Skeletal formula with numbering convention
Ball-and-stick molecular model
Space-filling molecular model
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Names

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

IUPAC name
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Identifiers#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

120-73-0 7pxY
ChEBI CHEBI:17258 7pxY
ChEMBL ChEMBL302239 7pxY
ChemSpider 1015 7pxY
Jmol-3D images Image
KEGG C15587 7pxY
MeSH Purine
PubChem Template:Chembox PubChem/format
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
Melting point Script error: No such module "convert".
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 14pxY verify (what is10pxY/10pxN?)
Infobox references

A purine is a heterocyclic aromatic organic compound. It consists of a pyrimidine ring fused to an imidazole ring. Purines, which include substituted purines and their tautomers, are the most widely occurring nitrogen-containing heterocycle in nature.[1]

Purines and pyrimidines make up the two groups of nitrogenous bases, including the two groups of nucleotide bases. Two of the four deoxyribonucleotides and two of the four ribonucleotides, the respective building-blocks of deoxyribonucleic acid - DNA, and ribonucleic acid - RNA, are purines.

Notable purines

There are many naturally occurring purines. Two of the five bases in nucleic acids, adenine (2) and guanine (3), are purines. In DNA, these bases form hydrogen bonds with their complementary pyrimidines thymine and cytosine, respectively. This is called complementary base pairing. In RNA, the complement of adenine is uracil instead of thymine.

Other notable purines are hypoxanthine (4), xanthine (5), theobromine (6), caffeine (7), uric acid (8) and isoguanine (9).



Aside from the crucial roles of purines (adenine and guanine) in DNA and RNA, purines are also significant components in a number of other important biomolecules, such as ATP, GTP, cyclic AMP, NADH, and coenzyme A. Purine (1) itself, has not been found in nature, but it can be produced by organic synthesis.

They may also function directly as neurotransmitters, acting upon purinergic receptors. Adenosine activates adenosine receptors.


The word purine (pure urine)[2] was coined by the German chemist Emil Fischer in 1884. He synthesized it for the first time in 1899.[3] The starting material for the reaction sequence was uric acid (8), which had been isolated from kidney stones by Scheele in 1776.[4] Uric acid (8) was reacted with PCl5 to give 2,6,8-trichloropurine (10), which was converted with HI and PH4I to give 2,6-diiodopurine (11). The product was reduced to purine (1) using zinc-dust.



Main article: Purine metabolism

Many organisms have metabolic pathways to synthesize and break down purines.

Purines are biologically synthesized as nucleosides (bases attached to ribose).

Accumulation of modified purine nucleotides is defective to various cellular processes, especially those involving DNA and RNA. To be viable, organisms possess a number of (deoxy)purine phosphohydrolases, which hydrolyze these purine derivatives removing them from the active NTP and dNTP pools. Deamination of purine bases can result in accumulation of such nucleotides as ITP, dITP, XTP and dXTP.[5]

Defects in enzymes that control purine production and breakdown can severely alter a cell’s DNA sequences, which may explain why people who carry certain genetic variants of purine metabolic enzymes have a higher risk for some types of cancer.

Purine Sources

Purines are found in high concentration in meat and meat products, especially internal organs such as liver and kidney. In general, plant-based diets are low in purines.[6] Examples of high-purine sources include: sweetbreads, anchovies, sardines, liver, beef kidneys, brains, meat extracts (e.g., Oxo, Bovril), herring, mackerel, scallops, game meats, beer (from the yeast) and gravy.

A moderate amount of purine is also contained in beef, pork, poultry, other fish and seafood, asparagus, cauliflower, spinach, mushrooms, green peas, lentils, dried peas, beans, oatmeal, wheat bran, wheat germ, and hawthorn.[7]

Higher levels of meat and seafood consumption are associated with an increased risk of gout, whereas a higher level of consumption of dairy products is associated with a decreased risk. Moderate intake of purine-rich vegetables or protein is not associated with an increased risk of gout.[8][9]

Laboratory synthesis

In addition to in vivo synthesis of purines in purine metabolism, purine can also be created artificially.

