Cynaropicrin: Difference between revisions

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'''Cynaropicrin''' is a [[sesquiterpene lactone]]<ref>{{cite journal | pmid= 14706635 | title = Cynaropicrin, a sesquiterpene lactone, as a new strong regulator of CD29 and CD98 functions | volume=313 | issue=4 | date=January 2004 | journal=Biochem. Biophys. Res. Commun. | pages=954–61 | doi=10.1016/j.bbrc.2003.12.026}}</ref> exhibiting a range of diverse bioactivities.<ref>Elsebai MF, Mocan A, Atanasov AG. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143615/ Cynaropicrin: A Comprehensive Research Review and Therapeutic Potential As an Anti-Hepatitis C Virus Agent]. Front Pharmacol. 2016 Dec 8;7:472. Review. [https://www.ncbi.nlm.nih.gov/pubmed/28008316 PubMed PMID: 28008316].</ref>
'''Cynaropicrin''' is a [[sesquiterpene lactone]]<ref>{{cite journal | pmid= 14706635 | title = Cynaropicrin, a sesquiterpene lactone, as a new strong regulator of CD29 and CD98 functions | volume=313 | issue=4 | date=January 2004 | journal=Biochem. Biophys. Res. Commun. | pages=954–61 | doi=10.1016/j.bbrc.2003.12.026}}</ref> exhibiting a range of diverse bioactivities.<ref>{{cite journal |last1=Elsebai |first1=MF |last2=Mocan |first2=A |last3=Atanasov |first3=AG |title=Cynaropicrin: A Comprehensive Research Review and Therapeutic Potential As an Anti-Hepatitis C Virus Agent |journal=Front Pharmacol |date=December 2016 |volume=8 |number=7 |page=472 |pmc=5143615 |pmid=28008316}}</ref>


==References==
==References==

Revision as of 05:53, 3 January 2017

Cynaropicrin
Names
IUPAC name
[(3aR,4S,6aR,8S,9aR,9bR)-8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate
Other names
Aguerin
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.216.734 Edit this at Wikidata
KEGG
  • InChI=1S/C19H22O6/c1-8-5-14(24-18(22)9(2)7-20)16-11(4)19(23)25-17(16)15-10(3)13(21)6-12(8)15/h12-17,20-21H,1-7H2/t12-,13-,14-,15-,16+,17+/m0/s1
    Key: KHSCYOFDKADJDJ-NQLMQOPMSA-N
  • InChI=1/C19H22O6/c1-8-5-14(24-18(22)9(2)7-20)16-11(4)19(23)25-17(16)15-10(3)13(21)6-12(8)15/h12-17,20-21H,1-7H2/t12-,13-,14-,15-,16+,17+/m0/s1
    Key: KHSCYOFDKADJDJ-NQLMQOPMBE
  • C=C1C[C@@H]([C@@H]2[C@@H]([C@@H]3[C@H]1C[C@@H](C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO
Properties
C19H22O6
Molar mass 346.379 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cynaropicrin is a sesquiterpene lactone[1] exhibiting a range of diverse bioactivities.[2]

References

  1. ^ "Cynaropicrin, a sesquiterpene lactone, as a new strong regulator of CD29 and CD98 functions". Biochem. Biophys. Res. Commun. 313 (4): 954–61. January 2004. doi:10.1016/j.bbrc.2003.12.026. PMID 14706635.
  2. ^ Elsebai, MF; Mocan, A; Atanasov, AG (December 2016). "Cynaropicrin: A Comprehensive Research Review and Therapeutic Potential As an Anti-Hepatitis C Virus Agent". Front Pharmacol. 8 (7): 472. PMC 5143615. PMID 28008316.