104615-28-3

Usage

Chemical structure

2-(2-Furanyl)-[1,2,4]triazolo[1,5-c]quinazoline-5-amine is a compound with a unique structure that includes a furanyl group and a triazoloquinazoline ring system.

Heterocyclic amine

It is a heterocyclic amine, meaning it contains a ring structure made up of different types of atoms, including nitrogen and oxygen.

Biological activities

The presence of the furanyl group and the triazoloquinazoline ring system in its structure suggests that it may possess interesting biological activities.

Pharmaceutical applications

These types of compounds are often studied for their potential pharmacological properties, and further research may reveal its potential as a drug candidate for various medical conditions.

Unexplored potential uses

The specific biological activities and potential uses of 2-(2-Furanyl)-[1,2,4]triazolo[1,5-c]quinazoline-5-amine have yet to be fully explored.

Upstream product

• 58314-88-8 N-ethoxymethylene-2-aminobenzonitrile 
• 1885-29-6 anthranilic acid nitrile 
• 153488-29-0 3-(2-furoylamino)-4-imino-3,4-dihydroquinazoline 
• 104615-73-8 2-(2-furyl)<1,2,4>triazolo<1,5-c>quinazoline-5(6H)-thione 
• 81431-98-3 2-cyanophenylisothiocyanate 
• 3326-71-4 2-furoic acid hydrazide 
• 1904-58-1 anthranilic acid hydrazide 
• 134-20-3 2-carbomethoxyaniline 
• 51282-48-5 furane-2-carboximidate de methyle 
• 617-90-3 2-furancarbonitrile 
• 420-04-2 CYANAMID 
• 104615-64-7 5-(2-aminophenyl)-3-(2-furyl)-1H-1,2,4-triazole 
• 104615-72-7 2-(2-furyl)-5-(methylthio)<1,2,4>triazolo<1,5-c>quinazoline 
• 593-85-1 diguanidine carbonate 

Relevant academic research and scientific papers

Synthesis and evaluation of adenosine antagonist activity of a series of [1,2,4]triazolo[1,5-c]quinazolines

A series of [1,2,4]triazolo[1,5-c]quinazolines were prepared in satisfactory yields by reaction of some derivatives of 2-aminobenzohydrazide with several hydrochlorides of aromatic amidines, and their binding affinities for the recombinant human adenosine A2A and A2B receptors were determined. None of the new compounds showed noteworthy affinity for these receptors, though a very high affinity for the A2A receptor and, consequently, a high level of A2A/A2B selectivity was revealed for one of the synthesized compounds.

Synthesis of Triazoloquinazoline and Triazolo-1,4-benzodiazepine Derivatives

Some triazoloquinazolin-5(6H)-ones 7, the corresponding isomers triazoloquinazolin-5(6H)-ones and the 5-amino derivatives 8,9 and 11 have been synthesized starting from the acylamidrazones 5.The preparation of 5H-triazol

Structure-Activity Profile of a Series of Novel Triazoloquinazoline Adenosine Antagonists

During a search for benzodiazepine receptor modulators, a highly potent adenosine antagonist (CGS 15943) was discovered.The compound was defined as resonance-stabilized hybrid of the canonical structures 9-chloro-2-(2-furyl)triazoloquinazoli