Containing more than one kind of atom joined in a ring.
heterocycle het'er·o·cy'cle (-sī'kəl) n.heterocyclic het'er·o·cy'clic n.
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Containing more than one kind of atom joined in a ring.
heterocycle het'er·o·cy'cle (-sī'kəl) n.Cyclic compounds in which the rings include at least one atom of an element different from the rest. Most types of heterocyclic compounds studied to date are organic compounds. An example of an organic heterocyclic compound is oxazoline (1); an example of an inorganic heterocyclic compound is the phosphonitrilic chloride (2). The smallest possible ring is three-membered, for example, ethylene oxide (3), but very 1




Naturally occurring heterocyclic compounds are extremely common as, for example, most alkaloids, sugars, vitamins, DNA and RNA, enzymic cofactors, plant pigments, many of the components of coal tar, many natural pigments (such as indigo, chlorophyll, hemoglobin, and the anthocyanins), antibiotics (such as penicillin and streptomycin), and some of the essential amino acids (for example, tryptophan), and many of the peptides (such as oxytocin). Some of the most important naturally occurring high polymers are heterocyclic, including starch and cellulose. The major groups of natural products that are not mainly heterocyclic are the fats and most of the terpenes, steroids, and essential α-amino acids, though exceptions do exist.
Heterocyclic compounds may be named systematically. Many heterocycles, however, have nonsystematic names that are usually preferred by practicing chemists over the systematic ones. In the systematic approach to nomenclature the ring size is denoted by the appropriate stem. For example, three-membered saturated rings without nitrogen would have a name ending in -irane. The nature of the heteroatom is denoted by such prefixes as oxa-, thia-, or aza-, for oxygen, sulfur, or nitrogen, respectively. Thus, ethylene oxide (3) becomes oxirane. A five-membered unsaturated ring would have a name ending in -ole. A six-membered unsaturated ring containing nitrogen would have a name ending in -ine according to this scheme. Actually, the trivial names for many systems are commonly accepted, and the systematic names are not often used.
For details about specific heterocyclic systems See also Furan; Heterocyclic polymer; Indole; Pyridine; Pyrimidine; Pyrrole.
For more information on heterocyclic compound, visit Britannica.com.
Having or pertaining to a closed chain or ring formation that includes atoms of different elements.
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.
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) |
| heteroatom | saturated | unsaturated |
|---|---|---|
| Nitrogen | azetidine | |
| Oxygen | oxetane |
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:
| heteroatom | saturated | unsaturated |
|---|---|---|
| Nitrogen | piperidine | pyridine |
| Oxygen | tetrahydropyran | pyran |
| Sulphur | Thiane | Thiine aka thiapyrane |
With two heteroatoms:
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.
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