Pyrrolo[3,2-c]pyridine derivatives as inhibitors of platelet aggregation was written by Altomare, C.;Summo, L.;Cellamare, S.;Varlamov, A. V.;Voskressensky, L. G.;Borisova, T. N.;Carotti, A.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2000.Safety of 1-Benzylpiperidin-4-one oxime This article mentions the following:
A series of pyrrolo[3,2-c]pyridines, isosteres of the antithrombotic drug ticlopidine, has been synthesized and evaluated in vitro for the ability to inhibit aggregation of human platelet-rich plasma induced by ADP. Structure-activity relationships showed their antiplatelet effects to be related to the lipophilicity. In the experiment, the researchers used many compounds, for example, 1-Benzylpiperidin-4-one oxime (cas: 949-69-9Safety of 1-Benzylpiperidin-4-one oxime).
1-Benzylpiperidin-4-one oxime (cas: 949-69-9) belongs to piperidine derivatives. The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper its spicy taste. Piperidine derivatives bearing a masked aldehyde function in the 蔚-position are easily transformed into quinolizidine compounds through intramolecular reductive amination.Safety of 1-Benzylpiperidin-4-one oxime
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem