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Showing 1-20 of 64 results
  1. A derivative of 3-(1,3-diarylallylidene)oxindoles inhibits dextran sulfate sodium-induced colitis in mice

    Background

    IA-0130 is a derivative of 3-(1,3-diarylallylidene)oxindoles, which is a selective estrogen receptor modulator (SERM). A previous study...

    Young-** Jeong, Hae-Ri Lee, ... Tae-Hwe Heo in Pharmacological Reports
    Article Open access 25 June 2024
  2. Medicinal Plants in Peru as a Source of Immunomodulatory Drugs Potentially Useful Against COVID-19

    The current COVID-19 pandemic, characterized by a highly contagious severe acute respiratory syndrome, led us to look for medicinal plants as an...

    Evelyn Maribel Condori Peñaloza, Sônia Soares Costa, Oscar Herrera-Calderon in Revista Brasileira de Farmacognosia
    Article 23 February 2023
  3. Recent progress in biologically active indole hybrids: a mini review

    The indole moiety is one of the most widespread heterocycles found in both natural products and biological systems. Indoles have important biological...

    Esraa Mahmoud, Alaa M. Hayallah, ... Mohamad Abdel-Aziz in Pharmacological Reports
    Article 20 May 2022
  4. Challenges and opportunities of develo** small-molecule therapies for age-related macular degeneration

    Age-related macular degeneration (AMD) is the leading cause of vision loss in senior adults. The disease can be categorized into two types: wet AMD...

    **ang Fei, Sooyun Jung, ... Seung-Yong Seo in Archives of Pharmacal Research
    Article 20 June 2024
  5. Synthesis of novel spirooxindole-pyrrolidines and evaluation of their cytotoxic activity

    Background

    A variety of spirooxindoles have demonstrated cytotoxic activity toward several cancer cell lines. This study investigates the cytotoxicity...

    Roman Sergeevich Tumskiy, Gennady Leonidovich Burygin, ... Iraida Nikolaevna Klochkova in Pharmacological Reports
    Article 15 December 2018
  6. Bioactive natural products from the genus Salinospora: a review

    Actinomycetes are an important source for bioactive secondary metabolites. Among them, the genus Salinispora is one of the first salt obligatory...

    Haerin Kim, Sohee Kim, ... Sang-Jip Nam in Archives of Pharmacal Research
    Article 25 November 2020
  7. DISCUSSION OF HERBAL DRUGS BASED ON THE BIOGENETIC CLASSIFICATION OF THEIR MAIN ACTIVE COMPONENTS

    Honey is prepared by honey-bees (Apis mellifera) from the nectar and honeydew of flowers. After chemical conversion by the gastric juices in the...
    Éva Szöke, Ágnes Kéry, Éva Lemberkovics in From Herbs to Healing
    Chapter 2023
  8. Current Strategies in Development of New Chromone Derivatives with Diversified Pharmacological Activities: A Review

    Chromone derivatives possess a spectrum of biological activities. Chromone has been recognized as a privileged structure for new drug invention and...

    Noor ul Amin Mohsin, Muhammad Irfan, ... Usman Saleem in Pharmaceutical Chemistry Journal
    Article 15 June 2020
  9. Monoterpenoid Indole Alkaloids from the Leaves of Alstonia scholaris

    A chemical investigation on the ethanol extract from the leaves of Alstonia scholaris led to the isolation of two new monoterpenoid indole alkaloids,...

    Jiang Hu, **a Mao, ... Junyou Shi in Chemistry of Natural Compounds
    Article 19 September 2018
  10. Thiadiazole derivatives as anticancer agents

    In spite of substantial progress made toward understanding cancer pathogenesis, this disease remains one of the leading causes of mortality. Thus,...

    Monika Szeliga in Pharmacological Reports
    Article Open access 03 September 2020
  11. Protein Glycation During Diabetes Mellitus and the Possibility of its Pharmacological Correction (Review)

    Non-enzymatic interaction of reducing sugars with free amines of proteins (Maillard reaction) leads to the formation of advanced glycation end...

