デオキシウリジン
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/02/13 11:05:51」(JST)
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Deoxyuridine |
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Identifiers |
CAS number |
951-78-0 Y |
PubChem |
640 |
ChemSpider |
13118 Y |
UNII |
W78I7AY22C Y |
MeSH |
Deoxyuridine |
ChEBI |
CHEBI:16450 N |
ChEMBL |
CHEMBL353955 N |
Jmol-3D images |
Image 1 |
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O=C/1NC(=O)N(\C=C\1)[C@@H]2O[C@@H]([C@@H](O)C2)CO
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InChI=1S/C9H12N2O5/c12-4-6-5(13)3-8(16-6)11-2-1-7(14)10-9(11)15/h1-2,5-6,8,12-13H,3-4H2,(H,10,14,15)/t5-,6+,8+/m0/s1 Y
Key: MXHRCPNRJAMMIM-SHYZEUOFSA-N Y
InChI=1/C9H12N2O5/c12-4-6-5(13)3-8(16-6)11-2-1-7(14)10-9(11)15/h1-2,5-6,8,12-13H,3-4H2,(H,10,14,15)/t5-,6+,8+/m0/s1
Key: MXHRCPNRJAMMIM-SHYZEUOFBK
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Properties |
Molecular formula |
C9H12N2O5 |
Molar mass |
228.202 |
N (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
Infobox references |
Deoxyuridine is a compound and a nucleoside. It is similar in chemical structure to uridine, but without the 2'-hydroxyl group.
Idoxuridine and Trifluridine are variants of deoxyuridine used as antiviral drugs. They are similar enough to be incorporated as part of DNA replication, but they possess side groups on the uracil component (an iodine and a CF3 group, respectively), that prevent base pairing.
Nucleic acid constituents
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Nucleobase |
- Purine
- Adenine
- Guanine
- Hypoxanthine
- Xanthine
- Purine analogue
- Pyrimidine
- Uracil
- Thymine
- Cytosine
- Pyrimidine analogue
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Nucleoside |
Ribonucleoside |
- Adenosine
- Guanosine
- 5-Methyluridine
- Uridine
- Cytidine
- Inosine
- Xanthosine
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Deoxyribonucleoside |
- Deoxyadenosine
- Deoxyguanosine
- Thymidine
- Deoxyuridine
- Deoxycytidine
- Deoxyinosine
- Deoxyxanthosine
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Nucleotide
(Nucleoside monophosphate) |
Ribonucleotide |
- AMP
- GMP
- m5UMP
- UMP
- CMP
- IMP
- XMP
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Deoxyribonucleotide |
- dAMP
- dGMP
- dTMP
- dUMP
- dCMP
- dIMP
- dXMP
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Cyclic nucleotide |
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Nucleoside diphosphate |
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Nucleoside triphosphate |
- ATP
- GTP
- m5UTP
- UTP
- CTP
- ITP
- XTP
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- dATP
- dGTP
- dTTP
- dUTP
- dCTP
- dITP
- dXTP
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- Biochemical families: carbohydrates
- alcohols
- glycoproteins
- glycosides
- lipids
- eicosanoids
- fatty acids / intermediates
- phospholipids
- sphingolipids
- steroids
- nucleic acids
- constituents / intermediates
- proteins
- Amino acids / intermediates
- tetrapyrroles / intermediates
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English Journal
- A new bioassay identifies proliferation ratios of fibroblasts and myofibroblasts.
- Vaughan MB1, Odejimi TD, Morris TL, Sawalha D, Spencer CL.
- Cell biology international.Cell Biol Int.2014 Aug;38(8):981-6. doi: 10.1002/cbin.10289. Epub 2014 May 6.
- Myofibroblasts are resident cells of wound healing, contractures and fibroses; these tissues are often referred to as fibroproliferative. Whether myofibroblasts themselves proliferate is of interest. Since many in vitro cultures are heterogeneous, staining in situ is required to identify the myofibr
- PMID 24764319
- Depletion of Kupffer cells modulates ethanol-induced hepatocyte DNA synthesis in C57Bl/6 mice.
