Trending Topics on Coumarin and Its Derivatives in 2020

molecules Review Trending Topics on Coumarin and Its Derivatives in 2020 Aitor Carneiro 1, Maria João Matos 1,2, Eugenio Uriarte 1,3 and Lourdes Santana 1,*   Citation: Carneiro, A.; Matos, M.J.; Uriarte, E.; Santana, L. Trending Topics on Coumarin and Its Derivatives in 2020. Molecules 2021, 26, 501. https://doi.org/10.3390/ molecules26020501 Academic Editor: Emerson F. Queiroz Received: 10 December 2020 Accepted: 15 January 2021 Published: 19 January 2021 Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). 1Departamento de Química Orgánica, Facultade de Farmacia, Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain; aitor[email protected] (A.C.); [email protected] (M.J.M.); [email protected] (E.U.) 2CIQUP/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Rua Campo Alegre 687, 4169-007 Porto, Portugal 3Instituto de Ciencias Químicas Aplicadas, Universidad Autónoma de Chile, 7500912 Santiago, Chile *Correspondence: lour[email protected]; Tel.: +34-881-814-936 Abstract: Coumarins are naturally occurring molecules with a versatile range of activities. Their structural and physicochemical characteristics make them a privileged scaffold in medicinal chemistry and chemical biology. Many research articles and reviews compile information on this important family of compounds. In this overview, the most recent research papers and reviews from 2020 are organized and analyzed, and a discussion on these data is included. Multiple electronic databases were scanned, including SciFinder, Mendeley, and PubMed, the latter being the main source of information. Particular attention was paid to the potential of coumarins as an important scaffold in drug design, as well as fluorescent probes for decaging of prodrugs, metal detection, and diagnostic purposes. Herein we do an analysis of the trending topics related to coumarin and its derivatives in the broad field of drug discovery. Keywords: coumarins; biological applications; drug discovery; fluorescent probes 1. Introduction Coumarins are molecules that belong to a very special family. Their conjugated double ring system makes them interesting molecules for different fields of research. Coumarins can be found in industry as cosmetics and perfume ingredients, as food additives, and especially in the pharmaceutical industry in the synthesis of a large number of synthetic pharmaceutical products [1]. This last application is the main focus of our overview. Coumarin (Figure 1) is found in nature in a wide variety of plants, particularly in high concentration in the tonka bean (Dipteryx odorata). It can also be found in sweet woodruff (Galium odoratum), vanilla grass (Anthoxanthum odoratum), and sweet grass (Hierochloe odorata), among others. This explains the great interest in the extraction and characterization techniques of natural coumarins, and in the synthesis of their derivatives. In addition, the simplicity of its chemical backbone is very attractive, as well as the reactivity of the benzene and pyrone rings. Conjugated double bonds are responsible for an electronic environment that plays a very important role in this family of compounds. Molecules 2021, 26, x FOR PEER REVIEW 2 of 16 Figure 1. Basic classification of coumarins: chemical structures of the three main classes. 2. Discussion Searching for the word “coumarin” in Mendeley, PubMed, and SciFinder in early November 2020, and filtering by year “2020”, more than a thousand references appeared. Another search was conducted in late December to include as much information as possible in this manuscript. A diversity of journals from different fields publishes research articles and reviews related to the biological interest of both plant extracts containing coumarins and/or synthetic molecules based on this scaffold. Hybrid molecules containing different pharmacophores [2,3] like piperazines or pyrazolines [4] are at the top of the list. For simplicity, in the current review the information is organized taking into account the potential pharmacological/biological applications of coumarin derivatives. 2.1. Anticancer Activity The activity of coumarins as anticancer agents is at the top of reviews published in 2020 [5–8], as well as research papers. Potent inhibitors (Figure 2, general structure I) of aldo–keto reductase (AKR) presenting an iminocoumarin scaffold, with activities between 25 and 56 nM, have been described for the treatment of prostatic cancer [9]. The design of sulfamide 3-benzylcoumarin hybrids bearing an oxadiazole ring at position 7 (Figure 2, general structure II) has allowed the preparation of new multitarget mitogen-activated protein kinase (MEK) inhibitors and nitric oxide (NO) donors, both with antiproliferative properties [10]. In other cases, the anticancer profile has been directed to other targets. Such is the case of new inhibitors of cyclin-dependent kinases, specifically CDK9, designing hybrids that incorporate an aminopyrimidine fragment to coumarin, both pharmacophores of known activity on these therapeutic targets [11]. We highlight here compound III (Figure 2), with high activity and selectivity for these receptors in comparison with other kinases. Other important targets for cancer treatment, especially lymphomas, are histone deacetylases (HDACs). A series of coumarins (Figure 2, general structure IV) exhibiting a hydroxamate structure similar to HDACi vorinostat (SAHA) has been