Category: 54-17-1

《Electrochemical performances of pyrolytic-cellulose for lithium and sodium ion batteries anodeã€?was written by Li, Lingfang; Chen, Dan; Su, Sichao; Zeng, Bin. Application of 54-17-1 And the article was included in Materials Express in 2020. The article conveys some information:

At present, due to the depletion of fossil fuels and increasingly serious environmental problems, more and more attention has been paid to the development and application of functional nanostructured materials as renewable energy storage materials. Herein, lithium and sodium storage properties of hard carbons (HC) prepared by pyrolyzing cellulose were investigated. The orderliness and bonding mode of hard carbon were analyzed by X-Ray Diffraction and XPS. Electrochem. properties were characterized by Cyclic Voltammetry, electrochem. Impedance Spectroscopy and charge-discharge test. Results showed that the cellulose-derived hard carbon had good lithium and sodium storage performance. The charge-discharge capacity was about 400 mAh/g and 240 mAh/g, resp., at a c.d. of 0.2 A/g, and capacity was also stable under high c.d. of 2 A/g. 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: 54-17-1Application of 54-17-1)

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

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Quality Control of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraolOn June 4, 2020, Xie, Huijun; Chen, Xiaoyu; Li, Miaomiao; Aisa, Haji Akber; Yuan, Tao published an article in Tetrahedron Letters. The article was 《Angustifolinoid B, a flavonoid glycoside dimer with cyclobutane from Elaeagnus angustifolia flowersã€? The article mentions the following:

A novel flavonoid glycoside dimer with an unprecedented cyclobutane moiety, named angustifolinoid B (1), was isolated from Elaeagnus angustifolia flowers. Its structure was determined by extensive spectroscopic anal. (HRMS, NMR) and chem. hydrolysis. The new dimer was formed via a [2 + 2] cycloaddition between two sym. tiliroside. Bioassay revealed that compound 1 showed significant α-glucosidase inhibitory activity with IC50 value at 4.40 μM. In the experiment, the researchers used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Quality Control 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.Quality Control of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

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Abdel-Wahhab, Mosaad A.; El-Nekeety, Aziza A.; Hathout, Amal S.; Salman, Asmaa S.; Abdel-Aziem, Sekena H.; Sabry, Bassem A.; Hassan, Nabila S.; Abdel-Aziz, Mohamed S.; Aly, Soher E.; Jaswir, Irwandi published an article in Toxicon. The title of the article was 《Bioactive compounds from Aspergillus niger extract enhance the antioxidant activity and prevent the genotoxicity in aflatoxin B1-treated ratsã€?HPLC of Formula: 54-17-1 The author mentioned the following in the article:

This study aimed to identify the bioactive compounds of the Et acetate extract of Aspergillus niger SH2-EGY using GC-MS and to evaluate their protective role against aflatoxin B1 (AFB1)-induced oxidative stress, genotoxicity and cytotoxicity in rats. Six groups of male Sprague-Dawley rats were treated orally for 4 wk included the control group, AFB1-treated group (80μg/kg b.w); fungal extract (FE)-treated groups at low (140) or high dose (280) mg/kg b.w and the groups treated with AFB1 plus FE at the two tested doses. The in vivo results showed that AFB1 significantly increased serum ALT, AST, creatinine, uric acid, urea, cholesterol, triglycerides, LDL, carcinoembryonic antigen, alpha-fetoprotein, interleukin-6, Malondialdehyde, nitric oxide, Bax, caspase-3 and P53 mRNA expression, chromosomal aberrations and DNA fragmentation. It decreased serum TP, albumin, HDL, Bcl-2 mRNA expression, hepatic and renal TAC, SOD and GPx content and induced histol. changes in the liver and kidney. FE prevented these disturbances in a dosage-dependent manner. It could be concluded that A. niger SH2-EGY extract is safe a promising agent for pharmaceutical and food industries. In the experimental materials used by the author, we found rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1HPLC of Formula: 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.HPLC of Formula: 54-17-1

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Recommanded Product: rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraolOn March 31, 2022, Wan, Jiang; Jiang, Chun-Xiao; Tang, Yu; Ma, Guang-Lei; Tong, Ying-Peng; Jin, Ze-Xin; Zang, Yi; E. A. Osman, Ezzat; Li, Jia; Xiong, Juan; Hu, Jin-Feng published an article in Bioorganic Chemistry. The article was 《Structurally diverse glycosides of secoiridoid, bisiridoid, and triterpene-bisiridoid conjugates from the flower buds of two Caprifoliaceae plants and their ATP-citrate lyase inhibitory activitiesã€? The article mentions the following:

