| 词条 | L-Deoxyribose |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 424873481 | Name = L-Deoxyribose | ImageFileL1 = L-Deoxyribose.png | ImageFileR1 = L-Deoxyribose chain.png | IUPACName = (3R,4S)-3,4,5-Trihydroxypentanal | OtherNames = 2-Deoxy-L-erythro-pentose; 2-Deoxy-L-ribose; L-2-Deoxyribose |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 18546-37-7 | PubChem = 6994527 | PubChem1 = 9855484 | PubChem1_Comment = hemiacetal | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 5362530 | ChemSpiderID1_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID1 = 8031184 | ChemSpiderID1_Comment = hemiacetal | SMILES = O=CC[C@@H](O)[C@@H](O)CO | SMILES1 = OC[C@@H]1OC(O)C[C@H]1O | SMILES1_Comment = hemiacetal | InChI = 1/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1 | InChIKey = ASJSAQIRZKANQN-UHNVWZDZBB | InChI1 = 1/C5H10O4/c6-2-4-3(7)1-5(8)9-4/h3-8H,1-2H2/t3-,4+,5?/m1/s1 | InChI1_Comment = hemiacetal | InChIKey1 = PDWIQYODPROSQH-OVEKKEMJBQ | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = ASJSAQIRZKANQN-UHNVWZDZSA-N | InChI3 = 1S/C5H10O4/c6-2-4-3(7)1-5(8)9-4/h3-8H,1-2H2/t3-,4+,5?/m1/s1 | InChI3_Comment = hemiacetal | InChIKey3 = PDWIQYODPROSQH-OVEKKEMJSA-N }} |Section2={{Chembox Properties | C=5 | H=10 | O=4 | Appearance = White solid | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} L-Deoxyribose is an organic compound with formula C5H10O4. It is a synthetic monosaccharide, a stereoisomer (mirror image) of the natural compound D-deoxyribose. L-Deoxyribose can be synthesized from D-galactose.[1] It has been used in chemical research, e.g. in the synthesis of mirror-image DNA.[2]References1. ^ SHI Zhen-Dan, YANG Bing-Hui, and WU Yu-Lin (2002), A stereospecific synthesis of L-deoxyribose, L-ribose and L-ribosides. Tetrahedron, volume 58, issue 16, pp. 3287–3296 {{DEFAULTSORT:Deoxyribose, L-}}{{organic-compound-stub}}2. ^ Hidehito Urata, Emiko Ogura, Keiko Shinohara, Yoshiaki Ueda and Masao Akagi (1992), Synthesis and properties of mirror-image DNA. Nucleic Acids Research, volume 20 issue 13, pp. 3325-3332 2 : Deoxy sugars|Aldopentoses |
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