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Home > Encyclopedia > 5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione

5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione

5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione structure

5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione 

structure
  • CAS No:

    17014-74-3

  • Formula:

    C9H16N4O6

  • Chemical Name:

    5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione

  • Synonyms:

    D-Ribitol,1-[(5-amino-1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidinyl)amino]-1-deoxy-;Uracil,5-amino-6-[(D-ribo-2,3,4,5-tetrahydroxypentyl)amino]-;1-[(5-Amino-1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidinyl)amino]-1-deoxy-D-ribitol;4-(Ribitylamino)-5-aminouracil;4-(1′-D-Ribitylamino)-5-amino-2,6-dihydroxypyrimidine;5-Amino-4-D-ribitylaminouracil;4-Ribitylamino-5-amino-2,6-dihydroxypyrimidine;5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

ChEBI: An aminouracil that is D-ribitol in which the hydroxy group at position 1 is substituted by the 6-amino group of 5,6-diaminouracil. Early intermediate in bacterial riboflavin synthesis.


Solid


5-amino-6-(D-ribitylamino)uracil is an aminouracil that is D-ribitol in which the hydroxy group at position 1 is substituted by the 6-amino group of 5,6-diaminouracil. Early intermediate in bacterial riboflavin synthesis. It has a role as a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a hydroxypyrimidine and an aminouracil. It derives from a ribitol.

5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione Basic Attributes

276.249

276.25

Characteristics

177

-3.2

Solid

1.67±0.1 g/cm3(Predicted)

Drug Information

5-amino-2,6-dioxo-4-ribitylaminopyrimidine

Computed Properties

Molecular Weight:276.25
XLogP3:-3.2
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:276.10698424
Monoisotopic Mass:276.10698424
Topological Polar Surface Area:177
Heavy Atom Count:19
Complexity:398
Defined Atom Stereocenter Count:3
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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