噻洛芬酸结构式
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常用名 | 噻洛芬酸 | 英文名 | Tiaprofenic Acid |
|---|---|---|---|---|
| CAS号 | 33005-95-7 | 分子量 | 260.30800 | |
| 密度 | 1.29 g/cm3 | 沸点 | 450.3ºC at 760 mmHg | |
| 分子式 | C14H12O3S | 熔点 | 96° (isopropyl ether) | |
| MSDS | N/A | 闪点 | 226.1ºC |
噻洛芬酸用途Tiaprofenic acid 是一种具有抗炎镇痛作用的口服非甾体抗炎药 (NSAID)。Tiaprofenic acid 通过抑制环氧化酶 (COX) 抑制前列腺素合成。Tiaprofenic acid 可用于治疗风湿性疾病。 |
| 中文名 | 噻洛芬酸 |
|---|---|
| 英文名 | Tiaprofenic Acid |
| 中文别名 | 异噻酮布洛芬 | 2-(5-苄氧基噻吩-2-基)丙酸 | 2-(5-苯甲氧基噻吩-2-基)丙酸 | 2-[5-(苯甲酰基)-2-噻吩基]丙酸 |
| 英文别名 | 更多 |
| 描述 | Tiaprofenic acid 是一种具有抗炎镇痛作用的口服非甾体抗炎药 (NSAID)。Tiaprofenic acid 通过抑制环氧化酶 (COX) 抑制前列腺素合成。Tiaprofenic acid 可用于治疗风湿性疾病。 |
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| 相关类别 | |
| 体内研究 | 雌性Lewis大鼠静脉注射(静脉注射)硫丙酸15mg/kg,持续输注0.02mg/min,持续6h。硫丙酸可显著降低血清硫酸盐浓度,提高硫酸盐清除率。肾脏再吸收硫酸盐的比例也显著降低[2]。 |
| 参考文献 |
| 密度 | 1.29 g/cm3 |
|---|---|
| 沸点 | 450.3ºC at 760 mmHg |
| 熔点 | 96° (isopropyl ether) |
| 分子式 | C14H12O3S |
| 分子量 | 260.30800 |
| 闪点 | 226.1ºC |
| 精确质量 | 260.05100 |
| PSA | 82.61000 |
| LogP | 3.16720 |
| InChIKey | GUHPRPJDBZHYCJ-UHFFFAOYSA-N |
| SMILES | CC(C(=O)O)c1ccc(C(=O)c2ccccc2)s1 |
| 外观性状 | 固体;White to Almost white powder to crystal |
| 折射率 | 1.612 |
| 储存条件 | 室温 |
| 水溶解性 | Practically insoluble in water, freely soluble in acetone, in ethanol (96 per cent) and in methylene chloride. |
| 危险品运输编码 | UN 2811 6.1/PG III |
|---|---|
| RTECS号 | XM7580000 |
| 包装等级 | III |
|
~95%
噻洛芬酸 33005-95-7 |
| 文献:Zhang, Shuguang; Huang, Shuang; Feng, Chengliang; Cai, Jin; Chen, Junqing; Ji, Min Journal of Chemical Research, 2013 , vol. 37, # 7 p. 406 - 408 |
|
~65%
噻洛芬酸 33005-95-7 |
| 文献:Sagami Chemical Research Center Patent: US4242519 A1, 1980 ; |
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The effect of terpenes on percutaneous absorption of tiaprofenic acid gel.
Arch. Pharm. Res. 33(11) , 1781-8, (2010) Tiaprofenic acid is a potent analgesic and nonsteroidal anti-inflammatory drug (NSAID) and like any other nonsteroidal anti-inflammatory drug, oral administration of the conventional dosage forms of t... |
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Time-resolved spectroscopic study of the photochemistry of tiaprofenic acid in a neutral phosphate buffered aqueous solution from femtoseconds to final products.
J. Phys. Chem. B 117(3) , 811-24, (2013) The photo-decarboxylation and overall reaction mechanism of tiaprofenic acid (TPA) was investigated by femtosecond transient absorption (fs-TA), nanosecond transient absorption (ns-TA), and nanosecond... |
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[New technologies in laparoscopic surgery].
Chirurg. 72(3) , 252-60, (2001) The technology associated with endoscopic surgery continues to evolve as a result of industrial R & D and research within academic surgical departments with interest in surgical endoscopic and remote ... |
| 2-(5-Benzoylthiophen-2-yl)propanoic acid |
| Tiaprofenic acid |
| 2-(5-Benzoylthiophen-2-yl)propionic Acid |