Tauroursodeoxycholic Acid (TUDCA)

製品コード：S3654 純度：99.97%

Tauroursodeoxycholic acid (TUDCA) is the taurine conjugate of ursodeoxycholic acid (UDCA) that acts as a mitochondrial stabilizer and anti-apoptotic agent in several models of neurodegenerative diseases, including AD, Parkinson's diseases (PD), and Huntington's diseases (HD).

CAS No. 14605-22-2

サイズ	価格(税別)	在庫状況
10mM (1mL in DMSO)	JPY 29500	国内在庫あり
25mg	JPY 22000	国内在庫あり
1g	JPY 145500	国内在庫なし(納期7~10日)

代表番号: 045-509-1970\|電子メール：[email protected] よく尋ねられる質問

文献中Selleckの製品使用例（30）

製品安全説明書

現在のバッチを見る：純度： 99.97%

99.97

Tauroursodeoxycholic Acid (TUDCA)関連製品

関連化合物ライブラリー	FDA-approved Drug Library Natural Product Library Neuronal Signaling Compound Library CNS-Penetrant Compound Library Anti-alzheimer Disease Compound Library	もっと見る

Apoptosis related阻害剤の選択性比較

Cell Data

Cell Lines	Assay Type	Concentration	Incubation Time	活性情報	PMID
HuH7	Cytoprotective assay	1 mM	24 hrs	Cytoprotective activity against DCA-induced cell death in human HuH7 cells assessed as increase in cell viability at 1 mM preincubated with cells followed by DCA addition measured after 24 hrs by MTT/INCELL assay	27729186
HEK293	Function assay		90 mins	Inhibition of human ATX expressed in HEK293 Flp-In cells assessed as decrease in choline release from LPC measured every 30 secs for 90 mins by HVA based fluorescence assay, IC50=10.3μM	28165241
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against tunicamycin-induced ER stress in human HuH7 cells assessed as inhibition of CHOP mRNA levels after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against DCA-induced ER stress in human HuH7 cells assessed as increase in XBPu mRNA levels after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against tunicamycin-induced ER stress in human HuH7 cells assessed as increase in XBPu mRNA levels after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against DCA-induced ER stress in human HuH7 cells assessed as inhibition of XBPs mRNA levels after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against tunicamycin-induced ER stress in human HuH7 cells assessed as inhibition of XBPs mRNA levels after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against tunicamycin-induced ER stress in human HuH7 cells assessed as reduction in XBPs/XBPu ratio after 6 hrs	27729186
HuH7	Cytoprotective assay		6 hrs	Cytoprotective activity against tunicamycin-induced ER stress in human HuH7 cells assessed as inhibition of BIP/GRP78 mRNA levels after 6 hrs	27729186
CHO cells	Function assay			Agonist activity at human TGR5 expressed in CHO cells by luciferase assay, EC50=30 μM	18307294
Sf9	Function assay			TP_TRANSPORTER: uptake in membrane vesicles from Bsep-expressing Sf9 cells, Km=4.1μM	10648470
MDCK	Function assay			TP_TRANSPORTER: uptake in Oatp3-expressing MDCK cells, Km=6.6μM	11093941
Sf9	Function assay			TP_TRANSPORTER: uptake in membrane vesicles isolated from Bsep-expressing Sf9 cells, Km=11.9μM	12404240
CHO	Function assay			TP_TRANSPORTER: uptake in Ntcp-expressing CHO cells, Km=14μM	9486191
COS	Function assay			TP_TRANSPORTER: inhibition of Taurocholate uptake in ASBT-expressing COS cells, Ki=28μM	9458785
HEK293	Function assay			Non-competitive inhibition of human ATX expressed in HEK293 Flp-In cells assessed as decrease in LPC hydrolysis by Lineweaver-Burk plot analysis	28165241
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生物活性

製品説明	Tauroursodeoxycholic acid (TUDCA) is the taurine conjugate of ursodeoxycholic acid (UDCA) that acts as a mitochondrial stabilizer and anti-apoptotic agent in several models of neurodegenerative diseases, including AD, Parkinson's diseases (PD), and Huntington's diseases (HD).

In Vitro
In vitro	Tauroursodeoxycholic acid (TUDCA) is an endogenous hydrophilic tertiary bile acid produces in humans at a low level. In ER stress conditions, TUDCA treatment of MSCs (mesenchymal stem cells) reduces the activation of ER stress-associated proteins, including GRP78, PERK, eIF2α, ATF4, IRE1α, JNK, p38, and CHOP, and inhibits the dissociation between GRP78 and PERK, resulting in reduced ER stress-mediated cell death. TUDCA treatment increases PrP^C (Cellular prion protein) expression. TUDCA regulates stem cell differentiation into various lineages such as adipogenic and osteogenic lineages. TUDCA attenuates ER stress, prevents unfolded protein response dysfunction, and stabilizes mitochondria. Under ER stress, treatment with TUDCA significantly increases the expression of BCL-2 and significantly decreases the expression of Bax, cleaved caspase-3, and cleaved PARP-1, compared with that of untreated cells^[1].
細胞実験	細胞株	Mesenchymal stem cells (MSCs)
	濃度	100 μM
	反応時間	30 min
	実験の流れ	MSCs are washed twice with phosphate buffer saline (PBS), and fresh α-MEM supplemented with 10% FBS is added. To investigate the apoptosis signaling pathway, MSCs are pretreated with TUDCA (100 μM) at 37 °C for 30 min and then treated with H2O2 (200 μM) for various times (0, 2, 4, 6, or 8 h). To assess another cell signaling pathway, MSCs are treated with an Akt inhibitor (10⁻⁶ M) for 30 min at 37 °C before treatment with TUDCA.
実験結果図	Methods	Biomarkers	結果図	PMID
	Western blot	p-Akt / Akt PrPc CHOP / Caspase-12 / Cleaved caspase-12 RIPK1 / RIPK3 / p-RIPK1 / p-RIPK3		28004805
	Growth inhibition assay	Cell viability		30038553

