D4407

2-Deoxy-D-galactose

98%

• Synonim(y): 2-Deoxy-D-lyxohexose
• Wzór empiryczny (zapis Hilla): C₆H₁₂O₅
• Numer CAS: 1949-89-9
• Masa cząsteczkowa: 164.16
• UNSPSC Code: 12352201
• NACRES: NA.22
• PubChem Substance ID: 24893869
• EC Number: 217-765-3
• Beilstein/REAXYS Number: 1723333
• MDL number: MFCD00014649

Właściwości

• Quality Segment: 200
• assay: 98%
• form: powder
• optical activity: [α]20/D +59.7°, c = 2 in H₂O
• color: white to off-white
• mp: 107 - 110 °C ((225 - 230 °F)), 107-110 °C (lit.)
• SMILES string: OC[C@H]1OC(O)C[C@@H](O)[C@H]1O
• InChI: 1S/C6H12O5/c7-2-4-6(10)3(8)1-5(9)11-4/h3-10H,1-2H2/t3-,4-,5?,6-/m1/s1
• InChI key: PMMURAAUARKVCB-DUVQVXGLSA-N

Opis

General description

2-Deoxy-D-galactose is a glucose analog that shows a wide range of biological activities such as inhibition of glycolysis and thereby tumor growth, interference with the biosynthetic processing of glycoproteins, antiviral activity, and hepatotoxicity. It is being extensively studied as trapping agents for phosphate and uridylate in mammalian cells due to its ability to interfere in the phosphate and nucleotide metabolism.

Application

• FUT1-mediated terminal fucosylation acts as a new target to attenuate renal fibrosis.: This research investigates the role of 2-deoxy-D-galactose in modulating terminal fucosylation processes, revealing potential therapeutic pathways for treating renal fibrosis and enhancing the understanding of kidney disease mechanisms (Luo et al., 2023).


• 2-D-gal Targets Terminal Fucosylation to Inhibit T-cell Response in a Mouse Skin Transplant Model.: Highlights the immunomodulatory potential of 2-deoxy-D-galactose in transplant medicine, showing how it can inhibit T-cell responses and contribute to the success of skin grafts, pointing towards new immunosuppressive treatments (Mao et al., 2023).


• Inhibition of Aberrant α(1,2)-Fucosylation at Ocular Surface Ameliorates Dry Eye Disease.: Explores the therapeutic effects of 2-deoxy-D-galactose in treating dry eye disease by modulating specific fucosylation pathways, potentially opening new avenues for ocular surface treatment strategies (Yoon et al., 2021).

Other Notes

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

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)