Biological importance of structurally diversified chromenes

M Costa, TA Dias, A Brito, F Proença - European journal of medicinal …, 2016 - Elsevier
Compounds incorporating the chromene scaffold are largely present in natural products and
display a wide variety of biological activities. Their low toxicity combined to the broad …

Irreversible inhibitors of serine, cysteine, and threonine proteases

JC Powers, JL Asgian, ÖD Ekici, KE James - Chemical reviews, 2002 - ACS Publications
Proteases or proteolytic enzymes form one of the largest and more important groups of
enzymes. Proteases selectively catalyze the hydrolysis of peptide bonds and can be divided …

Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins

A Maresca, C Temperini, L Pochet… - Journal of medicinal …, 2010 - ACS Publications
Coumarin derivatives were recently shown to constitute a totally new class of inhibitors of the
zinc metalloenzyme carbonic anhydrase (CA, EC 4.2. 1.1), being hydrolyzed within the CA …

The structure and pharmacological functions of coumarins and their derivatives

L Wu, X Wang, W Xu, F Farzaneh… - Current medicinal …, 2009 - ingentaconnect.com
Coumarins are of many different structures. They constitute an important class of
pharmacological agents possessing a range of different physiological activities including …

Recent advances and therapeutic journey of coumarins: current status and perspectives

KP Barot, SV Jain, L Kremer, S Singh… - Medicinal Chemistry …, 2015 - Springer
Coumarins are oxygen-containing molecules with specific benzopyrone nucleus. Different
coumarins are identified as antineurodegeneratives, anticoagulants, antioxidants …

Synthesis of new coumarin 3-(N-aryl) sulfonamides and their anticancer activity

NS Reddy, MR Mallireddigari, S Cosenza… - Bioorganic & medicinal …, 2004 - Elsevier
Synthesis of coumarin 3-(N-aryl) sulfonamides was accomplished either by Knoevenagel
condensation of anilinosulfonylacetic acids with suitable salicylaldehydes or by the reaction …

Factor XII/XIIa inhibitors: Their discovery, development, and potential indications

C Davoine, C Bouckaert, M Fillet, L Pochet - European Journal of Medicinal …, 2020 - Elsevier
Coagulation factor XII (FXII), a S1A serine protease, was discovered more than fifty years
ago. However, its in vivo functions and its three-dimensional structure started to be disclosed …

Synthesis and biological evaluation of novel coumarin derivatives with a 7-azomethine linkage

CA Kontogiorgis, DJ Hadjipavlou-Litina - Bioorganic & medicinal chemistry …, 2004 - Elsevier
The synthesis of several novel coumarin derivatives with a 7-azomethine linkage was
carried out starting from 7-formyl-coumarin. The compounds were tested in vivo for their anti …

3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo

I Kempen, D Papapostolou, N Thierry, L Pochet… - British Journal of …, 2003 - nature.com
In search for new anticancer agents, we have evaluated the antiinvasive and antimigrative
properties of recently developed synthetic coumarin derivatives among which two …

Coumarin and isocoumarin as serine protease inhibitors

L Pochet, R Frédérick… - Current pharmaceutical …, 2004 - ingentaconnect.com
Serine proteases are attractive targets for the design of enzyme inhibitors since they are
involved in the etiology of several diseases. Within the class of serine proteases, HLE is one …