In Vivo
In Vivo	TUDCA is effective for treating cholestatic liver diseases. It also has an ameliorating effect on several diseases, including neurodegenerative diseases, osteoarthritis, vascular diseases, and diabetes. In a murine hindlimb ischemia model, TUDCA-treated mesenchymal stem cells (MSCs) transplantation augments the blood perfusion ratio, vessel formation, and transplanted cell survival more than untreated MSC transplantation does. Augmented functional recovery following MSC transplantation is blocked by PrP^C downregulation^[1]. Several studies in animals have shown that TUDCA, an endogenous ambiphilic bile acid, can inhibit unfolded protein response dysfunction and ameliorate ER stress. TUDCA administration attenuates HDM-induced ER stress, airway inflammation, mucus metaplasia, airway remodeling, and methacholine-induced AHR^[2].
動物実験	動物モデル	House dust mite-induced allergic airway disease mouse model (background: C57BL/6 NJ mice)
	投与量	0.5, 1, and 5 mg/kg body wt
	投与経路	via the nasopharynx

NCT Number	Recruitment	Conditions	Sponsor/Collaborators	Start Date	Phases
臨床試験 (data from https://clinicaltrials.gov, updated on 2024-01-11)
NCT05753852	Recruiting	Amyotrophic Lateral Sclerosis	Humanitas Mirasole SpA\|University of Ulm\|University of Sheffield\|University Hospital Tours\|KU Leuven\|UMC Utrecht\|University of Dublin Trinity College\|Bruschettini S.r.l.\|Istituto Superiore di Sanità\|Motor Neurone Disease Association	October 25 2021	Phase 3
NCT04114292	Unknown status	Ulcerative Colitis	Washington University School of Medicine\|Crohn''s and Colitis Foundation	January 17 2019	Phase 1
NCT01899703	Completed	Cholestasis Intrahepatic	GlaxoSmithKline	March 10 2014	Phase 2

参考
[1] Yoon YM, et al. Sci Rep. 2016, 6:39838. [2] Siddesha JM, et al. Am J Physiol Lung Cell Mol Physiol. 2016, 310(11):L1243-59.

参考

化学情報

分子量	499.70	化学式	C₂₆H₄₅NO₆S
CAS No.	14605-22-2	SDF	Download Tauroursodeoxycholic Acid (TUDCA) SDFをダウンロードする
Smiles	CC(CCC(=O)NCCS(=O)(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	1年-80°Cin solvent
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	1个月-20°Cin solvent

In vitro
Batch:

DMSO : 100 mg/mL ( (200.12 mM)；吸湿したDMSOは溶解度を減少させます。新しいDMSOをご使用ください。)

Water : 100 mg/mL

Ethanol : 50 mg/mL

モル濃度計算器

in vivo
Batch:

Add solvents to the product individually and in order.

投与溶液組成計算機

実験計算

モル濃度計算器

質量	濃度	体積	分子量
=	×	×

希釈計算器分子量計算器

投与溶液組成計算機(クリア溶液)

ステップ１：実験データを入力してください。（実験操作によるロスを考慮し、動物数を1匹分多くして計算・調製することを推奨します）

投与量 mg/kg 動物平均体重 g 投与体積（動物毎）μL 動物数匹

ステップ２：投与溶媒の組成を入力してください。（ロット毎に適した溶解組成が異なる場合があります。詳細については弊社までお問い合わせください）

% DMSO + % + % Tween 80 + % ddH₂O

%DMSO+ %

計算結果：

投与溶媒濃度： mg/ml;

DMSOストック溶液調製方法： mg 試薬を μL DMSOに溶解する（濃度 mg/mL, 注：濃度が当該ロットのDMSO溶解度を超える場合はご連絡ください。 )

投与溶媒調製方法：Take μL DMSOストック溶液に μL PEG300，を加え、完全溶解後μL Tween 80，を加えて完全溶解させた後 μL ddH₂O，を加え完全に溶解させます。

投与溶媒調製方法：μL DMSOストック溶液に μL Corn oil，を加え、完全溶解。

注意：１.ストック溶液に沈殿、混濁などがないことをご確認ください；
２.順番通りに溶剤を加えてください。次のステップに進む前に溶液に沈殿、混濁などがないことを確認してから加えてください。ボルテックス、ソニケーション、水浴加熱など物理的な方法で溶解を早めることは可能です。

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Handling Instructions

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* 必須

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C6=C5/X	C6:	LOG(C6):
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C8=C7/X	C8:	LOG(C8):