published [12]. The compounds show inhibitory activity in the nanomolar range, being higher in the case of propyl or methoxypropyl derivatives. In addition, it is worth highlighting the design of hybrids in which one part of the molecule provides fluorescent properties, and another provides therapeutic action (theranostic). Such is the case of the fusion of a 7-aminocoumarin fluorescent ring with a chalcone fragment (Figure 2, compound V). This molecule is an inhibitor of thioredoxin reductases (TrxRs), presenting high antitumor activity (IC50 = 3.6 μM), and is also used as a diagnostic agent [13]. Coumarin scaffold fluorescence is being explored extensively in biomedicine, as described at the end of this review. The preparation of photo-triggered drug delivery systems (PTDDSs, Figure 2, general structure VI) has also been described, in which the chlorambucil pharmacophore is incorporated into more complex carbazole–coumarins (electron donor and electron acceptor fragments, respectively), carriers of a mitochondrial triphenylphosphonium ligand. O O R R = OCH 3, CH 3, OH, X, … Simple coumarins Pyranocoumarins Furocoumarins O OO O OO O O O O O O Figure 1. Basic classification of coumarins: chemical structures of the three main classes. Molecules 2021,26, 501. https://doi.org/10.3390/molecules26020501 https://www.mdpi.com/journal/molecules Molecules 2021,26, 501 2 of 15 This review is based on the most relevant literature that comprises new data from recent research articles and overviews on the development of new therapeutic solutions and fluorescent probes based on the coumarin scaffold. The research articles and reviews organized to prepare this manuscript have been compiled from various electronic databases, including SciFinder, Mendeley, and PubMed. The latter was the main source of information, due to its specificity in the biomedical field. 2. Discussion Searching for the word “coumarin” in Mendeley, PubMed, and SciFinder in early November 2020, and filtering by year “2020”, more than a thousand references appeared. Another search was conducted in late December to include as much information as possible in this manuscript. A diversity of journals from different fields publishes research articles and reviews related to the biological interest of both plant extracts containing coumarins and/or synthetic molecules based on this scaffold. Hybrid molecules containing different pharmacophores [ 2 , 3 ] like piperazines or pyrazolines [ 4 ] are at the top of the list. For simplicity, in the current review the information is organized taking into account the potential pharmacological/biological applications of coumarin derivatives. 2.1. Anticancer Activity The activity of coumarins as anticancer agents is at the top of reviews published in 2020 [ 5 – 8 ], as well as research papers. Potent inhibitors (Figure 2, general structure I ) of aldo–keto reductase (AKR) presenting an iminocoumarin scaffold, with activities between 25 and 56 nM, have been described for the treatment of prostatic cancer [ 9 ]. The design of sulfamide 3-benzylcoumarin hybrids bearing an oxadiazole ring at position 7 (Figure 2 , general structure II ) has allowed the preparation of new multitarget mitogen-activated protein kinase (MEK) inhibitors and nitric oxide (NO) donors, both with antiproliferative properties [ 10 ]. In other cases, the anticancer profile has been directed to other targets. Such is the case of new inhibitors of cyclin-dependent kinases, specifically CDK9, designing hybrids that incorporate an aminopyrimidine fragment to coumarin, both pharmacophores of known activity on these therapeutic targets [ 11 ]. We highlight here compound III (Figure 2) , with high activity and selectivity for these receptors in comparison with other kinases. Other important targets for cancer treatment, especially lymphomas, are histone deacetylases (HDACs). A series of coumarins (Figure 2, general structure IV ) exhibiting a hydroxamate structure similar to HDACi vorinostat (SAHA) has been published [ 12 ]. The compounds show inhibitory activity in the nanomolar range, being higher in the case of propyl or methoxypropyl derivatives. In addition, it is worth highlighting the design of hybrids in which one part of the molecule provides fluorescent properties, and another provides therapeutic action (theranostic). Such is the case of the fusion of a 7-aminocoumarin fluorescent ring with a chalcone fragment (Figure 2, compound V ). This molecule is an inhibitor of thioredoxin reductases (TrxRs), presenting high antitumor activity (IC 50 = 3.6 µ M), and is also used as a diagnostic agent [ 13 ]. Coumarin scaffold fluorescence is being explored extensively in biomedicine, as described at the end of this review. The preparation of photo-triggered drug delivery systems (PTDDSs, Figure 2, general structure VI) has also been described, in which the chlorambucil pharmacophore is incorporated into more complex carbazole–coumarins (electron donor and electron acceptor fragments, respectively), carriers of a mitochondrial triphenylphosphonium ligand. This system allows, by irradiation, the controlled release of the chemotherapeutic agent [14]. Finally, coumarins are widely used as ligands in the formation of metal complexes, as described in a very recent review [ 15 ] focusing on their application as anticancer agents. Such is the case of complexes with platinum, palladium, gold, copper, or ruthenium, many of which are