WordNet

street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
having the characteristics of an acid; "an acid reaction"

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/05/15 10:31:59」(JST)

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Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells.

van Heumen BW, Roelofs HM, Te Morsche RH, Marian B, Nagengast FM, Peters WH.SourceDepartment of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. b.vanheumen@mdl.umcn.nl
Experimental cell research.Exp Cell Res.2012 Apr 15;318(7):819-27. Epub 2012 Feb 14.
Chemoprevention would be a desirable strategy to avoid duodenectomy in patients with familial adenomatous polyposis (FAP) suffering from duodenal adenomatosis. We investigated the in vitro effects on cell proliferation, apoptosis, and COX-2 expression of the potential chemopreventives celecoxib and
PMID 22366264

Influenza A viral replication is blocked by inhibition of the inositol-requiring enzyme 1 (IRE1) stress pathway.

Hassan IH, Zhang MS, Powers LS, Shao JQ, Baltrusaitis J, Rutkowski DT, Legge K, Monick MM.SourceDepartment of Internal Medicine, University of Iowa, Iowa City, Iowa 52242, USA. ihab-hassan@uiowa.edu
The Journal of biological chemistry.J Biol Chem.2012 Feb 10;287(7):4679-89. Epub 2011 Dec 22.
Known therapies for influenza A virus infection are complicated by the frequent emergence of resistance. A therapeutic strategy that may escape viral resistance is targeting host cellular mechanisms involved in viral replication and pathogenesis. The endoplasmic reticulum (ER) stress response, also
PMID 22194594

Strain Differences in Deconjugation of Bile Acids in Bifidobacterium pseudocatenulatum Isolates

MARIAM Rezaei Sabet,YAP Keng Wai,LIM Long Chang,KHARIDAH Muhammad,SHUHAIMI Mustafa,ABDULLAH Sipat,ALI Abdul Manaf,ATIOAH Abdullah Nur,YAZID Abdul Manap
Bioscience and microflora 23(2), 93-98, 2004-04-01
… Six isolates of bifidobacteria with higher tolerance to 4.0% of bile were further evaluated for their ability to deconjugate different types of bile acids namely taurocholic acid (TC), glycocholic acid (GC), taurochenodeoxycholic acid (TCDC), glycochenodeoxycholic acid (GCDC), taurodeoxycholic acid (TDC), and glycodeoxycholic acid (GDC). …
NAID 10027995027

Triacylglycerol Lipase Participates in the Formation of n-Hexanal in Alfalfa Seedlings

Uno Chiharu,Hara Takashi,Joh Toshio
Food science and technology research 9(2), 185-189, 2003-05-01
… Taurodeoxycholic acid sodium salt (TDCA), an inhibitor of triacylglycerol lipase, inhibited the formation of n-hexanal by 36%. …
NAID 10012000683

Influence of Various Bile Acids on the Metabolism of Glycyrrhizin and Glycyrrhetic Acid by Ruminococcus sp. PO1-3 of Human Intestinal Bacteria

Akao Taiko
Biological & pharmaceutical bulletin 22(8), 787-793, 1999-08-15
… PO1-3,an intestinal bacterium isolated from human feces, metabolized glycyrrhizin (GL) to glycyrrhetic acid (GA) and GA to 3-oxo-glycyrrhetic acid (3-oxo-GA) and possessed GL β-D-glucuronidase and 3β-hydroxysteroid dehydrogenase (3β-HSD) involved in the metabolism of GL. …
NAID 110003639762

Taurodeoxycholic acid
Names
	IUPAC name 2-[[(4R)-4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10, 13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonic acid
Identifiers
CAS Registry Number	516-50-7
ChEBI	CHEBI:9410
ChEMBL	ChEMBL412272
ChemSpider	2015539
	InChI InChI=1S/C26H45NO6S/c1-16(4-9-24(30)27-12-13-34(31,32)33)20-7-8-21-19-6-5-17-14-18(28)10-11-25(17,2)22(19)15-23(29)26(20,21)3/h16-23,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17-,18-,19+,20-,21+,22+,23+,25+,26-/m1/s1 ; Key: AWDRATDZQPNJFN-VAYUFCLWSA-N ; InChI=1/C26H45NO6S/c1-16(4-9-24(30)27-12-13-34(31,32)33)20-7-8-21-19-6-5-17-14-18(28)10-11-25(17,2)22(19)15-23(29)26(20,21)3/h16-23,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17-,18-,19+,20-,21+,22+,23+,25+,26-/m1/s1; Key: AWDRATDZQPNJFN-VAYUFCLWBR ;
Jmol-3D images	Image
PubChem	2733768
	SMILES C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@@H]2[C@@]1([C@H](C[C@H]3[C@H]2CC[C@H]4[C@@]3(CC[C@H](C4)O)C)O)C ;
Properties
Chemical formula	C26H44NO6S-
Molar mass	498.70 g/mol
	Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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	Infobox references