Re-exploring promising α-glucosidase inhibitors for potential development into oral anti-diabetic drugs: Finding needle in the haystack

被引:235
作者
Ghani, Usman [1 ]
机构
[1] King Saud Univ, Coll Med, Dept Pathol, Clin Chem Unit, Riyadh 11461, Saudi Arabia
关键词
alpha-glucosidase inhibitors; Synthetic; Natural; Anti-diabetic drugs; Drug development; TYPE-2; DIABETES-MELLITUS; MEDICINE SALACIA-RETICULATA; SULFONIUM SULFATE STRUCTURE; HUMAN MALTASE GLUCOAMYLASE; GLYCOSIDASE INHIBITORS; POLYHYDROXYLATED PYRROLIDINE; BIOLOGICAL EVALUATION; ANTIHYPERGLYCEMIC ACTIVITY; HOMONOJIRIMYCIN ISOMERS; PYRROLIZIDINE ALKALOIDS;
D O I
10.1016/j.ejmech.2015.08.043
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Treatment of diabetes mellitus by oral alpha-glucosidase inhibitors is currently confined to acarbose, miglitol and voglibose marred by efficacy problems and unwanted side effects. Since the discovery of the drugs more than three decades ago, no significant progress has been made in the drug development area of anti-diabetic alpha-glucosidase inhibitors. Despite existence of a wide chemical diversity of alpha-glucosidase inhibitors identified to date, majority of them are simply piled up in publications and reports thus creating a haystack destined to be forgotten in the scientific literature without given consideration for further development into drugs. This review finds those "needles" in that haystack and lays groundwork for highlighting promising alpha-glucosidase inhibitors from the literature that may potentially become suitable candidates for pre-clinical or clinical trials while drawing attention of the drug development community to consider and take already-identified promising a-glucosidase inhibitors into the next stage of drug development. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:133 / 162
页数:30
相关论文
共 180 条
[1]
PREVALENCE AND HEALTH-CARE FEATURES OF HYPERGLYCEMIA IN SEMIURBAN-RURAL COMMUNITIES IN SOUTHERN SAUDI-ARABIA [J].
ABUZEID, HAH ;
ALKASSAB, ASK .
DIABETES CARE, 1992, 15 (04) :484-489
[2]
Hypoglycaemic activity of Alpinia galanga rhizome and its extracts in rabbits [J].
Akhtar, MS ;
Khan, MA ;
Malik, MT .
FITOTERAPIA, 2002, 73 (7-8) :623-628
[3]
Al-Nozha MM, 2004, SAUDI MED J, V25, P1603
[4]
AlNuaim AR, 1997, DIABETIC MED, V14, P595
[5]
Alzaid A., 2012, Br J Diabetes Vasc Dis, V12, P57, DOI [DOI 10.1177/1474651412444143, 10.1177/1474651412444143]
[6]
[Anonymous], 1991, TIBETAN MED
[7]
[Anonymous], 2006, ADV TRADIT MED, DOI DOI 10.3742/OPEM.2006.6.3.232
[8]
[Anonymous], HDB AFRICAN MED PLAN
[9]
Syntheses and biological activities of chalcone and 1,5-benzothiazepine derivatives:: Promising new free-radical scavengers, and esterase, urease, and α-glucosidase inhibitors [J].
Ansari, FL ;
Umbreen, S ;
Hussain, L ;
Makhmoor, T ;
Nawaz, SA ;
Lodhi, MA ;
Khan, SN ;
Shaheen, F ;
Choudhary, MI ;
Atta-ur-Rahman .
CHEMISTRY & BIODIVERSITY, 2005, 2 (04) :487-496
[10]
Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain [J].
Ardes-Guisot, Nicolas ;
Alonzi, Dominic S. ;
Reinkensmeier, Gabriele ;
Butters, Terry D. ;
Norez, Caroline ;
Becq, Frederic ;
Shimada, Yousuke ;
Nakagawa, Shinpei ;
Kato, Atsushi ;
Bleriot, Yves ;
Sollogoub, Matthieu ;
Vauzeilles, Boris .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2011, 9 (15) :5373-5388