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Assay Detail

CHEMBL809733

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

Functional
Cell free inhibiting activity against Streptococcus pneumoniae 5635(Wild type ribosomes for transcription/translation assay)
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Streptococcus pneumoniae
Confidence 1 — Organism
Curated By Intermediate

Target

Streptococcus pneumoniae (CHEMBL347)
Type ORGANISM
Organism Streptococcus pneumoniae

Publication

Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens.
Ma Z, Clark RF, Brazzale A, Wang S, Rupp MJ, Li L, Griesgraber G, Zhang S, Yong H, Phan LT, Nemoto PA, Chu DT, Plattner JJ, Zhang X, Zhong P, Cao Z, Nilius AM, Shortridge VD, Flamm R, Mitten M, Meulbroek J, Ewing P, Alder J, Or YS.
J Med Chem (2001) 44 : 4137 -4156
PubMed 11708916 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 6.91 7.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1741 CLARITHROMYCIN 4.0 1 7.05
CHEMBL529 AZITHROMYCIN 4.0 1 6.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1741 CLARITHROMYCIN IC50 = 90.0 nM 7.05
CHEMBL529 AZITHROMYCIN IC50 = 170.0 nM 6.77