D4407

2-Deoxy-D-galactose

98%

Manufacturer: Sigma Aldrich

CAS Number: 1949-89-9

Synonym(S): 2-Deoxy-D-lyxohexose

Select a Size

Pack Size SKU Availability Price
1 G D4407-1-G In Stock ₹ 7,317.70
5 G D4407-5-G In Stock ₹ 23,046.43

D4407 - 1 G

₹ 7,317.70

In Stock

Quantity

1

Base Price: ₹ 7,317.70

GST (18%): ₹ 1,317.186

Total Price: ₹ 8,634.886

Quality Level

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

Other Options

Image Product Name Manufacturer Price Range
50-186-4874
Sigma Aldrich Fine Chemicals Biosciences 2-Deoxy-D-galactose 98% | 1949-89-9 | MFCD00014649 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 30,500.43
D4407
2-Deoxy-D-galactose
Sigma Aldrich ₹ 7,317.70 - ₹ 23,046.43
CS-0142276
2-Deoxy-D-galactose
ChemScene ₹ 7,700.40 - ₹ 71,442.60
AI43604
1949-89-9 | 2-Deoxy-d-galactose
A2B Chem ₹ 6,673.68 - ₹ 78,030.72

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Description

  • 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.[1][2][3]
  • 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.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
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

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PMMURAAUARKVCB-DUVQVXGLSA-N

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Nc1ccc(cc1N)-c2ccc(N)c(N)c2

InChI:
1S/C12H14N4/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8/h1-6H,13-16H2

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HSTOKWSFWGCZMH-UHFFFAOYSA-N

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[Na+].CCCCC(CC)COC(=O)CC(C(=O)OCC(CC)CCCC)S([O-])(=O)=O

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BrCc1ccccc1CBr

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1S/C8H8Br2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H,5-6H2

InChI key:
KGKAYWMGPDWLQZ-UHFFFAOYSA-N