- API
Any substance that is represented for use in a drug and that, when used in the manufacturing, processing, or packaging ...
- Active Ingredient
Any component that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, ...
- CAS No.
Unique number assigned to a specific chemical (identified by its chemical name) by the American Chemical Society and ...
Alpha-L-Rhamnose
Catalog No. | PI0009 |
---|---|
CAS No. | 3615-41-6 |
Molecular Formula | C6H12O5 |
Molecular Weight | 164.16 |
Purity | 98% HPLC |
Package | 25 kg/drum |
Appearance | Powder |
Shelf Life | 2 years |
Safety Tips of Alpha-L-Rhamnose
Handling of alpha-l-rhamnose should only be performed by personnel trained and familiar with handling of potent active pharmaceutical ingredients. Moderate to severe irritant to the skin and eyes.
Related Applications
Sweeteners
Obesity has become a problem in the developed world. Special sweetener can increase the sweetness of foods and beverages but with much less calories, which is also beneficial for diabetes.
Related Researches
- 1. Updates on naringinase: structural and biotechnological aspects.
Puri M. Appl Microbiol Biotechnol 2012 Jan;93(1):49-60.
- 2. Studies on the conformational flexibility of α-L-rhamnose-containing oligosaccharides using 13C-site-specific labeling, NMR spectroscopy and molecular simulations: implications for the three-dimensional structure of bacterial rhamnan polysaccharides
Jonsson KH, et al. Org Biomol Chem 2012 Mar 28;10(12):2453-63.
- 3. Preparation, structure and anticoagulant activity of a low molecular weight fraction produced by mild acid hydrolysis of sulfated rhamnan from Monostroma latissimum.
Li H, et al. Bioresour Technol 2012 Jun;114:414-8.
- 4. Mandelalides A-D, cytotoxic macrolides from a new Lissoclinum species of South African tunicate.
Sikorska J, et al. J Org Chem 2012 Jul 20;77(14):6066-75.
- 5. Lateral gene transfer between the Bacteroidetes and Acidobacteria: the case of α-L-rhamnosidases.
Naumoff DG, et al. FEBS Lett 2012 Nov 2;586(21):3843-51.
- 6. Synthesis and anti-fungal activity of seven oleanolic acid glycosides.
Zhao H, et al. Molecules 2011 Jan 26;16(2):1113-28.
- 7. Triterpenoid saponins from Symplocos lancifolia.
Acebey-Castellon IL, et al. J Nat Prod 2011 Feb 25;74(2):163-8.
- 8. C5'-Alkyl Substitution Effects on Digitoxigenin α-l-Glycoside Cancer Cytotoxicity.
Wang HY, et al. ACS Med Chem Lett 2011 Apr 14;2(4):259-263.
- 9. Stereochemical survey of digitoxin monosaccharides: new anticancer analogues with enhanced apoptotic activity and growth inhibitory effect on human non-small cell lung cancer cell.
Wang HY, et al. ACS Med Chem Lett 2011 Jan 13;2(1):73-78.
- 10. Synthesis and Evaluation of the α-D-/α-L-Rhamnosyl and Amicetosyl Digitoxigenin Oligomers as Anti-tumor Agents.
Wang HY, et al. ACS Med Chem Lett 2011 Apr 14;2(4):264-269.