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Sodium (1R)-d-glucit-1-yl-sulfonate monohydrate.

Acta crystallographica. Section E, Structure reports online

Haines AH, Hughes DL.
PMID: 22589769
Acta Crystallogr Sect E Struct Rep Online. 2012 Apr 01;68:m377-8. doi: 10.1107/S1600536812007210. Epub 2012 Mar 07.

The title salt, Na(+)·C(6)H(13)O(9)S(-)·H(2)O, crystallizes with three independent cations, molecular anions and solvent water molecules in the asymmetric unit. This crystalline monohydrate addition product, formed by reaction of d-glucose and sodium hydrogen sulfite in water, forms a three-dimensional network...

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Haines AH, Hughes DL. Sodium (1R)-d-glucit-1-yl-sulfonate monohydrate. Acta Crystallogr Sect E Struct Rep Online. 2012;68:m377-8doi: 10.1107/S1600536812007210.
Haines, A. H., & Hughes, D. L. (2012). Sodium (1R)-d-glucit-1-yl-sulfonate monohydrate. Acta crystallographica. Section E, Structure reports online, 68m377-8. https://doi.org/10.1107/S1600536812007210
Haines, Alan H, and Hughes, David L. "Sodium (1R)-d-glucit-1-yl-sulfonate monohydrate." Acta crystallographica. Section E, Structure reports online vol. 68 (2012): m377-8. doi: https://doi.org/10.1107/S1600536812007210
Haines AH, Hughes DL. Sodium (1R)-d-glucit-1-yl-sulfonate monohydrate. Acta Crystallogr Sect E Struct Rep Online. 2012 Apr 01;68:m377-8. doi: 10.1107/S1600536812007210. Epub 2012 Mar 07. PMID: 22589769; PMCID: PMC3343795.
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WITHDRAWN: Corrigendum to "A lectin from the Chinese bird-hunting spider binds sialic acids".

Carbohydrate research

Siebert HC, Lu SY, Wechselberger R, Born K, Eckert T, Liang S, der Lieth CW, Jiménez-Barbero J, Schauer R, G Vliegenthart JF, Lütteke T, André S, Kaltner H, Gabius HJ, Kožár T.
PMID: 20176345
Carbohydr Res. 2010 Feb 20; doi: 10.1016/j.carres.2009.12.027. Epub 2010 Feb 20.

The Publisher regrets that this article is an accidental duplication of an article that has already been published, doi: 10.1016/j.carres.2010.01.003. The duplicate article has therefore been withdrawn.

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Siebert HC, Lu SY, Wechselberger R, et al. WITHDRAWN: Corrigendum to "A lectin from the Chinese bird-hunting spider binds sialic acids". Carbohydr Res. 2010;doi: 10.1016/j.carres.2009.12.027.
Siebert, H. C., Lu, S. Y., Wechselberger, R., Born, K., Eckert, T., Liang, S., der Lieth, C. W., Jiménez-Barbero, J., Schauer, R., G Vliegenthart, J. F., Lütteke, T., André, S., Kaltner, H., Gabius, H. J., & Kožár, T. (2010). WITHDRAWN: Corrigendum to "A lectin from the Chinese bird-hunting spider binds sialic acids". Carbohydrate research, . https://doi.org/10.1016/j.carres.2009.12.027
Siebert, Hans-Christian, et al. "WITHDRAWN: Corrigendum to "A lectin from the Chinese bird-hunting spider binds sialic acids"." Carbohydrate research vol. (2010). doi: https://doi.org/10.1016/j.carres.2009.12.027
Siebert HC, Lu SY, Wechselberger R, Born K, Eckert T, Liang S, der Lieth CW, Jiménez-Barbero J, Schauer R, G Vliegenthart JF, Lütteke T, André S, Kaltner H, Gabius HJ, Kožár T. WITHDRAWN: Corrigendum to "A lectin from the Chinese bird-hunting spider binds sialic acids". Carbohydr Res. 2010 Feb 20; doi: 10.1016/j.carres.2009.12.027. Epub 2010 Feb 20. PMID: 20176345.
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Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6.

Carbohydrate research

Morelli L, Bernardi A, Sattin S.
PMID: 24690674
Carbohydr Res. 2014 May;390:33-41. doi: 10.1016/j.carres.2014.03.006. Epub 2014 Mar 13.

Hsp90 (Heat shock protein-90) is a chaperone protein and an established anti-apoptotic target in cancer therapy. Most of the known small-molecule inhibitors that have shown potent antitumor activity target the Hsp90 N-terminal domain and directly inhibit its ATP-ase activity....

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Morelli L, Bernardi A, Sattin S. Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6. Carbohydr Res. 2014;390:33-41doi: 10.1016/j.carres.2014.03.006.
Morelli, L., Bernardi, A., & Sattin, S. (2014). Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6. Carbohydrate research, 39033-41. https://doi.org/10.1016/j.carres.2014.03.006
Morelli, Laura, et al. "Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6." Carbohydrate research vol. 390 (2014): 33-41. doi: https://doi.org/10.1016/j.carres.2014.03.006
Morelli L, Bernardi A, Sattin S. Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6. Carbohydr Res. 2014 May;390:33-41. doi: 10.1016/j.carres.2014.03.006. Epub 2014 Mar 13. PMID: 24690674.
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Dissolution behavior of cellulose in a novel cellulose solvent.

Carbohydrate research

Lin L, Tsuchii K.
PMID: 34952277
Carbohydr Res. 2021 Dec 18;511:108490. doi: 10.1016/j.carres.2021.108490. Epub 2021 Dec 18.

We have found that cellulose can be dissolved rapidly in the mixed solvent of tetrabutylammonium acetate (TBAA) and a polar aprotic solvents (PAS) at 50 °C and the obtained cellulose solution could be regenerated into cellulose film and fiber....

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Lin L, Tsuchii K. Dissolution behavior of cellulose in a novel cellulose solvent. Carbohydr Res. 2021;511:108490doi: 10.1016/j.carres.2021.108490.
Lin, L., & Tsuchii, K. (2021). Dissolution behavior of cellulose in a novel cellulose solvent. Carbohydrate research, 511108490. https://doi.org/10.1016/j.carres.2021.108490
Lin, Lianzhen, and Tsuchii, Kaname. "Dissolution behavior of cellulose in a novel cellulose solvent." Carbohydrate research vol. 511 (2021): 108490. doi: https://doi.org/10.1016/j.carres.2021.108490
Lin L, Tsuchii K. Dissolution behavior of cellulose in a novel cellulose solvent. Carbohydr Res. 2021 Dec 18;511:108490. doi: 10.1016/j.carres.2021.108490. Epub 2021 Dec 18. PMID: 34952277.
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Plausible role of chitosan in drug and gene delivery against resistant breast cancer cells.

Carbohydrate research

Nandgude T, Pagar R.
PMID: 34146935
Carbohydr Res. 2021 Aug;506:108357. doi: 10.1016/j.carres.2021.108357. Epub 2021 Jun 04.

Breast cancer is the highest global spread of invasive cancer in women. While significant progress has been made in breast cancer, diagnostic and therapeutic effective prevention and treatment options remain scarce. Concerning chitosan-based chemotherapeutic therapies, the studies reported cell...

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Nandgude T, Pagar R. Plausible role of chitosan in drug and gene delivery against resistant breast cancer cells. Carbohydr Res. 2021;506:108357doi: 10.1016/j.carres.2021.108357.
Nandgude, T., & Pagar, R. (2021). Plausible role of chitosan in drug and gene delivery against resistant breast cancer cells. Carbohydrate research, 506108357. https://doi.org/10.1016/j.carres.2021.108357
Nandgude, Tanaji, and Pagar, Roshani. "Plausible role of chitosan in drug and gene delivery against resistant breast cancer cells." Carbohydrate research vol. 506 (2021): 108357. doi: https://doi.org/10.1016/j.carres.2021.108357
Nandgude T, Pagar R. Plausible role of chitosan in drug and gene delivery against resistant breast cancer cells. Carbohydr Res. 2021 Aug;506:108357. doi: 10.1016/j.carres.2021.108357. Epub 2021 Jun 04. PMID: 34146935.
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Isolation, characterization and prediction of biologically active glycoside compounds quercetin-3-rutinoside from the fruits of Ficus sycomorus.

