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Assay Detail

CHEMBL1248094

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

ADMET
Inhibition of human recombinant CYP1A2 preincubated for 10 mins
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Cytochrome P450 1A2 (CHEMBL3356)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design and synthesis of novel tricyclic benzoxazines as potent 5-HT(1A/B/D) receptor antagonists leading to the discovery of 6-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-4H-imidazo[5,1-c][1,4]benzoxazine-3-carboxamide (GSK588045).
Bromidge SM, Arban R, Bertani B, Bison S, Borriello M, Cavanni P, Dal Forno G, Di-Fabio R, Donati D, Fontana S, Gianotti M, Gordon LJ, Granci E, Leslie CP, Moccia L, Pasquarello A, Sartori I, Sava A, Watson JM, Worby A, Zonzini L, Zucchelli V.
J Med Chem (2010) 53 : 5827 -5843
PubMed 20590088 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.70 6.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1241639 1 6.00
CHEMBL1241737 1 5.40
CHEMBL1241738 1 -
CHEMBL1241546 1 -
CHEMBL1241736 1 -
CHEMBL1241824 1 -
CHEMBL1241912 1 -
CHEMBL1241913 1 -
CHEMBL1241998 1 -
CHEMBL1242081 1 -
CHEMBL1242345 1 -
CHEMBL1242533 1 -
CHEMBL1242623 1 -
CHEMBL1242717 1 -
CHEMBL1241642 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1241639 IC50 = 1000.0 nM 6.00
CHEMBL1241737 IC50 = 4000.0 nM 5.40
CHEMBL1241738 IC50 > 10000.0 nM -
CHEMBL1241546 IC50 > 5000.0 nM -
CHEMBL1241736 IC50 > 5000.0 nM -
CHEMBL1241824 IC50 > 10000.0 nM -
CHEMBL1241912 IC50 > 9000.0 nM -
CHEMBL1241913 IC50 > 9000.0 nM -
CHEMBL1241998 IC50 > 8000.0 nM -
CHEMBL1242081 IC50 > 7000.0 nM -
CHEMBL1242345 IC50 > 10000.0 nM -
CHEMBL1242533 IC50 > 6000.0 nM -
CHEMBL1242623 IC50 > 10000.0 nM -
CHEMBL1242717 IC50 > 10000.0 nM -
CHEMBL1241642 IC50 < 2000.0 nM -