98123-77-4

Upstream product

• 51935-42-3 1-chloro-4-hydrazinophthalazine 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 87540-60-1 6-(2-methoxy)ethoxy-3-(4'-methoxyphenyl)-1,2,4-triazolo<3,4-a>phthalazine 
• 87539-86-4 N-(2-hydroxypropyl)-3-(4-methoxyphenyl)-N-methyl-1,2,4-triazolo[3,4-a]phthalazin-6-amine 
• 87540-22-5 L 16317 
• 98123-78-5 6-ethylthio-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-a]phthalazine 
• 898804-92-7 4-[3-(4-Methoxyphenyl)-[1,2,4]triazolo[3,4-a]phthalazin-6-ylamino]-benzonitrile 
• 882983-10-0 N-[3-(4-methoxyphenyl)-[1,2,4]triazolo[3,4-a]phthalazin-6-yl]-benzene-1,4-diamine 
• 98123-79-6 6-Ethanesulfonyl-3-(4-methoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine 
• 87540-59-8 ethyl 4-<<3-(4'-methoxyphenyl)-1,2,4-triazolo<3,4-a>phthalazine-6-yl>-oxy>butanoate 
• 87540-57-6 2-<<3-(4-'methoxyphenyl)-1,2,4-triazolo<3,4-a>phthalazin-6-yl>-oxy>-ethanol 
• 87540-56-5 6-ethoxy-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-a]phthalazine 
• 87540-94-1 6-hydroxy-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-a]phthalazine 
• 87540-58-7 4-<<3-(4-methoxyphenyl)-1,2,4-triazolo<3,4-a>phthalazin-6-yl>-oxy>butanol 
• 87540-02-1 3-(4-Methoxy-phenyl)-6-pyrrolidin-1-yl-[1,2,4]triazolo[3,4-a]phthalazine 
• 897662-74-7 (4-Methoxyphenyl)-[3-(4-methoxyphenyl)-[1,2,4]triazolo[3,4-a]phthalazin-6-yl]-amine 

Relevant academic research and scientific papers

Triazolophthalazines

The compounds of formula I in which R1 and R2 have the meanings as given in the description are novel effective PDE2 inhibitors.

Triazolophthalazines

The compounds of formula (I) in which R1, R2 and R3 have the meanings as given in the description are novel effective PDE2 inhibitors.

Triazolophthalazines

The compounds of formula (I) in which R1, R2 and R3 have the meanings as given in the description are novel effective PDE2 inhibitors.

6-(Alkylamino)-3-aryl-1,2,4-triazolophthalazines. A New Class of Benzodiazepine Receptor Ligands

Some 6-(alkylamino)-3-aryl-1,2,4-triazolophthalazines have been shown to displace diazepam from rat brain specific binding sites, in vitro, with Ki (nM) values comparable to those of reference benzodiazepines and to have anticonvulsant (