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M6882

Sigma-Aldrich

Methyl α-D-mannopyranoside

≥99.0% (HPLC)

Sinonimo/i:

α-Methyl D-mannoside

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About This Item

Formula empirica (notazione di Hill):
C7H14O6
Numero CAS:
617-04-9
Peso molecolare:
194.18
Beilstein:
81566
Numero CE:
210-502-3
Numero MDL:
MFCD00063262
Codice UNSPSC:
12352201
ID PubChem:
24897124
NACRES:
NA.25

Saggio

≥99.0% (HPLC)

Forma fisica

powder

Attività ottica

[α]20/D 77.0 to 82.0°, c = 1-10% (w/v) in water

tecniche

HPLC: suitable

Colore

white to off-white

Punto di fusione

193-196 °C (lit.)

Solubilità

water: 100 mg/mL, clear, colorless

Temperatura di conservazione

15-25°C

Stringa SMILE

CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

InChI

1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
HOVAGTYPODGVJG-VEIUFWFVSA-N

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Descrizione generale

Methyl α-D-mannopyranoside is a competitor inhibitor of the binding of mannose by Escherichia coli.

Applicazioni

Methyl α-D-mannopyranoside has been used to synthesize a series of tri- and tetrahydroxylated seven-membered iminosugars in a study that worked towards a stable noeuromycin analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose binding site of pradimicin A.

Altre note

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

404.1 °F

Punto d’infiammabilità (°C)

206.74 °C

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Allyl α-D-mannopyranoside 95%

Sigma-Aldrich

772208

Allyl α-D-mannopyranoside

METHYL 2,3-DI-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-GLUCOPYRANOSIDE AldrichCPR

T282243

METHYL 2,3-DI-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-GLUCOPYRANOSIDE

M Aronson et al.
The Journal of infectious diseases, 139(3), 329-332 (1979-03-01)
Methyl alpha-D-mannopyranoside (alpha MM), a competitor inhibitor of the binding of mannose by Escherichia coli, was tested for its ability to prevent infection of the urinary tract of mice with infective strains of the organisms. Injection of the bacteria in
Yu Nakagawa et al.
Journal of the American Chemical Society, 133(43), 17485-17493 (2011-09-29)
Pradimicin A (PRM-A) is an actinomycete-derived antibiotic with the lectin-like property of being able to recognize D-mannopyranoside (Man) in the presence of Ca(2+) ion. PRM-A and its derivatives have been attracting a great deal of attention as the only family
Julia Deschamp et al.
Bioorganic & medicinal chemistry, 20(2), 641-649 (2010-10-26)
Noeuromycin is a highly potent albeit unstable glycosidase inhibitor due to its hemiaminal function. While stable D-gluco-like analogs have been reported, no data are available for D-manno-like structures. A series of tri- and tetrahydroxylated seven-membered iminosugars displaying either a D-manno-or
Oliver Schwardt et al.
Bioorganic & medicinal chemistry, 19(21), 6454-6473 (2011-10-04)
Urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) is one of the most prevalent infectious diseases. Particularly affected are women, who have a 40-50% risk to experience at least one symptomatic UTI episode at some time during their
Karen T Welch et al.
Bioorganic & medicinal chemistry letters, 18(24), 6573-6575 (2008-11-08)
A virtual screening approach was used to identify new glycomimetics. The National Cancer Institute Diversity Set was docked into the carbohydrate binding site of the lectin concanavalin A (ConA). The resulting poses were analyzed and 19 molecules were tested for
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