共 114 条
Chalcones and their therapeutic targets for the management of diabetes: Structural and pharmacological perspectives
被引:200
作者:

Mahapatra, Debarshi Kar
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Guru Ghasidas Vishwavidyalaya Cent Univ, Inst Pharmaceut Sci, Bilaspur 495009, Chhattisgarh, India Guru Ghasidas Vishwavidyalaya Cent Univ, Inst Pharmaceut Sci, Bilaspur 495009, Chhattisgarh, India

Asati, Vivek
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Guru Ghasidas Vishwavidyalaya Cent Univ, Inst Pharmaceut Sci, Bilaspur 495009, Chhattisgarh, India Guru Ghasidas Vishwavidyalaya Cent Univ, Inst Pharmaceut Sci, Bilaspur 495009, Chhattisgarh, India

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[1] Guru Ghasidas Vishwavidyalaya Cent Univ, Inst Pharmaceut Sci, Bilaspur 495009, Chhattisgarh, India
关键词:
Chalcone;
Diabetes;
DPP-4;
alpha-Glucosidase;
PPAR-gamma;
PTP1B;
TYROSINE-PHOSPHATASE;
1B;
ALPHA-GLUCOSIDASE INHIBITORS;
PROLIFERATOR-ACTIVATED RECEPTORS;
ALDOSE REDUCTASE INHIBITORS;
BIOLOGICAL EVALUATION;
ANGELICA-KEISKEI;
ANTIHYPERGLYCEMIC ACTIVITY;
BROUSSONETIA-PAPYRIFERA;
SULFONAMIDE CHALCONE;
INSULIN-RESISTANCE;
D O I:
10.1016/j.ejmech.2015.01.051
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Diabetes Mellitus (DM) is the fastest growing metabolic disorder affecting about 387 million people across the globe and is estimated to affect 592 million people by year 2030. The search for newer antidiabetic agents is the foremost need to control the accelerating diabetic population. Several natural and (semi) synthetic chalcones deserve the credit of being potential candidates that act by modulating the therapeutic targets PPAR-gamma, DPP-4, alpha-glucosidase, PTP1B, aldose reductase, and stimulate insulin secretion and tissue sensitivity. In this review, a comprehensive study (from January 1977 to October 2014) of anti-diabetic chalcones, their molecular targets, structure activity relationships (SARs), mechanism of actions (MOAs) and patents have been described. The compounds which showed promising activity and have a well-defined MOAs, SARs must be considered as prototype for the design and development of potential anti-diabetic agents. They should be evaluated critically at all clinical stages to ensure their therapeutic and toxicological profile to meet the demand of diabetics. (C) 2015 Elsevier Masson SAS. All rights reserved.
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页码:839 / 865
页数:27
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