348618-22-4

Upstream product

• 348618-21-3 1-(2-chloroethoxy)-4,5-bis(chloromethyl)-2-methoxybenzene 
• 90-05-1 2-methoxy-phenol 
• 53815-60-4 1-(2-chloroethoxy)-2-methoxybenzene 
• 127-09-3 sodium acetate 

Downstream Products

• 1393907-11-3 8-methoxy-9-[2-(4-benzylpiperazino)ethoxy]-(13aS)-1,2,3,13a-tetrahydro-5H-pyrrolo[2,1-c][1,4]naphthodiazepin-5-one 
• 1393910-24-1 C₃₄H₄₄N₄O₅S₂ 
• 1393910-25-2 C₃₄H₄₆N₄O₃S₂ 
• 1393907-12-4 8-methoxy-9-[2-(4-phenylpiperazino)ethoxy]-(13aS)-1,2,3,13a-tetrahydro-5H-pyrrolo[2,1-c][1,4]naphthodiazepin-5-one 
• 1393910-26-3 C₃₃H₄₂N₄O₅S₂ 
• 1393910-27-4 C₃₃H₄₄N₄O₃S₂ 
• 348618-24-6 4-(2-chloroethoxy)-5-methoxyphthalaldehyde 
• 348618-23-5 [4-(2-chloroethoxy)-2-(hydroxymethyl)-5-methoxyphenyl]methanol 

Relevant academic research and scientific papers

Pyrrolo[2,1-c][1,4]naphthodiazepine Linked Piperazine Compounds and a Process for the Preparation Thereof

The present invention provides a compound of general formula A, useful as potential antitumour agents against five human cancer cell lines. The present invention further provides a process for the preparation of pyrrolo[2,1-c][1,4]naphthodiazepine linked substituted piperazine conjugates attached through different alkane spacers of general formula A. (Formula I) General formula A. Where R=R′=(Formula II). n=1-9 and R″=methyl, ethyl, acetyl, benzyl, piperinoyl, 4-fluorophenyl, 4-chlorophenyl, 4-methoxyphenyl, pyridyl, pyrimidyl

PYRROLO [2,1-C]1,4]NAPHTHODIAZEPINE LINKED PIPERAZINE COMPOUNDS AND A PROCESS FOR THE PREPARATION THEREOF

The present invention provides a compound of general formula A, useful as potential antitumour agents against five human cancer cell lines. The present invention further provides a process for the preparation of pyrrolo[2,1-c][1,4]naphthodiazepine linked substituted piperazine conjugates attached through different alkane spacers of general formula A. (Formula I) General formula A. Where R= R'= (Formula II). n=1-9 and R''= methyl, ethyl, acetyl, benzyl, piperinoyl, 4-fluorophenyl, 4-chlorophenyl, 4-methoxyphenyl, pyridyl, pyrimidyl

4-Anilino-7,8-dialkoxybenzo[g]quinoline-3-carbonitriles as potent Src kinase inhibitors

It has been previously reported that appropriately substituted 4-anilinoquinoline-3-carbonitriles are potent inhibitors of Src kinase, with biological activity in vitro and in vivo. Structural modifications to these compounds have been explored, providing

Tricyclic protein kinase inhibitors

This invention provides compounds of formula 1, having the structure which are useful as inhibitors of protein tyro sine kinase and are antiproliferative agents.