Record Information |
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Version | 2.0 |
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Created at | 2005-11-16 15:48:42 UTC |
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Updated at | 2021-06-29 00:46:55 UTC |
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NP-MRD ID | NP0000678 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | 5-Thymidylic acid |
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Description | 5-Thymidylic acid (conjugate base thymidylate), also known as thymidine monophosphate (TMP), deoxythymidine monophosphate (dTMP), or deoxythymidylic acid (conjugate base deoxythymidylate), is a nucleotide that is used as a monomer in DNA. It is an ester of phosphoric acid with the nucleoside thymidine. DTMP consists of a phosphate group, the pentose sugar deoxyribose, and the nucleobase thymine. Unlike the other deoxyribonucleotides, thymidine monophosphate often does not contain the "deoxy" prefix in its name; nevertheless, its symbol often includes a "d" ("dTMP"). 5-Thymidylic acid belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with a monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. The neutral species of 5-Thymidylic acid (2'-deoxythymidine 5'-monophosphate). 5-Thymidylic acid exists in all living species, ranging from bacteria to humans. Within humans, 5-thymidylic acid participates in a number of enzymatic reactions. In particular, 5-thymidylic acid and dihydrofolic acid can be biosynthesized from dUMP and 5,10-methylene-THF by the enzyme thymidylate synthase. In addition, 5-thymidylic acid can be converted into dTDP; which is catalyzed by the enzyme thymidylate synthase. In humans, 5-thymidylic acid is involved in pyrimidine metabolism. Outside of the human body, 5-Thymidylic acid has been detected, but not quantified in several different foods, such as common buckwheats, corn salad, garden cress, squashberries, and star fruits. |
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Structure | CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=O InChI=1S/C10H15N2O8P/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(20-8)4-19-21(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,11,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1 |
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Synonyms | Value | Source |
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(DT)1 | ChEBI | 5'-Thymidylic acid | ChEBI | 5'-TMP | ChEBI | 5-Methyl-dUMP | ChEBI | Deoxyribosylthymine monophosphate | ChEBI | Ribothymidine 5'-monophosphate | ChEBI | Thymidine 5'-(dihydrogen phosphate) | ChEBI | Thymidine 5'-phosphate | ChEBI | Thymidine 5'-phosphoric acid | ChEBI | Thymidine monophosphate | ChEBI | Thymidine-5'-monophosphoric acid | ChEBI | THYMIDINE-5'-phosphATE | ChEBI | Thymidylate | ChEBI | Thymidylic acid | ChEBI | TMP | ChEBI | Deoxythymidine 5'-phosphate | Kegg | Deoxythymidylic acid | Kegg | 5'-Thymidylate | Generator | Deoxyribosylthymine monophosphoric acid | Generator | Ribothymidine 5'-monophosphoric acid | Generator | Thymidine 5'-(dihydrogen phosphoric acid) | Generator | Thymidine monophosphoric acid | Generator | Thymidine-5'-monophosphate | Generator | THYMIDINE-5'-phosphoric acid | Generator | Deoxythymidine 5'-phosphoric acid | Generator | Deoxythymidylate | Generator | 5-Thymidylate | Generator | 2'-Deoxythymidine 5'-monophosphate | HMDB | 5'-dTMP | HMDB | Deoxy TMP | HMDB | Deoxythymidine 5'-monophosphate | HMDB | Deoxythymidine monophosphate | HMDB | Deoxythymydilate | HMDB | Deoxythymydilic acid | HMDB | dTMP | HMDB | Thymidine 5'-monophosphate | HMDB | Thymidine 5'-phosphorate | HMDB | Thymidine 5'MP | HMDB | Thymidine mononucleotide | HMDB | Thymidine phosphate | HMDB | Thymidine-5'-monophosphorate | HMDB | Thymidylic acids | HMDB | Acids, thymidylic | HMDB | Acid, thymidylic | HMDB | monoPhosphate, thymidine | HMDB |
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Chemical Formula | C10H15N2O8P |
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Average Mass | 322.2085 Da |
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Monoisotopic Mass | 322.05660 Da |
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IUPAC Name | {[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy}phosphonic acid |
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Traditional Name | thymidylate |
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CAS Registry Number | 365-07-1 |
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SMILES | CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=O |
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InChI Identifier | InChI=1S/C10H15N2O8P/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(20-8)4-19-21(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,11,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1 |
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InChI Key | GYOZYWVXFNDGLU-XLPZGREQSA-N |
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Experimental Spectra |
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| Spectrum Type | Description | Depositor Email | Depositor Organization | Depositor | Deposition Date | View |
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1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 2D NMR | [1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Predicted Spectra |
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| Not Available | Chemical Shift Submissions |
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| Not Available | Species |
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Species of Origin | |
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Species Where Detected | |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with a monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. |
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Kingdom | Organic compounds |
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Super Class | Nucleosides, nucleotides, and analogues |
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Class | Pyrimidine nucleotides |
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Sub Class | Pyrimidine deoxyribonucleotides |
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Direct Parent | Pyrimidine 2'-deoxyribonucleoside monophosphates |
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Alternative Parents | |
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Substituents | - Pyrimidine 2'-deoxyribonucleoside monophosphate
- Pyrimidone
- Monoalkyl phosphate
- Hydropyrimidine
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Pyrimidine
- Alkyl phosphate
- Heteroaromatic compound
- Vinylogous amide
- Tetrahydrofuran
- Lactam
- Secondary alcohol
- Urea
- Oxacycle
- Azacycle
- Organoheterocyclic compound
- Hydrocarbon derivative
- Organic oxide
- Organooxygen compound
- Organonitrogen compound
- Organopnictogen compound
- Organic oxygen compound
- Alcohol
- Organic nitrogen compound
- Aromatic heteromonocyclic compound
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Molecular Framework | Aromatic heteromonocyclic compounds |
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External Descriptors | |
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Physical Properties |
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State | Solid |
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Experimental Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Predicted Properties | |
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General References | - Gribaudo G, Riera L, Caposio P, Maley F, Landolfo S: Human cytomegalovirus requires cellular deoxycytidylate deaminase for replication in quiescent cells. J Gen Virol. 2003 Jun;84(Pt 6):1437-41. [PubMed:12771412 ]
- Seno T, Ayusawa D, Shimizu K, Koyama H, Takeishi K, Hori T: Thymineless death and genetic events in mammalian cells. Basic Life Sci. 1985;31:241-63. [PubMed:3888175 ]
- Terai C, Carson DA: Pyrimidine nucleotide and nucleic acid synthesis in human monocytes and macrophages. Exp Cell Res. 1991 Apr;193(2):375-81. [PubMed:1706277 ]
- Gribaudo G, Riera L, Lembo D, De Andrea M, Gariglio M, Rudge TL, Johnson LF, Landolfo S: Murine cytomegalovirus stimulates cellular thymidylate synthase gene expression in quiescent cells and requires the enzyme for replication. J Virol. 2000 Jun;74(11):4979-87. [PubMed:10799571 ]
- Zhang X, Zhang J, Guo G, Mao X, Hu Y, Zou Q: Crystal structure of a flavin-dependent thymidylate synthase from Helicobacter pylori strain 26695. Protein Pept Lett. 2012 Nov;19(11):1225-30. doi: 10.2174/092986612803217105. [PubMed:22512654 ]
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