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Merck

C6240

Sigma-Aldrich

CITCO

≥98% (HPLC), solid

别名:

6-(4-氯苯基)咪唑并[2,1-b][1,3]噻唑-5-甲醛O-(3,4-二氯苄基)肟

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About This Item

经验公式(希尔记法):
C19H12N3OCl3S
分子量:
436.74
MDL號碼:
分類程式碼代碼:
12352203
PubChem物質ID:
NACRES:
NA.77

化驗

≥98% (HPLC)

形狀

solid

儲存條件

desiccated

溶解度

DMSO: soluble 28 mg/mL
H2O: insoluble

儲存溫度

−20°C

SMILES 字串

Clc1ccc(cc1)-c2nc3sccn3c2\C=N\OCc4ccc(Cl)c(Cl)c4

InChI

1S/C19H12Cl3N3OS/c20-14-4-2-13(3-5-14)18-17(25-7-8-27-19(25)24-18)10-23-26-11-12-1-6-15(21)16(22)9-12/h1-10H,11H2/b23-10+

InChI 密鑰

ZQWBOKJVVYNKTL-AUEPDCJTSA-N

一般說明

CITCO是一种咪唑并噻唑衍生物。它刺激人类组成型雄烷受体(CAR)核易位。

應用

CITCO已用于小鼠组成型雄烷受体(CAR)和人CAR的激活。

生化/生理作用

CITCO是组成型雄烷受体(CAR)激动剂;核受体NR113激动剂。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Tadeja Režen et al.
Drug metabolism and disposition: the biological fate of chemicals, 45(8), 974-976 (2017-05-26)
Statins are well known lipid lowering agents that inhibit the enzyme 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase. They also activate drug metabolism but their exact receptor-mediated action has not been proven so far. We tested whether atorvastatin and rosuvastatin are direct ligands of
Susanne Johansson et al.
Clinical pharmacology in drug development, 6(5), 466-475 (2017-03-17)
Tenapanor (RDX5791, AZD1722) is an inhibitor of sodium/hydrogen exchanger isoform 3 in development for the treatment of constipation-predominant irritable bowel syndrome and the treatment of hyperphosphatemia in patients with chronic kidney disease on dialysis. We aimed to investigate whether tenapanor
Constitutive androstane receptor agonist CITCO inhibits growth and expansion of brain tumour stem cells
Chakraborty S , et al.
British Journal of Cancer, 104(3), 448-448 (2011)
Constitutive androstane receptor (Car)-driven regeneration protects liver from failure following tissue loss
Tschuor C, et l.
Journal of Hepatology, 65(1), 66-74 (2016)
Congrong Niu et al.
Frontiers in pharmacology, 11, 620197-620197 (2021-02-09)
The induction potentials of ligand-activated nuclear receptors on metabolizing enzyme genes are routinely tested for new chemical entities. However, regulations of drug transporter genes by the nuclear receptor ligands are underappreciated, especially in differentiated human hepatocyte cultures. In this study

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