cynarine (Q1763092)

(1S,3S,4R,5S)-3-[(Z)-3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy-1-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxycyclohexane-1-carboxylic acid

Cynarin (English)

5 October 2016

2 references

inferred from InChIKey

(1S,3R,4R,5R)-1,3-bis({[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-4,5-dihydroxycyclohexane-1-carboxylic acid

inferred from InChI

1 reference

1 reference

1,3-Dicaffeoylquinic acid

1 reference

inferred from InChI

chemical formula

C₂₅H₂₄O₁₂

1 reference

Cynarin (English)

19 November 2016

C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O

1 reference

Cynarin (English)

19 November 2016

C1[C@H]([C@@H]([C@@H](C[C@]1(C(=O)O)OC(=O)/C=C/C2=CC(=C(C=C2)O)O)OC(=O)/C=C/C3=CC(=C(C=C3)O)O)O)O

1 reference

Thiazinedione from xanthium strumarium

Cynarin (English)

19 November 2016

3 references

Inhibition of γ-irradiation-induced oxidation of chlorogenate by 1,3-dicaffeoylquinate in Xanthium occidentale

Bioactivity-guided fractionation for anti-inflammatory and analgesic properties and constituents of Xanthium strumarium L

Cynara scolymus

5 references

HPLC Evaluation of the Active Constituents in the Newly Introduced Romanian Strain of Cynara scolymus Cultivated in Egypt

Electrospray characterization of selected medicinal plant extracts

Flavonoids of Cynara scolymus possess potent xanthinoxidase inhibitory activity in vitro but are devoid of hypouricemic effects in rats after oral application

High-performance liquid chromatography of caffeoylquinic acid derivatives of Cynara scolymus L. leaves

Prevention of taurolithocholate-induced hepatic bile canalicular distortions by HPLC-characterized extracts of artichoke (Cynara scolymus) leaves

Sarcandra glabra

1 reference

Chemical profiling of bioactive constituents in Sarcandra glabra and its preparations using ultra‐high‐pressure liquid chromatography coupled with LTQ Orbitrap mass spectrometry

Centella asiatica

1 reference

The anti-thrombotic active constituents from Centella asiatica

sweet potato

1 reference

New polyphenol derivative in Ipomoea batatas tubers and its antioxidant activity

Saussurea involucrata

1 reference

Chemical constituents from the cell cultures of Saussurea involucrata

Coffea canephora

1 reference

Coffee bean dicaffeoylquinic acids

Echinacea purpurea

4 references

Evaluation of Major Caffeic Acid Derivatives inEchinacea purpureaDietary Supplements by HPLC with Photodiode Array Detection and Electrospray Mass Spectrometry

Simultaneous analysis of alkamides and caffeic acid derivatives for the identification of Echinacea purpurea, Echinacea angustifolia, Echinacea pallida and Parthenium integrifolium roots

Phytochemical variation in echinacea from roots and flowerheads of wild and cultivated populations

Echinacea standardization: analytical methods for phenolic compounds and typical levels in medicinal species.

Echinacea angustifolia

7 references

Characterization of Antiviral Activities inEchinacea. Root Preparations

Quality assessment of herbal preparations as a precondition of pharmacological and clinical studies

Comparison of chemical components and antioxidants capacity of different Echinacea species

Simultaneous analysis of alkamides and caffeic acid derivatives for the identification of Echinacea purpurea, Echinacea angustifolia, Echinacea pallida and Parthenium integrifolium roots

Phytochemical variation within populations of Echinacea angustifolia (Asteraceae)

Analytical aspects of drugs of natural origin

Echinacea standardization: analytical methods for phenolic compounds and typical levels in medicinal species.

Echinacea pallida

3 references

Characterization of Antiviral Activities inEchinacea. Root Preparations

Phytochemical variation in echinacea from roots and flowerheads of wild and cultivated populations

Echinacea standardization: analytical methods for phenolic compounds and typical levels in medicinal species.

Helichrysum italicum

1 reference

Dicaffeolyquinic acids from Helichrysum italicum and Achillea cartilaginea

Achillea cartilaginea

1 reference

Dicaffeolyquinic acids from Helichrysum italicum and Achillea cartilaginea

Xanthium chinense

1 reference

Inhibition of γ-irradiation-induced oxidation of chlorogenate by 1,3-dicaffeoylquinate in Xanthium occidentale

Matricaria chamomilla

1 reference

Characterization ofMatricaria recutita L. Flower extracts by HPLC-MS and HPLC-DAD analysis

Echinacea atrorubens

1 reference

Phytochemical variation in echinacea from roots and flowerheads of wild and cultivated populations

Artemisia caruifolia

1 reference

Inhibitory effects on HIV-1 protease of tri-p-coumaroylspermidine from Artemisia caruifolia and related amides

