Mario Di Braccio scite author profile

Multi-membered N-heterocycles R 0690 1,5-Benzodiazepines. Part 13. Substituted 4H-[1,2,4]Triazolo[4,3-a][1,5]benzodiazepin-5-amines and 4H-Imidazo[1,2-a][1,5]benzodiazepin-5-amines as Analgesic, Antiinflammatory and/or Antipyretic Agents with Low Acute Toxicity. -A series of benzodiazepines is prepared and tested for pharmacological activity. Compounds (XIII) and (XV) show remarkable analgesic, anti-inflammatory and antipyretic activities at doses devoid of acute adverse effects. -(GROSSI, G.; DI BRACCIO, M.; ROMA*, G.; BALLABENI, V.; TOGNOLINI, M.; CALCINA, F.; BAROCELLI, E.; Eur.

show abstract

In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors

Pisani

Farina

Nicolotti

et al. 2015

European Journal of Medicinal Chemistry

View full text Add to dashboard Cite

Coumarin, chromone, and 4(3H)-pyrimidinone novel bicyclic and tricyclic derivatives as antiplatelet agents: synthesis, biological evaluation, and comparative molecular field analysis

Roma

Braccio

Carrieri

et al. 2003

Bioorganic & Medicinal Chemistry

View full text Add to dashboard Cite

1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity

Roma

Grossi

Braccio

et al. 2008

European Journal of Medicinal Chemistry

View full text Add to dashboard Cite

1,5-Benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandinE2production

Fruscella

Sottocorno

Braccio

et al. 2001

Pharmacological Research

View full text Add to dashboard Cite

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

hi@scite.ai

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Mario Di Braccio

1,5-Benzodiazepines. Part XII. Synthesis and biological evaluation of tricyclic and tetracyclic 1,5-benzodiazepine derivatives as nevirapine analogues

1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities

Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors

1,5‐Benzodiazepines. Part 13. Substituted 4H‐[1,2,4]Triazolo[4,3‐a][1,5]benzodiazepin‐5‐amines and 4H‐Imidazo[1,2‐a][1,5]benzodiazepin‐5‐amines as Analgesic, Antiinflammatory and/or Antipyretic Agents with Low Acute Toxicity.

In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors

Coumarin, chromone, and 4(3H)-pyrimidinone novel bicyclic and tricyclic derivatives as antiplatelet agents: synthesis, biological evaluation, and comparative molecular field analysis

1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity

1,5-Benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandinE2production

Contact Info

Product

Resources

About