Category: 54-17-1

Maeda, Haruka; Tsuyama, Taku; Takabe, Keiji; Kamitakahara, Hiroshi; Takano, Toshiyuki published their research in Journal of Wood Science on December 31 ,2019. The article was titled 《Preparation and properties of a coniferin enantiomer》.Safety of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol The article contains the following contents:

L-Coniferin (1L), which is an enantiomer of natural coniferin (D-coniferin (1D)), was prepared from L-glucose according to the conventional method for compound 1D. The reactivity of L-glucose and its derivatives was found to be almost same as that of the corresponding D-glucose and its derivatives during the preparation for compound 1L. Compound 1L showed resistance toward enzymic hydrolysis by com. β-glucosidase from Almond. However, unlike compound 1D, compound 1L was not transported across the membrane obtained from differentiating xylem of a hybrid poplar in the present assay. The result suggested for the first time that the D-/L-configuration of the glucose moiety of coniferin is an important factor affecting coniferin transport across the membrane. In the experiment, the researchers used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Safety of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Safety of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

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Burcat, Alexander published their research in Combustion and Flame on December 31 ,2020. The article was titled 《Thermochemistry of computed gaseous energetic compounds: Cellulose nitrate》.Application In Synthesis of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol The article contains the following contents:

The thermochem. of gaseous Cellulose, Cellulosedinitrate and Cellulosetrinitrate basic cells, was calculated and is presented as numerical values and as NASA-7-term polynomials. The problem of representing and calculating thermochem. values of cell polymers is discussed. In the experiment, the researchers used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Application In Synthesis of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is the monohydrate form of the alpha isoform of D-glucopyranose, a synthetic simple monosaccharide that is used as an energy source.Application In Synthesis of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

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Nachtigall, Carsten; Berger, Christiane; Kovanovic, Tijana; Wefers, Daniel; Jaros, Doris; Rohm, Harald published their research in Food Hydrocolloids on December 31 ,2019. The article was titled 《Shear induced molecular changes of exopolysaccharides from lactic acid bacteria》.Electric Literature of C6H12O6 The article contains the following contents:

Exopolysaccharide (EPS) producing lactic acid bacteria are known for their pos. effect on the texture of fermented dairy products, with their high water binding capacity causing changes in rheol. and syneresis reduction During manufacture, product texture is affected by shearing with an unknown impact on the properties of the EPS. By subjecting aqueous solutions of viscosity enhancing EPS from Streptococcus thermophilus DGCC7710 or dextran to defined shear treatments with a Microfluidizer, a cell disruption system or a toothed ring dispersion unit to apply different energy input, we investigated macromol. properties and the behavior in solution Despite the breakage of covalent bonds, spectroscopic NMR analyses revealed that repeating unit structure remained unchanged, whereas changes in macromol. properties such as intrinsic viscosity, hydrodynamic volume, and mol. mass strongly depended on energy input. The decrease of the dynamic viscosity of the polysaccharide solutions was significantly related to the observed decrease in mol. mass, and the impact of the EPS on technofunctional properties such as contribution to gel stiffness during acid gel formation was also affected. The results therefore indicate that mech. energy input through shearing should be considered because product texture may be altered as a consequence of a mech. breakdown of EPS mols. The experimental part of the paper was very detailed, including the reaction process of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Electric Literature of C6H12O6)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Electric Literature of C6H12O6

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In 2019,Natural Product Research included an article by Zhu, Zhen-Yuan; Chen, Chun-Juan; Sun, Hui-Qing; Chen, Li-Jing. COA of Formula: C6H12O6. The article was titled 《Structural characterisation and ACE-inhibitory activities of polysaccharide from Gastrodia elata Blume》. The information in the text is summarized as follows:

The structural properties and Angiotensin-I converting enzyme (ACE) inhibition activities of a polysaccharide (PGE) extracted from Gastrodia elata Blume were investigated. PGE was extracted using hot water and purified by Sephadex G-200 followed by ultra-filtration. The structural characterization of PGE was analyzed by FT-IR, NMR spectroscopy, sp. rotation determination, periodate oxidation-smith degradation, methylation anal., GC-MS and Congo red test. The results revealed that PGE was composed by glucose, with an average mol. weight of 1.54 × 103 kDa. The structure of PGE was 1→3 and 1→4,6-branched-glucopyranose that had a linear backbone of (1 → 4)-linked-D-glucopyranose (Glcp). ACE-inhibitory activity results showed that PGE was efficient to inhibit ACE and the IC50 value was 0.66 mg/mL. In the experiment, the researchers used many compounds, for example, rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1COA of Formula: C6H12O6)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.COA of Formula: C6H12O6

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Bahramzadeh, Saman; Tabarsa, Mehdi; You, SangGuan; Li, Changsheng; Bita, Seraj published an article on February 1 ,2019. The article was titled 《Purification, structural analysis and mechanism of murine macrophage cell activation by sulfated polysaccharides from Cystoseira indica》, and you may find the article in Carbohydrate Polymers.Computed Properties of C6H12O6 The information in the text is summarized as follows:

Sulfated polysaccharides were isolated and purified from the water extract of Cystoseira indica using DEAE Sepharose Fast Flow column to evaluate their structure and macrophage stimulating capacity. Crude and fractionated polysaccharides, CIF1 and CIF2, were mostly composed of neutral sugars (73.1%-78.6%) with relatively lower amounts of acidic sugars (1.3%-9.0%) and sulfate esters (6.9%-9.7%). The polymer chains of polysaccharides were mainly built of different levels of glucose (2.1%-30.8%), fucose (17.2%-24.4%), mannose (17.8%-20.6%) and galactose (16.7%-17.3%). The weight average mol. weight (Mw) of polysaccharides varied between 573.1 × 103 g/mol to 1146.6 × 103 g/mol. The CIF2 polysaccharide, as the most immunostimulating polysaccharide, remarkably induced the release of nitric oxide and inflammatory cytokines including TNF-α, IL-1β, IL-6 and IL-10 from RAW264.7 murine macrophage cells through NF-κB and MAPKs transduction signaling pathways via cell surface TLR4. The interconnections of sugars in CIF2 polysaccharide were complex with (1→3)-fucopyranose, (1→2,3,4)-glucopyranose, (→1)-galactopyranose, (→1)-xylopyranose, (1→2)-rhamnopyranose and (1→2,3)-mannopyranose units being the most predominant residues. After reading the article, we found that the author used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Computed Properties of C6H12O6)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Computed Properties of C6H12O6

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Recommanded Product: 54-17-1On March 1, 2021, Bridi, Raquel; Lino von Poser, Gilsane; Gomez, Miguel; Andia, Marcelo E.; Oyarzun, Juan Esteban; Nunez, Paula; Vasquez Arias, Ariadsna Jael; Espinosa-Bustos, Christian published an article in Journal of Ethnopharmacology. The article was 《Hepatoprotective species from the Chilean medicinal flora: Junellia spathulata (Verbenaceae)》. The article mentions the following:

