InChI=1S/C9H16N4O6/c10- 5- 7(12- 9(19) 13- 8(5) 18) 11- 1- 3(15) 6(17) 4(16) 2- 14/h3- 4,6,14- 17H,1- 2,10H2,(H3,11,12,13,18,19) /t3- ,4+,6- /m0/s1 |
XKQZIXVJVUPORE-RPDRRWSUSA-N |
Nc1c(NC[C@H](O)[C@H](O)[C@H](O)CO)[nH]c(=O)[nH]c1=O |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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Saccharomyces cerevisiae
(NCBI:txid4932)
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Source: yeast.sf.net
See:
PubMed
|
Escherichia coli
(NCBI:txid562)
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See:
PubMed
|
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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View more via ChEBI Ontology
1-[(5-amino-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)amino]-1-deoxy-D-ribitol
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4-(1-D-Ribitylamino)-5-amino-2,6-dihydroxypyrimidine
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KEGG COMPOUND
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5-A-RU
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ChEBI
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5-amino-2,6-dioxo-4-ribitylaminopyrimidine
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ChemIDplus
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5-Amino-6-(1-D-ribitylamino)uracil
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KEGG COMPOUND
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5-amino-6-(D-ribitylamino)uracil
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UniProt
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5-amino-6-(D-ribitylamino)uracil
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KEGG COMPOUND
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5-amino-6-ribitylamino-2,4-(1H,3H)pyrimidinedione
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ChemIDplus
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5-Amino-6-ribitylaminouracil
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KEGG COMPOUND
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5-arpd
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ChemIDplus
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6-(1-D-Ribitylamino)-5-amino-2,4-dihydroxypyrimidine
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KEGG COMPOUND
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6-(1-D-Ribitylamino)-5-aminouracil
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KEGG COMPOUND
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17014-74-3
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CAS Registry Number
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ChemIDplus
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33063
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Reaxys Registry Number
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Reaxys
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