他氟前列素

• 常用名: 他氟前列素
• 英文名: Tafluprost
• CAS号: 209860-87-7
• 分子量: 452.531
• 密度: 1.2±0.1 g/cm3
• 沸点: 552.9±50.0 °C at 760 mmHg
• 分子式: C₂₅H₃₄F₂O₅
• 熔点: N/A
• 闪点: 288.2±30.1 °C

他氟前列素用途

Tafluprost(AFP-168)是抗青光眼前列腺素(PG)类似物。

他氟前列素名称

• 中文名: 他氟前列素
• 英文名: tafluprost
• 中文别名: (5Z)-7-[(1R,2R,3R,5S)-2-[(1E)-3,3-二氟-4-苯氧基-1-丁烯-1-基]-3,5-二羟基环戊基]-5-庚烯酸异丙酯

他氟前列素生物活性

• 描述: Tafluprost(AFP-168)是抗青光眼前列腺素(PG)类似物。
• 相关类别:
  信号通路 >> 其他 >> 其他
  研究领域 >> 其他
• 参考文献:

  [1]. Kuwayama, Y. and A. Nomura, Prospective observational post-marketing study of tafluprost for glaucoma and ocular hypertension: short-term efficacy and safety. Adv Ther, 2014. 31(4): p. 461-71.

  [2]. Kumagami, T., et al., Comparison of corneal safety and intraocular pressure-lowering effect of tafluprost ophthalmic solution with other prostaglandin ophthalmic solutions. J Ocul Pharmacol Ther, 2014. 30(4): p. 340-5.

  [3]. Inoue, K., A. Tanaka, and G. Tomita, Effects of tafluprost treatment for 3 years in patients with normal-tension glaucoma. Clin Ophthalmol, 2013. 7: p. 1411-6.

他氟前列素物理化学性质

• 密度: 1.2±0.1 g/cm3
• 沸点: 552.9±50.0 °C at 760 mmHg
• 分子式: C₂₅H₃₄F₂O₅
• 分子量: 452.531
• 闪点: 288.2±30.1 °C
• 精确质量: 452.237427
• PSA: 75.99000
• LogP: 4.23
• InChIKey: WSNODXPBBALQOF-VEJSHDCNSA-N
• SMILES: CC(C)OC(=O)CCCC=CCC1C(O)CC(O)C1C=CC(F)(F)COc1ccccc1
• 外观性状: 粉末
• 蒸汽压: 0.0±1.6 mmHg at 25°C
• 折射率: 1.549
• 储存条件: -20℃

他氟前列素靶点实验

查看更多实验

实验名称：Binding affinity towards human ADRA2A in an in vitro assay with cellular components m... 来源：ChEMBL 靶标：Alpha-2A adrenergic receptor External Id：CHEMBL5291736

实验名称：Binding affinity towards human GABRA1 in an in vitro assay with cellular components m... 来源：ChEMBL 靶标：Gamma-aminobutyric acid receptor subunit gamma-2 External Id：CHEMBL5291799

实验名称：Binding affinity towards human PGR in an in vitro assay with cellular components meas... 来源：ChEMBL 靶标：Progesterone receptor External Id：CHEMBL5291863

实验名称：Antagonist activity at human ADRA1A in an in vitro cell-based assay measured by fluor... 来源：ChEMBL 靶标：Alpha-1A adrenergic receptor External Id：CHEMBL5291731

实验名称：Binding affinity towards human ESR1 in an in vitro cell free assay (CRO assay) measur... 来源：ChEMBL 靶标：Estrogen receptor External Id：CHEMBL5291792

实验名称：Binding affinity towards human ADORA3 (agonistic activity) in an in vitro assay with ... 来源：ChEMBL 靶标：Adenosine receptor A3 External Id：CHEMBL5291728

实验名称：Compound was evaluated for inhibition of human PDE3A in an in vitro cell free assay m... 来源：ChEMBL 靶标：cGMP-inhibited 3',5'-cyclic phosphodiesterase 3A External Id：CHEMBL5291856

实验名称：Binding affinity towards human OPRM1 in an in vitro assay with cellular components me... 来源：ChEMBL 靶标：Mu-type opioid receptor External Id：CHEMBL5291855

实验名称：Agonist activity at human ADRA1A in an in vitro cell-based assay (CRO assay) measured... 来源：ChEMBL 靶标：Alpha-1A adrenergic receptor External Id：CHEMBL5291730

实验名称：Compound was evaluated for inhibition of human F2 in an in vitro cell free assay meas... 来源：ChEMBL 靶标：Prothrombin External Id：CHEMBL5291794

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他氟前列素英文别名

• Tapros
• MK-2452
• propan-2-yl (Z)-7-[(1R,2R,3R,5S)-2-[(E)-3,3-difluoro-4-phenoxybut-1-enyl]-3,5-dihydroxycyclopentyl]hept-5-enoate
• Saflutan
• AFP-168
• Isopropyl (5Z)-7-{(1R,2R,3R,5S)-2-((1E)-3,3-difluoro-4-phenoxybut-1-enyl)-3,5-dihydroxycyclopentyl}hept-5-enoate
• Taflotan
• Tafluprost
• Isopropyl (5Z)-7-{(1R,2R,3R,5S)-2-[(1E)-3,3-difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl}-5-heptenoate
• UNII-1O6WQ6T7G3
• Zioptan