D-(+)-Mannose

D-(+)-Mannose Structure
D-(+)-Mannose structure
Common Name D-(+)-Mannose
CAS Number 10030-80-5 Molecular Weight 180.156
Density 1.6±0.1 g/cm3 Boiling Point 527.1±50.0 °C at 760 mmHg
Molecular Formula C6H12O6 Melting Point 129-131ºC(lit.)
MSDS Chinese USA Flash Point 286.7±26.6 °C

Structure and bioactivity of a polysaccharide extracted from protocorm-like bodies of Dendrobium huoshanense.

Int. J. Biol. Macromol. 72 , 664-72, (2014)

The crude polysaccharides of Dendrobium huoshanense were fractionated by anion-exchange chromatography and gel permeation chromatography, giving one homogeneous fraction DHP-4A with molecular weight of 2.32 × 10(5)Da. UV spectrum indicated that there was no e...

Functional assessment of mouse complement pathway activities and quantification of C3b/C3c/iC3b in an experimental model of mouse renal ischaemia/reperfusion injury

J. Immunol. Methods 419 , 25-34, (2015)

The complement system is an essential component of our innate immunity, both for the protection against infections and for proper handling of dying cells. However, the complement system can also contribute to tissue injury and inflammatory responses. In view ...

Lactobacillus pentosus B231 Isolated from a Portuguese PDO Cheese: Production and Partial Characterization of Its Bacteriocin.

Probiotics Antimicrob Proteins 6 , 95-104, (2014)

Bacteriocin B231 produced by Lactobacillus pentosus, isolated from an artisanal raw cow's milk protected designation of origin Portuguese cheese, is a small protein with an apparent relative mass of about 5 kDa and active against a large number of Listeria mo...

Chiral separation of D/L-aldoses by micellar electrokinetic chromatography using a chiral derivatization reagent and a phenylboronic acid complex.

Anal. Bioanal. Chem 407 , 6201-6, (2015)

A novel method was developed for D/L-isomeric separation of aldopentoses and aldohexoses as their (S)-(+)-4-(N,N-dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole derivatives using phenylboronate buffer containing sodium dodecyl sulfate a...

A versatile route to L-hexoses: synthesis of L-mannose and L-altrose.

Org. Lett. 8 , 4863-4866, (2006)

[reaction: see text] An efficient route for the synthesis of orthogonally protected l-sugars has been opened up, starting from the heterocyclic homologating agent 1 and 2,3-O-isopropylidene-l-glyceraldehyde (2). Our synthetic path enables the synthesis of a 2...

Substrate specificity of galactokinase from Streptococcus pneumoniae TIGR4 towards galactose, glucose, and their derivatives.

Bioorg. Med. Chem. Lett. 22 , 3540-3, (2012)

Galactokinases (GalKs) have attracted significant research attention for their potential applications in the enzymatic synthesis of unique sugar phosphates. The galactokinase (GalKSpe4) cloned from Streptococcus pneumoniae TIGR4 presents a remarkably broad su...