1096481-48-9Relevant articles and documents
Synthesis and anti-oomycete activity of novel quinazolin- and benzothiazol-6-yloxyacetamides: Potent aza-analogs and five-ring analogs of quinoline fungicides
Beaudegnies, Renaud,Quaranta, Laura,Murphy Kessabi, Fiona,Lamberth, Clemens,Knauf-Beiter, Gertrud,Fraser, Torquil
, p. 444 - 452 (2016)
Novel quinazolin- and benzothiazol-6-yloxyacetamides show excellent in vivo activity against the three economically most important Oomycete pathogens Phytophthora infestans, Plasmopara viticola and Pythium ultimum. They are polar analogs of known quinolin-6-yloxyacetamides, which are not active against the soil-borne damping-off disease caused by Pythium ultimum. The Bogert quinazoline synthesis, an almost forgotten heterocyclization technique, proved to be highly useful for the concise construction of required quinazolin-6-ol building blocks.
HETEROBICYCLIC AMIDES AS INHIBITORS OF CD38
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Paragraph 0498, (2021/02/05)
The present invention relates to heterobicyclic amides and related compounds which are inhibitors of CD38 and are useful in the treatment of cancer.