    A. A. Spasov, O. A. Solov’eva, V. A. Kuznetsova in Pharmaceutical Chemistry Journal
    Article 01 September 2017
  12. Toxicity and antinociceptive effects of Hamelia patens

    Many medicinal herbs are used in folk medicine without taking into account their toxicity. Hamelia patens Jacq. (Rubiaceae), a Mexican endemic...

    Angel Josabad Alonso-Castro, Sarahi Balleza-Ramos, ... Candy Carranza-Álvarez in Revista Brasileira de Farmacognosia
    Article Open access 31 March 2015
  13. The catechol-O-methyltransferase inhibitory potential of Z-vallesiachotamine by in silico and in vitro approaches

    Z -Vallesiachotamine is a monoterpene indole alkaloid that has a β- N -acrylate group in its structure. This class of compounds has already been...

    Carolina dos Santos Passos, Luiz Carlos Klein-Júnior, ... Amélia Teresinha Henriques in Revista Brasileira de Farmacognosia
    Article Open access 26 July 2015
  14. In vitro and in vivo antifungal activity, liver profile test, and mutagenic activity of five plants used in traditional Mexican medicine

    Berberis hartwegii Benth ., Berberidaceae, Hameliapatens Jacq.,Rubiaceae, Dendropanaxarboreus (L.)Decne & Planch., Araliaceae, Erythrina herbacea L.,...

    Jorge Cornejo-Garrido, Martha Salinas-Sandoval, ... Cynthia Ordaz-Pichardo in Revista Brasileira de Farmacognosia
    Article Open access 14 February 2015
  15. Marine organisms as source of extracts to disrupt bacterial communication: bioguided isolation and identification of quorum sensing inhibitors from Ircinia felix

    tIn this study, 39 extracts from marine organisms were evaluated as quorum sensing inhibitors, collected in the Colombian Caribbean Sea and the...

    Jairo Quintana, José Brango-Vanegas, ... Carmenza Duque in Revista Brasileira de Farmacognosia
    Article Open access 29 April 2015
  16. Asymmetric synthesis and evaluation of α-quaternary chiral lactam derivatives as novel anticancer agents

    Asymmetric synthesis of α-quaternary chiral lactam derivatives as novel anticancer agents and evaluation of their cytotoxic potentials and spectrums...

    Hwanhyuk Lee, Su Jung Hwang, ... Yohan Park in Archives of Pharmacal Research
    Article 02 November 2013
  17. Biochemical and pharmacological characterization of isatin and its derivatives: from structure to activity

    Isatin, k1H-indole-2,3-dione, kis a heterocyclic compound of significant importance in medicinal chemistry. It is a synthetically versatile molecule,...

    Parvaneh Pakravan, Soheila Kashanian, ... Frances J. Harding in Pharmacological Reports
    Article 01 March 2013
  18. Synthesis, screening and antimicrobial activity evaluation of spiro indolothiazolidinone, oxazolidinone and azetidene derivatives of benzenesulfonyl chloride

    In an attempt to find a new class of antimicrobial agents, a series of indolothiazolidinone, oxazolidinone, and azetidene analogs of benzenesulfonyl...

    Hrushikesh Deokar, Jyotsna Chaskar, Atul Chaskar in Pharmaceutical Chemistry Journal
    Article 01 October 2012
  19. New 8-aminoalkyl derivatives of purine-2,6-dione with arylalkyl, allyl or propynyl substituents in position 7, their 5-HT1A, 5-HT2A, and 5-HT7 receptor affinity and pharmacological evaluation

    Background

    Our previous studies in a group of arylpiperazine derivatives of 1,3-dimethyl-3,7-dihydro-purine-2,6-diones, aimed at chemical...

    Grażyna Chłoń-Rzepa, Paweł Żmudzki, ... Paweł Zajdel in Pharmacological Reports
    Article 01 January 2013
  20. Synthesis of novel isatin-thiazoline and isatin-benzimidazole conjugates as anti-breast cancer agents

    A series of new isatin-thiazoline 3a–h and isatin-benzimidazole 4a–h derivatives were synthesized via condensation of isatin Mannich bases 2a–h with...

    Azza T. Taher, Nadia A. Khalil, Eman M. Ahmed in Archives of Pharmacal Research
    Article 01 October 2011
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