GLPBio

5-Amino-6-(D-ribitylamino)uracil (hydrochloride)

Catalog No.: GC45355Purity:>85.00%Synonyms: 5-Amino-6-ribitylamino-2,4(1H,3H)-Pyrimidinedione; 5-Amino-ribityl-Uracil; 5-A-RU

Products are for research use only. Not for human use. We do not sell to patients.


5-Amino-6-(D-ribitylamino)uracil (hydrochloride)
Cas No.: 134452-11-2
500μgQuote
$160.00
1mgQuote
$305.00

Citations

No citations are currently available for this product. Below are selected publications citing GlpBio products.
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

Description

5-Amino-6-(D-ribitylamino)uracil (5-A-RU) is a derivative of uracil and a precursor to riboflavin.1,2 It reacts non-enzymatically with dihydroxy acetone, methylglyoxal, or glyoxal to activate mucosal-associated invariant T (MAIT) cells isolated from iVα19-Tg and iVα19Vβ6-DTg mice.2 5-A-RU (100 nM, i.p.), when administered in combination with methylglyoxal, activates MAIT cells in iVα19 Cα-/--Tg mice. It is also a substrate for F0 synthase, an enzyme involved in the biosynthesis of the energy metabolism cofactor F420 in archaea, bacteria, and eukaryotes.1

References
1. Decamps, L., Philmus, B., Benjdia, A., et al. Biosynthesis of F0, precursor of the F420 cofactor, requires a unique two radical-SAM domain enzyme and tyrosine as substrate. J. Am. Chem. Soc. 134(44), 18173-18176 (2012).
2. Soudais, C., Samassa, F., Sarkis, M., et al. In vitro and in vivo analysis of the gram-negative bacteria-derived riboflavin precursor derivatives activating mouse MAIT cells. J. Immunol. 194(10), 4641-4649 (2015).

Product Documents

Purity:>85.00%Appearance:A solid

Chemical Properties

CAS No.
134452-11-2
Synonyms
5-Amino-6-ribitylamino-2,4(1H,3H)-Pyrimidinedione; 5-Amino-ribityl-Uracil; 5-A-RU
SMILES
O=C(C(N)=C(NC[C@H](O)[C@H](O)[C@H](O)CO)N1)NC1=O.Cl.Cl
Molecular Formula
C9H16N4O6.2HCl
Molecular Weight
349.2
Solubility
DMSO: Slightly Soluble,Water: Slightly Soluble
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

Reviews

Review for 5-Amino-6-(D-ribitylamino)uracil (hydrochloride)

Rating: 5
  • 5 Star100%
  • 4 Star0%
  • 3 Star0%
  • 2 Star0%
  • 1 Star0%