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Assay Detail

CHEMBL5229752

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

Functional
Cytotoxicity against human DU-145 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 DU-145
Confidence 1 — Organism
Curated By Autocuration

Target

DU-145 (CHEMBL613508)
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 7.20 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL451147 RENIERAMYCIN M 1 8.40
CHEMBL5273157 1 8.22
CHEMBL452709 SAFRAMYCIN A 1 8.10
CHEMBL5169402 1 7.50
CHEMBL5191895 1 7.30
CHEMBL468488 RENIERAMYCIN S 1 7.14
CHEMBL5285549 1 6.85
CHEMBL5275238 1 6.17
CHEMBL5289736 1 5.14
CHEMBL5279287 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL451147 RENIERAMYCIN M IC50 = 4.0 nM 8.40
CHEMBL5273157 IC50 = 6.0 nM 8.22
CHEMBL452709 SAFRAMYCIN A IC50 = 8.0 nM 8.10
CHEMBL5169402 IC50 = 32.0 nM 7.50
CHEMBL5191895 IC50 = 50.0 nM 7.30
CHEMBL468488 RENIERAMYCIN S IC50 = 72.0 nM 7.14
CHEMBL5285549 IC50 = 140.0 nM 6.85
CHEMBL5275238 IC50 = 680.0 nM 6.17
CHEMBL5289736 IC50 = 7300.0 nM 5.14
CHEMBL5279287 IC50 > 20000.0 nM -