190912-49-3 Usage
Uses
Used in Pharmaceutical and Biochemical Industries:
HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a drug delivery agent for enhancing the solubility and bioavailability of various pharmaceutical compounds. Its ability to form stable complexes with drugs allows for controlled release and targeted delivery, improving the therapeutic efficacy of medications.
Used in Synthesis of Glycoconjugates:
In the field of biochemistry, HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE serves as a key building block for the synthesis of glycoconjugates, which are essential for various biological processes, including cell recognition, signaling, and immune response modulation.
Used in Antibacterial and Antiviral Applications:
HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE has been studied for its potential antibacterial and antiviral properties. Its ability to interact with bacterial and viral components can inhibit their growth and replication, making it a promising candidate for the development of new antimicrobial and antiviral agents.
Used in Cancer Therapy:
HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE has been explored for its role in cancer therapy. Its unique chemical structure allows it to target cancer cells selectively, leading to the inhibition of tumor growth and metastasis. It can also be used in combination with other anticancer drugs to enhance their therapeutic effects.
Used in Cosmetic Formulations and Skincare Products:
In the cosmetic industry, HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used for its moisturizing and emulsifying properties. Its ability to retain moisture and improve the texture of cosmetic products makes it a valuable ingredient in skincare formulations, contributing to healthier and more radiant skin.
Overall, HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE has a wide range of applications in different industries, including pharmaceuticals, biochemistry, cosmetics, and more, due to its unique chemical structure and diverse properties.
Check Digit Verification of cas no
The CAS Registry Mumber 190912-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,9,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 190912-49:
(8*1)+(7*9)+(6*0)+(5*9)+(4*1)+(3*2)+(2*4)+(1*9)=143
143 % 10 = 3
So 190912-49-3 is a valid CAS Registry Number.
190912-49-3Relevant academic research and scientific papers
N-Acetylmuramyl-L-Alanyl-D-Isoglutamine Glycosides: Effect of Glycoside Bond Configuration and Aglycone on Biological Activity
Zemlyakov,Tsikalov,Kalyuzhin,Kur'yanov,Chirva
, p. 286 - 292 (2007/10/03)
Hexyl, octyl, and cyclohexyl β-glycosides and heptyl and cyclohexyl α-glycosides of muramyl dipeptide (MDP) were synthesized. Tests in vitro and in vivo revealed lower immunostimulating activities of MDP α-glycosides in comparison with the corresponding β-glycosides and MDP itself. In the case of alkyl β-glycosides, differences in hydrocarbon chain lengths (C4-C8) and in aglycone (aliphatic chain and aliphatic or aromatic ring) exerted no substantial effect on the immunostimulating activity.
Alkylating agents from sugars. Alkyl hexopyranoside derivatives as carrier systems for chlorambucil
Iglesias-Guerra, Fernando,Candela, Jose I.,Bautista, Juan,Alcudia, Felipe,Vega-Perez, Jose M.
, p. 71 - 84 (2007/10/03)
Chlorambucil derivatives involving alkyl 2-aminodeoxy sugars have been synthesized in good yield by coupling the chlorambucil moiety to positions C-2 or C-3 of the sugar, directly or via a spacer. The starting material was easily available from 2-acetamido-2-deoxy-D-glucose. The final compounds were tested for cytotoxicity, and some of those that presented the best results were studied for inhibition of cell proliferation. Copyright (C) 1999 Elsevier Science Ltd.
Chemical synthesis of N-acetylglucosamine derivatives and their use as glycosyl acceptors by the Mesorhizobium loti chitin oligosaccharide synthase NodC
Kamst, Eric,Zegelaar-Jaarsveld, Korien,Van Der Marel, Gijs A.,Van Boom, Jacques H.,Lugtenberg, Ben J.J.,Spaink, Herman P.
, p. 176 - 189 (2007/10/03)
Rhizobial bacteria synthesize lipo-chitin oligosaccharide signal molecules (Nod factors) that are essential for the formation of symbiotic organs on the roots of host plants, a process known as nodulation. Biosynthesis of the chitin oligosaccharide moiety
Synthesis of a SLex mimic: a potential E-selectin binding antagonist
Heskamp, B. M.,Veeneman, G. H.,Marel, G. A. van der,Boeckel, C. A. A. van,Boom, J. H. van
, p. 398 - 402 (2007/10/03)
Iodonium-ion-assisted condensation of methyl 4,7,8,9-tetra-O-acetyl-N-acetyl-2-O--α-D-neuraminate (15) with hexyl 2-acetamido-6-O-benzyl-3-O-(tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-β-D-glucopyranoside (12) furnished, after de
