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Home > Encyclopedia > METHYL-ALPHA-D-MANNOPYRANOSIDE

METHYL-ALPHA-D-MANNOPYRANOSIDE

METHYL-ALPHA-D-MANNOPYRANOSIDE structure

METHYL-ALPHA-D-MANNOPYRANOSIDE 

structure
  • CAS No:

    617-04-9

  • Formula:

    C7H14O6

  • Chemical Name:

    METHYL-ALPHA-D-MANNOPYRANOSIDE

  • Synonyms:

    Methyl α-D-mannopyranoside,α-Methyl D-mannoside;Methyl α-D-maopyranoside;1-O-Methyl-α-D-Mannopyranoside;NSC 1225;alpha-Methyl-D-mannoside Methyl alpha-D-Mannoside;Methyl α-D-mannopyranoside Supplement;Methyl-α-D-mannopyranoside≥ 99% (Assay);α-Methyl-D-mannopyranoside α-Methylmannoside

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

White Cyrstalline Solid


Methyl alpha-D-mannoside is a methyl mannoside having alpha-configuration at the anomeric centre. It is a methyl mannoside and an alpha-D-mannoside.


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

METHYL-ALPHA-D-MANNOPYRANOSIDE Basic Attributes

194.18

194.18

81566

210-502-3

White to off-white or slightly grayish

29400090

Characteristics

99.4

-2.2

White to off-white or slightly grayish Crystalline Powder

1.2501 (rough estimate)

193-196 °C(lit.)

250.62°C (rough estimate)

189.1±27.9 °C

79.5 ° (C=4, H2O)

It is easily soluble in methanol, water. Insoluble in ether.

Refrigerator

0Pa at 20℃

Not classified

12.92±0.70(Predicted)

Sealed in dry,2-8°C

Safety Information

NONH for all modes of transport

3

Xi,F

22-24/25-16

Xi,F

Irritant

10

Drug Information

alpha-methyl-D-mannose

METHYL-ALPHA-D-MANNOPYRANOSIDE Use and Manufacturing

Biochemical research. An eluent used in affinity chromatography to dissociate concanavalin A glycoprotein complexes. Binding avidin to endogenous lectin


Methyl a-D-mannopyranoside Is a competitor inhibitor of the binding of mannose by Escherichia coli. It is also used as a pharmaceutical raw material, health care product and intermediate. It is also been used as Animal Pharmaceuticals.


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.

Computed Properties

Molecular Weight:194.18
XLogP3:-2.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:194.07903816
Monoisotopic Mass:194.07903816
Topological Polar Surface Area:99.4
Heavy Atom Count:13
Complexity:163
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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