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heterocyclic

  (hĕt'ə-rō-sī'klĭk, -sĭk'lĭk) pronunciation
adj.

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.
 
 
Sci-Tech Encyclopedia: Heterocyclic compounds

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

2
3
large rings are possible, as in the crown ethers, for example, 18-crown-6 (4). 4
The cycle may contain only single bonds and is thus saturated; it may include one or more double bonds; or it may possess aromatic unsaturation characteristics of benzene, that is, it is heteroaromatic. Heterocyclic compounds can contain more than one ring, either heterocyclic or homocyclic.

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.


 
Britannica Concise Encyclopedia: heterocyclic compound

Any of a class of organic compounds whose molecules contain one or more rings of atoms with at least one atom (the heteroatom) being an element other than carbon, most frequently oxygen, nitrogen, or sulfur. As in regular cyclic hydrocarbons, such heterocyclic rings may include single, double, or triple bonds or be aromatic (see covalent bond; aromatic compound), and the compound may contain one or more single rings or have fused rings (in which adjoining rings share two carbon atoms). Compounds having five-membered heterocyclic rings include chlorophyll, hemoglobin, indigo, tryptophan, and certain polymers. Those with six-membered heterocyclic rings include pyridine, pyridoxine (vitamin B6; see vitamin B complex), vitamin E, quinine, and the pyran nucleus, which is found in sugars and the anthocyanin pigments. Nicotine and morphine have both five- and six-membered heterocyclic rings; some antibiotics (e.g., penicillin) have two different heteroatoms in their rings. Other important heterocyclic compounds are pyrimidines, which occur in barbiturates, and purines, which occur in caffeine and related compounds; pyrimidine and purine are the parent compounds of the nucleic acids.

For more information on heterocyclic compound, visit Britannica.com.

 
Veterinary Dictionary: heterocyclic

Having or pertaining to a closed chain or ring formation that includes atoms of different elements.

 
Wikipedia: heterocyclic compound
Pyridine a simple heterocyclic compound
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:

6-membered rings

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

With two heteroatoms:

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

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

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Copyrights:

Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2007. Published by Houghton Mifflin Company. All rights reserved.  Read more
Sci-Tech Encyclopedia. McGraw-Hill Encyclopedia of Science and Technology. Copyright © 2005 by The McGraw-Hill Companies, Inc. All rights reserved.  Read more
Britannica Concise Encyclopedia. Britannica Concise Encyclopedia. © 2006 Encyclopædia Britannica, Inc. All rights reserved.  Read more
Veterinary Dictionary. Saunders Comprehensive Veterinary Dictionary 3rd Edition. Copyright © 2007 by D.C. Blood, V.P. Studdert and C.C. Gay, Elsevier. All rights reserved.  Read more
Wikipedia. This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Heterocyclic compound" Read more

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