Therapeutic potentials of microalgae and their bioactive compounds on diabetes mellitus

K Tamel Selvan, JA Goon, S Makpol, JK Tan - Marine Drugs, 2023 - mdpi.com
Diabetes mellitus is a metabolic disorder characterized by hyperglycemia due to impaired
insulin secretion, insulin resistance, or both. Oxidative stress and chronic low-grade …

[HTML][HTML] DPP-IV Inhibitory Peptide against In Vitro Gastrointestinal Digestion Derived from Goat's Milk Protein and Its Activity Enhancement via Amino Acid Substitution

B He, Y Lian, H Xue, Y Zhou, Y Wei, J Ma, Y Tan… - Foods, 2024 - pmc.ncbi.nlm.nih.gov
Goat milk protein can release a variety of bioactive peptides after digestion, while most of
them are digested into free amino acids or dipeptides via the GI tract. We investigated the …

[HTML][HTML] Angular-Substituted [1, 4] Thiazino [3, 4-a] Isoquinolines: Biological Evaluation and In Silico Studies on DPP-IV Inhibition

A Pashev, V Petrov, A Pesheva, L Petrova… - International Journal of …, 2024 - mdpi.com
Recent studies have discovered that aryl-substituted pyrido [2, 1-a] isoquinolines have the
potential to be highly active DPP IV inhibitors. In previous studies, we reported a novel …

Bis (benzimidazol‐2‐yl) amine‐Based DPP‐4 Inhibitors Potentially Suitable for Combating Diabetes and Associated Nervous System Alterations

K Tomović Pavlović, BS Ilić, L Leitzbach… - Chemistry & …, 2024 - Wiley Online Library
Abstract Bis (benzimidazol‐2‐yl) amine scaffold is not present in dipeptidyl peptidase‐4
(DPP‐4) inhibitors published so far. Herein, the inhibitory potential of bis (benzimidazol‐2 …

Identification of small-molecule glucokinase activator for type-2-diabetes treatment: a structure-based virtual screening approach

M Malini, R Thilagavathi, J Vennila, B Malgija… - Molecular …, 2023 - Taylor & Francis
ABSTRACT Glucokinase (GK, EC 2.7. 1.2) is a crucial enzyme that catalyses the conversion
of glucose to glucose-6-phosphate. It is used to treat type-2 diabetes (T2D), a serious …

Predictive bioactivity of compounds from Vitis gracilis leaf extract to counteract doxorubicin-induced cardiotoxicity via sirtuin 1 and adenosine monophosphate …

P Santoso, S Ilyas, YH Midoen, R Maliza… - Journal of Applied …, 2024 - japsonline.com
Doxorubicin is a potent chemotherapy drug. However, it is known to cause cardiotoxicity via
inhibition of sirtuin 1 (SIRT1) and adenosine monophosphate protein kinase (AMPK) activity …

Evaluation of N10-substituted acridone-based derivatives as AKT inhibitors against breast cancer cells: in vitro and molecular docking studies

TT Yadav, PD Patil, GM Shaikh, MS Kumar… - 3 Biotech, 2023 - Springer
A series of N 10-substituted acridone-2-carboxamide derivatives were synthesized and
evaluated for their potent anti-cancer agents targeting AKT kinase. In vitro cytotoxicity activity …

[HTML][HTML] Design and synthesis of new coumarin-1, 2, 3-triazole hybrids as new antidiabetic agents: In vitro α-amylase, α-glucosidase inhibition, anti-inflammatory, and …

VC Barangi, LA Shastri, PK Chowdegowda… - European Journal of …, 2024 - eurjchem.com
The current study focuses on the synthesis of coumarin-triazole hybrids (7i-t) starting from 4-
hydroxy benzaldehyde or 4-hydroxyacetophenone (1a-b) and propargyl bromide. On the …