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Assay Detail

CHEMBL4678656

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

Functional
Reversal of resistance to paclitaxel-induced cytotoxicity in human KB 3-1 cells assessed as paclitaxel IC50 at 4 uM pre-incubated for 4 hrs followed by paclitaxel addition and measured after 72 hrs by MTT assay (Rvb = 4.54 +/- 1.59 nM)
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type KB 3-1
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Structure-Based Design, Synthesis, and Biological Evaluation of New Triazolo[1,5-a]Pyrimidine Derivatives as Highly Potent and Orally Active ABCB1 Modulators.
Wang S,Wang SQ,Teng QX,Yang L,Lei ZN,Yuan XH,Huo JF,Chen XB,Wang M,Yu B,Chen ZS,Liu HM
J Med Chem (2020) 63 : 15979 -15996
PubMed 33280384 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.42 8.42

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL6966 VERAPAMIL 4.0 1 8.42

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL6966 VERAPAMIL IC50 = 3.84 nM 8.42