The ethanolic extracts of the dried flower buds of two Caprifoliaceae plants, Lonicera japonica and Abelia x grandiflora, showed considerable inhibitory activities against ATP (ATP)-citrate lyase (ACL), a new promising drug target for the treatment of metabolic disorders. Bioassay-guided purification in conjunction with HPLC-PDA profiling led to the isolation and characterization of thirty-five (1-35) and fourteen (1-14) structurally diverse compounds from the above two plant extracts, resp. Compounds 1-9 and 1-6 are previously undescribed glycosides. Their structures were elucidated on the basis of spectroscopic data, electronic CD (ECD), and single crystal X-ray diffraction analyses. In particular, lonicejaposide A (1) has an unprecedented skeleton generated through the coupling of C-7 in secologanin with C-2 in phenylacetaldehyde via an aldol condensation. Abeliflorosides A (1) and B (2) are hitherto unknown glycosides of triterpene and bisiridoid conjugates constructed through the formation of a 1,3-dioxane moiety. All the isolates were evaluated for their inhibitory activities against ACL. Compounds 9, 25-28, 31, 1, 2, and 14 displayed significant inhibitory effects, with IC50 values ranging from 0.1 to 14.2 μM. The interactions of selected compounds possessing different structure features (e.g., 9, 25, 31, and 2) with ACL were thereafter performed by employing mol. docking studies. In addition, compound 2, the most complex triterpene-bisiridoid conjugate glycoside reported herein, also inhibited acetyl-CoA carboxylase 1 (ACC1), with an IC50 value of 7.9 μM. The dried material of the flower buds of L. japonica (honeysuckle) is a well-known traditional oriental medicine (i.e., Flos Lonicerae Japonicae, FLJ) and has long been used in large quantities. The above findings not only provide new insights for the development of multipurpose utilization of FLJ in healthcare community, but also provide profitable clues indicating that the flower buds of A. x grandiflora might be a potential alternative to FLJ in the traditional Chinese medicine market.rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Recommanded Product: rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol) was used in this study.

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: rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

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Synthetic Route of C6H12O6On October 31, 2019 ,《Initial pyrolysis mechanism of cellulose revealed by in-situ DRIFT analysis and theoretical calculation》 appeared in Combustion and Flame. The author of the article were Dai, Gongxin; Wang, Kaige; Wang, Guanyu; Wang, Shurong. The article conveys some information:

Cellulose is one of the major components of biomass. The study on its pyrolysis process will be beneficial to the in-depth understanding of biomass pyrolysis mechanism. In this work, in-situ diffuse reflectance IR Fourier transform spectroscopy (in-situ DRIFT) combined with two-dimensional perturbation correlation IR spectroscopy (2D-PCIS) was first used to characterize the evolution process of the functional groups in cellulose during pyrolysis. The results showed that the degradation of carbon skeleton was prior to the dehydration of free hydroxyls after the destruction of hydrogen bond networks during pyrolysis. The thermal stability of C-O in cellulose followed by the order of glycosidic bond Synthetic Route 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.Synthetic Route of C6H12O6

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Formula: C6H12O6On September 15, 2021 ,《Chemical structure and anti-inflammatory activity of a branched polysaccharide isolated from Phellinus baumii》 was published in Carbohydrate Polymers. The article was written by Sun, Yuqing; Huo, Jinxi; Zhong, Shi; Zhu, Jianxun; Li, Yougui; Li, Xiaojun. The article contains the following contents:

Phellinus baumii is used to treat inflammatory bowel disease (IBD) and gastroenteritis. In this study, a 46 kDa heteropolysaccharide SHPS-1 was isolated from fruiting bodies of P. baumii. SHPS-1 consisted of arabinose, mannose, glucose, and galactose at a molar ratio of 2.2:15.7:49.3:32.8. SHPS-1 had a backbone containing 1,3-linked β-D-Glcp and 1,6-linked α-D-Galp residues, and Araf, Manp and Galp units were attached as oligosaccharidic side chains to the backbone at C-6 of some glucopyranoses. SHPS-1 decreased phosphorylation level of STAT-1 and expression levels of STAT-1 targeted genes such as iNOS and TNF-α in lipopolysaccharide-stimulated macrophage RAW 264.7 cells. Furthermore, SHPS-1 promoted the expression of IL-10 and macrophage mannose receptor CD 206, markers of tissue repairing macrophages. SHPS-1 alleviated ulcerative colitis in mice by decreasing pro-inflammatory genes and increasing anti-inflammatory and tissue repairing genes. Collectively, SHPS-1 polysaccharide from P. baumii had anti-inflammatory activity and can potentially treat IBD. In the experiment, the researchers used rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Formula: 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.Formula: C6H12O6

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In 2022,Natural Product Research included an article by Feng, Jie; Zhao, Danyang; Xu, Qiannan; Liu, Xiangzhong; Zhou, Mi; Ye, Xiansheng; Lin, Ting; Wang, Guanghui; Sun, Cuiling; Ding, Rong; Tian, Wenjing; Chen, Haifeng. HPLC of Formula: 54-17-1. The article was titled 《A new phenolic glycoside from Trollius chinensis Bunge with anti-inflammatory and antibacterial activities》. The information in the text is summarized as follows:

A undescribed phenolic glycoside, trochinenol A, was isolated from the flowers of Trollius chinensis Bunge and the structure was identified by spectroscopic methods. Its anti-inflammatory and antibacterial effects were investigated by broth microdilution and NF-κB reporter gene assays. Consequently, compound exhibited an appreciable effect against Staphylococcus aureus with the MIC value of 6.25μg/mL. Besides, it showed moderate effect against TNFα-induced activation of NF-κB pathway. The experimental process involved the reaction of rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1HPLC of Formula: 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.HPLC of Formula: 54-17-1

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《A new megastigmane glucoside and other constituents fromDesmodium gangeticum》 was published in Journal of Chemistry in 2020. These research results belong to Dang, Hau Viet; Do, Giang Hoang; Ngo, Phuong Thi; Nguyen, Tien Dat; Le, Ha Minh. Application of 54-17-1 The article mentions the following:

A new megastigmane glycoside, gangeticoside (1), and three known compounds leonuriside A (2), Me benzoate 2-O-β-D-glucopyranoside (3), and tortoside A (4) were isolated from the aerial part of Desmodium gangeticum. Their structures were determined by 1D and 2D NMR spectra. The isolated compounds were evaluated for their inhibitory effect on NO production in LPS-stimulated RAW264.7 cells. Among them, compounds 1, 2, and 3 exhibited strong effect with the IC50 values of 22.3, 15.6, 7.3 μM, resp. 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: 54-17-1Application of 54-17-1)

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

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Related Products of 54-17-1On March 31, 2021, Moret, Florian; Delorme, Gael; Clement, Gilles; Grosjean, Claire; Lemaitre-Guillier, Christelle; Trouvelot, Sophie; Adrian, Marielle; Fontaine, Florence published an article in Physiologia Plantarum. The article was 《Esca-affected grapevine leaf metabolome is clone- and vintage-dependent》. The article mentions the following:

Esca is a complex grapevine trunk disease caused by wood-rotting ascomycetes and basidiomycetes and leading to several foliar and wood symptoms. Given that the esca expression can be influenced by several environmental, physiol., and genetic factors, foliar symptoms are inconsistent in incidence and prevalence and may appear 1 yr but not the following. We have previously reported a clone-dependent expression of the disease in cv Chardonnay. Owing to metabolome anal., we could discriminate the metabolite fingerprint of green leaves collected on diseased vines of clones 76 and 95. These clone-dependent fingerprints were year-dependent in intensity and nature. The present work was conducted to determine if the clone-dependent disease expression observed is specific to Chardonnay or if it also occurs in another cultivar. A plot located in the Jura vineyard (France) and planted with both 1004 and 1026 clones of Trousseau, a cultivar highly susceptible to esca, was thus selected and studied during 2017 and 2018. A year-dependent variation of the symptoms expression was first observed and a possible relationship with rainfall is hypothesized and discussed. Moreover, a higher percentage of the clone 1026 vines expressed disease, compared to the 1004 ones, suggesting the higher susceptibility of this clone. Finally, metabolomic analyzes of the remaining green leaves (i.e, without symptom expression) of partial esca-apoplectic vines allowed us to confirm a clone-dependent metabolic response to the disease. The metabolite fingerprints obtained differed in nature and intensity to those previously reported for Chardonnay and also between years. In the experimental materials used by the author, we found 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 the monohydrate form of the alpha isoform of D-glucopyranose, a synthetic simple monosaccharide that is used as an energy source.Related Products of 54-17-1

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In 2021,Antioxidants included an article by Saravanakumar, Kandasamy; Park, SeonJu; Sathiyaseelan, Anbazhagan; Mariadoss, Arokia Vijaya Anand; Park, Soyoung; Kim, Seong-Jung; Wang, Myeong-Hyeon. Name: rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol. The article was titled 《Isolation of Polysaccharides from Trichoderma harzianum with Antioxidant, Anticancer, and Enzyme Inhibition Properties》. The information in the text is summarized as follows:

In this work, a total of six polysaccharides were isolated from culture filtrate (EPS1, EPS2) and mycelia (IPS1-IPS4) of Trichoderma harzianum. The HPLC anal. results showed that EPS1, EPS2, IPS1, and IPS2 were composed of mannose, ribose, glucose, galactose, and arabinose. The FT-IR, 1H, and 13C NMR chem. shifts confirmed that the signals in EPS1 mainly consist of (1→4)-linked α-d-glucopyranose. EPS1 and IPS1 showed a smooth and clean surface, while EPS2, IPS2, and IPS3 exhibited a microporous structure. Among polysaccharides, EPS1 displayed higher ABTS+ (47.09 ± 2.25% and DPPH (26.44 ± 0.12%) scavenging activities, as well as higher α-amylase (69.30 ± 1.28%) and α-glucosidase (68.22 ± 0.64%) inhibition activity than the other polysaccharides. EPS1 exhibited high cytotoxicity to MDA-MB293 cells, with an IC50 of 0.437 mg/mL, and this was also confirmed by cell staining and FACS assays. These results report the physicochem. and bioactive properties of polysaccharides from T. harzianum. In the experimental materials used by the author, we found rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol(cas: 54-17-1Name: 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.Name: rel-(3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

Referemce:
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