1,5-Dicaffeoylquinic acid

Modify Date: 2024-01-02 19:46:55

1,5-Dicaffeoylquinic acid Structure
1,5-Dicaffeoylquinic acid structure
Common Name 1,5-Dicaffeoylquinic acid
CAS Number 30964-13-7 Molecular Weight 516.451
Density 1.6±0.1 g/cm3 Boiling Point 819.9±65.0 °C at 760 mmHg
Molecular Formula C25H24O12 Melting Point 225-227 °C
MSDS Chinese USA Flash Point 278.1±27.8 °C

 Use of 1,5-Dicaffeoylquinic acid


Cynarin is an antichoke agent with a variety of biological activities including antioxidant, antihistamic and antiviral activities.

 Names

Name 1,3-dicaffeoylquinic acid
Synonym More Synonyms

 1,5-Dicaffeoylquinic acid Biological Activity

Description Cynarin is an antichoke agent with a variety of biological activities including antioxidant, antihistamic and antiviral activities.
Related Catalog
In Vitro Cynarin inhibits taste receptors, making water to be sweet. It has been shown to have some pharmacological properties including hypocholesterolemic, hepatoprotective, antiviral, antibacterial, and antihistamic effects. Cynarin has marked antioxidant, anticholinergic, reducing ability, radical-scavenging, and metal-binding activities. Cynarin demonstrates 87.72% inhibition of linoleic acid lipid peroxidation at 30 mg/mL concentration. Cynarin exhibits effective DMPD+, ABTS+/sup>, O2-, DPPH1, and H2O2 scavenging effects, reducing capabilities and Fe2+ chelating effects. IC50 and Ki of cynarin for acetylcholinesterase enzyme inhibition are 243.67nM and 39.34±13.88 nM, respectively[1]. Cynarin is a potential immunosuppressant that blocks the interaction between the CD28 of T-cell receptor and CD80 of antigen presenting cells. Cynarin blocks about 87% of the CD28-dependent "signal 2" pathway of T-cell activation under the condition of one to one ratio of T-cell and B-cell. Cynarin binds to the "G-pocket" of CD28 and thus interrupts the site of interaction between CD28 and CD80[2].
Cell Assay The cytotoxicity of cynarin treatment of T-cells is measured by MTT colorimetric assay. 100 μL Jurkat cells are incubated with cynarin (0-1000 μg/mL) for 24 h at 37°C. The cell solution is then centrifuged and the supernatant removed. 200 μL of MTT is added and the cell solution is incubated again for 4 h at 37°C. 200 μL of DMSO lysis buffer is added into the cell medium and the concentration of dissolved MTT crystals is measured by plate reader at 560 nm[2].
References

[1]. Topal M, et al. Antioxidant, antiradical, and anticholinergic properties of cynarin purified from the Illyrian thistle (Onopordum illyricum L.). J Enzyme Inhib Med Chem. 2016;31(2):266-75.

[2]. Dong GC, et al. Blocking effect of an immuno-suppressive agent, cynarin, on CD28 of T-cell receptor. Pharm Res. 2009 Feb;26(2):375-81.

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 819.9±65.0 °C at 760 mmHg
Melting Point 225-227 °C
Molecular Formula C25H24O12
Molecular Weight 516.451
Flash Point 278.1±27.8 °C
Exact Mass 516.126770
PSA 211.28000
LogP 1.64
Vapour Pressure 0.0±3.1 mmHg at 25°C
Index of Refraction 1.719
Storage condition 2-8°C

 Safety Information

RIDADR NONH for all modes of transport
HS Code 2932999099

 Customs

HS Code 2932999099
Summary 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles5

More Articles
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.

Chem. Res. Toxicol. 23 , 171-83, (2010)

Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental...

Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

J. Med. Chem. 51 , 6740-51, (2008)

The work provides a new model for the prediction of the MAO-A and -B inhibitor activity by the use of combined complex networks and QSAR methodologies. On the basis of the obtained model, we prepared ...

Natural product inhibitors of protein-protein interactions mediated by Src-family SH2 domains.

Bioorg. Med. Chem. Lett. 19 , 3305-9, (2009)

In this Letter, we report the natural products salvianolic acid A, salvianolic acid B, and caftaric acid as inhibitors of the protein-protein interactions mediated by the SH2 domains of the Src-family...

 Synonyms

Listrocol
Acido,1,4-dicaffeilchinico
(1R,3R,4S,5R)-1,3-Bis{[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]oxy}-4,5-dihydroxycyclohexanecarboxylic acid
[1R-(1a,3a,4a,5b)]-1,3-Bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-4,5-dihydroxycyclohexanecarboxylic Acid
1,5-Dicaffeoylquinic acid
1,3-DICAFFEOYLQUINIC ACID
1,3-O-Dicaffeoylquinic acid
(1R,3R,4S,5R)-1,3-Bis{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-4,5-dihydroxycyclohexanecarboxylic acid
1-Carboxy-4,5-dihydroxy-1,3-cyclohexylenebis-(3,4-dihydroxycinnamate)
3,4-Dihydroxycinnamic Acid 1-Carboxy-4,5-dihydroxy-1,3-cyclohexylene Ester
CINARINE
1,4-Dicaffeylquinic acid
MFCD00075714
Caffeic Acid 1-Carboxy-4,5-dihydroxy-1,3-cyclohexylene Ester
Cinarcaf
Cyclohexanecarboxylic acid, 1,3-bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1R,3R,4S,5R)-
1,5-Dicaffeylquinic Acid
Cynarine
Cynara scolymus L,
Quinic Acid 1,5-Dicaffeic Ester
Plemocil
Cynarin
CINARAN
EINECS 214-655-7
Dicaffeoylquinic Acid, 1,3-
Top Suppliers:I want be here





Get all suppliers and price by the below link:

1,5-Dicaffeoylquinic acid suppliers


Price: $150/10mM*1mLinDMSO

Reference only. check more 1,5-Dicaffeoylquinic acid price