Carbohydrate research

Al-Shabibi MHS, Al-Touby SSJ, Hossain MA.
PMID: 34864403
Carbohydr Res. 2021 Nov 30;511:108483. doi: 10.1016/j.carres.2021.108483. Epub 2021 Nov 30.

Ficus sycomorus (F. sycomorus) is a medicinal plant which has been used traditionally for its medicinal benefits as metabolic, cardiovascular, respiratory, antispasmodic and anti-inflammatory remedy. Therefore the present work was designed to isolate and characterize antibacterial compounds from the...

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Al-Shabibi MHS, Al-Touby SSJ, Hossain MA. Isolation, characterization and prediction of biologically active glycoside compounds quercetin-3-rutinoside from the fruits of Ficus sycomorus. Carbohydr Res. 2021;511:108483doi: 10.1016/j.carres.2021.108483.
Al-Shabibi, M. H. S., Al-Touby, S. S. J., & Hossain, M. A. (2021). Isolation, characterization and prediction of biologically active glycoside compounds quercetin-3-rutinoside from the fruits of Ficus sycomorus. Carbohydrate research, 511108483. https://doi.org/10.1016/j.carres.2021.108483
Al-Shabibi, Maryam Hamed Said, et al. "Isolation, characterization and prediction of biologically active glycoside compounds quercetin-3-rutinoside from the fruits of Ficus sycomorus." Carbohydrate research vol. 511 (2021): 108483. doi: https://doi.org/10.1016/j.carres.2021.108483
Al-Shabibi MHS, Al-Touby SSJ, Hossain MA. Isolation, characterization and prediction of biologically active glycoside compounds quercetin-3-rutinoside from the fruits of Ficus sycomorus. Carbohydr Res. 2021 Nov 30;511:108483. doi: 10.1016/j.carres.2021.108483. Epub 2021 Nov 30. PMID: 34864403.
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Streamlined access to carbohydrate building blocks: Methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside.

Carbohydrate research

Shrestha G, Kashiwagi GA, Stine KJ, Demchenko AV.
PMID: 34856429
Carbohydr Res. 2021 Nov 26;511:108482. doi: 10.1016/j.carres.2021.108482. Epub 2021 Nov 26.

Presented herein is an improved synthesis of a common 3-OH glycosyl acceptor. This compound is a building block that is routinely synthesized by many research groups to be used in glycosylation refinement studies. The only known direct synthesis by...

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Shrestha G, Kashiwagi GA, Stine KJ, et al. Streamlined access to carbohydrate building blocks: Methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside. Carbohydr Res. 2021;511:108482doi: 10.1016/j.carres.2021.108482.
Shrestha, G., Kashiwagi, G. A., Stine, K. J., & Demchenko, A. V. (2021). Streamlined access to carbohydrate building blocks: Methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside. Carbohydrate research, 511108482. https://doi.org/10.1016/j.carres.2021.108482
Shrestha, Ganesh, et al. "Streamlined access to carbohydrate building blocks: Methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside." Carbohydrate research vol. 511 (2021): 108482. doi: https://doi.org/10.1016/j.carres.2021.108482
Shrestha G, Kashiwagi GA, Stine KJ, Demchenko AV. Streamlined access to carbohydrate building blocks: Methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside. Carbohydr Res. 2021 Nov 26;511:108482. doi: 10.1016/j.carres.2021.108482. Epub 2021 Nov 26. PMID: 34856429.
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Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditions.

