BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 26406581)

  • 1. Synthesis and Evaluation of Novel Triterpene Analogues of Ursolic Acid as Potential Antidiabetic Agent.
    Wu P; Zheng J; Huang T; Li D; Hu Q; Cheng A; Jiang Z; Jiao L; Zhao S; Zhang K
    PLoS One; 2015; 10(9):e0138767. PubMed ID: 26406581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and biological evaluation of novel ursolic acid analogues as potential α-glucosidase inhibitors.
    Wu PP; Zhang BJ; Cui XP; Yang Y; Jiang ZY; Zhou ZH; Zhong YY; Mai YY; Ouyang Z; Chen HS; Zheng J; Zhao SQ; Zhang K
    Sci Rep; 2017 Mar; 7():45578. PubMed ID: 28358057
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis and biological evaluation of novel oleanolic acid analogues as potential α-glucosidase inhibitors.
    Zhong YY; Chen HS; Wu PP; Zhang BJ; Yang Y; Zhu QY; Zhang CG; Zhao SQ
    Eur J Med Chem; 2019 Feb; 164():706-716. PubMed ID: 30677669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In vitro and in vivo evaluation of the antidiabetic activity of ursolic acid derivatives.
    Wu PP; Zhang K; Lu YJ; He P; Zhao SQ
    Eur J Med Chem; 2014 Jun; 80():502-8. PubMed ID: 24813878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Furofuran lignans as a new series of antidiabetic agents exerting α-glucosidase inhibition and radical scarvenging: Semisynthesis, kinetic study and molecular modeling.
    Worawalai W; Doungwichitrkul T; Rangubpit W; Taweechat P; Sompornpisut P; Phuwapraisirisan P
    Bioorg Chem; 2019 Jun; 87():783-793. PubMed ID: 30978603
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of indole derivatives as diabetics II inhibitors and enzymatic kinetics study of α-glucosidase and α-amylase along with their in-silico study.
    Taha M; Alrashedy AS; Almandil NB; Iqbal N; Anouar EH; Nawaz M; Uddin N; Chigurupati S; Wadood A; Rahim F; Das S; Venugopal V; Nawaz F; Khan KM
    Int J Biol Macromol; 2021 Nov; 190():301-318. PubMed ID: 34481854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis, in vitro evaluation and molecular docking studies of biscoumarin thiourea as a new inhibitor of α-glucosidases.
    Zawawi NK; Taha M; Ahmat N; Ismail NH; Wadood A; Rahim F; Rehman AU
    Bioorg Chem; 2015 Dec; 63():36-44. PubMed ID: 26432614
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis, in vitro evaluation and molecular docking studies of novel triazine-triazole derivatives as potential α-glucosidase inhibitors.
    Wang G; Peng Z; Wang J; Li X; Li J
    Eur J Med Chem; 2017 Jan; 125():423-429. PubMed ID: 27689725
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis, docking and ADMET studies of novel chalcone triazoles for anti-cancer and anti-diabetic activity.
    Chinthala Y; Thakur S; Tirunagari S; Chinde S; Domatti AK; Arigari NK; K V N S S; Alam S; Jonnala KK; Khan F; Tiwari A; Grover P
    Eur J Med Chem; 2015 Mar; 93():564-73. PubMed ID: 25743216
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluation and docking of indole sulfonamide as a potent inhibitor of α-glucosidase enzyme in streptozotocin -induced diabetic albino wistar rats.
    Taha M; Imran S; Salahuddin M; Iqbal N; Rahim F; Uddin N; Shehzad A; Khalid Farooq R; Alomari M; Mohammed Khan K
    Bioorg Chem; 2021 May; 110():104808. PubMed ID: 33756236
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Potential α-glucosidase inhibitor from Hylotelephium erythrostictum.
    Quan YS; Zhang XY; Yin XM; Wang SH; Jin LL
    Bioorg Med Chem Lett; 2020 Dec; 30(24):127665. PubMed ID: 33152378
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exploring efficacy of natural-derived acetylphenol scaffold inhibitors for α-glucosidase: Synthesis, in vitro and in vivo biochemical studies.
    Yu X; Zhang F; Liu T; Liu Z; Dong Q; Li D
    Bioorg Med Chem Lett; 2020 Dec; 30(23):127528. PubMed ID: 32920141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Triterpenic Acids as Non-Competitive α-Glucosidase Inhibitors from
    Ur Rehman N; Halim SA; Al-Azri M; Khan M; Khan A; Rafiq K; Al-Rawahi A; Csuk R; Al-Harrasi A
    Biomolecules; 2020 May; 10(5):. PubMed ID: 32408614
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Semi-synthesis of C28-modified triterpene acid derivatives from maslinic acid or corosolic acid as potential α-glucosidase inhibitors.
    Liu X; Zang X; Yin X; Yang W; Huang J; Huang J; Yu C; Ke C; Hong Y
    Bioorg Chem; 2020 Apr; 97():103694. PubMed ID: 32120080
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biscoumarin-1,2,3-triazole hybrids as novel anti-diabetic agents: Design, synthesis, in vitro α-glucosidase inhibition, kinetic, and docking studies.
    Asgari MS; Mohammadi-Khanaposhtani M; Kiani M; Ranjbar PR; Zabihi E; Pourbagher R; Rahimi R; Faramarzi MA; Biglar M; Larijani B; Mahdavi M; Hamedifar H; Hajimiri MH
    Bioorg Chem; 2019 Nov; 92():103206. PubMed ID: 31445191
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.
    Rahim F; Malik F; Ullah H; Wadood A; Khan F; Javid MT; Taha M; Rehman W; Ur Rehman A; Khan KM
    Bioorg Chem; 2015 Jun; 60():42-8. PubMed ID: 25955493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel tetrahydrobenzo[b]thiophen-2-yl)urea derivatives as novel α-glucosidase inhibitors: Synthesis, kinetics study, molecular docking, and in vivo anti-hyperglycemic evaluation.
    Xie HX; Zhang J; Li Y; Zhang JH; Liu SK; Zhang J; Zheng H; Hao GZ; Zhu KK; Jiang CS
    Bioorg Chem; 2021 Oct; 115():105236. PubMed ID: 34411978
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of new clioquinol derivatives as potent α-glucosidase inhibitors; molecular docking, kinetic and structure-activity relationship studies.
    Wali S; Atia-Tul-Wahab ; Ullah S; Khan MA; Hussain S; Shaikh M; Atta-Ur-Rahman ; Choudhary MI
    Bioorg Chem; 2022 Feb; 119():105506. PubMed ID: 34896920
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exploring the inhibitory action of betulinic acid on key digestive enzymes linked to diabetes via in vitro and computational models: approaches to anti-diabetic mechanisms.
    Salau VF; Erukainure OL; Aljoundi A; Akintemi EO; Elamin G; Odewole OA
    SAR QSAR Environ Res; 2024 May; 35(5):411-432. PubMed ID: 38764437
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis, α-glucosidase inhibition, and molecular docking studies of novel N-substituted hydrazide derivatives of atranorin as antidiabetic agents.
    Duong TH; Paramita Devi A; Tran NM; Phan HV; Huynh NV; Sichaem J; Tran HD; Alam M; Nguyen TP; Nguyen HH; Chavasiri W; Nguyen TC
    Bioorg Med Chem Lett; 2020 Sep; 30(17):127359. PubMed ID: 32738998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.