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  1. Article ; Online: Insights on the antiradical capacity and mechanism of phytocannabinoids: H-abstraction and electron transfer processes in physiological media and the influence of the acid-base equilibrium.

    Boulebd, Houssem

    Phytochemistry

    2023  Volume 208, Page(s) 113608

    Abstract: Phytocannabinoids are natural products primarily isolated from Cannabis sativa that exhibit the typical C21 terpenophenolic skeleton. This class of compounds has been shown to be effective in the treatment of various oxidation-related diseases, which has ...

    Abstract Phytocannabinoids are natural products primarily isolated from Cannabis sativa that exhibit the typical C21 terpenophenolic skeleton. This class of compounds has been shown to be effective in the treatment of various oxidation-related diseases, which has made their antioxidant properties the focus of increasing interest. In the present contribution, the primary antioxidant properties of eight representative phytocannabinoids have been systematically studied against a variety of biologically significant radical species using the density functional theory (DFT) method. The findings demonstrated that phytocannabinoids, in water at physiological pH, exhibit excellent radical scavenging capacity, mainly exerted by the single electron transfer (SET) process from the deprotonated state. In contrast, phytocannabinoids are moderate radical scavengers in non-polar environment via the formal hydrogen atom transfer (fHAT) process. Among the compounds examined, cannabichromene (CBC) and cannabifuran (CBF) had the greatest free radical scavenging capacity in water, surpassing even common antioxidants like BHT and Trolox. CBF is expected to have potent antiradical action toward peroxyl radicals, alkoxy radicals, and nitrogen dioxide in water at physiological pH. These results provide supporting evidence that phytocannabinoids may be useful in scavenging harmful free radicals in physiological environments.
    MeSH term(s) Antioxidants/chemistry ; Free Radical Scavengers/chemistry ; Acid-Base Equilibrium ; Electrons ; Free Radicals/chemistry ; Water/chemistry
    Chemical Substances Antioxidants ; Free Radical Scavengers ; Free Radicals ; Water (059QF0KO0R)
    Language English
    Publishing date 2023-02-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113608
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Insights on the antiradical capacity and mechanism of phytocannabinoids: H-abstraction and electron transfer processes in physiological media and the influence of the acid-base equilibrium

    Boulebd, Houssem

    Phytochemistry. 2023 Apr., v. 208 p.113608-

    2023  

    Abstract: Phytocannabinoids are natural products primarily isolated from Cannabis sativa that exhibit the typical C21 terpenophenolic skeleton. This class of compounds has been shown to be effective in the treatment of various oxidation-related diseases, which has ...

    Abstract Phytocannabinoids are natural products primarily isolated from Cannabis sativa that exhibit the typical C21 terpenophenolic skeleton. This class of compounds has been shown to be effective in the treatment of various oxidation-related diseases, which has made their antioxidant properties the focus of increasing interest. In the present contribution, the primary antioxidant properties of eight representative phytocannabinoids have been systematically studied against a variety of biologically significant radical species using the density functional theory (DFT) method. The findings demonstrated that phytocannabinoids, in water at physiological pH, exhibit excellent radical scavenging capacity, mainly exerted by the single electron transfer (SET) process from the deprotonated state. In contrast, phytocannabinoids are moderate radical scavengers in non-polar environment via the formal hydrogen atom transfer (fHAT) process. Among the compounds examined, cannabichromene (CBC) and cannabifuran (CBF) had the greatest free radical scavenging capacity in water, surpassing even common antioxidants like BHT and Trolox. CBF is expected to have potent antiradical action toward peroxyl radicals, alkoxy radicals, and nitrogen dioxide in water at physiological pH. These results provide supporting evidence that phytocannabinoids may be useful in scavenging harmful free radicals in physiological environments.
    Keywords Cannabis sativa ; acid-base balance ; antioxidants ; density functional theory ; electron transfer ; free radicals ; hydrogen ; nitrogen dioxide ; plant biochemistry ; skeleton ; Cannabaceae ; Phytocannabinoids ; DFT calculations ; Antioxidant activity ; Kinetic study
    Language English
    Dates of publication 2023-04
    Publishing place Elsevier Ltd
    Document type Article ; Online
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113608
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Structure-activity relationship of antioxidant prenylated (iso)flavonoid-type compounds: quantum chemistry and molecular docking studies.

    Boulebd, Houssem

    Journal of biomolecular structure & dynamics

    2021  Volume 40, Issue 20, Page(s) 10373–10382

    Abstract: Prenylated (iso)flavonoid-type compounds are a subclass of natural flavonoids that have been reported to exhibit good antioxidant properties. In the present paper, the structure-activity relationship of three typical prenylated (iso)flavonoids namely 8- ... ...

