| 词条 | 5,6-Dihydroxycytosine |
| 释义 |
| ImageFile = 5,6-Dihydroxycytosine.svg | ImageSize = 150px | ImageAlt = | IUPACName = 6-Amino-5-hydroxy-2,4(1H,3H)-pyrimidinedione | OtherNames = 6-Amino-2,4,5-trihydroxypyrimidine; Isouramil | Section1 = {{Chembox Identifiers | CASNo = 3914-34-9 | PubChem = 77518 | ChemSpiderID = 69925 | SMILES = c1(c([nH]c(=O)[nH]c1=O)N)O | InChI=1S/C4H5N3O3/c5-2-1(8)3(9)7-4(10)6-2/h8H,(H4,5,6,7,9,10) | InChIKey=SPOYOCCBDWULRZ-UHFFFAOYSA-N | Section2 = {{Chembox Properties | C=4|H=5|N=3|O=3 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}5,6-Dihydroxycytosine can be formed from treatment of DNA with osmium tetroxide.[1] References1. ^{{cite journal | pmid = 3741404 |pmc=1146717|title=Formation of cytosine glycol and 5,6-dihydroxycytosine in deoxyribonucleic acid on treatment with osmium tetroxide|journal=The Biochemical Journal|volume=235|issue=2|pages=531–6|year=1986|author1=Dizdaroglu|first1=M|last2=Holwitt|first2=E|last3=Hagan|first3=M. P.|last4=Blakely|first4=W. F.|doi=10.1042/bj2350531}} {{DEFAULTSORT:Dihydroxycytosine, 5,6-}}{{Organic-compound-stub}} 3 : DNA|Biochemistry|Pyrimidinediones |
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