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特立氟胺

更新时间:2025-08-20 19:13:27

特立氟胺结构式
特立氟胺结构式
品牌特惠专场
常用名 特立氟胺 英文名 teriflunomide
CAS号 108605-62-5 分子量 270.207
密度 1.4±0.1 g/cm3 沸点 363.0±42.0 °C at 760 mmHg
分子式 C12H9F3N2O2 熔点 N/A
MSDS 美版 闪点 173.3±27.9 °C
符号 GHS07
GHS07
信号词 Warning

 特立氟胺用途


(E/Z)-Teriflunomide((E/Z)-A77 1726)是来氟米特(HY-B0083)的活性代谢物。来氟米特是一种免疫调节剂,可通过抑制线粒体酶二氢乳清酸脱氢酶(DHODH)发挥作用。来氟米特可用于类风湿性关节炎(RA)的研究[1]。

 特立氟胺名称

中文名 2-氰基-3-羟基-N-[4-(三氟甲基)苯基]-2-丁烯酰胺
英文名 2-Cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)but-2-enamide,teriflunomide
中文别名 特立氟胺
英文别名 更多

 特立氟胺生物活性

描述 (E/Z)-Teriflunomide((E/Z)-A77 1726)是来氟米特(HY-B0083)的活性代谢物。来氟米特是一种免疫调节剂,可通过抑制线粒体酶二氢乳清酸脱氢酶(DHODH)发挥作用。来氟米特可用于类风湿性关节炎(RA)的研究[1]。
相关类别

 特立氟胺物理化学性质

密度 1.4±0.1 g/cm3
沸点 363.0±42.0 °C at 760 mmHg
分子式 C12H9F3N2O2
分子量 270.207
闪点 173.3±27.9 °C
精确质量 270.061615
PSA 73.12000
LogP 0.71
外观性状 白色固体
蒸汽压 0.0±0.9 mmHg at 25°C
折射率 1.552
储存条件 +2C to +8C
分子结构

1、摩尔折射率:60.59

2、摩尔体积(cm3/mol):189.6

3、等张比容(90.2K):492.1

4、表面张力(dyne/cm):45.3

5、介电常数:无可用的

6、极化率(10-24cm3):24.02

7、单一同位素质量:270.061612 Da

8、标称质量:270 Da

9、平均质量:270.2073 Da

计算化学

1.疏水参数计算参考值(XlogP):3.3

2.氢键供体数量:2

3.氢键受体数量:6

4.可旋转化学键数量:2

5.互变异构体数量:8

6.拓扑分子极性表面积73.1

7.重原子数量:19

8.表面电荷:0

9.复杂度:426

10.同位素原子数量:0

11.确定原子立构中心数量:0

12.不确定原子立构中心数量:0

13.确定化学键立构中心数量:1

14.不确定化学键立构中心数量:0

15.共价键单元数量:1

 特立氟胺安全信息

符号 GHS07
GHS07
信号词 Warning
危害声明 H302
危害码 (欧洲) Xn
风险声明 (欧洲) 22
危险品运输编码 NONH for all modes of transport

 特立氟胺文献26

更多文献
Hepatic cytochrome P450s attenuate the cytotoxicity induced by leflunomide and its active metabolite A77 1726 in primary cultured rat hepatocytes.

Toxicol. Sci. 122(2) , 579-86, (2011)

The Black Box Warning section of the U.S. drug label for leflunomide was recently updated to include stronger warnings about potential hepatotoxicity from this novel anti-arthritis drug. Because metab...

Respiratory syncytial virus inhibits lung epithelial Na+ channels by up-regulating inducible nitric-oxide synthase.

J. Biol. Chem. 284(11) , 7294-306, (2009)

Respiratory syncytial virus (RSV) infection has been shown to reduce Na+-driven alveolar fluid clearance in BALB/c mice in vivo. To investigate the cellular mechanisms by which RSV inhibits amiloride-...

Induction of EMT-like phenotypes by an active metabolite of leflunomide and its contribution to pulmonary fibrosis.

Cell Death Differ. 17(12) , 1882-95, (2010)

Drug-induced interstitial lung disease (ILD), particularly pulmonary fibrosis, is a serious clinical concern and myofibroblasts have been suggested to have a major role, with it recently being reveale...

 特立氟胺靶点实验

查看更多实验

实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
实验名称:Primary qHTS for Identification of Small Molecule Activators of Huntingtin-Antisense ...
来源:NCGC
External Id:huntington-HTTAS8-p1-FF-overN
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-keats_OPM1-m4-1
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-OC1MY5-m4-1
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-KMS_34-m4-1
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-keats_L363-m4-1
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-keats_OCIMY7-m4-1
实验名称:Primary qHTS for Identification of Small Molecule Inhibitors of Huntingtin Promoter A...
来源:NCGC
External Id:huntington-HTT2-p1-FF-overN
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-MM1R-m4-1
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 特立氟胺英文别名

2-Butenamide (2-cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]
(2Z)-2-(Hydroxy{[4-(trifluoromethyl)phenyl]amino}methylene)-3-oxobutanenitrile
2-Cyano-3-hydroxy-N-(4-trifluoromethylphenyl)crotonamide
Teriflunomide
2-Cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)but-2-enamide
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