    Abstract Prenylated (iso)flavonoid-type compounds are a subclass of natural flavonoids that have been reported to exhibit good antioxidant properties. In the present paper, the structure-activity relationship of three typical prenylated (iso)flavonoids namely 8-prenyldaidzein (Per), Licoflavone (Lic), and erysubin F (Ery) have been determined using DFT (density functional theory)-based calculations and molecular docking studies. As result, the CH bond of the prenyl substituent was found to be the most thermodynamically favorable site for trapping free radicals in the gas phase and lipid physiological environments. While the OH bond of the B-ring seems to be more reactive in water. HAT (hydrogen atom transfer) and SPLET (sequential proton loss electron transfer) play a decisive role in the antiradical activity of the studied compounds in lipid and polar physiological environments, respectively. All of the studied compounds exhibit strong binding affinity to both xanthine oxidase and inducible nitric oxide synthase enzymes by forming several hydrogen bonds and hydrophobic interactions with their respective catalytic sites. These results suggest that (iso)flavonoid-type compounds are promising radical scavengers and antioxidants. Communicated by Ramaswamy H. Sarma.
    MeSH term(s) Antioxidants/chemistry ; Flavonoids/chemistry ; Molecular Docking Simulation ; Structure-Activity Relationship ; Protons ; Lipids ; Thermodynamics ; Free Radical Scavengers
    Chemical Substances Antioxidants ; Flavonoids ; Protons ; Lipids ; Free Radical Scavengers
    Language English
    Publishing date 2021-06-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 49157-3
    ISSN 1538-0254 ; 0739-1102
    ISSN (online) 1538-0254
    ISSN 0739-1102
    DOI 10.1080/07391102.2021.1943529
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Are thymol, rosefuran, terpinolene and umbelliferone good scavengers of peroxyl radicals?

    Boulebd, Houssem

    Phytochemistry

    2021  Volume 184, Page(s) 112670

    Abstract: DFT-based computational calculations have been used to investigate the hydroperoxyl radical scavenging activity of four essential oil constituents namely thymol (Thy), rosefuran (Ros), terpinolene (Ter), and umbelliferone (Umb). Different reaction ... ...

    Abstract DFT-based computational calculations have been used to investigate the hydroperoxyl radical scavenging activity of four essential oil constituents namely thymol (Thy), rosefuran (Ros), terpinolene (Ter), and umbelliferone (Umb). Different reaction mechanisms including formal hydrogen transfer (FHT), radical adduct formation (RAF), sequential proton loss electron transfer (SPLET), and sequential electron transfer proton transfer (SETPT) have been examined in the gas phase and physiological environments. It was found that the HOO radical scavenging activity of these compounds is strongly influenced by the environment, which becomes more important in water than pentyl ethanoate. According to the overall reaction rate constants, the phenolic compounds Thy and Umb are predicted to exhibit excellent activity in aqueous solution. Umb with an overall rate constant of 1.44 × 10
    MeSH term(s) Antioxidants ; Cyclohexane Monoterpenes ; Free Radical Scavengers ; Thymol ; Umbelliferones
    Chemical Substances Antioxidants ; Cyclohexane Monoterpenes ; Free Radical Scavengers ; Umbelliferones ; Thymol (3J50XA376E) ; terpinolene (N9830X5KSL)
    Language English
    Publishing date 2021-01-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2021.112670
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Modeling the peroxyl radical scavenging behavior of Carnosic acid: Mechanism, kinetics, and effects of physiological environments.

    Boulebd, Houssem

    Phytochemistry

    2021  Volume 192, Page(s) 112950

    Abstract: Carnosic acid (CA), a phenolic diterpene and abietane-type compound, is a potent natural antioxidant with medical benefits. The present paper elucidates, for the first time, the kinetics and the exact mechanism of the peroxyl radical scavenging activity ... ...

    Abstract Carnosic acid (CA), a phenolic diterpene and abietane-type compound, is a potent natural antioxidant with medical benefits. The present paper elucidates, for the first time, the kinetics and the exact mechanism of the peroxyl radical scavenging activity of CA in the gas phase and under physiological conditions. According to the obtained results, the reaction of CA with HOO
    MeSH term(s) Abietanes/pharmacology ; Antioxidants/pharmacology ; Free Radical Scavengers/pharmacology ; Kinetics ; Peroxides
    Chemical Substances Abietanes ; Antioxidants ; Free Radical Scavengers ; Peroxides ; perhydroxyl radical (3170-83-0) ; salvin (LI791SXT24)
    Language English
    Publishing date 2021-09-13
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2021.112950
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The role of benzylic-allylic hydrogen atoms on the antiradical activity of prenylated natural chalcones: a thermodynamic and kinetic study.

    Boulebd, Houssem

    Journal of biomolecular structure & dynamics

    2020  Volume 39, Issue 6, Page(s) 1955–1964

    Abstract: Prenylated chalcones are a family of natural chalcones that have been reported to exhibit a high antioxidant activity. In this paper, the density functional calculations are carried out to study, systematically, the antiradical properties of four ... ...

