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Revision as of 10:16, 29 November 2010 editNono64 (talk | contribs)Autopatrolled, Pending changes reviewers, Rollbackers96,246 editsm Hydroxycinnamic acid template← Previous edit Latest revision as of 19:56, 20 December 2023 edit undoJWBE (talk | contribs)Extended confirmed users10,126 edits removed Category:Vinylogous carboxylic acids using HotCat 
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{{chembox {{Chembox
| Verifiedfields = changed
|ImageFile1=Cynarine.svg
| Watchedfields = changed
|ImageSize1=200px
| verifiedrevid = 399494542
|ImageFile2=Cynarine3d.png
| ImageFile1 = Cynarine.svg
|ImageSize2=200px
| ImageFile2 = Cynarine3d.png
|IUPACName=(1''R'',3''R'',4''S'',5''R'')-1,3-bis<nowiki>oxy]-4,5-dihydroxycyclohexane-1-carboxylic acid | PIN = (1''R'',3''R'',4''S'',5''R'')-1,3-Bis{oxy}-4,5-dihydroxycyclohexane-1-carboxylic acid
|OtherNames=1,5-Dicaffeoylquinic acid; Cynarin; Cinarin; Cinarine | OtherNames = 1,5-Dicaffeoylquinic acid; Cynarin; Cinarin; Cinarine
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|changed|CAS}}
| CASNo=30964-13-7 | CASNo = 212891-05-9
| PubChem=5281769 | PubChem = 5281769
| SMILES=C1(((C1(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
| ChEMBL_Ref = {{ebicite|changed|EBI}}
}}
| ChEMBL = 2105478
| SMILES = C1(((C1(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
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 4445082
| InChI = 1/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
| InChIKey = YDDUMTOHNYZQPO-RVXRWRFUBT
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = YDDUMTOHNYZQPO-RVXRWRFUSA-N
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = 85D81U9JAV
}}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| C=25|H=25|O=12 | C=25|H=24|O=12
| Appearance= | Appearance =
| Density= | Density =
| MeltingPt= | MeltingPt =
| BoilingPt= | BoilingPt =
| Solubility= | Solubility =
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards =
| FlashPt= | FlashPt =
| AutoignitionPt =
| Autoignition=
}} }}
}} }}


'''Cynarine''' is a ] and a biologically active chemical constituent of ].<ref>{{cite journal | doi = 10.1038/1741062a0 | pmid = 13214078 | title = Constitution of Cynarine, the Active Principle of the Artichoke | year = 1954 | last1 = Panizzi | first1 = Luigi | last2 = Scarpati | first2 = Maria Luisa | journal = Nature | volume = 174 | issue = 4440 | pages = 1062}}</ref> Chemically, it is an ester formed from ] and two units of ]. '''Cynarine''' is a ] ] and a biologically active chemical constituent of ] (''Cynara cardunculus'').<ref>{{cite journal |doi = 10.1038/1741062a0 |pmid = 13214078 |title = Constitution of Cynarine, the Active Principle of the Artichoke |year = 1954 |last1 = Panizzi |first1 = Luigi |last2 = Scarpati |first2 = Maria Luisa |journal = Nature |volume = 174 |issue = 4440 |pages = 1062–3|s2cid = 4254603 |doi-access = free }}</ref>


Chemically, it is an ] formed from ] and two units of ].
==References==

== See also ==
* ]

== References ==
{{reflist}} {{reflist}}


{{Hydroxycinnamic acid}} {{Hydroxycinnamic acid}}


] ]
] ]
]
] ]
{{aromatic-stub}}

{{polyphenol-stub}}

]
]