also used as described below, in the design of antimicrobial agents. Molecules 2021,26, 501 3 of 15 Molecules 2021, 26, x FOR PEER REVIEW 3 of 16 This system allows, by irradiation, the controlled release of the chemotherapeutic agent [14]. Figure 2. Structures of coumarin derivatives as anticancer agents. Finally, coumarins are widely used as ligands in the formation of metal complexes, as described in a very recent review [15] focusing on their application as anticancer agents. Such is the case of complexes with platinum, palladium, gold, copper, or ruthenium, many of which are also used as described below, in the design of antimicrobial agents. Within the group of compounds with anticancer activity, coumarins exhibiting an antiglioma profile may be highlighted. Simple coumarins such as osthole, umbelliferone, esculin, and 4-hydroxycoumarin, combined with sorafenib (a kinase inhibitor drug approved for the treatment of primary kidney cancer, advanced primary liver cancer, FLT3- ITD positive acute myeloid leukemia (AML), and radioactive iodine-resistant advanced thyroid carcinoma) were studied [16]. The same group also studied a combination of the same simple coumarins with temozolomide (used in the treatment of brain tumors such as glioblastoma multiforme or anaplastic astrocytoma) [17]. 2.2. Antimicrobial Activity There is also an abundant bibliography related to the interest of coumarins as antimicrobials. Most of the projects are still inspired by the classic antibiotic novobiocin. There are several works in which antibacterial activity is found due to the presence of an azole ring introduced in different positions of the coumarin system. Articles have been published recently on the antibacterial activity of azole–coumarins, as well as 3/4/7 substituted arylcoumarins (Figure 3, general structures VII and VIII), especially active on Gram-pos- itive and negative bacteria according to substitution patterns [15,18–20]. In other cases, thiazolidinedione–coumarin hybrids have been described (Figure 3, general structure IX) that show activity on methicillin-resistant Staphylococcus aureus (MRSA) [21]. Interestingly, coumarin metal complexes also show antibacterial activity. Such is the case of 3-arylcoumarins that present general structures X (Figure 3), coordinated with Re(I), active against MRSA in nanomolar concentrations [22]; or the complexes of general Figure 2. Structures of coumarin derivatives as anticancer agents. Within the group of compounds with anticancer activity, coumarins exhibiting an antiglioma profile may be highlighted. Simple coumarins such as osthole, umbelliferone, esculin, and 4-hydroxycoumarin, combined with sorafenib (a kinase inhibitor drug approved for the treatment of primary kidney cancer, advanced primary liver cancer, FLT3- ITD positive acute myeloid leukemia (AML), and radioactive iodine-resistant advanced thyroid carcinoma) were studied [ 16 ]. The same group also studied a combination of the same simple coumarins with temozolomide (used in the treatment of brain tumors such as glioblastoma multiforme or anaplastic astrocytoma) [17]. 2.2. Antimicrobial Activity There is also an abundant bibliography related to the interest of coumarins as antimicrobials. Most of the projects are still inspired by the classic antibiotic novobiocin. There are several works in which antibacterial activity is found due to the presence of an azole ring introduced in different positions of the coumarin system. Articles have been published recently on the antibacterial activity of azole–coumarins, as well as 3/4/7 substituted arylcoumarins (Figure 3, general structures VII and VIII ), especially active on Gram-positive and negative bacteria according to substitution patterns [ 15 , 18 – 20 ]. In other cases, thiazolidinedione–coumarin hybrids have been described (Figure 3, general structure IX ) that show activity on methicillin-resistant Staphylococcus aureus (MRSA) [ 21 ]. Interestingly, coumarin metal complexes also show antibacterial activity. Such is the case of 3-arylcoumarins that present general structures X (Figure 3), coordinated with Re( I ), active against MRSA in nanomolar concentrations [ 22 ]; or the complexes of general structure XI , a coordination of coumarin–quinoline hybrids with Cu( I ), with activity against Flavobacterium psychrophilum, a Gram-negative bacterium that causes significant septicemia in fish, causing devastating economic problems in aquaculture [23]. Molecules 2021,26, 501 4 of 15 Molecules 2021, 26, x FOR PEER REVIEW 4 of 16 structure XI, a coordination of coumarin–quinoline hybrids with Cu(I), with activity against Flavobacterium psychrophilum, a Gram-negative bacterium that causes significant septicemia in fish, causing devastating economic problems in aquaculture [23]. Figure 3. Structures of coumarin derivatives as antimicrobial agents. In addition to the antibacterial activity, in a recent and comprehensive review on coumarins, activity against protozoa of the genus Leishmania was described [24]. The most promising compounds are prenylated, glycosylated, furan/pyranocoumarins, or simple hydroxy- or methoxy-substituted coumarins, along with the natural coumarin mammea A/BB (Figure 3, structure XII). Derivatives of this natural product have been prepared and substitutions at positions 6 and 8, as well as the phenyl ring at position 4, turned out to be mandatory for the studied activity. This structure–activity relationship (SAR) study led to the synthesis of the simplest and most lipophilic analogue XIII (Figure 3), the most promising member of the group as an antileishmanial agent. Similar structures, some also derived of the Mammea genus, have been evaluated against Mycobacterium tuberculosis, an activity that also shows simpler synthetic analogues derived from 4-hydroxycoumarin (Figure 3, general structure XIV) [25]. Finally, it is worth mentioning two articles reported this year on the design and preparation of coumarin derivatives with potential antiviral activity. This is the case of the dual hybrid inhibitors inspired by the antiviral activity of calanolide, known as reverse transcriptase (RT) inhibitor. With this in mind, dual inhibitors of HIV-1 RT and protease (PR) have been designed, in which the coumarin fragment responsible for RT activity is linked to the fragment of the antiretroviral darunavir, active against PR of the HIV, through different amide, carbamate, or amine linkers (Figure 3, general structure XV) [26]. Figure 3. Structures of coumarin derivatives as antimicrobial agents. In addition to the antibacterial activity, in a recent and comprehensive review on coumarins, activity against protozoa of the genus Leishmania was described [ 24 ]. The most promising compounds are prenylated, glycosylated, furan/pyranocoumarins, or simple hydroxy- or methoxy-substituted coumarins, along with the natural coumarin mammea A/BB (Figure 3, structure XII ). Derivatives of this natural product have been prepared and substitutions at positions 6 and 8, as well as the phenyl ring at position 4, turned out to be mandatory for the studied activity. This structure–activity relationship (SAR) study led to the synthesis of the simplest and most lipophilic analogue XIII (Figure 3), the most promising member of the group as an antileishmanial agent. Similar structures, some also derived of the Mammea genus, have been evaluated against Mycobacterium tuberculosis, an activity that also shows simpler synthetic analogues derived from 4-hydroxycoumarin (Figure 3, general structure XIV) [25]. Finally, it is worth mentioning two articles reported this year on the design and preparation of coumarin derivatives with potential antiviral activity. This is the case of the dual hybrid inhibitors inspired by the antiviral activity of calanolide, known as reverse transcriptase (RT) inhibitor. With this in mind, dual inhibitors of HIV-1 RT and protease (PR) have been designed, in which the coumarin fragment responsible for RT activity is linked to the fragment of the antiretroviral darunavir, active against PR of the HIV, through different amide, carbamate, or amine linkers (Figure 3, general structure XV ) [ 26 ]. The second case described the introduction of a piperidine ring through a linker in position 7 of the coumarin scaffold, originating compounds with outstanding activity against certain filoviruses such as Marburg virus (MARV) or Ebolavirus (EBOV). From the SAR studied, it is interesting to highlight the role of substitution in para position with a trifluoromethoxy Molecules 2021,26, 501 5 of 15 group that originated compound XVI (Figure 3) with IC 50 = 0.5 µ M and 1.2 µ M against EBOV and MARV, respectively [27]. 2.3. Antioxidant and Anti-Inflammatory Activities Although we have found very few publications related to these activities, in some cases the antioxidant activity of coumarin derivatives of both natural [ 28 ] and synthetic [ 29 ] origin has been reported. This is the case of NOs inhibitors, an activity described for coumarins that bind through different linkers to phenolic fragments capable of acting as radical scavengers (Figure 4, general structure XVII ), hybrids that can therefore be used in the treatment of immunomodulatory diseases. Molecules 2021, 26, x FOR PEER REVIEW 5 of 16 The second case described the introduction of a piperidine ring through a linker in position 7 of the coumarin scaffold, originating compounds with outstanding activity against certain filoviruses such as Marburg virus (MARV) or Ebolavirus (EBOV). From the SAR studied, it is interesting to highlight the role of substitution in para position with a trifluoromethoxy group that originated compound XVI (Figure 3) with IC50 = 0.5 μM and 1.2 μM against EBOV and MARV, respectively [27]. 2.3. Antioxidant and Anti-Inflammatory Activities Although we have found very few publications related to these activities, in some cases the antioxidant activity of coumarin derivatives of both natural [28] and synthetic [29] origin has been reported. This is the case of NOs inhibitors, an activity described for coumarins that bind through different linkers to phenolic fragments capable of acting as radical scavengers (Figure 4, general structure XVII), hybrids that can therefore be used in the treatment of immunomodulatory diseases. Regarding the anti-inflammatory activity, it is worth mentioning a review on the coumarins of natural origin (simple coumarins, prenylcoumarins, furocoumarins, coumestans, and benzocoumarins) with a detailed anti-inflammatory activity due to the activation of the nuclear factor erythroid 2-related factor 2 (Nrf2 factor) that protects cells against stress oxidative [30]. In other cases, the anti-inflammatory activity found for coumarin esters (Figure 4, general structure XVIII) as inhibitors of the Kallikrein-related peptidase 9 (KLK9) involved in inflammatory processes of the skin is reported [31]. Finally, the replacement of the carboxylic group by a sulfone or sulfoxide group (Figure 4, general structure XIX) gives rise to new inhibitors of cyclooxygenase-2 (COX-2) with activities comparable, in many cases, to indomethacin [32]. Figure 4. Structures of coumarin derivatives as antioxidant and anti-inflammatory agents. 