89374-41-4

Upstream product

• 49609-84-9 2-Chloronicotinoyl chloride 
• 89374-20-9 2-Chloronicotinoyl Isothiocyanate 
• 2942-59-8 2-chloronicotinic acid 
• 89374-29-8 1-(2-Chloro-pyridine-3-carbonyl)-3-(4-methoxy-phenyl)-thiourea 

Downstream Products

• 190843-54-0 2-[N-benzyl-N-(4-methoxyphenyl)amino]-4H-pyrido[3,2-e]-1,3-thiazin-4-one 
• 190843-41-5 2-[(4-methoxyphenyl)(methyl)amino]-4H-pyrido[3,2-e][1,3]thiazin-4-one 
• 190843-51-7 2-[ethyl(4-methoxyphenyl)amino]-4H-pyrido[3,2-e][1,3]thiazin-4-one 
• 190843-61-9 2-[N-allyl-N-(4-methoxyphenyl)amino]-4H-pyrido[3,2-e]-1,3-thiazin-4-one 
• 190843-52-8 2-[N-isopropyl-N-(4-methoxyphenyl)amino]-4H-pyrido[3,2-e]-1,3-thiazin-4-on 
• 190843-53-9 2-[N-butyl-N-(4-methoxyphenyl)amino]-4H-pyrido[3,2-e]-1,3-thiazin-4-one 
• 190843-43-7 2-[N-(4-methoxyphenyl)-N-propylamino]-4H-pyrido[3,2-e]-1,3-thiazin-4-one 

Relevant academic research and scientific papers

4 H - pyrido [3, 2 - e] [1, 3] thiazine - 4 - ketone derivative and its application

The invention relates to the technical field of medicines, discloses a novel 4H-pyridino-[3,2-e][1,3]thiazine-4-ketone derivate and an application thereof, and designs and synthesizes a series of novel-structure 4H-pyridino-[3,2-e][1,3]thiazine-4-ketone c

Synthesis, structure-activity relationships, and anticonvulsant activities of 2-amino-4H-pyrido[3,2-e][1,3]thiazin-4-one derivatives as orally active AMPA receptor antagonists

As part of a program aimed at discovering orally active 2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid (AMPA) receptor antagonists, we screened our compound library and identified 2-[allyl(4-methylphenyl)amino]-4H-pyrido[3,2-e][1,3]thiazin-4-on