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Assay Detail

CHEMBL3420058

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Physicochemical
Antioxidant activity assessed as inhibition of ABTS free radical scavenging activity after 10 mins by spectrophotometry relative to control
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Physicochemical
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Publication

Design, synthesis and biological evaluation of quinazoline derivatives as anti-trypanosomatid and anti-plasmodial agents.
Mendoza-Martínez C, Correa-Basurto J, Nieto-Meneses R, Márquez-Navarro A, Aguilar-Suárez R, Montero-Cortes MD, Nogueda-Torres B, Suárez-Contreras E, Galindo-Sevilla N, Rojas-Rojas Á, Rodriguez-Lezama A, Hernández-Luis F.
Eur J Med Chem (2015) 96 : 296 -307
PubMed 25899334 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.02 5.32

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3415778 1 5.32
CHEMBL546890 1 5.24
CHEMBL3415776 1 5.20
CHEMBL3415777 1 5.20
CHEMBL6885 QUINAZOLINE-2,4,6-TRIAMINE 1 5.17
CHEMBL3415775 1 5.15
CHEMBL3415942 1 5.13
CHEMBL153 TROLOX 1 4.96
CHEMBL196 ASCORBIC ACID 4.0 1 4.95
CHEMBL3989727 VITAMIN E 4.0 1 4.83
CHEMBL3415944 1 4.61
CHEMBL3415945 1 4.47
CHEMBL3415943 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3415778 IC50 = 4750.0 nM 5.32
CHEMBL546890 IC50 = 5720.0 nM 5.24
CHEMBL3415776 IC50 = 6290.0 nM 5.20
CHEMBL3415777 IC50 = 6380.0 nM 5.20
CHEMBL6885 QUINAZOLINE-2,4,6-TRIAMINE IC50 = 6780.0 nM 5.17
CHEMBL3415775 IC50 = 7040.0 nM 5.15
CHEMBL3415942 IC50 = 7360.0 nM 5.13
CHEMBL153 TROLOX IC50 = 10920.0 nM 4.96
CHEMBL196 ASCORBIC ACID IC50 = 11250.0 nM 4.95
CHEMBL3989727 VITAMIN E IC50 = 14840.0 nM 4.83
CHEMBL3415944 IC50 = 24460.0 nM 4.61
CHEMBL3415945 IC50 = 33910.0 nM 4.47
CHEMBL3415943 IC50 = 113950.0 nM -