Purine (1) is obtained in good yield when formamide is heated in an open vessel at 170 °C for 28 hours.[10]


This remarkable reaction and others like it have been discussed in the context of the origin of life.[11]

Oro, Orgel and co-workers have shown that four molecules of HCN tetramerize to form diaminomaleodinitrile (12), which can be converted into almost all natural-occurring purines.[12][13][14][15][16] For example, five molecules of HCN condense in an exothermic reaction to make Adenine, especially in the presence of ammonia.


The Traube purine synthesis (1900) is a classic reaction (named after Wilhelm Traube) between an amine-substituted pyrimidine and formic acid.[17]

Traube purine synthesis

See also


  1. ^ Rosemeyer, H (2004). Chemistry & Biodiversity 1: 361. doi:10.1002/cbdv.200490033.  Missing or empty |title= (help)
  2. ^ McGuigan, Hugh (1921). An Introduction To Chemical Pharmacology. P. Blakiston's Sons & Co. p. 283. Retrieved July 18, 2012. 
  3. ^ Fischer, E (1899). Berichte der Deutschen Chemischen Gesellschaft 32: 2550.  Missing or empty |title= (help)
  4. ^ Scheele, V. Q. (1776). "Examen Chemicum Calculi Urinari". Opuscula 2: 73. 
  5. ^ Davies O, Mendes P, Smallbone K, Malys N (2012). "Characterisation of multiple substrate-specific (d)ITP/(d)XTPase and modelling of deaminated purine nucleotide metabolism". BMB Reports 45 (4): 259–64. PMID 22531138. doi:10.5483/BMBRep.2012.45.4.259. 
  6. ^
  7. ^ Gout Diet: Limit High Purine Foods
  8. ^ NEJM - Purine-Rich Foods, Dairy and Protein Intake, and the Risk of Gout in Men
  9. ^ [1], USDA on bone health
  10. ^ Yamada, H.; Okamoto, T. (1972). "A One-step Synthesis of Purine Ring from Formamide". Chemical & Pharmaceutical Bulletin 20 (3): 623. doi:10.1248/cpb.20.623. 
  11. ^ Saladino; Crestini, Claudia; Ciciriello, Fabiana; Costanzo, Giovanna; Mauro, Ernesto et al. (2006). "About a Formamide-Based Origin of Informational Polymers: Syntheses of Nucleobases and Favourable Thermodynamic Niches for Early Polymers". Origins of Life and Evolution of Biospheres 36 (5–6): 523–531. Bibcode:2006OLEB...36..523S. PMID 17136429. doi:10.1007/s11084-006-9053-2. 
  12. ^ Sanchez, R. A.; Ferris, J. P.; Orgel, L. E. (1967). "Studies in prebiotic synthesis. II. Synthesis of purine precursors and amino acids from aqueous hydrogen cyanide". Journal of Molecular Biology 30 (2): 223–53. PMID 4297187. doi:10.1016/S0022-2836(67)80037-8. 
  13. ^ Ferris, J. P.; Orgel, L. E. (1966). Journal of the American Chemical Society 88 (5): 1074. doi:10.1021/ja00957a050.  Missing or empty |title= (help)
  14. ^ Ferris, J. P.; Kuder, J. E.; Catalano, O. W.; Kuder; Catalano (1969). "Photochemical Reactions and the Chemical Evolution of Purines and Nicotinamide Derivatives". Science 166 (3906): 765–6. Bibcode:1969Sci...166..765F. PMID 4241847. doi:10.1126/science.166.3906.765. 
  15. ^ Oro, J.; Kamat, J. S.; Kamat (1961). "Amino-acid Synthesis from Hydrogen Cyanide under Possible Primitive Earth Conditions". Nature 190 (4774): 442–3. Bibcode:1961Natur.190..442O. PMID 13731262. doi:10.1038/190442a0. 
  16. ^ Houben-Weyl, Vol . E5, p. 1547[full citation needed]
  17. ^ Hassner, Alfred; Stumer, C. (2002). Organic Syntheses Based on Name Reactions (2nd ed.). Elsevier. ISBN 0-08-043259-X. 

External links

Lua error in Module:Authority_control at line 346: attempt to index field 'wikibase' (a nil value).