File:Thymin.svg · Wikimedia Commons · See Wikimedia Commons
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Sign in to saveAlso known as 5-methylpyrimidine-2,4(1H,3H)-dione, 2,4-dihydroxy-5-methylpyrimidine, 5-methyl-2,4(1H,3H)-pyrimidinedione, 5-methyluracil, Thymin, 2,4(1H,3H)-Pyrimidinedione, 5-methyl-, 5-Methyl-2,4-dihydroxypyrimidine, 5-Methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
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OverviewAI-generated
Thymine is a chemical compound with the IUPAC name 5-methyl-1H-pyrimidine-2,4-dione. Its chemical formula is C₅H₆N₂O₂, and it has a mass of 126.043. The substance features a melting point of 317. In terms of molecular properties, thymine has a charge of 0, an xlogp value of -0.6, and a topological polar surface area of 58.2. It contains two hydrogen bond donors and two hydrogen bond acceptors.
The compound is associated with a weight of 126.11. Its canonical SMILES notation is CC1=CNC(=O)NC1=O. Thymine is referenced by 566 other encyclopedia articles. Additionally, there are 18572 PubMed entries associated with the query for thymine.
Synthesized by Vinony from 18 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C5H6N2O2
- Molecular weight
- 126.11 g/mol
- IUPAC name
- 5-methyl-1H-pyrimidine-2,4-dione
- SMILES
- CC1=CNC(=O)NC1=O
- InChIKey
- RWQNBRDOKXIBIV-UHFFFAOYSA-N
- XLogP
- -0.6
- Polar surface area
- 58.2 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Research
18,572 papers- Thymine methyls and DNA-protein interactions.ReviewNucleic acids research · 1987Ivarie RDOI: 10.1093/nar/15.23.9975
- A new method for sequencing DNA.Proceedings of the National Academy of Sciences of the United States of America · 1977Maxam AM, Gilbert WDOI: 10.1073/pnas.74.2.560
- Thymine-Modified Silicones: A Bioinspired Approach to Cross-Linked, Recyclable Silicone Polymers.Biomacromolecules · 2023Voigt LJ, Tucker KE, Zelisko PMDOI: 10.1021/acs.biomac.3c00185
- Thymine dissociation and dimer formation: A Raman and synchronous fluorescence spectroscopic study.Proceedings of the National Academy of Sciences of the United States of America · 2021Nagpal A, Dhankhar D, Cesario TC et al.DOI: 10.1073/pnas.2025263118
- The Radiation Stability of Thymine in Solid H(2)O.Astrobiology · 2020Materese CK, Gerakines PA, Hudson RLDOI: 10.1089/ast.2019.2199
- Photocrosslinking Probes Proximity of Thymine Modifiers Tethering Excitonically Coupled Dye Aggregates to DNA Holliday Junction.Molecules (Basel, Switzerland) · 2022Basu S, Cervantes-Salguero K, Yurke B et al.DOI: 10.3390/molecules27134006
- [Thymine dimerization and survival of bacteria].Journal of molecular biology · 1962WACKER A, DELLWEG H, JACHERTS DDOI: 10.1016/s0022-2836(62)80022-9
- Thymine and thymidine synthesis.Biochimica et biophysica acta · 1956BARNER HD, COHEN SS, GREEN MDOI: 10.1016/0006-3002(56)90252-9
via PubMed
Gallery (7)
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