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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. Pyrimidine metabolism - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine_metabolism

    RNA is composed of pyrimidine and purine nucleotides, both of which are necessary for reliable information transfer, and thus natural selection and Darwinian evolution. Becker et al. showed how pyrimidine nucleosides can be synthesized from small molecules and ribose, driven solely by wet-dry cycles. [11]

  4. Category:Pyrimidines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyrimidines

    Pyrimidines are organic compounds that contain the pyrimidine base structure. Subcategories. This category has the following 9 subcategories, out of 9 total. A.

  5. 4-Amino-5-hydroxymethyl-2-methylpyrimidine - Wikipedia

    en.wikipedia.org/wiki/4-Amino-5-hydroxymethyl-2...

    Within the field of biochemistry, 4-amino-5-hydroxymethyl-2-methylpyrimidine (HMP) also known as toxopyrimidine together with its mono phosphate (HMP-P) and pyrophosphate (HMP-PP) esters are biogenetic precursors to the important biochemical cofactor thiamine pyrophosphate (TPP), a derivative of thiamine (vitamin B 1).

  6. 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. They are the most widely occurring nitrogen-containing heterocycles in nature. [1]

  7. Pyrimidinedione - Wikipedia

    en.wikipedia.org/wiki/Pyrimidinedione

    Pyrimidinediones are a class of chemical compounds characterized by a pyrimidine ring substituted with two carbonyl groups. Examples include naturally occurring metabolites : Trivial name

  8. Pyrimidine dimer - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine_dimer

    The 6–4 photoproduct (6–4 pyrimidine–pyrimidone, or 6–4 pyrimidine–pyrimidinone) is an alternate dimer configuration consisting of a single covalent bond linking the carbon at the 6 (C6) position of one pyrimidine ring and carbon at the 4 (C4) position of the adjoining base's ring. [11]

  9. Cytidine triphosphate - Wikipedia

    en.wikipedia.org/wiki/Cytidine_triphosphate

    Cytidine triphosphate (CTP) is a pyrimidine nucleoside triphosphate.CTP, much like ATP, consists of a ribose sugar, and three phosphate groups.The major difference between the two molecules is the base used, which in CTP is cytosine.