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Assay Detail

CHEMBL4381889

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

Functional
Growth inhibition of human 1321N1 cells incubated for 72 hrs by MTT assay
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Synthesis of Novel Potent Archazolids: Pharmacology of an Emerging Class of Anticancer Drugs.
Scheeff S, Rivière S, Ruiz J, Abdelrahman A, Schulz-Fincke AC, Köse M, Tiburcy F, Wieczorek H, Gütschow M, Müller CE, Menche D.
J Med Chem (2020) 63 : 1684 -1698
PubMed 31990540 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 8.30 9.84

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL411767 ARCHAZOLID B 1 9.84
CHEMBL241106 ARCHAZOLID A 1 9.60
CHEMBL4471610 1 9.12
CHEMBL4593430 1 8.67
CHEMBL4460252 1 8.59
CHEMBL290814 BAFILOMYCIN A1 1 8.51
CHEMBL1784269 ARCHAZOLID F 1 8.35
CHEMBL4549217 1 6.53
CHEMBL4447903 1 5.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL411767 ARCHAZOLID B IC50 = 0.145 nM 9.84
CHEMBL241106 ARCHAZOLID A IC50 = 0.253 nM 9.60
CHEMBL4471610 IC50 = 0.757 nM 9.12
CHEMBL4593430 IC50 = 2.16 nM 8.67
CHEMBL4460252 IC50 = 2.58 nM 8.59
CHEMBL290814 BAFILOMYCIN A1 IC50 = 3.06 nM 8.51
CHEMBL1784269 ARCHAZOLID F IC50 = 4.51 nM 8.35
CHEMBL4549217 IC50 = 296.0 nM 6.53
CHEMBL4447903 IC50 = 3050.0 nM 5.52