Heterocyclic compound

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File:Pyridine simple structure.png
Pyridine a simple heterocyclic compound

Heterocyclic compounds are organic compounds that contain a ring structure containing atoms in addition to carbon, such as sulfur, oxygen or nitrogen, as part of the ring. They may be either simple aromatic rings or non-aromatic rings. Some examples are pyridine (C5H5N), pyrimidine (C4H4N2) and dioxane (C4H8O2).

Note that compounds such as cyclopropane, an anaesthetic with explosive properties, and cyclohexane, a solvent, are not heterocyclic, they are merely cycloalkanes. The suffix '-cyclic' implies a ring structure, while 'hetero' refers to an atom other than carbon, as above. Many heterocyclic compounds, including some amines, are carcinogenic.

Heterocyclic chemistry is the chemistry branch dealing exclusively with synthesis, properties and applications of heterocycles especially vital to drug design.

3-membered rings

Heterocycles with three atoms in the ring are more reactive because of ring strain. Those containing one heteroatom are generally stable. Those with two heteroatoms are more likely to occur as reactive intermediates. Common 3-membered heterocycles are:

heteroatom saturated unsaturated
Nitrogen aziridine
Oxygen ethylene oxide (epoxides, oxiranes) oxirene
Sulphur thiirane (episulfides)

4-membered rings

heteroatom saturated unsaturated
Nitrogen azetidine
Oxygen oxetane

5-membered rings

With heterocycles containing five atoms, the unsaturated compounds are frequently more stable because of aromaticity.

heteroatom saturated unsaturated
Nitrogen dihydropyrrole (pyrroline) & tetrahydropyrrole (pyrrolidine) pyrrole
Oxygen dihydrofuran & tetrahydrofuran furan
Sulphur dihydrothiophene & tetrahydrothiophene thiophene (thiole)
Arsenic arsole

With two heteroatoms:

  • The azoles:
    • Two N: pyrazole & imidazole
    • Three N: triazole
    • Four N: tetrazole
    • One N and one O: oxazole & isoxazole
    • One N and one S: thiazole & isothiazole
  • Two S: Dithiolane

6-membered rings

heteroatom saturated unsaturated
Nitrogen piperidine pyridine
Oxygen tetrahydropyran pyran
Sulphur Thiane Thiine aka thiapyrane

With two heteroatoms:

  • Two N: Pyridazine, Pyrimidine, and Pyrazine are the 1,2-, 1,3-, and 1,4-isomers, respectively.
  • Two N: Piperazine
  • One N and one O: Oxazines
  • One N and one S: Thiazine
  • Two S: Dithiane
  • Two O: Dioxane

Heterocyclic amines and cancer

Some heterocyclic amines (HCAs) found in cooked meat are known carcinogens. Research has shown that cooking certain meats at high temperatures creates chemicals that are not present in uncooked meats. For example, heterocyclic amines are the carcinogenic chemicals formed from the cooking of muscle meats such as beef, pork, fowl, and fish. HCAs form when amino acids and creatine (a chemical found in muscles) react at high cooking temperatures. Researchers have identified 17 different HCAs resulting from the cooking of muscle meats that may pose human cancer risk.[1] NCI's Division of Cancer Epidemiology and Genetics found a link between individuals with stomach cancer and the consumption of cooked meat, and other studies for colorectal, pancreatic, and breast cancer is associated with high intakes of well-done, fried, or barbecued meats. Other sources of protein (milk, eggs, tofu, and organ meats such as liver) have very little or no HCA content naturally or when cooked.

References
ISBN links support NWE through referral fees

  1. Heterocyclic Amines in Cooked Meats. National Cancer Institute (15 Sep 2004). Retrieved 2007-08-09.

External links

ar:حلقة غير متجانسة ca:Compost heterocíclic cs:Heterocyklické sloučeniny de:Heterocyclen es:Compuesto heterocíclico fr:Hétérocycle it:Composto eterociclico he:תרכובת הטרוציקלית mk:Хетероциклично соединение nl:Heterocyclische verbinding ja:複素環式化合物 pl:Związki heterocykliczne ru:Гетероциклические соединения sk:Heterocyklická zlúčenina fi:Heterosyklinen yhdiste sv:Heterocykliska föreningar uk:Гетероциклічні сполуки zh:杂环化合物