2.4. Adenosine Ligands The affinity of the coumarin system for adenosine receptors has also been published recently. The 3-arylcoumarins (Figure 5, compound XX) have been described as antagonists of hA3 receptors, showing a high affinity (in the low nanomolar range) and selectivity for this subtype [33], while the 3-aroylcoumarins (Figure 5, general structure XXI) have been described as dual hA1/hA3 antagonists in the low micromolar range [34]. These works are aligned with the already known potential of these derivatives as modulators of the different adenosine receptors, published in the last decade. Figure 5. Structures of coumarin derivatives as adenosine ligands. Figure 4. Structures of coumarin derivatives as antioxidant and anti-inflammatory agents. Regarding the anti-inflammatory activity, it is worth mentioning a review on the coumarins of natural origin (simple coumarins, prenylcoumarins, furocoumarins, coumestans, and benzocoumarins) with a detailed anti-inflammatory activity due to the activation of the nuclear factor erythroid 2-related factor 2 (Nrf2 factor) that protects cells against stress oxidative [ 30 ]. In other cases, the anti-inflammatory activity found for coumarin esters (Figure 4, general structure XVIII ) as inhibitors of the Kallikrein-related peptidase 9 (KLK9) involved in inflammatory processes of the skin is reported [ 31 ]. Finally, the replacement of the carboxylic group by a sulfone or sulfoxide group (Figure 4, general structure XIX ) gives rise to new inhibitors of cyclooxygenase-2 (COX-2) with activities comparable, in many cases, to indomethacin [32]. 2.4. Adenosine Ligands The affinity of the coumarin system for adenosine receptors has also been published recently. The 3-arylcoumarins (Figure 5, compound XX ) have been described as antagonists of hA 3 receptors, showing a high affinity (in the low nanomolar range) and selectivity for this subtype [ 33 ], while the 3-aroylcoumarins (Figure 5, general structure XXI ) have been described as dual hA 1 /hA 3 antagonists in the low micromolar range [ 34 ]. These works are aligned with the already known potential of these derivatives as modulators of the different adenosine receptors, published in the last decade. Molecules 2021, 26, x FOR PEER REVIEW 5 of 16 The second case described the introduction of a piperidine ring through a linker in position 7 of the coumarin scaffold, originating compounds with outstanding activity against certain filoviruses such as Marburg virus (MARV) or Ebolavirus (EBOV). From the SAR studied, it is interesting to highlight the role of substitution in para position with a trifluoromethoxy group that originated compound XVI (Figure 3) with IC50 = 0.5 μM and 1.2 μM against EBOV and MARV, respectively [27]. 2.3. Antioxidant and Anti-Inflammatory Activities Although we have found very few publications related to these activities, in some cases the antioxidant activity of coumarin derivatives of both natural [28] and synthetic [29] origin has been reported. This is the case of NOs inhibitors, an activity described for coumarins that bind through different linkers to phenolic fragments capable of acting as radical scavengers (Figure 4, general structure XVII), hybrids that can therefore be used in the treatment of immunomodulatory diseases. Regarding the anti-inflammatory activity, it is worth mentioning a review on the coumarins of natural origin (simple coumarins, prenylcoumarins, furocoumarins, coumestans, and benzocoumarins) with a detailed anti-inflammatory activity due to the activation of the nuclear factor erythroid 2-related factor 2 (Nrf2 factor) that protects cells against stress oxidative [30]. In other cases, the anti-inflammatory activity found for coumarin esters (Figure 4, general structure XVIII) as inhibitors of the Kallikrein-related peptidase 9 (KLK9) involved in inflammatory processes of the skin is reported [31]. Finally, the replacement of the carboxylic group by a sulfone or sulfoxide group (Figure 4, general structure XIX) gives rise to new inhibitors of cyclooxygenase-2 (COX-2) with activities comparable, in many cases, to indomethacin [32]. Figure 4. Structures of coumarin derivatives as antioxidant and anti-inflammatory agents. 2.4. Adenosine Ligands The affinity of the coumarin system for adenosine receptors has also been published recently. The 3-arylcoumarins (Figure 5, compound XX) have been described as antagonists of hA3 receptors, showing a high affinity (in the low nanomolar range) and selectivity for this subtype [33], while the 3-aroylcoumarins (Figure 5, general structure XXI) have been described as dual hA1/hA3 antagonists in the low micromolar range [34]. These works are aligned with the already known potential of these derivatives as modulators of the different adenosine receptors, published in the last decade. Figure 5. Structures of coumarin derivatives as adenosine ligands. Figure 5. Structures of coumarin derivatives as adenosine ligands. 