Carbohydrate research

Jana S, Crich D.
PMID: 34959032
Carbohydr Res. 2021 Dec 21;511:108494. doi: 10.1016/j.carres.2021.108494. Epub 2021 Dec 21.

We describe the novel oxidative fragmentation of methyl (5-acetamido-4,7,8,9-tetra-O-acetyl-5-deoxy-3-O-trifluoromethanesulfonyl-β-D-erythro-L-gluco-2-nonulopyranos)onate 2 on stirring with sodium nitrite in DMF to give the novel 3-acetamido-2,5,6,7-tetra-O-acetyl-d-glycero-d-galacto-heptono-1,4-lactone 3 in excellent yield. Stirring of the same triflate with sodium carbonate on the other hand affords...

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Jana S, Crich D. Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditions. Carbohydr Res. 2021;511:108494doi: 10.1016/j.carres.2021.108494.
Jana, S., & Crich, D. (2021). Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditions. Carbohydrate research, 511108494. https://doi.org/10.1016/j.carres.2021.108494
Jana, Santanu, and Crich, David. "Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditions." Carbohydrate research vol. 511 (2021): 108494. doi: https://doi.org/10.1016/j.carres.2021.108494
Jana S, Crich D. Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditions. Carbohydr Res. 2021 Dec 21;511:108494. doi: 10.1016/j.carres.2021.108494. Epub 2021 Dec 21. PMID: 34959032.
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1,6-heptadiynes based cyclopolymerization functionalized with mannose by post polymer modification for protein interaction.

Carbohydrate research

Kumar P, Kanjilal P, Das R, Dash TK, Mohanan M, Le TN, Rao NV, Mukhopadhyay B, Shunmugam R.
PMID: 34280802
Carbohydr Res. 2021 Oct;508:108397. doi: 10.1016/j.carres.2021.108397. Epub 2021 Jul 12.

Carbohydrate functionalized polymers or Glycopolymers have earned a great deal of interest in recent times for their potential biomedical applications. In the present study, a mannose containing glycopolymer was synthesized by cyclopolymerization of malonic acid derivative using second generation...

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Kumar P, Kanjilal P, Das R, et al. 1,6-heptadiynes based cyclopolymerization functionalized with mannose by post polymer modification for protein interaction. Carbohydr Res. 2021;508:108397doi: 10.1016/j.carres.2021.108397.
Kumar, P., Kanjilal, P., Das, R., Dash, T. K., Mohanan, M., Le, T. N., Rao, N. V., Mukhopadhyay, B., & Shunmugam, R. (2021). 1,6-heptadiynes based cyclopolymerization functionalized with mannose by post polymer modification for protein interaction. Carbohydrate research, 508108397. https://doi.org/10.1016/j.carres.2021.108397
Kumar, Pawan, et al. "1,6-heptadiynes based cyclopolymerization functionalized with mannose by post polymer modification for protein interaction." Carbohydrate research vol. 508 (2021): 108397. doi: https://doi.org/10.1016/j.carres.2021.108397
Kumar P, Kanjilal P, Das R, Dash TK, Mohanan M, Le TN, Rao NV, Mukhopadhyay B, Shunmugam R. 1,6-heptadiynes based cyclopolymerization functionalized with mannose by post polymer modification for protein interaction. Carbohydr Res. 2021 Oct;508:108397. doi: 10.1016/j.carres.2021.108397. Epub 2021 Jul 12. PMID: 34280802.
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Synthesis of fluorinated thiodigalactoside analogues.

Carbohydrate research

St-Gelais J, Leclerc C, Giguère D.
PMID: 34837848
Carbohydr Res. 2021 Nov 20;511:108481. doi: 10.1016/j.carres.2021.108481. Epub 2021 Nov 20.

In this work, we report the first synthesis of fluorinated thiodigalactoside analogues. We used tri-isopropylsilyl thioglycosides as masked glycosyl thiol nucleophiles for the elaboration of two monofluorinated heterodimers, one difluorinated homodimer, and one difluorinated heterodimer. Moreover, we also present...

