251 related articles for article (PubMed ID: 25087634)
1. Synthesis and biological evaluation of 3-styrylchromone derivatives as free radical scavengers and α-glucosidase inhibitors.
Takao K; Ishikawa R; Sugita Y
Chem Pharm Bull (Tokyo); 2014; 62(8):810-5. PubMed ID: 25087634
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and Biological Evaluation of 3-Benzylidene-4-chromanone Derivatives as Free Radical Scavengers and α-Glucosidase Inhibitors.
Takao K; Yamashita M; Yashiro A; Sugita Y
Chem Pharm Bull (Tokyo); 2016; 64(8):1203-7. PubMed ID: 27477661
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Synthesis and biological evaluation of piperic acid amides as free radical scavengers and α-glucosidase inhibitors.
Takao K; Miyashiro T; Sugita Y
Chem Pharm Bull (Tokyo); 2015; 63(5):326-33. PubMed ID: 25948326
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and biological evaluation of novel benzyl-substituted flavones as free radical (DPPH) scavengers and α-glucosidase inhibitors.
Kumar GS; Tiwari AK; Rao VR; Prasad KR; Ali AZ; Babu KS
J Asian Nat Prod Res; 2010 Nov; 12(11):978-84. PubMed ID: 21061220
[TBL] [Abstract][Full Text] [Related]
6. alpha-Glucosidase inhibitory antihyperglycemic activity of substituted chromenone derivatives.
Raju BC; Tiwari AK; Kumar JA; Ali AZ; Agawane SB; Saidachary G; Madhusudana K
Bioorg Med Chem; 2010 Jan; 18(1):358-65. PubMed ID: 19932027
[TBL] [Abstract][Full Text] [Related]
7. A trisaccharide phenylethanoid glycoside from Scrophularia flava Grau with potential anti-type 2 diabetic properties by inhibiting α-glucosidase enzyme and decreasing oxidative stress.
Hamedi A; Pasdaran A; Pasdaran A
Bioorg Chem; 2020 Jun; 99():103776. PubMed ID: 32276136
[TBL] [Abstract][Full Text] [Related]
8. Synthesis and in vitro evaluation of chlorogenic acid amides as potential hypoglycemic agents and their synergistic effect with acarbose.
Cardullo N; Floresta G; Rescifina A; Muccilli V; Tringali C
Bioorg Chem; 2021 Dec; 117():105458. PubMed ID: 34736132
[TBL] [Abstract][Full Text] [Related]
9. Chemistry, Alpha-glucosidase and Radical Scavenging Properties of Uranyl(VI) Hydrazide Complexes.
Akhter P; Ashiq U; Jamal RA; Shaikh Z; Mahroof-Tahir M; Lateef M; Badar R
Med Chem; 2019; 15(8):923-936. PubMed ID: 30760191
[TBL] [Abstract][Full Text] [Related]
10. Antioxidant and α-Glucosidase Inhibitory Constituents from Hornstedtia Species of Malaysia.
Hashim SE; Sirat HM; Yen KH; Ismail IS; Matsuki SN
Nat Prod Commun; 2015 Sep; 10(9):1561-3. PubMed ID: 26594759
[TBL] [Abstract][Full Text] [Related]
11. Synthesis, in vitro α-glucosidase inhibitory activity and docking studies of novel chromone-isatin derivatives.
Wang G; Chen M; Qiu J; Xie Z; Cao A
Bioorg Med Chem Lett; 2018 Jan; 28(2):113-116. PubMed ID: 29208524
[TBL] [Abstract][Full Text] [Related]
12. Tyramine Derivatives as Potent Therapeutics for Type 2 Diabetes: Synthesis and
Bashir MA; Javaid K; Shaikh M; Choudhary MI; Siddiqui H
Med Chem; 2020; 16(8):1124-1135. PubMed ID: 32003674
[TBL] [Abstract][Full Text] [Related]
13. Anti-inflammatory, free radical scavenging and alpha-glucosidase inhibitory activities of Hamelia patens and its chemical constituents.
Jiménez-Suárez V; Nieto-Camacho A; Jiménez-Estrada M; Alvarado Sánchez B
Pharm Biol; 2016 Sep; 54(9):1822-30. PubMed ID: 26731099
[TBL] [Abstract][Full Text] [Related]
14. Synthesis, biological evaluation and molecular docking studies of chromone hydrazone derivatives as α-glucosidase inhibitors.
Wang G; Chen M; Wang J; Peng Y; Li L; Xie Z; Deng B; Chen S; Li W
Bioorg Med Chem Lett; 2017 Jul; 27(13):2957-2961. PubMed ID: 28506754
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and in vitro α-glucosidase inhibition of novel dihydropyrano[3,2-c]quinoline derivatives as potential anti-diabetic agents.
Nikookar H; Mohammadi-Khanaposhtani M; Imanparast S; Faramarzi MA; Ranjbar PR; Mahdavi M; Larijani B
Bioorg Chem; 2018 Apr; 77():280-286. PubMed ID: 29421703
[TBL] [Abstract][Full Text] [Related]
16. The multi-targets integrated fingerprinting for screening anti-diabetic compounds from a Chinese medicine Jinqi Jiangtang Tablet.
Chang YX; Ge AH; Donnapee S; Li J; Bai Y; Liu J; He J; Yang X; Song LJ; Zhang BL; Gao XM
J Ethnopharmacol; 2015 Apr; 164():210-22. PubMed ID: 25698248
[TBL] [Abstract][Full Text] [Related]
17. Quercitylcinnamates, a new series of antidiabetic bioconjugates possessing α-glucosidase inhibition and antioxidant.
Rattanangkool E; Kittikhunnatham P; Damsud T; Wacharasindhu S; Phuwapraisirisan P
Eur J Med Chem; 2013 Aug; 66():296-304. PubMed ID: 23811091
[TBL] [Abstract][Full Text] [Related]
18. Inhibitors of α-glucosidase and α-amylase from Cyperus rotundus.
Tran HH; Nguyen MC; Le HT; Nguyen TL; Pham TB; Chau VM; Nguyen HN; Nguyen TD
Pharm Biol; 2014 Jan; 52(1):74-7. PubMed ID: 24044731
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Identification of highly potent α-glucosidase inhibitory and antioxidant constituents from Zizyphus rugosa bark: enzyme kinetic and molecular docking studies with active metabolites.
Sichaem J; Aree T; Lugsanangarm K; Tip-Pyang S
Pharm Biol; 2017 Dec; 55(1):1436-1441. PubMed ID: 28320255
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