2.5. Enzymatic Inhibitory Activity: α -Glucosidase, Carbonic Anhydrase, Tyrosinase, Sulfatase, and Xanthine Oxidase The activity of coumarin derivatives on α -glucosidase was also reviewed in 2020 [ 35 ], in a study in which the influence of the substitution pattern was evaluated, and an important SAR was established. In addition to α -glucosidase, aldehyde dehydroge- Molecules 2021,26, 501 6 of 15 nase 1A1 (ALDH1A1) is another target for the treatment of diabetes and obesity, and 3-amidocoumarins have been described as inhibitors of this enzyme, with compound XXII (Figure 6) being a very promising derivative (IC 50 = 3.87 mM) [ 36 ]. This activity has also recently been found for hybrids of coumarin and cinnamic acid, with compound XXIII (Figure 6) being described as a very promising derivative (IC50 = 12.98 mM) [37]. Molecules 2021, 26, x FOR PEER REVIEW 6 of 16 2.5. Enzymatic Inhibitory Activity: α-Glucosidase, Carbonic Anhydrase, Tyrosinase, Sulfatase, and Xanthine Oxidase The activity of coumarin derivatives on α-glucosidase was also reviewed in 2020 [35], in a study in which the influence of the substitution pattern was evaluated, and an important SAR was established. In addition to α-glucosidase, aldehyde dehydrogenase 1A1 (ALDH1A1) is another target for the treatment of diabetes and obesity, and 3-amidocou- marins have been described as inhibitors of this enzyme, with compound XXII (Figure 6) being a very promising derivative (IC50 = 3.87 mM) [36]. This activity has also recently been found for hybrids of coumarin and cinnamic acid, with compound XXIII (Figure 6) being described as a very promising derivative (IC50 = 12.98 mM) [37]. Closely related to these structures, works have been published on coumarin derivatives with inhibitory activity on carbonic anhydrase IX and XII. These are coumarins that incorporate arylacrylamide substituents at position 3 (Figure 6, general structure XXIV) that showed inhibitory activity in the nanomolar range [38]. In other cases, anhydrase inhibitory activity was reported for hybrids connected by a methyleneoxy linker at position 7, oxadiazole heterocycles [39] that the same authors extend to the triazole ring (Figure 6, general structure XXV) [40]. These last structures are closely related to others that present tyrosinase inhibitory activity in the sub-micromolar range. This is the case of coumarins (umbelliferone and other phenolic analogues) that incorporate a kojic acid fragment through a triazole linker at position 4 (Figure 6, compound XXVI), both fragments with demonstrated tyrosinase inhibitory activity [41]. Likewise, the introduction of a sulfamate group in the coumarin scaffold originates a hybrid prototype (Figure 6, general structure XXVII) that presents a high inhibitory activity of the steroid sulfatase (best compound of the series with IC50 = 0.13 μM), which is of interest in the treatment of hormone-dependent breast cancers [42]. During 2020, 3-phenylcoumarins were also studied as xanthine oxidase inhibitors [43]. Methoxy and nitro substituents were introduced into the framework. The best compound in the series proved to be 3-(4-methoxyphenyl)-6-nitrocoumarin, with an IC50 = 8.4 μM, being also non-cytotoxic in B16F10 cells. Figure 6. Structures of coumarin derivatives as enzymatic inhibitors. 2.6. Anti-Neurodegenerative Diseases Activity: MAO and AChE/BChE Inhibitors Figure 6. Structures of coumarin derivatives as enzymatic inhibitors. Closely related to these structures, works have been published on coumarin derivatives with inhibitory activity on carbonic anhydrase IX and XII . These are coumarins that incorporate arylacrylamide substituents at position 3 (Figure 6, general structure XXIV ) that showed inhibitory activity in the nanomolar range [ 38 ]. In other cases, anhydrase inhibitory activity was reported for hybrids connected by a methyleneoxy linker at position 7, oxadiazole heterocycles [ 39 ] that the same authors extend to the triazole ring (Figure 6, general structure XXV) [40]. These last structures are closely related to others that present tyrosinase inhibitory activity in the sub-micromolar range. This is the case of coumarins (umbelliferone and other phenolic analogues) that incorporate a kojic acid fragment through a triazole linker at position 4 (Figure 6, compound XXVI ), both fragments with demonstrated tyrosinase inhibitory activity [41]. Likewise, the introduction of a sulfamate group in the coumarin scaffold originates a hybrid prototype (Figure 6, general structure XXVII ) that presents a high inhibitory activity of the steroid sulfatase (best compound of the series with IC 50 = 0.13 µ M), which is of interest in the treatment of hormone-dependent breast cancers [42]. During 2020, 3-phenylcoumarins were also studied as xanthine oxidase inhibitors [ 43 ]. Methoxy and nitro substituents were introduced into the framework. The best compound in the series proved to be 3-(4-methoxyphenyl)-6-nitrocoumarin, with an IC 50 = 8.4 µ M, being also non-cytotoxic in B16F10 cells. 