Saltar al contenido
Merck
Todas las fotos(4)

Documentos

M4670

Sigma-Aldrich

D-Mannosamine hydrochloride

≥98% (HPLC)

Sinónimos:

2-Amino-2-deoxy-D-mannose hydrochloride

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(4)

About This Item

Fórmula empírica (notación de Hill):
C6H13NO5 · HCl
Número de CAS:
5505-63-5
Peso molecular:
215.63
Beilstein:
3914860
Número CE:
226-847-8
Número MDL:
MFCD00064557
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
24896935
NACRES:
NA.25

origen biológico

crab (shell)
shrimp shells

Análisis

≥98% (HPLC)

formulario

powder

técnicas

HPLC: suitable

color

white

mp

168 °C (dec.) (lit.)

solubilidad

water: 50 mg/mL, clear, colorless to faintly yellow

temp. de almacenamiento

2-8°C

cadena SMILES

Cl[H].N[C@@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O

InChI

1S/C6H13NO5.ClH/c7-3-5(10)4(9)2(1-8)12-6(3)11;/h2-6,8-11H,1,7H2;1H/t2-,3+,4-,5-,6?;/m1./s1

Clave InChI

QKPLRMLTKYXDST-OHXGPSCHSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Categorías relacionadas

Aplicación

D-Mannosamine hydrochloride can be used for the synthesis of non-natural ManNAc analogs for the expression of thiols on cell-surface sialic acids. It has been used in a study to investigate the synthesis and high-throughput screening of N-acetyl-β-hexosaminidase inhibitor libraries targeting osteoarthritis.

Otras notas

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

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Los clientes también vieron

Slide 1 of 2

1 of 2

D-Mannose 6-phosphate sodium salt ≥98% (HPLC)

Sigma-Aldrich

M3655

D-Mannose 6-phosphate sodium salt

D(+)Galactosamine, Hydrochloride A powerful inhibitor of hepatic RNA synthesis. Increases the adherence of polymorphonuclear leukocytes to hepatic endothelial cells and induces superoxide production. Induces hepatic damage, causing macrophage infiltration.

Millipore

34539-M

D(+)Galactosamine, Hydrochloride

Srinivasa-Gopalan Sampathkumar et al.
Nature protocols, 1(5), 2377-2385 (2007-04-05)
The sialic acid biosynthetic pathway in mammalian cells utilizes N-acetyl-D-mannosamine (ManNAc) as a natural metabolic precursor and has the remarkable ability to biosynthetically process non-natural ManNAc analogs. Herein, we describe a recipe-style protocol for the synthesis of the novel peracetylated
Junjie Liu et al.
The Journal of organic chemistry, 69(19), 6273-6283 (2004-09-11)
C1 Nitrogen iminocyclitols are potent inhibitors of N-acetyl-beta-hexosaminidases. Given hexosaminidases' important roles in osteoarthritis, we developed two straightforward and efficient syntheses of C1 nitrogen iminocyclitols from two readily available starting materials, D-mannosamine hydrochloride and the microbial oxidation product of fructose.
Christopher Brigham et al.
Journal of bacteriology, 191(11), 3629-3638 (2009-03-24)
We characterized the nanLET operon in Bacteroides fragilis, whose products are required for the utilization of the sialic acid N-acetyl neuraminic acid (NANA) as a carbon and energy source. The first gene of the operon is nanL, which codes for
Tal Gefen et al.
Vaccine, 28(51), 8197-8202 (2010-09-30)
Passive immunization with cross-species antibodies triggers the patient's immune response, thereby preventing repeated treatment. Mannosamine-biotin adduct (MBA) has been described as a masking agent for immunogenic reduction and here, the immunogenicity and biological activity of MBA-coated horse anti-viper venom (hsIgG)
Alyaa Ibrahim et al.
Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 13(2), 128-135 (2010-09-08)
An improved HPLC method with fluorescence detection was developed and validated for determination of glucosamine in human and rat biological samples. Aliquot of 0.1 mL plasma was spiked with mannosamine HCl as the internal standard (IS); proteins were precipitated with
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico