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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/04/10 11:47:00」(JST)

English Journal

Comparative evaluation of in vitro efficacy of colesevelam hydrochloride tablets.

Krishnaiah YS, Yang Y, Bykadi S, Sayeed VA, Khan MA.SourceDivision of Product Quality Research, Office of Testing and Research, Office of Pharmaceutical Sciences, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring , MD , USA and.
Drug development and industrial pharmacy.Drug Dev Ind Pharm.2013 Jun 27. [Epub ahead of print]
Abstract Context: Colesevelam hydrochloride is used as an adjunct to diet and exercise to reduce elevated low-density lipoprotein (LDL) cholesterol in patients with primary hyperlipidemia as well as to improve glycemic control in patients with type 2 diabetes. This is likely to result in submission
PMID 23805883

Porcine pancreatic lipase related protein 2 has high triglyceride lipase activity in the absence of colipase.

Xiao X, Ross LE, Sevilla WA, Wang Y, Lowe ME.SourceDepartment of Pediatrics, Children's Hospital of Pittsburgh of the University of Pittsburgh Medical Center, Pittsburgh, PA 15224, USA.
Biochimica et biophysica acta.Biochim Biophys Acta.2013 Jun 13;1831(9):1435-1441. doi: 10.1016/j.bbalip.2013.06.002. [Epub ahead of print]
Efficient dietary fat digestion is essential for newborns who consume more dietary fat per body weight than at any other time of life. In many mammalian newborns, pancreatic lipase related protein 2 (PLRP2) is the predominant duodenal lipase. Pigs may be an exception since PLRP2 expression has been
PMID 23770034

Separation of phthalates by cyclodextrin modified micellar electrokinetic chromatography: Quantitation in perfumes.

Pérez-Fernández V, González MJ, García MÁ, Marina ML.SourceDepartment of Analytical Chemistry, Faculty of Chemistry, University of Alcalá, Spain. Electronic address: virginia.perezf@uah.es.
Analytica chimica acta.Anal Chim Acta.2013 Jun 11;782:67-74. doi: 10.1016/j.aca.2013.03.072. Epub 2013 Apr 22.
A new CE method has been developed for the simultaneous separation of a group of parent phthalates. Due to the neutral character of these compounds, the addition of several bile salts as surfactants (sodium cholate (SC), sodium deoxycholate (SDC), sodium taurodeoxycholate (STDC), sodium taurocholate
PMID 23708286

村田慶史,中村倫子,小藤恭子,磯部隆史,岸利弘
日本食品科学工学会誌 : Nippon shokuhin kagaku kogaku kaishi = Journal of the Japanese Society for Food Science and Technology 58(9), 428-432, 2011-09-15
α-リポ酸（ALA）を用いたキトサンの塩，CS-ALAを調製し，一次胆汁酸あるいは二次胆汁酸の吸着，並びにALA放出挙動を調べた．また，CA-ALAを含有したアルギン酸カルシウムゲルビーズ（Alg-Ca）の調製と経口摂取用の担体としての機能についても検討した．一次胆汁酸であるタウロコール酸の溶液中において，CS-ALAはALAを放出すると同時にその胆汁酸を吸着し，また，二次胆汁酸のタウロデオキシコ …
NAID 10029722638

リンク元	「taurodeoxycholic acid」「タウロデオキシコール酸」

Taurodeoxycholic acid
	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 number	516-50-7
PubChem	2733768
ChemSpider	2015539
ChEBI	CHEBI:9410
ChEMBL	CHEMBL412272
Jmol-3D images	Image 1
	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 ;
	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 ;
Properties
Molecular formula	C26H44NO6S-
Molar mass	498.70 g/mol
	(verify) (what is: /?); Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
	Infobox references