L-(+)-ERGOTHIONEINE CAS NO.497-30-3

The Chinese name for ergothione is 2-mercaptohistidine betaine, which is synonymous with 2-mercaptohistidine betaine in Chinese; Ergothionein liposomes; Super antioxidant ergothionein; Pine mushroom extract; Ergothionein; (S) 3- (2-Thio-2,3-dihydro-1H-imidazol-4-yl) -2- (trimethylammonium) propionate; Ergothione/2-mercaptohistidine betaine; The English name for ergothione is L - (+) - Ergothionine, and its English synonym is L - (+) - Ergothionine INNERSALT; ERGOLD; 2-MERCAPTOHISTIDINEBETAINE; (S)-ALPHA-CARBOXY-2,3-DIHYDRO-N,N,N-TRIMETHYL-2-THIOXO-1H-IMIDAZOLE-4-ETHANAMINIUMINNERSALT; THIONEINE; (S)-[1-carboxy-2-(2-mercaptoimidazol-4-yl)ethyl]trimethylammoniumhydroxide; 1H-Imidazole-4-ethanaminium,.alpha.-carboxy-2,3-dihydro-N,N,N-trimethyl-2-thioxo-,innersalt,(.alpha.S)-; 3- (2-sulfanylidene-1,3-dihydroimidazol-4-yl) -2-trimethylammonio-propanoate CAS number 497-30-3 Molecular formula C9H15N3O2S Molecular weight 229.3 EINECS number 207-843-5 Related category synthesis; Fermented products; Cosmetic additives; anti-aging; Standard products; Ergothionein -0.5%; Chemical raw materials; Whitening and freckle removal; High purity reagents; Cosmetic functional ingredient additives - whitening and anti-aging ingredients; Intermediates&FineChemicals; Pharmaceuticals; Sulfur&SeleniumCompounds; Heterocycles; Cosmetics raw materials; Cosmetic functional raw material additive - Bose Einstein; Cosmetic functional raw material additives; Daily chemical products; Ergothionein; Raw materials; Research materials; Organic raw materials; Chemical reagent Mol file 497-30-3. mol Structural formula: Ergothione Due to properties Melting point 275-277 ° C (dec.) Density 1.2541 (roughness) Refractive index 1.6740 (estimate) Storage conditions -20 ° C Solubility in water (up to 10mg/ml) Acidity coefficient (pKa) 1.706 ± 0.32 (predicted) Form: White solid. Color: white or off white, pH+47 ^ o (c=1inwater), biogenic fungi fungi fungi fungi fungi (Ascomycota) fungi (Basidiomycota), water solubility: 50mg/mL, clear, colorless stability: maintain stability within 1 year from the date of purchase. The aqueous solution can be stored at -20 ° C for no more than 1 day. InChIInChI=1/C9H15N3O2S/c1-12(2,3)7(8(13)14)4-6-5-10-9(15)11-6/h5,7H,4H2,1-3H3,(H2-,10,11,13,14,15)/t7-/s3InChIKeySSISHJJTAXXQAX-KChemicalbookPOCXSGKNA-NSMILES[N+](C)(C)(C)[C@@H](CC1=CNC(S)=N1)C([O-])=O|&1:4,r|EPA Chemical Substance Information 1 H-Imidazole-4-ethanaminium,.alpha.-carboxy-2,3-dihydro-N,N,N-trimethyl-2-thioxo-,innersalt,(.alpha.S)-(497-30-3) Introduction to the uses and synthesis methods of ergothionein. Ergothionein is a natural antioxidant that can protect cells in the human body and is an important active substance in the body. Natural antioxidants are safe, non-toxic, and have become a hot research topic. As a natural antioxidant, ergothionein has entered people's field of vision. It has various physiological functions such as clearing free radicals, detoxification, maintaining DNA biosynthesis, normal cell growth, and cellular immunity. Ergothionein is a natural molecule isolated from the rye ergot fungus and later discovered in rat red blood cells, liver, and many other animal tissues. Its antioxidant properties can provide potential for composite therapy, or it can be used as a food additive or cosmetic. Application: L-ergothionein is a natural molecule isolated from the rye ergot fungus and later discovered in rat red blood cells, liver, and many other animal tissues. Its antioxidant properties can provide therapeutic potential for the compound, or it can be used as a food additive or cosmetic. The principle of action is that ergothionein is transported to the important "energy factory" mitochondria through the transport protein OCTN1 on the cell membrane and mitochondrial membrane, exerting antioxidant function, inhibiting DNA damage, effectively protecting against UV damage, protecting cells, and preventing photoaging. At the same time, it has the ability to eliminate free radicals, reduce lipid peroxidation, and promote the body's own antioxidant