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St-Gelais J, Leclerc C, Giguère D. Synthesis of fluorinated thiodigalactoside analogues. Carbohydr Res. 2021;511:108481doi: 10.1016/j.carres.2021.108481.
St-Gelais, J., Leclerc, C., & Giguère, D. (2021). Synthesis of fluorinated thiodigalactoside analogues. Carbohydrate research, 511108481. https://doi.org/10.1016/j.carres.2021.108481
St-Gelais, Jacob, et al. "Synthesis of fluorinated thiodigalactoside analogues." Carbohydrate research vol. 511 (2021): 108481. doi: https://doi.org/10.1016/j.carres.2021.108481
St-Gelais J, Leclerc C, Giguère D. Synthesis of fluorinated thiodigalactoside analogues. Carbohydr Res. 2021 Nov 20;511:108481. doi: 10.1016/j.carres.2021.108481. Epub 2021 Nov 20. PMID: 34837848.
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Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain.

Carbohydrate research

Ennemoser M, Pum A, Kungl A.
PMID: 34837849
Carbohydr Res. 2021 Nov 17;511:108480. doi: 10.1016/j.carres.2021.108480. Epub 2021 Nov 17.

A wide variety of diseases throughout the mammalian organism is characterized by abnormal deposition of various components of the extracellular matrix (ECM), including the heterogeneous family of glycosaminoglycans (GAGs), which contribute considerably to the ECM architecture as part of...

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Ennemoser M, Pum A, Kungl A. Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain. Carbohydr Res. 2021;511:108480doi: 10.1016/j.carres.2021.108480.
Ennemoser, M., Pum, A., & Kungl, A. (2021). Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain. Carbohydrate research, 511108480. https://doi.org/10.1016/j.carres.2021.108480
Ennemoser, Maria, et al. "Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain." Carbohydrate research vol. 511 (2021): 108480. doi: https://doi.org/10.1016/j.carres.2021.108480
Ennemoser M, Pum A, Kungl A. Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain. Carbohydr Res. 2021 Nov 17;511:108480. doi: 10.1016/j.carres.2021.108480. Epub 2021 Nov 17. PMID: 34837849.
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Design, synthesis, and preliminary immunopotentiating activity of new analogues of nojirimycin.

Carbohydrate research

Thangarasu AK, Sambyal S, Kumar HMS, Lankalapalli RS.
PMID: 34798489
Carbohydr Res. 2021 Nov 14;511:108479. doi: 10.1016/j.carres.2021.108479. Epub 2021 Nov 14.

Three new classes of nojirimycin analogues viz. N-alkyl with C1-substituent (4-phenylbutyl), N-substituted 1-deoxynojirimycin and its congener δ-lactam, and a 4-phenylbutyl-β-C-glycoside were designed and synthesized for immunological studies. The resulting diverse compound library exhibited proliferation of B Cells and T...

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Thangarasu AK, Sambyal S, Kumar HMS, et al. Design, synthesis, and preliminary immunopotentiating activity of new analogues of nojirimycin. Carbohydr Res. 2021;511:108479doi: 10.1016/j.carres.2021.108479.
Thangarasu, A. K., Sambyal, S., Kumar, H. M. S., & Lankalapalli, R. S. (2021). Design, synthesis, and preliminary immunopotentiating activity of new analogues of nojirimycin. Carbohydrate research, 511108479. https://doi.org/10.1016/j.carres.2021.108479
Thangarasu, Arun K, et al. "Design, synthesis, and preliminary immunopotentiating activity of new analogues of nojirimycin." Carbohydrate research vol. 511 (2021): 108479. doi: https://doi.org/10.1016/j.carres.2021.108479
Thangarasu AK, Sambyal S, Kumar HMS, Lankalapalli RS. Design, synthesis, and preliminary immunopotentiating activity of new analogues of nojirimycin. Carbohydr Res. 2021 Nov 14;511:108479. doi: 10.1016/j.carres.2021.108479. Epub 2021 Nov 14. PMID: 34798489.
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