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Merck

375004

Sigma-Aldrich

2,4-噻唑烷二酮

technical grade, 90%

别名:

2,4(3H,5H)-噻唑二酮, 2,4-二氧代-1,3-噻唑烷, 2,4-二氧代噻唑烷, 2-羟基-4,5-二氢-1,3-噻唑-4-酮, 噻唑-2,4-二酮, 噻唑啉-2,4-二酮, 噻唑烷二酮 (6CI)

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About This Item

经验公式(希尔记法):
C3H3NO2S
CAS号:
分子量:
117.13
Beilstein:
110700
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

technical grade

化驗

90%

mp

125-127 °C (lit.)

SMILES 字串

O=C1CSC(=O)N1

InChI

1S/C3H3NO2S/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)

InChI 密鑰

ZOBPZXTWZATXDG-UHFFFAOYSA-N

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一般說明

2,4-噻唑烷二酮是一种著名的过氧化物酶体增殖物激活受体(PPAR)激活剂。它对衰老过程的影响通过使用来自Fischer 344大鼠的肾脏已被报道。2,4-噻唑烷二酮的耦合物文库已通过Knoevenagel缩合以及后续使用氢气和Pd/C催化剂的还原反应而合成得到。已经报道了各种芳香醛与聚乙二醇-300中的2,4-噻唑烷二酮的Knoevenagel缩合。

應用

2,4-噻唑烷二酮可通过超声促进的羟醛缩合反应用于十六个5-亚芳基-2,4-噻唑烷二酮的合成。它可作为起始材料用于合成具有抗高血糖活性的药物。

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

Eyeshields, Gloves, type N95 (US)


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Suzanne V Arnold et al.
Circulation. Heart failure, 12(6), e005855-e005855 (2019-05-28)
Background Thiazolidinediones (rosiglitazone, pioglitazone) are oral insulin-sensitizing medications used in type 2 diabetes mellitus that reduce glucose with minimal risk of hypoglycemia and potential benefits on atherosclerosis. However, thiazolidinediones can cause fluid retention thereby increasing the risk of heart failure-a
Tien-Jyun Chang et al.
Pharmacogenetics and genomics, 21(12), 829-836 (2011-09-22)
This study aimed to analyze the association of thiazolidinedione (TZD)-related edema with genetic and clinical variables and develop a simple points system to predict the risk of developing TZD-related edema. Fifty-eight (21.6%) of 268 individuals who received TZD for type
A Koch et al.
British journal of pharmacology, 166(3), 1018-1032 (2012-01-10)
PPARγ agonists [thiazolidinediones (TZDs)] are known to exert anti-fibrotic effects in the kidney. In addition, we previously demonstrated that sphingosine kinase 1 (SK-1) and intracellular sphingosine-1-phosphate (S1P), by reducing the expression of connective tissue growth factor (CTGF), have a protective
Sabrina Heng et al.
Bioorganic & medicinal chemistry, 19(24), 7453-7463 (2011-11-15)
We present a new class of inhibitors of pancreatic cholesterol esterase (CEase) based on 'priviledged' 5-benzylidenerhodanine and 5-benzylidene-2,4-thiazolidinedione structural scaffolds. The lead structures (5-benzylidenerhodanine 4a and 5-benzylidene-2,4-thiazolidinedione 4b) were identified in an in-house screening and these inhibited CEase with some
K M Schoenberg et al.
Journal of dairy science, 94(11), 5523-5532 (2011-10-29)
Administration of peroxisome proliferator-activated receptor gamma (PPARγ) ligands, thiazolidinediones (TZD), to prepartum dairy cattle has been shown to improve dry matter intake and decrease circulating nonesterified fatty acids (NEFA) around the time of calving. The objective of this work was

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