Chilean population relies on medicinal plants for treating a wide range of illnesses, especially those of the gastrointestinal system. Junellia spathulata (Gillies & Hook.) Moldenke var. spathulata (Verbenaceae), called as “”verbena-azul-de-cordilleira””, is a medicinal plant native to Argentina and Chile traditionally used for treating digestive disorders. Although the species of the genus are important as therapeutic resources for the Andean population, the plants are very scarcely studied. The purpose of the present study was to find out the main constituents and investigate the protective effect of J. spathulata against oxidative stress induced by the potent oxidant 2,2-azobis (2-amidinopropane) dihydrochloride (AAPH) in human hepatoblastoma cells.The crude methanol extract of J. spathulata and an iridoid obtained by chromatog. processes were tested to access the hepatoprotective effect and cytotoxicity in HepG2 cell. In addition, the reducing power of the samples and their ability to scavenge free radicals were evaluated using FRAP and ORAC assay systems. The iridoid asperuloside, the main compound of the crude methanol extract of J. spathulata, was isolated and identified by means of NMR anal. The crude methanol extract of J. spathulata and asperuloside protected HepG2 cells against oxidative damage triggered by AAPH-derived free radicals. This effect can be credited to the ability of the extract and asperuloside to protect the liver cells from chem.-induced injury, which might be correlated to their free radical scavenging potential. This study exptl. evidenced the ethnopharmacol. usefulness of J. spathulata as a treatment of digestive disorders. Our result could stimulate further investigations of hepatoprotective agents in other Chilean Junellia species. After reading the article, we found that the author used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Recommanded Product: 54-17-1)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Recommanded Product: 54-17-1

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Product Details of 54-17-1On November 30, 2020 ,《Thermal, Morphological, and Functional Characterization of Gros Michel Banana Starch Modified with Octenyl Succinic Anhydride》 appeared in Starch/Staerke. The author of the article were Quintero-Castano, Victor D.; Bello-Perez, Luis A.; Alvarez-Barreto, Cristina I.; Castellanos-Galeano, Francisco J.; Rodriguez-Garcia, Mario E.. The article conveys some information:

Banana is a food crop produced extensively in Colombia for fresh consumption. This fruit in the green state has a large amount of starch, which-unlike other Musaceae-has a small granule size that makes it attractive for use in the food industry. This work characterizes physicochem., morphol., structurally, and functionally isolated and modified starches from Gros Michel banana. This characterization uses techniques like SEM, XRD, FTIR, DSC, RVA, and HPLC. The results show a morphol. change, given that the granules display superficial adherence of small masses. The IR spectra shows mol. vibrations in the modified starch at 1578 and 1745 cm-1; the X-ray diffraction patterns show alteration of the 3D starch structure, given that it changes in large proportion from a hexagonal to a monoclinic conformation after the modification. The maximum viscosities obtained via RVA change from 1380 cP for the isolated starch to 1247 cP for the modified starch. The amylopectin/amylose ratio is altered after the modification, going from 75/25 to 87/13. Modified starches are a viable alternative for use in the food industry as additives to stabilize emulsions that do not need high processing temperatures In the part of experimental materials, we found many familiar compounds, such as rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Product Details of 54-17-1)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Product Details of 54-17-1

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Related Products of 54-17-1On March 31, 2019, Gabr, S. K.; Bakr, R. O.; Mostafa, E. S.; El-Fishawy, A. M.; El-Alfy, T. S. published an article in South African Journal of Botany. The article was 《Antioxidant activity and molecular docking study of Erythrina neillii polyphenolics》. The article mentions the following:

Species of genus Erythrina have a great contribution in folk medicine; various species are utilized as a tranquilizer, to treat insomnia, inflammation and colic. Besides, Erythrina species have reported antioxidant, hepatoprotective and anxiolytic activities. Erythrina × neillii is a hybrid obtained through a cross between E. herbacea L. and E. humeana Spreng. It has not been well-studied for its chem. or biol. profile; therefore it represents an interesting field of study. In this study, seven phenolic compounds; two hydrolysable tannins (1,3), one phenolic acid (2) and four known flavonoids (4-7) were isolated and characterized for the first time in E × neillii and Erythrina genus except for vitexin (7). Isolated compounds were assessed for their antioxidant activities using ORAC assay. 2″”-O-galloyl orientin (6) exhibited the highest activity followed by 2″”-O-galloyl vitexin (5). Flexible mol. docking on heme oxygenase, an important stress protein that is involved in cellular protection, antioxidant and anti-inflammatory activities, justified the antioxidant activity of the isolated compounds The best scoring was observed with 2″”-O-galloyl orientin forming four binding interactions with residues, Arg 136 (two interactions), Met34 and Gly139. Erythrina × neillii offered powerful and available antioxidant beside significantly active phytoconstituents. After reading the article, we found that the author used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Related Products of 54-17-1)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is oxidized in various tissues under either aerobic or anaerobic conditions through glycolysis; the oxidation reaction produces carbon dioxide, water, and ATP.Related Products of 54-17-1

