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  2. Pyrimidine - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine

    Pyrimidine (C 4 H 4 N 2; / p ɪ ˈ r ɪ. m ɪ ˌ d iː n, p aɪ ˈ r ɪ. m ɪ ˌ d iː n /) is an aromatic, heterocyclic, organic compound similar to pyridine (C 5 H 5 N). [3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has nitrogen atoms at positions 1 and 3 in the ring.

  3. Purine - Wikipedia

    en.wikipedia.org/wiki/Purine

    Purine is a heterocyclic aromatic organic compound that consists of two rings (pyrimidine and imidazole) fused together.It is water-soluble.Purine also gives its name to the wider class of molecules, purines, which include substituted purines and their tautomers.

  4. Uracil - Wikipedia

    en.wikipedia.org/wiki/Uracil

    The amide tautomer is referred to as the lactam structure, while the imidic acid tautomer is referred to as the lactim structure. These tautomeric forms are predominant at pH 7. The lactam structure is the most common form of uracil. Uracil tautomers: Amide or lactam structure (left) and imide or lactim structure (right)

  5. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [ 6 ] Each of the base pairs in a typical double- helix DNA comprises a purine and a pyrimidine: either an A paired with a T or a C paired with a G.

  6. Uridine - Wikipedia

    en.wikipedia.org/wiki/Uridine

    Uridine (symbol U or Urd) is a glycosylated pyrimidine analog containing uracil attached to a ribose ring (or more specifically, a ribofuranose) via a β-N 1-glycosidic bond.The analog is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine.

  7. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    The nitrogen (N)-containing aromatic rings can be separated into basic aromatic rings that are easily protonated, and form aromatic cations and salts (e.g., pyridinium), and non-basic aromatic rings. In the basic aromatic rings, the lone pair of electrons is not part of the aromatic system and extends in the plane of the ring.

  8. Cytosine - Wikipedia

    en.wikipedia.org/wiki/Cytosine

    [4] [5] A structure was proposed in 1903, and was synthesized (and thus confirmed) in the laboratory in the same year. In 1998, cytosine was used in an early demonstration of quantum information processing when Oxford University researchers implemented the Deutsch–Jozsa algorithm on a two qubit nuclear magnetic resonance quantum computer ...

  9. Dihydrouridine - Wikipedia

    en.wikipedia.org/wiki/Dihydrouridine

    Thus, while pseudouridine and 2′-O-methylations stabilize the local RNA structure, D does the opposite. [ 2 ] The tRNAs of organisms that grow at low temperatures ( psychrophiles ) have high 5,6-dihydrouridine levels (40-70% more on average) which provides the necessary local flexibility of the tRNA at or below the freezing point.