    Abstract Prenylated chalcones are a family of natural chalcones that have been reported to exhibit a high antioxidant activity. In this paper, the density functional calculations are carried out to study, systematically, the antiradical properties of four prenylated natural chalcones namely isobavachalcone (
    MeSH term(s) Antioxidants ; Chalcone ; Chalcones/pharmacology ; Hydrogen ; Thermodynamics
    Chemical Substances Antioxidants ; Chalcones ; Chalcone (5S5A2Q39HX) ; Hydrogen (7YNJ3PO35Z)
    Language English
    Publishing date 2020-03-20
    Publishing country England
    Document type Journal Article
    ZDB-ID 49157-3
    ISSN 1538-0254 ; 0739-1102
    ISSN (online) 1538-0254
    ISSN 0739-1102
    DOI 10.1080/07391102.2020.1740791
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Theoretical insights into the antioxidant activity of moracin T.

    Boulebd, Houssem

    Free radical research

    2020  Volume 54, Issue 4, Page(s) 221–230

    Abstract: Moracin T is a natural product isolated ... ...

    Abstract Moracin T is a natural product isolated from
    MeSH term(s) Antioxidants/chemistry ; Benzofurans/chemistry ; Chromans/chemistry ; Free Radicals/chemistry ; Humans ; Models, Molecular ; Morus/chemistry ; Peroxides/chemistry ; Plant Extracts/chemistry ; Stilbenes/chemistry ; Thermodynamics
    Chemical Substances Antioxidants ; Benzofurans ; Chromans ; Free Radicals ; Peroxides ; Plant Extracts ; Stilbenes ; 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (S18UL9710X)
    Language English
    Publishing date 2020-04-13
    Publishing country England
    Document type Journal Article
    ZDB-ID 1194130-3
    ISSN 1029-2470 ; 1071-5762
    ISSN (online) 1029-2470
    ISSN 1071-5762
    DOI 10.1080/10715762.2020.1747616
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Computational assessment of the primary and secondary antioxidant potential of alkylresorcinols in physiological media.

    Boulebd, Houssem / Spiegel, Maciej

    RSC advances

    2023  Volume 13, Issue 42, Page(s) 29463–29476

    Abstract: Alkylresorcinols are a group of natural phenolic compounds found in various foods such as whole grain cereals, bread, and certain fruits. They are known for their beneficial health effects, such as anti-inflammatory and anti-cancer properties. This study ...

    Abstract Alkylresorcinols are a group of natural phenolic compounds found in various foods such as whole grain cereals, bread, and certain fruits. They are known for their beneficial health effects, such as anti-inflammatory and anti-cancer properties. This study aimed to evaluate the antioxidant activity of two typical alkylresorcinols namely olivetol and olivetolic acid (Oli and OliA) under physiological conditions. The free radical scavenging capacity of Oli and OliA toward oxygenated free radicals (HO˙ and HOO˙ radicals) was investigated using thermodynamic and kinetic calculations. The results revealed that Oli and OliA are potent scavengers of HO˙ radical in both polar and lipid media, acting exclusively
    Language English
    Publishing date 2023-10-09
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra05967g
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Examination of the Antioxidant Activity of Psoralidin: Computational Mechanistic Study and Impact on the ROS Level in Human Keratinocytes.

    Boulebd, Houssem / Pereira, David M

    The Journal of organic chemistry

    2023  Volume 88, Issue 9, Page(s) 5745–5751

    Abstract: Psoralidin ( ...

    Abstract Psoralidin (
    MeSH term(s) Humans ; Antioxidants/pharmacology ; Reactive Oxygen Species ; Benzofurans ; Keratinocytes
    Chemical Substances Antioxidants ; psoralidin (G16ZUQ069L) ; Reactive Oxygen Species ; Benzofurans
    Language English
    Publishing date 2023-04-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/acs.joc.3c00193
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: DFT study of the antiradical properties of some aromatic compounds derived from antioxidant essential oils: C-H bond vs. O-H bond.

    Boulebd, Houssem

    Free radical research

    2019  Volume 53, Issue 11-12, Page(s) 1125–1134

    Abstract: This paper describes a theoretical comparative study of the antiradical properties of six aromatic compounds namely eugenol ( ...

    Abstract This paper describes a theoretical comparative study of the antiradical properties of six aromatic compounds namely eugenol (
    MeSH term(s) Antioxidants/chemistry ; Density Functional Theory ; Free Radicals/chemistry ; Hydrocarbons, Aromatic/chemistry ; Molecular Structure ; Oils, Volatile/chemistry
    Chemical Substances Antioxidants ; Free Radicals ; Hydrocarbons, Aromatic ; Oils, Volatile
    Language English
    Publishing date 2019-11-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 1194130-3
    ISSN 1029-2470 ; 1071-5762
    ISSN (online) 1029-2470
    ISSN 1071-5762
    DOI 10.1080/10715762.2019.1690652
    Database MEDical Literature Analysis and Retrieval System OnLINE

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