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Recommanded Product: 54-17-1On March 31, 2019, Ye, Luxin; Huang, Binge; Lin, YiJing; Chen, Fan; Li, Jie; Huang, Peng; Sheen, Xiuwei published an article in Latin American Journal of Pharmacy. The article was 《Effect of codeine on urine metabolism in rats》. The article mentions the following:

Codeine, a commonly used cough drug, belongs to opioids, which is used more by drug abusers as an addictive substance. Except tablets, some other preparations of codeine are relatively easy to obtain, and at present in the youth codeine addicts have reached a large number due to cough drug abuse. In order to further comprehend the mechanism of codeine, the effects of codeine on the metabolic pathway of rats were studied by searching the relative relationship between metabolites (urine) and physiol. and pathol. changes. The metabolites were analyzed by gas chromatog.-mass spectrometer, the data were processed by principal component anal. (PCA) and PLS-DA by SIMCA-P 13.0 software, and statistical anal. by SPSS18.0 software. The results indicated that codeine induced metabolic disorder, and Metabolomics could provide a useful tool for the metabolic changes of rats. The results came from multiple reactions, including the reaction of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Recommanded Product: 54-17-1)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is the monohydrate form of the alpha isoform of D-glucopyranose, a synthetic simple monosaccharide that is used as an energy source.Recommanded Product: 54-17-1

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Application of 54-17-1On October 31, 2020 ,《New caryophyllene-type sesquiterpene and flavonol tetraglycoside with sixteen known compounds from sword bean (Canavalia gladiata)》 was published in Food Science and Biotechnology. The article was written by An, Hyun Jeong; Kim, Eun Hee; Lee, Hyoung Jae; Cho, Jeong-Yong; Moon, Jae-Hak. The article contains the following contents:

Eighteen compounds including new caryophyllene-type sesquiterpene and flavonol tetraglycoside were purified and isolated from sword beans (Canavalia gladiata). Two new compounds, (Z,1R,7S,9S)-7-hydroxy-11,11-dimethyl-8-methylenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid (2) and kaempferol-7-O-α-L-dirhamnopyranosyl(1 → 2;1 → 6)-O-β-D-glucopyranosyl(1 → 2)-O-α-L-rhamnopyranoside (9), were identified. Other known compounds including Me gallate (1), (2S,3S,4E,8E)-2-aminooctadeca-4,8-diene-1,3-diol 1-O-β-D-glucopyranoside (3), (2S,3S,4E,8Z)-2-aminooctadeca-4,8-diene-1,3-diol 1-O-β-D-glucopyranoside (4), lupeol (5), trilinolein (6), 1,6-di-O-galloyl β-D-glucopyranoside (7), N-(2-methoxybenzoyl)homoserine (8), dihydrophaseic acid (10), dillenetin (11), kaempferol-7-O-[2-O-β-D-glucopyranosyl-6-O-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside (12), canavalioside (13), kaempferol-3-O-[2-O-β-D-glucopyranosyl-6-O-α-L-rhamnopyranosyl]-β-D-glucopyranoside (14), kaempferol-3-O-(2,6-O-α-L-dirhamnopyranosyl)-β-D-glucopyranoside (15), kaempferol-3-O-rutinoside (16), gladiatoside A1 (17), and gladiatoside B1 (18) were identified. The chem. structures of these compounds were determined by ESI-MS and NMR analyses. In the experiment, the researchers used many compounds, for example, rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Application of 54-17-1)

rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1) is the monohydrate form of the alpha isoform of D-glucopyranose, a synthetic simple monosaccharide that is used as an energy source.Application of 54-17-1

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Alcohol – Wikipedia,
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