5-A-RU hydrochloride

Modify Date: 2025-08-24 21:54:32

5-A-RU hydrochloride Structure
5-A-RU hydrochloride structure
Common Name 5-A-RU hydrochloride
CAS Number 134452-11-2 Molecular Weight 312.71
Density N/A Boiling Point N/A
Molecular Formula C9H17ClN4O6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of 5-A-RU hydrochloride


5-A-RU hydrochloride (5-Amino-6-(D-ribitylamino)uracil hydrochloride), a precursor of bacterial Riboflavin, is a mucosal-associated invariant T (MAIT) cells activator. 5-A-RU hydrochloride forms potent MAIT-activating antigens via non-enzymatic reactions with small molecules, such as glyoxal and methylglyoxal, which are derived from other metabolic pathways[1][2][3].

 Names

Name 5-A-RU hydrochloride

 5-A-RU hydrochloride Biological Activity

Description 5-A-RU hydrochloride (5-Amino-6-(D-ribitylamino)uracil hydrochloride), a precursor of bacterial Riboflavin, is a mucosal-associated invariant T (MAIT) cells activator. 5-A-RU hydrochloride forms potent MAIT-activating antigens via non-enzymatic reactions with small molecules, such as glyoxal and methylglyoxal, which are derived from other metabolic pathways[1][2][3].
Related Catalog
In Vitro The MAIT antigens formed by the reactions between 5-A-RU hydrochloride and glyoxal/methylglyoxal are simple adducts, 5-(2-oxoethylideneamino)-6-D-ribitylaminouracil (5-OE-RU) and 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU), respectively, which bound to MR1 as shown by crystal structures of MAIT TCR ternary complexes[1]. 5-A-RU hydrochloride presents in diverse bacteria and yeast as well as plants. 5-A-RU plays an important role in MAIT cell activation, MR1 could not be refolded efficiently with 5-ARU alone. 5-A-RU is a precursor for MAIT cell ligand[2]. 5-A-RU hydrochloride can react extemporaneously with glyoxal and methylglyoxal to generate pyrimidine adducts that activate mouse MAIT cells from STg (iVa19) and DTg (iVa19Vb6) animals[3].
In Vivo 5-A-RU hydrochloride (100 nM; i.p.; 18 hours) and methylglyoxal (MeG) are mixed extemporaneously, MAIT cells are activated in iVa19 Cα-/- Tg mice (generated on the C57BL/6 background)[3].
References

[1]. Corbett AJ, et al. T-cell activation by transitory neo-antigens derived from distinct microbial pathways. Nature. 2014 May 15;509(7500):361-5.

[2]. Eckle SB, et al. Recognition of Vitamin B Precursors and Byproducts by Mucosal Associated Invariant T Cells.

[3]. Soudais C, et al. In Vitro and In Vivo Analysis of the Gram-Negative Bacteria-Derived Riboflavin PrecursorDerivatives Activating Mouse MAIT Cells. J Immunol. 2015 May 15;194(10):4641-9.

 Chemical & Physical Properties

Molecular Formula C9H17ClN4O6
Molecular Weight 312.71
InChIKey VGAFXPBLNINPEY-ZUOBHZEMSA-N
SMILES Cl.Nc1c(NCC(O)C(O)C(O)CO)[nH]c(=O)[nH]c1=O
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here

Get all suppliers and price by the below link:

5-A-RU hydrochloride suppliers

5-A-RU hydrochloride price

Related Compounds: More...
5-A-RU-PABC-Val-Cit-Fmoc
2677841-58-4
Pyrazolo[1,5-a]pyrimidin-3-amine hydrochloride
232600-78-1
Pyrazolo[1,5-a]pyridin-3-ylamine hydrochloride
136548-72-6
Imidazo[1,5-a]pyridin-1-amine hydrochloride
2803477-10-1
Pyrazolo[1,5-a]pyridin-2-ylmethanol hydrochloride (1:1)
1187932-28-0
IMidazo[1,5-a]pyridin-1-ylmethanamine hydrochloride
1187932-15-5
pyrazolo[1,5-a]pyridin-2-ylmethanamine hydrochloride
1187931-45-8
pyrazolo[1,5-a]pyridin-3-ylmethanamine,hydrochloride
1351659-25-0
Octahydroimidazolidino[1,5-a]piperazin-3-onehydrochloride
1376340-66-7
Phenyl (2-(4-(4-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)carbamate
877632-75-2
N-cyclopentyl-N'-{2-[4-(2-fluorophenyl)piperazin-1-yl]-2-(furan-2-yl)ethyl}ethanediamide
877632-79-6
N-{2-[4-(2-fluorophenyl)piperazin-1-yl]-2-(furan-2-yl)ethyl}-N'-[(4-methylphenyl)methyl]ethanediamide
877632-80-9
N1-(4-chlorobenzyl)-N2-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)oxalamide
877632-81-0
N1-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)-N2-propyloxalamide
877632-82-1
N1-allyl-N2-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)oxalamide
877632-83-2
N1-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)-N2-isopentyloxalamide
877632-84-3
N1-(2-(dimethylamino)ethyl)-N2-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)oxalamide
877632-85-4
N1-cyclohexyl-N2-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)oxalamide
877632-86-5
N1-butyl-N2-(2-(4-(2-fluorophenyl)piperazin-1-yl)-2-(furan-2-yl)ethyl)oxalamide
877632-87-6