enzymes. In terms of antioxidant ability, ergothionein is a strong contender that can compete against competitors of the same type, such as the formidable Coenzyme Q10 and Adiponem. The distribution range of ergothionein is found in certain tissues and organs of mammals, mainly in red blood cells (about 1-2 mmol/L) and semen of certain animals. Although there is no experimental research indicating that animals can synthesize this substance, there are certainly pathways for the absorption and retention of ergothionein in animal cells. For carnivores, ergotamine in animal tissues can provide dietary needs, and research has found that it is present in cereal plants. Ergothionein is a powerful hypochlorous acid scavenger (HOCl), and although many compounds can react with hypochlorous acid, few can react as rapidly as ergothionein. A1 anti protease inhibitors (APIs), such as elastase, are particularly sensitive to hypochlorous acid, and physiological concentrations of ergotamine can effectively protect APIs against inactivation caused by hypochlorous acid. As neutrophils are the main source of hypochlorous acid in the body, one of their functions is to protect red blood cells from harm from neutrophils in normal functioning or pathological inflammatory sites. The application of ergothionein has a wide range of uses and market prospects in fields such as organ transplantation, cell preservation, medicine, food and beverage, functional foods, animal feed, cosmetics, and biotechnology. It is also a highly protective and non-toxic natural antioxidant for cells, which is not easily oxidized in water, allowing its concentration in certain tissues to reach mmol and stimulating the cell's natural antioxidant defense system. Among numerous antioxidants, ergotamine is particularly unique because it can chelate heavy metal ions, which can protect red blood cells in the body from free radical damage. Ergothionine, a biologically active derivative of histidine betaine, is synthesized by certain bacteria and fungi. Ergothionene is commonly considered an antioxidant

The Chinese name for ergothione is 2-mercaptohistidine betaine, which is synonymous with 2-mercaptohistidine betaine in Chinese; Ergothionein liposomes; Super antioxidant ergothionein; Pine mushroom extract; Ergothionein; (S) 3- (2-Thio-2,3-dihydro-1H-imidazol-4-yl) -2- (trimethylammonium) propionate; Ergothione/2-mercaptohistidine betaine; The English name for ergothione is L - (+) - Ergothionine, and its English synonym is L - (+) - Ergothionine INNERSALT; ERGOLD; 2-MERCAPTOHISTIDINEBETAINE; (S)-ALPHA-CARBOXY-2,3-DIHYDRO-N,N,N-TRIMETHYL-2-THIOXO-1H-IMIDAZOLE-4-ETHANAMINIUMINNERSALT; THIONEINE; (S)-[1-carboxy-2-(2-mercaptoimidazol-4-yl)ethyl]trimethylammoniumhydroxide; 1H-Imidazole-4-ethanaminium,.alpha.-carboxy-2,3-dihydro-N,N,N-trimethyl-2-thioxo-,innersalt,(.alpha.S)-; 3- (2-sulfanylidene-1,3-dihydroimidazol-4-yl) -2-trimethylammonio-propanoate CAS number 497-30-3 Molecular formula C9H15N3O2S Molecular weight 229.3 EINECS number 207-843-5 Related category synthesis; Fermented products; Cosmetic additives; anti-aging; Standard products; Ergothionein -0.5%; Chemical raw materials; Whitening and freckle removal; High purity reagents; Cosmetic functional ingredient additives - whitening and anti-aging ingredients; Intermediates&FineChemicals; Pharmaceuticals; Sulfur&SeleniumCompounds; Heterocycles; Cosmetics raw materials; Cosmetic functional raw material additive - Bose Einstein; Cosmetic functional raw material additives; Daily chemical products; Ergothionein; Raw materials; Research materials; Organic raw materials; Chemical reagent Mol file 497-30-3. mol Structural formula: Ergothione Due to properties Melting point 275-277 ° C (dec.) Density 1.2541 (roughness) Refractive index 1.6740 (estimate) Storage conditions -20 ° C Solubility in water (up to 10mg/ml) Acidity coefficient (pKa) 1.706 ± 0.32 (predicted) Form: White solid. Color: white or off white, pH+47 ^ o (c=1inwater), biogenic fungi fungi fungi fungi fungi (Ascomycota) fungi (Basidiomycota), water solubility: 50mg/mL, clear, colorless stability: maintain stability within 1 year from the date of purchase. The aqueous solution can be stored at -20 ° C for no more than 1 day. InChIInChI=1/C9H15N3O2S/c1-12(2,3)7(8(13)14)4-6-5-10-9(15)11-6/h5,7H,4H2,1-3H3,(H2-,10,11,13,14,15)/t7-/s3InChIKeySSISHJJTAXXQAX-KChemicalbookPOCXSGKNA-NSMILES[N+](C)(C)(C)[C@@H](CC1=CNC(S)=N1)C([O-])=O|&1:4,r|EPA Chemical Substance Information 1 H-Imidazole-4-ethanaminium,.alpha.