Potential antidiabetic activity of naturally occurring compounds by enzyme α-glucosidase inhibition

被引:0
|
作者
Islam, S. [1 ]
机构
[1] Univ Arkansas, Dept Agr, Pine Bluff, AR 71601 USA
关键词
natural compounds; antidiabetic; inhibition; anthocyanins; polyphenols; thiols; ACID;
D O I
10.17660/ActaHortic.2015.1106.26
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Fourteen naturally occurring compounds and two derivatives of naturally occurring compounds were tested for inhibitory activity with the enzyme alpha-glucosidase. These compounds included anthocyanins, thiol derivatives, and cinnamic acid. Acarbose was used as the standard. Rutin and tannic acid displayed the highest inhibitory effect (almost 90%), whereas thiols had a neglected effect. Compared to acarbose, rutin and tannic inhibitory effects were 1.6% higher. Concerning anthocyanins, pelargodin had a comparable effect as acarbose and the other anthocyanins tested displayed a less effect. More generally, the ortho-diphenolic structures as aglycones or free forms, such as cyanidin, caffeic acid and quercetin, were less active certainly due to their high oxidability in the test solutions. The glycosylation confer a better stability to the polyphenol, found in rutin, and contribute to a better effect.
引用
收藏
页码:169 / 173
页数:5
相关论文
共 50 条
  • [21] Naturally occurring bitter compounds
    Opletal, Lubomir
    Copikova, Jana
    Uher, Michal
    Lapcik, Oldrich
    Moravcova, Jitka
    Drasar, Pavel
    CHEMICKE LISTY, 2007, 101 (11): : 895 - 906
  • [22] Naturally Occurring Astringent Compounds
    Copikova, Jana
    Wimmer, Zdenek
    Lapcik, Oldrich
    Cahlikova, Lucie
    Opletal, Lubomir
    Moravcova, Jitka
    Drasar, Pavel
    CHEMICKE LISTY, 2014, 108 (11): : 1053 - 1057
  • [23] Antidiabetic potential of Asparagus racemosus Willd leaf extracts through inhibition of α-amylase and α-glucosidase
    Vadivelan, R.
    Krishnan, R. Gopala
    Kannan, R.
    JOURNAL OF TRADITIONAL AND COMPLEMENTARY MEDICINE, 2019, 9 (01): : 1 - 4
  • [24] In vitro evaluation of α-glucosidase inhibitor and antioxidant activity of Lactobacillus isolates and their antidiabetic potential
    Puspawati, Ni Nyoman
    Antara, Nyoman Semadi
    Permana, I. Dewa Gde Mayun
    Sukrama, I. Dewa Made
    MALAYSIAN JOURNAL OF MICROBIOLOGY, 2022, 18 (02) : 192 - 203
  • [25] Investigation of α-glucosidase and α-amylase inhibition for antidiabetic potential of agarwood (Aquilaria malaccensis) leaves extract
    Wibowo, Syahputra
    Wardhani, Sunia Kusuma
    Hidayati, Lisna
    Wijayanti, Nastiti
    Matsuo, Koichi
    Costa, Jessica
    Nugraha, Yudhi
    Siregar, Josephine Elizabeth
    Nuringtyas, Tri Rini
    BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY, 2024, 58
  • [26] Benzoylquinazolinone derivatives as new potential antidiabetic agents: α-Glucosidase inhibition, kinetic, and docking studies
    Mohammadi-Khanaposhtani, Maryam
    Yahyavi, Hoda
    Imanparast, Somaye
    Harandi, Fereshte Nazemi
    Faramarzi, Mohammad Ali
    Foroumadi, Alireza
    Larijani, Bagher
    Biglar, Mahmood
    Mahdavi, Mohammad
    JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2020, 67 (05) : 856 - 863
  • [27] Research progress of indole compounds with potential antidiabetic activity
    Zhu, Yuqian
    Zhao, Jinran
    Luo, Longbiao
    Gao, Yang
    Bao, He
    Li, Pengfei
    Zhang, Hailong
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2021, 223
  • [28] STUDY OF NATURALLY-OCCURRING PHENOLIC-COMPOUNDS AS POTENTIAL ANTIOXIDANTS
    PENDSE, RA
    HO, CT
    DESHPANDE, VH
    PENDSE, AD
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1992, 204 : 147 - AGFD
  • [29] Naturally Occurring Exosome Vesicles as Potential Delivery Vehicle for Bioactive Compounds
    Akuma, Precious
    Okagu, Ogadimma D.
    Udenigwe, Chibuike C.
    FRONTIERS IN SUSTAINABLE FOOD SYSTEMS, 2019, 3
  • [30] Antidiabetic potential and enzyme kinetics of benzothiazole derivatives and their non-bonded interactions with α-glucosidase and α-amylase
    Ninad V. Puranik
    Hemalata M. Puntambekar
    Pratibha Srivastava
    Medicinal Chemistry Research, 2016, 25 : 805 - 816