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Chenodeoxycholic acid-13C

MCE 國際站：Chenodeoxycholic acid-13C

品牌：MedChemExpress (MCE)

貨號：HY-76847S2

CAS：52918-92-0

中文名稱：鵝去氧膽酸-13C

Synonyms：鵝去氧膽酸-13C; CDCA-13C

純度：≥98.0%

存儲條件：4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

運輸條件：美國大陸的室溫；其他地方可能有所不同。

產(chǎn)品活性：Chenodeoxycholic acid-13C 是一種 13C 標記的 Chenodeoxycholic Acid。Chenodeoxycholic Acid 是一種疏水初級膽汁酸，能夠活化核受體 FXR，該受體與膽固醇代謝有關。

生物活性：鵝去氧膽酸-13C 是 13C 標記的鵝去氧膽酸。鵝去氧膽酸是一種疏水性初級膽汁酸，可激活參與膽固醇代謝的核受體 (FXR)。

體外：氫、碳和其他元素的穩(wěn)定重同位素已被整合到藥物分子中，主要用作藥物開發(fā)過程中定量的示蹤劑。氘化因其可能影響藥物的藥代動力學和代謝特征而受到關注[1]。MCE 尚未獨立證實這些方法的準確性。它們僅供參考。

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參考文獻：

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
[2]. Stauffer AT, et al. Chenodeoxycholic acid and deoxycholic acid inhibit 11 beta-hydroxysteroid dehydrogenase type 2 and cause cortisol-induced transcriptional activation of the mineralocorticoid receptor. J Biol Chem. 2002 Jul 19;277(29):26286-92
[3]. Casaburi I, et al. Chenodeoxycholic acid through a TGR5-dependent CREB signaling activation enhances cyclin D1 expression and promotes human endometrial cancer cell proliferation. Cell Cycle. 2012 Jul 15;11(14):2699-710
[4]. Kawabe Y, et al. The molecular mechanism of the induction of the low density lipoprotein receptor by chenodeoxycholic acid in cultured human cells. Biochem Biophys Res Commun. 1995 Mar 8;208(1):405-11.
[5]. Ao M, et al. Chenodeoxycholic acid stimulates Cl(-) secretion via cAMP signaling and increases cystic fibrosis transmembrane conductance regulator phosphorylation in T84 cells. Am J Physiol Cell Physiol. 2013 Aug 15;305(4):C447-56
[6]. Noh K, et al. Farnesoid X receptor activation by chenodeoxycholic acid induces detoxifying enzymes through AMP-activated protein kinase and extracellular signal-regulated kinase 1/2-mediated phosphorylation of CCAAT/enhancer binding protein β. Drug Metab