| Record Information |
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| Version | 2.0 |
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| Creation Date | 2012-05-31 14:19:58 -0600 |
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| Update Date | 2015-06-03 17:19:00 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | Se-Adenosylselenomethionine |
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| Description | Se-Adenosylselenomethionine is an intermediate in Selenoamino acid metabolism. Se-Adenosylselenomethionine is converted from Selenomethionine via the enzyme S-adenosylmethionine synthetase (EC 2.5.1.6). It is then |
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| Structure | |
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| Synonyms: | Not Available |
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| Chemical Formula: | C15H23N6O5Se |
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| Weight: | Average: 446.34
Monoisotopic: 447.089514704 |
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| InChI Key: | GGJFWMOVUFBSIN-YDBXVIPQSA-O |
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| InChI: | InChI=1S/C15H22N6O5Se/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/p+1/t7?,8-,10-,11-,14-,27?/m1/s1 |
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| CAS number: | Not Available |
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| IUPAC Name: | (3-amino-3-carboxypropyl)({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl})methylselanium |
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| Traditional IUPAC Name: | se-adenosylselenomethionine |
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| SMILES: | C[Se+](CCC(N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives. |
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| Kingdom | Organic compounds |
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| Super Class | Nucleosides, nucleotides, and analogues |
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| Class | 5'-deoxyribonucleosides |
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| Sub Class | Not Available |
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| Direct Parent | 5'-deoxyribonucleosides |
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| Alternative Parents | |
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| Substituents | - 5'-deoxyribonucleoside
- N-glycosyl compound
- Glycosyl compound
- Pentose monosaccharide
- 6-aminopurine
- Alpha-amino acid
- Alpha-amino acid or derivatives
- Imidazopyrimidine
- Purine
- Aminopyrimidine
- N-substituted imidazole
- Monosaccharide
- Pyrimidine
- Imidolactam
- Imidazole
- Tetrahydrofuran
- Heteroaromatic compound
- Azole
- Secondary alcohol
- 1,2-diol
- Amino acid or derivatives
- Amino acid
- Oxacycle
- Azacycle
- Carboxylic acid derivative
- Carboxylic acid
- Organoheterocyclic compound
- Selenoether
- Monocarboxylic acid or derivatives
- Organic oxide
- Organopnictogen compound
- Alcohol
- Carbonyl group
- Organic oxygen compound
- Organic nitrogen compound
- Amine
- Primary amine
- Primary aliphatic amine
- Hydrocarbon derivative
- Organoselenium compound
- Organooxygen compound
- Organonitrogen compound
- Organic cation
- Aromatic heteropolycyclic compound
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| Molecular Framework | Aromatic heteropolycyclic compounds |
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| External Descriptors | Not Available |
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| Physical Properties |
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| State: | Solid |
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| Charge: | 1 |
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| Melting point: | Not Available |
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| Experimental Properties: | |
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| Predicted Properties | |
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| Biological Properties |
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| Cellular Locations: | Cytoplasm |
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| Reactions: | |
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| SMPDB Pathways: | Not Available |
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| KEGG Pathways: | Not Available |
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| EcoCyc Pathways: | Not Available |
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| Concentrations |
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| Not Available |
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| Spectra |
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| Spectra: | |
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| References |
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| References: | - Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510
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| Synthesis Reference: | Not Available |
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| Material Safety Data Sheet (MSDS) | Not Available |
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| Links |
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| External Links: | | Resource | Link |
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| CHEBI ID | Not Available | | HMDB ID | HMDB11118 | | Pubchem Compound ID | 24892761 | | Kegg ID | C05691 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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