Thymine
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| Names | |||
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| IUPAC name
5-Methylpyrimidine-2,4(1H,3H)-dione
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| Other names
5-methyluracil
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| Identifiers | |||
65-71-4  |
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| ChEBI | CHEBI:17821  |
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| ChEMBL | ChEMBL993 |
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| ChemSpider | 1103 |
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| 4581 | |||
| Jmol 3D model | Interactive image | ||
| MeSH | Thymine | ||
| PubChem | 1135 | ||
| UNII | QR26YLT7LT |
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| Properties | |||
| C5H6N2O2 | |||
| Molar mass | 126.12 g·mol−1 | ||
| Density | 1.23 g cm−3 (calculated) | ||
| Melting point | 316 to 317 °C (601 to 603 °F; 589 to 590 K) | ||
| Boiling point | 335 °C (635 °F; 608 K) (decomposes) | ||
| Acidity (pKa) | 9.7 | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 verify (what is ?) |
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| Infobox references | |||
Thymine /ˈθaɪmᵻn/ (T, Thy) is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T. The others are adenine, guanine, and cytosine. Thymine is also known as 5-methyluracil, a pyrimidine nucleobase. In RNA, thymine is replaced by the nucleobase uracil. Thymine was first isolated (from calves' thymus glands) in 1893 by Albrecht Kossel and Albert Neumann.[1]
Derivation
As the name suggests, thymine may be derived by methylation of uracil at the 5th carbon. In RNA, thymine is replaced with uracil in most cases. In DNA, thymine (T) binds to adenine (A) via two hydrogen bonds, thus stabilizing the nucleic acid structures.
Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is synonymous with the term thymidine. Thymidine can be phosphorylated with one, two, or three phosphoric acid groups, creating, respectively, TMP, TDP, or TTP (thymidine mono-, di-, or triphosphate).
One of the common mutations of DNA involves two adjacent thymines or cytosine, which, in presence of ultraviolet light, may form thymine dimers, causing "kinks" in the DNA molecule that inhibit normal function.
Thymine could also be a target for actions of 5-fluorouracil (5-FU) in cancer treatment. 5-FU can be a metabolic analog of thymine (in DNA synthesis) or uracil (in RNA synthesis). Substitution of this analog inhibits DNA synthesis in actively dividing cells.
Thymine bases are frequently oxidized to hydantoins over time after the death of an organism.[2]
Thymine is a nuclear base.
Theoretical aspects
In March 2015, NASA scientists reported that, for the first time, complex DNA and RNA organic compounds of life, including uracil, cytosine and thymine, have been formed in the laboratory under outer space conditions, using starting chemicals, such as pyrimidine, found in meteorites. Pyrimidine, like polycyclic aromatic hydrocarbons (PAHs), the most carbon-rich chemical found in the Universe, may have been formed in red giants or in interstellar dust and gas clouds, according to the scientists.[3]
See also
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References
- ↑ Albrecht Kossel and Albert Neumann (1893) "Ueber das Thymin, ein Spaltungsproduct der Nucleïnsäure" (On thymine, a cleavage product of nucleic acid), Berichte der Deutschen Chemischen Gesellschaft zu Berlin, 26 : 2753-2756. From p. 2754: "Wir bezeichnen diese Substanz als Thymin." (We designate this substance as "thymine" [because it was initially obtained from the thymus glands of calves].)
- ↑ Hofreiter M., Serre D., Poinar H.N., Kuch M., and Paabo S. Nature Reviews Genetics (2001) 2:353.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
