(1R,3S,4R,5S)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid

Modify Date: 2024-01-06 06:22:54

(1R,3S,4R,5S)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid Structure
(1R,3S,4R,5S)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid structure
Common Name (1R,3S,4R,5S)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid
CAS Number 5746-55-4 Molecular Weight 338.31
Density 1.6±0.1 g/cm3 Boiling Point 613.2±55.0 °C at 760 mmHg
Molecular Formula C16H18O8 Melting Point N/A
MSDS N/A Flash Point 227.0±25.0 °C

 Use of (1R,3S,4R,5S)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid


5-O-(E)-p-Coumaroylquinic acid, a quinic acid derivative, is a potent phytochemical agent against hepatitis B virus[1].

 Names

Name 3-O-p-Coumaroylquinic acid

  Biological Activity

Description 5-O-(E)-p-Coumaroylquinic acid, a quinic acid derivative, is a potent phytochemical agent against hepatitis B virus[1].
Related Catalog
In Vitro 5-O-(E)-p-Coumaroylquinic acid (compound 12) 降低了 HepG2.2.15 培养物释放的成熟 HBV 颗粒中的 HBV DNA 水平降低了 HepG2.2.15 培养物释放的成熟 HBV 颗粒中的 HBV DNA 水平。
References

[1]. Kim KH, et, al. Isolation of quinic acid derivatives and flavonoids from the aerial parts of Lactuca indica L. and their hepatoprotective activity in vitro. Bioorg Med Chem Lett. 2007 Dec 15;17(24):6739-43.  

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 613.2±55.0 °C at 760 mmHg
Molecular Formula C16H18O8
Molecular Weight 338.31
Flash Point 227.0±25.0 °C
Exact Mass 338.100159
LogP 0.10
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.662
Storage condition -20°C
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