEMBL5169402 1 7.50
CHEMBL5191895 1 7.09
CHEMBL468488 RENIERAMYCIN S 1 6.80
CHEMBL5285549 1 6.64
CHEMBL5275238 1 5.92
CHEMBL5289736 1 5.66
CHEMBL5279287 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL451147 RENIERAMYCIN M IC50 = 18.0 nM 7.75
CHEMBL452709 SAFRAMYCIN A IC50 = 20.0 nM 7.70
CHEMBL5273157 IC50 = 27.0 nM 7.57
CHEMBL5169402 IC50 = 32.0 nM 7.50
CHEMBL5191895 IC50 = 82.0 nM 7.09
CHEMBL468488 RENIERAMYCIN S IC50 = 160.0 nM 6.80
CHEMBL5285549 IC50 = 230.0 nM 6.64
CHEMBL5275238 IC50 = 1200.0 nM 5.92
CHEMBL5289736 IC50 = 2200.0 nM 5.66
CHEMBL5279287 IC50 > 20000.0 nM -