- 関
- 3-O-methyl-D-glucose
WordNet
- the 15th letter of the Roman alphabet (同)o
- the blood group whose red cells carry neither the A nor B antigens; "people with type O blood are universal donors" (同)type_O, group O
PrepTutorEJDIC
- 《呼び掛けの名前の前につけて》『おお』,あ / (驚き・恐れ・喜び・苦痛などを表して)『おお』,ああ,まあ / 《肯定・否定を強めて》
- oxygenの化学記号
- ohmオーム / Old
- osmiumの化学記号
English Journal
- Selective sodium-dependent glucose transporter 1 inhibitors block glucose absorption and impair glucose-dependent insulinotropic peptide release.
- Dobbins RL1, Greenway FL2, Chen L3, Liu Y3, Breed SL3, Andrews SM3, Wald JA3, Walker A3, Smith CD3.
- American journal of physiology. Gastrointestinal and liver physiology.Am J Physiol Gastrointest Liver Physiol.2015 Jun 1;308(11):G946-54. doi: 10.1152/ajpgi.00286.2014. Epub 2015 Mar 12.
- GSK-1614235 and KGA-2727 are potent, selective inhibitors of the SGLT1 sodium-dependent glucose transporter. Nonclinical (KGA-2727) and clinical (GSK-1614235) trials assessed translation of SGLT1 inhibitor effects from rats to normal human physiology. In rats, KGA-2727 (0.1 mg/kg) or vehicle was giv
- PMID 25767259
- Caffeine inhibits glucose transport by binding at the GLUT1 nucleotide-binding site.
- Sage JM1, Cura AJ2, Lloyd KP1, Carruthers A3.
- American journal of physiology. Cell physiology.Am J Physiol Cell Physiol.2015 May 15;308(10):C827-34. doi: 10.1152/ajpcell.00001.2015. Epub 2015 Feb 25.
- Glucose transporter 1 (GLUT1) is the primary glucose transport protein of the cardiovascular system and astroglia. A recent study proposes that caffeine uncompetitive inhibition of GLUT1 results from interactions at an exofacial GLUT1 site. Intracellular ATP is also an uncompetitive GLUT1 inhibitor
- PMID 25715702
- Return of the glucoreceptor: Glucose activates the glucose-sensing receptor T1R3 and facilitates metabolism in pancreatic β-cells.
- Kojima I1, Nakagawa Y1, Ohtsu Y1, Hamano K1, Medina J1, Nagasawa M1.
- Journal of diabetes investigation.J Diabetes Investig.2015 May;6(3):256-63. doi: 10.1111/jdi.12304. Epub 2014 Dec 15.
- Subunits of the sweet taste receptor, namely T1R2 and T1R3, are expressed in mouse pancreatic islets. Quantitatively, the expression of messenger ribonucleic acid for T1R2 is much lower than that of T1R3, and immunoreactive T1R2 is in fact undetectable. Presumably, a homodimer of T1R3 could function
- PMID 25969708
Japanese Journal
- Identification of more than 200 glucose-responsive Arabidopsis genes none of which responds to 3-O-methylglucose or 6-deoxyglucose
- VILLADSEN D
- Plant Mol Biol 55, 467-477, 2004
- NAID 80017150747
- Effect of the Opioid Antagonist Naloxone on the Regional Metabolic Rate for Glucose in the Conscious Rat Brain
- SUZUKI Toyofumi,TOMONO Kazuo,HANANO Manabu
- Biological & pharmaceutical bulletin 22(11), 1217-1221, 1999-11-15
- … For quantitative evaluation of the functional activity in brain, the regional cerebral metabolic rate for glucose (rCMR_<glc>) was measured by the double tracer technique, using [^<14>C]2-deoxyglucose and [^3H]3-O-methylglucose. …
- NAID 110003639578
Related Links
- "3-O-Methylglucose" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are ... A non-metabolizable glucose analogue that is not phosphorylated by ...
- 3-O-Methylglucose (n.) 1. (MeSH) A non-metabolizable glucose analogue that is not phosphorylated by hexokinase. 3-O-Methylglucose is used as a marker to assess ... Webmaster Solution Alexandria A windows (pop-into) of ...
Related Pictures
★リンクテーブル★
| リンク元 | 「3-O-メチルグルコース」 |
| 関連記事 | 「O」「Os」 |
「3-O-メチルグルコース」
「O」
- 同
- 食道入口部