- Owumi SE1, Corthals SM, Uwaifo AO, Kamendulis LM, Klaunig JE.
- Environmental toxicology.Environ Toxicol.2014 Aug;29(8):867-75. doi: 10.1002/tox.21814. Epub 2012 Sep 20.
- Kupffer cells (KCs) are important in hepatic homeostasis and responses to xenobiotics. KCs are activated on interaction with endotoxin, releasing cytokines, and reactive oxygen species normally associated with increased gene expression, cellular growth, or hepatic injury. Ethanol-induced endotoxemia
- PMID 22996800
- Effects of 5'-fluoro-2-deoxyuridine on mitochondrial biology in Caenorhabditis elegans.
- Rooney JP1, Luz AL1, González-Hunt CP1, Bodhicharla R1, Ryde IT1, Anbalagan C1, Meyer JN2.
- Experimental gerontology.Exp Gerontol.2014 Aug;56:69-76. doi: 10.1016/j.exger.2014.03.021. Epub 2014 Apr 3.
- 5-Fluoro-2'-deoxyuridine (FUdR) is a DNA synthesis inhibitor commonly used to sterilize Caenorhabditis elegans in order to maintain a synchronized aging population of nematodes, without contamination by their progeny, in lifespan experiments. All somatic cells in the adult nematode are post-mitotic
- PMID 24704715
Japanese Journal
- Identification of tympanic border cells as slow-cycling cells in the cochlea.
- Taniguchi Mirei,Yamamoto Norio,Nakagawa Takayuki,Ogino Eriko,Ito Juichi
- PloS one 7(10), 2012-10-31
- … In this study, using the exogenous proliferation marker, 5'-bromo-2'-deoxyuridine (BrdU) in combination with the endogenous proliferation marker Ki-67, we identified tympanic border cells. …
- NAID 120004945149
- Luteolin Inhibits Angiotensin II-Induced Human Umbilical Vein Endothelial Cell Proliferation and Migration Through Downregulation of Src and Akt Phosphorylation
- Zhu Manyi,Chen Dan,Li Dongye,Ding Hong,Zhang Tian,Xu Tongda,Zhang Yanbin
- Circulation Journal, 2012
- … Analysis using methyl thiazolyl tetrazolium and 5-ethynyl-2'-deoxyuridine revealed that 25μmol/L luteolin had a particularly inhibitory effect on the AngII-induced proliferation of HUVECs. …
- NAID 130002491327
- Neuroprotective Capabilities of Tanshinone IIA against Cerebral Ischemia/Reperfusion Injury via Anti-apoptotic Pathway in Rats
- Chen Yanlin,Wu Xuemei,Yu Shanshan [他],Fauzee Nilufer Jasmine Selimah,Wu Jingxian,Li Lan,Zhao Jing,Zhao Yong
- Biological and Pharmaceutical Bulletin 35(2), 164-170, 2012
- … Fewer terminal deoxyribonucleotidyl transferase-mediated deoxyuridine triphosphate biotin nick-end labeling (TUNEL)-positive cells were found in the penumbra of the treated group, but they were significantly more common in the vehicle group. …
- NAID 130001872289
Related Links
- ウィキペディアの英語版でDeoxyuridineという用語が挙げてありますが、そこでは、以下の意味で使われています。Deoxyuridine is a compound and a nucleoside. It is similar in chemical structure to uridine, but without the 2'-hydroxyl group. ...
- [5-Iodo-2'-deoxyuridine] [54-42-2] | 価格や在庫、物性値などの詳細情報ページです。 ... ・川口の在庫は即日,つくばの在庫は2〜3日以内の出荷となります。・詳細につきましては,お手数ですが営業部までお問い合わせください。
★リンクテーブル★
[★]
デオキシウリジン一リン酸
- 関
- dUMP
[★]
ブロモデオキシウリジン BrdU
[★]
5-フルオロデオキシウリジン