Thymine () (symbol T or Thy) is one of the four nucleotide bases 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 in 1893 by Albrecht Kossel and Albert Neumann from calf thymus glands, hence its name.
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InChI=1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9) |
RWQNBRDOKXIBIV-UHFFFAOYSA-N |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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Escherichia coli
(NCBI:txid562)
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See:
PubMed
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Cordyceps sinensis
(NCBI:txid72228)
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Found in
mycelium
(BTO:0001436).
Ethanolic extract of dried mycelia
See:
PubMed
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Homo sapiens
(NCBI:txid9606)
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See:
DOI
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Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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View more via ChEBI Ontology
Outgoing
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thymine
(CHEBI:17821)
has role
Escherichia coli metabolite
(CHEBI:76971)
thymine
(CHEBI:17821)
has role
human metabolite
(CHEBI:77746)
thymine
(CHEBI:17821)
has role
mouse metabolite
(CHEBI:75771)
thymine
(CHEBI:17821)
is a
pyrimidine nucleobase
(CHEBI:26432)
thymine
(CHEBI:17821)
is a
pyrimidone
(CHEBI:38337)
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Incoming
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α-putrescinylthymine
(CHEBI:132931)
has functional parent
thymine
(CHEBI:17821)
(2-O,3-C-methylene-5-O-phosphonoarabinofuranosyl)thymine
(CHEBI:46007)
has functional parent
thymine
(CHEBI:17821)
(2-O,3-ethane-1,2-diyl-5-O-phosphonoarabinofuranosyl)thymine
(CHEBI:45967)
has functional parent
thymine
(CHEBI:17821)
1-(2,3-dideoxy-6-O-phosphono-β-D-erythro-hexopyranosyl)thymine
(CHEBI:46508)
has functional parent
thymine
(CHEBI:17821)
1-(2-O-methyl-5-O-phosphono-β-D-arabinofuranosyl)thymine
(CHEBI:45953)
has functional parent
thymine
(CHEBI:17821)
1-(2-deoxy-2-fluoro-5-O-phosphono-β-D-arabinofuranosyl)thymine
(CHEBI:45806)
has functional parent
thymine
(CHEBI:17821)
1-[(1S,2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)bicyclo[3.1.0]hexan-2-yl]thymine
(CHEBI:46026)
has functional parent
thymine
(CHEBI:17821)
1-[(1S,3S,4R,5S)-3-hydroxy-4-(hydroxymethyl)bicyclo[3.1.0]hexan-1-yl]thymine
(CHEBI:45586)
has functional parent
thymine
(CHEBI:17821)
1-[(2-hydroxyethoxy)methyl]-6-(phenylsulfanyl)thymine
(CHEBI:43060)
has functional parent
thymine
(CHEBI:17821)
5,6-dihydrothymine
(CHEBI:27468)
has functional parent
thymine
(CHEBI:17821)
5-formyluracil
(CHEBI:80961)
has functional parent
thymine
(CHEBI:17821)
6-(1,3-dihydroxyisobutyl)thymine
(CHEBI:41485)
has functional parent
thymine
(CHEBI:17821)
6-(3-hydroxypropyl)thymine
(CHEBI:43299)
has functional parent
thymine
(CHEBI:17821)
6-{[(4R,5R)-4-(hydroxymethyl)thymin-5-yl]methyl}thymine
(CHEBI:45366)
has functional parent
thymine
(CHEBI:17821)
N-[2-(methylamino)ethyl]-N-[(thymin-1-yl)acetyl]glycine
(CHEBI:46063)
has functional parent
thymine
(CHEBI:17821)
[(1R,2S,3S,5S)-5-hydroxy-2-methyl-3-(thymin-1-yl)cyclopentyl]methyl dihydrogen phosphate
(CHEBI:45942)
has functional parent
thymine
(CHEBI:17821)
[(1R,4S,6S)-6-hydroxy-4-(thymin-1-yl)cyclohex-2-en-1-yl]methyl dihydrogen phosphate
(CHEBI:43121)
has functional parent
thymine
(CHEBI:17821)
methylthymine
(CHEBI:134101)
has functional parent
thymine
(CHEBI:17821)
stavudine
(CHEBI:63581)
has functional parent
thymine
(CHEBI:17821)
telbivudine
(CHEBI:63624)
has functional parent
thymine
(CHEBI:17821)
thymidine
(CHEBI:17748)
has functional parent
thymine
(CHEBI:17821)
thymine glycol
(CHEBI:29128)
has functional parent
thymine
(CHEBI:17821)
thymin-1-yl group
(CHEBI:30757)
is substituent group from
thymine
(CHEBI:17821)
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2,4-dihydroxy-5-methylpyrimidine
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NIST Chemistry WebBook
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5-methyl-2,4(1H,3H)-pyrimidinedione
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NIST Chemistry WebBook
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5-methylpyrimidine-2,4(1H,3H)-dione
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IUPAC
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5-Methyluracil
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KEGG COMPOUND
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5-methyluracil
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NIST Chemistry WebBook
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T
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ChEBI
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Thy
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CBN
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Thymin
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ChemIDplus
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Thymine
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KEGG COMPOUND
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THYMINE
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PDBeChem
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thymine
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UniProt
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C00001511
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KNApSAcK
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C00178
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KEGG COMPOUND
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DB03462
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DrugBank
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TDR
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PDBeChem
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Thymine
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Wikipedia
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View more database links |
278790
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Gmelin Registry Number
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Gmelin
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607626
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Beilstein Registry Number
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Beilstein
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65-71-4
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CAS Registry Number
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KEGG COMPOUND
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65-71-4
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CAS Registry Number
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ChemIDplus
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65-71-4
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CAS Registry Number
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NIST Chemistry WebBook
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Shetlar MD, Basus VJ (2013) The photochemistry of thymine in frozen aqueous solution: trimeric and minor dimeric products. Photochemistry and photobiology 89, 631-639 [PubMed:23237383] [show Abstract] Early work identified three compounds, namely the c,s cyclobutane dimer, the so-called (6-4) photoproduct (5-hydroxy-6-4'-(5-methylpyrimidin-2'-one)-5,6-dihydrothymine) and a trimer hydrate, as products formed upon UV irradiation of thymine in frozen aqueous solution. More recent work has shown that an (α-4) product, namely α-4'-(5'-methylpyrimidine-2'-one)-thymine, is a likely product formed under these reaction conditions. During a thorough reinvestigation of the photochemistry of Thy in ice at -78.5°C, we found that a variety of other products could be detected. In addition to the c,s dimer, the other three known cyclobutane dimers, namely the c,a, t,s and t,a forms, are produced, although in considerably smaller amounts. The so-called "spore product" of thymine (5,6-dihydro-5-(α-thyminyl)thymine) is likewise formed. Two other dimers have been identified as minor products; one of these has been determined to be 5-(thymin-3-yl)-5,6-dihydrothymine and the other has been tentatively assigned to be a (5-4) adduct (6-hydroxy-5-4'-(5-methylpyrimidin-2'-one)-5,6-dihydrothymine). Compounds with the behavior expected of true trimeric compounds have been isolated via HPLC and characterized by mass spectrometry and photochemical behavior. One of these materials, putatively containing an oxetane ring, decomposes thermally to a secondary trimeric product that is then converted into the known trimer hydrate. |
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