2.6. Anti-Neurodegenerative Diseases Activity: MAO and AChE/BChE Inhibitors The role played by coumarin derivatives as agents that exhibit biological activities associated with neurodegenerative diseases, such as Alzheimer’s disease, is very important. Throughout this year, a large number of manuscripts related to this field have been found. Due to the multidirectional nature of these diseases, there are also many works on hybrid coumarins directed at different pharmacological targets, such as monoamine oxidase B Molecules 2021,26, 501 7 of 15 (MAO-B) or acetylcholinesterase (AChE), amyloid aggregation, or oxidative stress, among others. Hybrids of general structure XXVIII (Figure 7) have been described, in which the rasagiline fragment with MAO-B inhibitory activity and neuroprotection properties is incorporated into the coumarin scaffold also with demonstrated MAO-B inhibitory activity, antioxidant, and neuroprotective properties [ 44 ]. The incorporation at position 3 of a pyridazine ring (Figure 7, general structure XXIX ) is another case of hybrid structures as selective MAO-B inhibitors [ 45 ]. The incorporation of isoxazole-type heterocycles in carboxamide–coumarins (Figure 7, general structure XXX ) allowed obtaining derivatives with significant inhibitory activities of AChE/BuChE and beta-secretase 1 (BACE1) [ 46 ]. In other cases, taking into account the importance of metals in the pathogenesis of Alzheimer’s disease, a pyridinone fragment (Figure 7, general structure XXXI ) with iron-chelating properties was incorporated [47]. Molecules 2021, 26, x FOR PEER REVIEW 9 of 16 Figure 7. Structures of coumarin derivatives as anti-neurodegenerative diseases agents. 2.7. Anticoagulant Activity The classic anticoagulant effect of specific coumarin derivatives, based on acenocoumarol and warfarin, also remains one of the classic applications for this family. During 2020, a review on this topic was published [55]. 2.8. Fluorescent Probes In addition to the interest of coumarins as a versatile scaffold in drug design, the important role that this scaffold plays as fluorescent probes to detect metals, enzymes, and biomaterials, among others, should be highlighted [56–59]. These fluorescent probes have a great imaging potential for the diagnosis of several pathologies. O O H N XXVIII XN N OO XXIX O OO XXX H N O N O R O O N H O R NO OH XXXI 2 O O O XXXII NN N NN N R R OMe OMe O O O XXXIV N O O O XXXIII R R= H, Me, Et R= H, X, NO 2 , OMe, Me R= H, Me, OEt, OPr, Me, CH 2 -Ar H, X n n=2-6 n n=3,5 R= H, X, OMe, Me OO XXXV O O R 1 R 1 = H, Me, OH, OMe, Br R 2 = H, Me, OMe. OEt, R 2 8 6 OO R 2 8 7 S R 1 R 1 = H, Br R 2 = H, OH N H R, Ar O R= Me, Et, iPr,iBut, tBut Ar= Ph, 2 Thiophen, 2 Furan XXXVI XXXVII Figure 7. Structures of coumarin derivatives as anti-neurodegenerative diseases agents. Molecules 2021,26, 501 8 of 15 Other multitarget structures are the benzotriazole–coumarin (Figure 7, general structure XXXII ) and carbazole–coumarin (Figure 7, general structure XXXIII ) hybrids [ 48 , 49 ]. In both cases, the molecules show antioxidant activity, as well as AChE and β -amyloid aggregation inhibitory properties. Finally, it is worth mentioning another type of hybrid, this time a furocoumarin that incorporates two fragments of resveratrol (Figure 7, general structure XXXIV ) [ 50 ]. Compounds containing this scaffold present AChE and BACE1 inhibitory properties related to the furocoumarin fragment, and antioxidant (radical scavenging) and COX-2 inhibition, related to the resveratrol [50]. The 7-amidocoumarins (Figure 7, general structure XXXV ) have recently been published for their potential against monoamine oxidase A (hMAO-A), hMAO-B, hBACE1, hAChE, and butyrylcholinesterase (hBuChE) [ 51 ]. The research project is based on a screening of compounds with potential activity against Alzheimer’s and Parkinson’s diseases, since these multifactorial pathologies share some of their pharmacological targets. Five derivatives of the studied series were described as potent and selective hMAO-B inhibitors in the nanomolar range; six turned out to be hMAO-A inhibitors in the low micromolar range; one showed inhibitory activity of hBACE1, and another one hAChE inhibitory activity, both in the micromolar range. In addition to the enzymatic inhibition, all of the studied molecules proved to be non-cytotoxic to neurons in the motor cortex. As a main conclusion, results suggest that by modulating the substitution pattern at position 7 of the scaffold, selective or multitarget molecules can be achieved. The 3-arylcoumarins are a family of compounds with proven activity on different targets related to neurodegenerative diseases, especially Alzheimer’s and Parkinson’s diseases, the two most prevalent. In the last decade, several manuscripts described very promising activities of this scaffold, both as selective and multitarget compounds. SAR studies were performed, and important conclusions were drawn based on the substitution patterns in the main scaffold. Due to the large number of molecules based on this scaffold currently synthetized and studied as hMAO inhibitors, in 2020 a theoretical work was published comparing different QSAR models and docking calculations, in order to predict the hMAO-B activity of the 3-arylcoumarins [ 52 ]. Based on the predictions, a small series of compounds was synthetized and evaluated against both hMAO-A and hMAO-B, and the most promising models were validated. Selective activities were found in the low nanomolar range against this isoenzyme for 6 and 8 methyl-substituted 3-arylcoumarins, also presenting methoxy groups or bromine atoms in different positions of the 3-phenyl ring (Figure 7, general structure XXXVI ). These advancements may represent robust tools in the design of potent and selective derivatives. Analogues of 3-phenylcoumarins were also published during 2020. The discovery and optimization of 3-thiophenylcoumarins (Figure 7, general structure XXXVII ) as novel and promising agents against Parkinson’s disease