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Merck

67770

Millipore

メチル α-D-マンノピラノシド

≥99.0%, suitable for microbiology, enables differentiation between species of Listeria

別名:

α-メチル D-マンノシド

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About This Item

実験式(ヒル表記法):
C7H14O6
CAS番号:
分子量:
194.18
Beilstein:
81566
EC Number:
MDL番号:
UNSPSCコード:
41106212
PubChem Substance ID:
NACRES:
NA.85

品質水準

アッセイ

≥99.0% (sum of enantiomers, HPLC)
≥99.0%

形状

powder

光学活性

[α]20/D 77.0 to 82.0°, c = 10% in H2O

分子量

194.18 g/mol

mp

187-195 °C
193-196 °C (lit.)

溶解性

H2O: 0.1 g/mL, clear, colorless

アプリケーション

microbiology

SMILES記法

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

InChI Key

HOVAGTYPODGVJG-VEIUFWFVSA-N

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詳細

Methyl α-D-mannopyranoside is a compound that belongs to the class of organic compounds known as o-glycosyl compounds. It is used for the differentiation of Listeria species, Listeria monocytogenes, Listeria innocua, and Listeria welshimeri can ferment the sugar, producing acid which can be identified using an appropriate pH indicator. It has been used to synthesize a series of tri- and tetrahydroxylated seven-membered imino sugars in a study that worked towards a stable Noeuromycin (glycosyl cation mimic that strongly inhibits glycosidases) analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose-binding site of Pradimicin A. (antifungal agent)

アプリケーション

Methyl α-D-mannopyranoside can be used to identify different species of Listeria based on their ability to ferment the sugar.

その他情報

アビジンと内因性レクチンとの好ましくない結合が生じます

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

404.1 °F

引火点(℃)

206.74 °C

個人用保護具 (PPE)

Eyeshields, Gloves, type N95 (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

67770-BULK:
67770-VAR:
67770-25G:
67770-100G:
67770-500G:


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Prevention of nonspecific binding of avidin.
R C Duhamel et al.
Methods in enzymology, 184, 201-207 (1990-01-01)
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
Su Yu et al.
BMC gastroenterology, 9, 58-58 (2009-07-25)
GP2 is the major membrane protein present in the pancreatic zymogen granule, and is cleaved and released into the pancreatic duct along with exocrine secretions. The function of GP2 is unknown. GP2's amino acid sequence is most similar to that
Rafael Maldonado-Hernández et al.
Analytical biochemistry, 610, 113887-113887 (2020-08-09)
Over the past 10 years we have been developing a multi-attribute analytical platform that allows for the preparation of milligram amounts of functional, high-pure, and stable Torpedo (muscle-type) nAChR detergent complexes for crystallization purpose. In the present work, we have

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