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Mushroom tyrosinase: recent prospects.
- S. Seo, V. Sharma, Niti Sharma
- Chemistry, MedicineJournal of agricultural and food chemistry
- 12 April 2003
A study on the importance of tyrosinase, especially that derived from mushroom, and describes its biochemical character and inhibition and activation by the various chemicals obtained from natural and synthetic origins with its clinical and industrial importance in the recent prospects.
Screening of some medicinal plants for anti-lipase activity.
Chaenomeles Sinensis: A Potent α-and β-Glucosidase Inhibitor
The fruits of Chaenomeles sinensis may prove as potent natural anti-diabetic source with noteworthy α-glucosidase and β-glUCosid enzyme inhibitions, because the inhibition of these enzymes provide a strong biochemical basis for the management of type II diabetes by controlling glucose absorption.
1,2,3,4,6-penta-O-galloyl-β-d-glucose: A cholinesterase inhibitor from Terminalia chebula
Antihyperglycemic, antihyperlipidemic, and antioxidant effects of Chaenomeles sinensis fruit extract in streptozotocin-induced diabetic rats
The rising incidence of diabetes mellitus (DM) is alarming and becoming a major health problem worldwide, which is mainly associated with hyperglycemia, abnormal lipid, and antioxidant profiles.…
Feeling of Cold Hands and Feet is a Highly Heritable Phenotype
Model-fitting analyses suggested that in the best fitting model, additive genetic and nonshared environmental variance including measurement error were 64% (95% CI: 55%-72%) and 36% (28%-45%), respectively.
Green Synthesis of Silver Nanoparticles using Bidens Frondosa Extract and their Tyrosinase Activity
- Q. Abbas, M. Saleem, S. Seo
- Materials ScienceIranian journal of pharmaceutical research : IJPR
- 1 June 2017
The eco-friendly synthesis, characterization and their tyrosinase activity of silver nanoparticles (AgNPs) using aqueous extract of Bidens frondosa is reported and may be considered as potential candidate for the production of medical and cosmetic products.
Hybrid Pharmacophoric Approach in the Design and Synthesis of Coumarin Linked Pyrazolinyl as Urease Inhibitors, Kinetic Mechanism and Molecular Docking
Coumarinyl pyrazolinyl thioamide derivatives 5a – 5q showed significant activity against Urease enzyme and also exhibited good antioxidant potential and it was found that compound 5n inhibits urease enzymes by non‐competitive mode of inhibition.
Antidiabetic and antiacetylcholinesterase effects of ethyl acetate fraction of Chaenomeles sinensis (Thouin) Koehne fruits in streptozotocin-induced diabetic rats.
Effect of 1,2,3,4,6-penta-O-galloyl-beta-D-glucose on elastase and hyaluronidase activities and its type II collagen expression.
- Song-Ja Kim, S. Sancheti, S. Sancheti, B. Um, Seon-Mi Yu, S. Seo
- BiologyActa poloniae pharmaceutica
- 1 March 2010
It can be concluded that PGG may prove to be an active ingredient in cosmeceutical and pharmaceutical formulations, and that it definitely merits further in vivo investigations.