Screening System for the Maillard Reaction Inhibitor from Natural Product Extracts
スポンサーリンク
概要
- 論文の詳細を見る
An assay for the Maillard reaction has been developed to screen efficiently inhibitors from natural resources such as extracts of plants. The fluorometric analysis of fluorescent material based on advanced glycation endproducts (AGEs) was applied to measurement of an inhibitory index of the Maillard reaction to detect all of the inhibitors at each step of the complicated reaction. To solve the two major problems, slowness of the reaction rate and the existence of interfering substances such as quencher and fluorescent material in the screening sources, we devised the following procedures. Slowness of the reaction rate was solved by raising the reaction temperature to 60℃ at which the conformation of bovine serum albumin (BSA) did not change greatly. To remove the interfering substances, AGEs-BSA was precipitated from the reaction mixture. Thus, an efficient assay system by measuring the fluorescent intensity based on AGEs was established to isolate the glycation inhibitors from natural product extracts.
- 公益社団法人日本薬学会の論文
- 2002-12-01
著者
-
MATSUURA Nobuyasu
Biotechnology Research Center,Toyama Prefectural University
-
Matsuura N
Toyama Prefectural Univ. Toyama Jpn
-
Sasaki Chihiro
Biotechnology Research Center Toyama Prefecture University
-
UBUKATA Makoto
Biotechnology Research Center, Toyama Prefectural University
-
Matsuura Nobuyasu
Biotechnology Research Center Toyama Prefectural University
-
Matsuura Nobuyasu
Biotechnology Research Center Toyama Prefecture University
-
HASEGAWA Junichi
Ichimaru Pharcos Co., Ltd.
-
Ubukata Makoto
Biotechnology Research Center Toyama Prefecture University
-
Aradate Tadashi
Biotechnology Research Center, Toyama Prefecture University
-
Kojima Hiroyuki
Ichimaru Pharcos Co. Ltd.
-
Ohara Mitsuharu
Ichimaru Pharcos Co. Ltd.
-
Aradate Tadashi
Biotechnology Research Center Toyama Prefecture University
-
Ubukata Makoto
Biotechnology Research Center Toyama Prefectural University
-
Hasegawa J
Ichimaru Pharcos Co. Ltd.
-
Hasegawa Junichi
Ichimaru Pharcos Co. Ltd.
関連論文
- Tannins and Related Polyphenols,HIV Reverse Transcriptase Inhibitors, from Rosa woodsii
- New Types of Liposidomycins that Inhibit Bacterial Peptidoglycan Synthesis and are Produced by Streptomyces II. Isolation and Structure Elucidaion
- Acetophthalidin, a Novel Inhibitor of Mammalian Cell Cycle, Produced by a Fungus Isolated from a Sea Sediment
- Structure-Activity Relationship within a Series of Degradation Products of Tautomycin
- Tryprostatins A and B, Novel Mammalian Cell Cycle Inhibitors Produced by Aspergillus fumigatus
- A Pharmacophore Model of Tautomycin, an Inhibitor of Protein Phosphatases I and 2A
- Synthesis and Activity of Pyrimidinylpropenamide Antibiotics : The Alkyl Analogues of Sparsomycin(Organic Chemistry)
- Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : II. Isolation, Physicochemical Properties and Structural Elucidation
- Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : I. Screening, Taxonomy, Fermentation and Biological Activities
- Indocardazostatin, a Novel Inhibitor of NGF-induced Neurite Outgrowth from Rat Pheochromocytoma PC12 Cells
- Stilbenoids in Lianas of Gnetum parvifolium
- Stilbenoids in Lianas of Gnetum parvifolium
- New Hydrolyzable Tannins, Shephagenins A and B, from Shepherdia argentea as HIV-1 Reverse Transcriptase Inhibitors
- Sparoxomycins A1 and A2, New Inducers of the Flat Reversion of NRK Cells Transformed by Temperature Sensitive Rous Sarcoma Virus I. Taxonomy of the Producing Organism, Fermentation and Biological Activity
- Synthetic Studies of Proanthocyanidins. Highly Stereoselective Synthesis of the Catechin Dimer, Procyanidin-B3(Organic Chemistry)
- Interaction of Phytoestrogens with Estrogen Receptors α and β(II)
- Screening System for the Maillard Reaction Inhibitor from Natural Product Extracts
- Facile Synthesis of Cyanogen Glycosides (R)-Prunasin, Linamarin and (S)-Heterodendrin
- Tannins and Related Polyphenols, HIV Reverse Transcriptase Inhibitors, from Rosa woodsii(Natural Medicine Note)
- A Shotrcut and Stereoselective Synthesis of 1-β-Alkyl-2-deoxy-D-ribose Derivatives via Wittig-Horner-Emmons Reaction