-carboxy-2,3-dihydro-N,N,N-trimethyl-2-thioxo-,innersalt,(.alpha.S)-(497-30-3) Introduction to the uses and synthesis methods of ergothionein. Ergothionein is a natural antioxidant that can protect cells in the human body and is an important active substance in the body. Natural antioxidants are safe, non-toxic, and have become a hot research topic. As a natural antioxidant, ergothionein has entered people's field of vision. It has various physiological functions such as clearing free radicals, detoxification, maintaining DNA biosynthesis, normal cell growth, and cellular immunity. Ergothionein is a natural molecule isolated from the rye ergot fungus and later discovered in rat red blood cells, liver, and many other animal tissues. Its antioxidant properties can provide potential for composite therapy, or it can be used as a food additive or cosmetic. Application: L-ergothionein is a natural molecule isolated from the rye ergot fungus and later discovered in rat red blood cells, liver, and many other animal tissues. Its antioxidant properties can provide therapeutic potential for the compound, or it can be used as a food additive or cosmetic. The principle of action is that ergothionein is transported to the important "energy factory" mitochondria through the transport protein OCTN1 on the cell membrane and mitochondrial membrane, exerting antioxidant function, inhibiting DNA damage, effectively protecting against UV damage, protecting cells, and preventing photoaging. At the same time, it has the ability to eliminate free radicals, reduce lipid peroxidation, and promote the body's own antioxidant enzymes. In terms of antioxidant ability, ergothionein is a strong contender that can compete against competitors of the same type, such as the formidable Coenzyme Q10 and Adiponem. The distribution range of ergothionein is found in certain tissues and organs of mammals, mainly in red blood cells (about 1-2 mmol/L) and semen of certain animals. Although there is no experimental research indicating that animals can synthesize this substance, there are certainly pathways for the absorption and retention of ergothionein in animal cells. For carnivores, ergotamine in animal tissues can provide dietary needs, and research has found that it is present in cereal plants. Ergothionein is a powerful hypochlorous acid scavenger (HOCl), and although many compounds can react with hypochlorous acid, few can react as rapidly as ergothionein. A1 anti protease inhibitors (APIs), such as elastase, are particularly sensitive to hypochlorous acid, and physiological concentrations of ergotamine can effectively protect APIs against inactivation caused by hypochlorous acid. As neutrophils are the main source of hypochlorous acid in the body, one of their functions is to protect red blood cells from harm from neutrophils in normal functioning or pathological inflammatory sites. The application of ergothionein has a wide range of uses and market prospects in fields such as organ transplantation, cell preservation, medicine, food and beverage, functional foods, animal feed, cosmetics, and biotechnology. It is also a highly protective and non-toxic natural antioxidant for cells, which is not easily oxidized in water, allowing its concentration in certain tissues to reach mmol and stimulating the cell's natural antioxidant defense system. Among numerous antioxidants, ergotamine is particularly unique because it can chelate heavy metal ions, which can protect red blood cells in the body from free radical damage. Ergothionine, a biologically active derivative of histidine betaine, is synthesized by certain bacteria and fungi. Ergothionene is commonly considered an antioxidant