have been described [ 53 ]. This study explores, for the first time, the potential of these structures as in vitro and in vivo agents against this disease. The inhibitory activities of hMAO-A and hMAO-B, antioxidant profile, neurotoxicity in neurons of the motor cortex, and neuroprotection against hydrogen peroxide production were studied. The in vivo effect on locomotor activity was also evaluated by an open field test (OFT) for the most potent, selective and reversible hMAO-B inhibitor of the series: 3-(4 0 -bromothiophen-2 0 -yl)-7-hydroxycoumarin (IC 50 = 140 nM). In reserpinized mice pre-treated with levodopa and benserazide, this molecule exhibited a slightly better in vivo profile than selegiline, currently a therapeutic option for Parkinson’s disease. The results suggested that the 7-position substitution of the coumarin scaffold is interesting for enzyme inhibition. Furthermore, the presence of a catechol at positions 7 and 8 exponentially increases the antioxidant potential and the neuroprotective properties. The neuroprotective effects of xanthotoxin and umbelliferone on streptozotocin (STZ)- induced cognitive dysfunction in rats were evaluated [ 54 ]. Alzheimer’s disease was induced in these animals and both compounds were administrated, proving to prevent cognitive deficits in the Morris water maze and object recognition tests. In addition, both compounds reduced the activity of hippocampal AChE and the level of malondialdehyde, Molecules 2021,26, 501 9 of 15 increasing the glutathione content. These coumarins also modulated neuronal cell death by reducing the level of proinflammatory cytokines, inhibiting the overexpression of inflammatory markers (nuclear factor κ B and cyclooxygenase II ), and upregulating the expression of NF- κ B inhibitor (I κ B- α ). An attenuation of cognitive dysfunction by these compounds was observed. This effect can at least be attributed to the inhibition of AChE and the reduction of oxidative stress, neuroinflammation, and neuronal loss, opening a new door for these classic coumarins. 2.7. Anticoagulant Activity The classic anticoagulant effect of specific coumarin derivatives, based on acenocoumarol and warfarin, also remains one of the classic applications for this family. During 2020, a review on this topic was published [55]. 2.8. Fluorescent Probes In addition to the interest of coumarins as a versatile scaffold in drug design, the important role that this scaffold plays as fluorescent probes to detect metals, enzymes, and biomaterials, among others, should be highlighted [ 56 – 59 ]. These fluorescent probes have a great imaging potential for the diagnosis of several pathologies. Coumarins are being used in the selective detection of metals such as copper (Figure 8 , general structure XXXVIII ) [ 60 ] or its determination in drinking water (Figure 8, compound XXXIX ) [ 61 , 62 ]. A recent review focuses on the detection of iron in water and its applications [ 63 ]. Other works study the fluorescence determination of the presence of silver in aqueous medium (Figure 8, compound XL ) [ 64 ]. In the case of mercury, there are also published works in which the selective determination in water is studied (Figure 8, general structure XLI ) [ 65 ]. In some cases, this determination is selective, but in this case, the innovative methodology can be applied over a wide pH range (Figure 8, compound XLII) [66]. In some cases, these metal complexes serve as probes for the detection of biothiols, as in the case of copper complexes with benzothiazoles (Figure 8, compound XLIII ) used in the determination of cysteines [ 67 ], or coumarin–quinoline complexes used in the detection of glutathione (Figure 8, compound XLIV ) [ 68 ]. In other cases, aromatization to form the coumarin ring is used as a fluorescence test to detect the superoxide anion (Figure 8, compound XLV) [69]. In addition to the determination of metals, in many cases coumarin derivatives are used as fluorescence probes for the detection of hypochlorite, as in the case of coumarin– thiophene complexes (Figure 8, compound XLVI ) [ 70 ] or of 2-thiocoumarins in which the presence of ClO– allows the formation of a fluorescent coumarin (Figure 8, compound XLVII) [71]. Coumarins can also be used as photocleavable linkers in the controlled release of drugs or biomaterials. This is the case of the in vivo photolysis of the microtubule inhibitor 4- pyridinomethylcoumarin (Figure 8, compound XLVIII ) [ 72 ]. 7-Hydroxymethyl substituted aminocoumarins are used as iron complexes (Figure 8, general structures XLIX and L ), and can be used to photochemotherapeutically target the mitochondria in the treatment of cancer [60,73]. Other reviews report on the use of 7-hydroxycoumarin and its derivatives in determining the activity of cytochromes P450 (CYP) enzymes [ 74 ] as well as 7-aminocoumarin derivatives in determining amino acids from serine or cysteine proteases [ 58 ]. In other cases, they are used to detect the metabolism of mitochondrial cysteines, the oxidation of which is a measure of cellular oxidative stress (Figure 8, compound LI ) [ 75 ]. The use of the chiral coumarin-BINOL hybrid allows the enantioselective detection of amino acids (Figure 8, compound LII ) [ 76 ]. Finally, coumarins can be used for easy detection of bacterial carbapenamases in which the coumarin fluorophore binds to the carbapenemic structure via a reactive linker (Figure 8, general structure LIII) [77,78].