Xanthium occidentale

1 reference

Inhibition of γ-irradiation-induced oxidation of chlorogenate by 1,3-dicaffeoylquinate in Xanthium occidentale

Artemisia carvifolia

1 reference

Inhibitory effects on HIV-1 protease of tri-p-coumaroylspermidine from Artemisia caruifolia and related amides

Chamomilla recutita

1 reference

Characterization ofMatricaria recutita L. Flower extracts by HPLC-MS and HPLC-DAD analysis

Artemisia annua

2 references

Chemical constituents from Artemisia annua

Artemisia annua L.: Essential oil and acetone extract composition and antioxidant capacity

Foeniculum vulgare

1 reference

Separation and characterization of phenolic compounds in fennel (Foeniculum vulgare) using liquid chromatography-negative electrospray ionization tandem mass spectrometry.

Phaseolus vulgaris

1 reference

Alpha-amylase, α-glucosidase and lipase inhibiting activities of polyphenol-rich extracts from six common bean cultivars of Southern Italy, before and after cooking.

Morus alba

1 reference

The novel contributors of anti-diabetic potential in mulberry polyphenols revealed by UHPLC-HR-ESI-TOF-MS/MS.

potato

1 reference

Metabolite profiling of red and blue potatoes revealed cultivar and tissue specific patterns for anthocyanins and other polyphenols.

Cynara cardunculus

7 references

Electrospray characterization of selected medicinal plant extracts

HPLC Evaluation of the Active Constituents in the Newly Introduced Romanian Strain of Cynara scolymus Cultivated in Egypt

High-performance liquid chromatography of caffeoylquinic acid derivatives of Cynara scolymus L. leaves

Flavonoids of Cynara scolymus possess potent xanthinoxidase inhibitory activity in vitro but are devoid of hypouricemic effects in rats after oral application

Prevention of taurolithocholate-induced hepatic bile canalicular distortions by HPLC-characterized extracts of artichoke (Cynara scolymus) leaves

Pharmacological Studies of Artichoke Leaf Extract and Their Health Benefits

Metabolomics driven analysis of artichoke leaf and its commercial products via UHPLC-q-TOF-MS and chemometrics

subject has role

cholagogues and choleretics

1 reference

Medical Subject Headings

MeSH descriptor ID

C100257

InChI=1S/C25H24O12/c26-15-5-1-13(9-17(15)28)3-7-21(31)36-20-12-25(24(34)35,11-19(30)23(20)33)37-22(32)8-4-14-2-6-16(27)18(29)10-14/h1-10,19-20,23,26-30,33H,11-12H2,(H,34,35)/b7-3+,8-4+/t19-,20-,23+,25-/m1/s1

15 March 2018

Identifiers

InChI

1 reference

Cynarin (English)

19 November 2016

2 references

Cynarin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

212891-05-9

2 references

Global Substance Registration System

UNII

85D81U9JAV

cynarine (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=212891-05-9

8 April 2021

1 reference

Cynarine (English)

19 November 2016

2 references

Cynarin (English)

19 November 2016

Reaxys registry number

3189399

1 reference

1,3-dicaffeoylquinic acid (English)

5 October 2016

ChEBI ID

520

mapping relation type

2 references

CYNARIN (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C25H24O12/c26-15-5-1-13(9-17(15)28)3-7-21(31)36-20-12-25(24(34)35,11-19(30)23(20)33)37-22(32)8-4-14-2-6-16(27)18(29)10-14/h1-10,19-20,23,26-30,33H,11-12H2,(H,34,35)/b7-3+,8-4+/t19-,20-,23+,25-/m1/s1

1 reference

CYNARIN (English)

19 November 2016

2 references

inferred from InChIKey

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00928

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00930

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00932

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00934

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00936

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00937

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00929

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00931

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00935

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-Fiocruz-FIO00933

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_ReSpect-PM000305

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_ReSpect-PM000306

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

splash10-014i-0003090000-1ab78c464c6821c3c81b

0 references

splash10-0udo-0909000000-8a10d11a75c14fd8e76e

0 references

splash10-0ufr-0709000000-d243d562bc47fda8d64c

0 references

splash10-0uxr-0009050000-e5af379611e857605383

0 references

splash10-0udi-0089000000-c1ebd23a9bc153e7e5a1

0 references

DSSTox substance ID

DTXSID301309674

1 reference

MeSH descriptor ID

C100257

1 reference

Medical Subject Headings

MeSH descriptor ID

C100257

Human Metabolome Database ID

14 March 2018

HMDB0030093

2 references

inferred from InChIKey

1 reference

Global Substance Registration System

1,3-dicaffeoylquinic acid (English)

5 October 2016

2 references

UNII

85D81U9JAV

cynarine (English)

19 November 2016

0 references

1 reference

1 reference