Misplaced Pages

Iridin: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively
Page 1
Page 2
← Previous editContent deleted Content addedVisualWikitext
Revision as of 10:27, 19 February 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit Latest revision as of 10:19, 24 May 2024 edit undoCitation bot (talk | contribs)Bots5,416,934 edits Add: bibcode, authors 1-1. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Superegz | Category:O-methylated isoflavones‎ | #UCB_Category 7/16 
(32 intermediate revisions by 23 users not shown)
Line 1: Line 1:
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 405874526
| Watchedfields = changed
| verifiedrevid = 414762471
| Name = Iridin | Name = Iridin
| ImageFile = Iridin2.svg | ImageFile = Iridin2.svg
| ImageSize = 300px | ImageSize = 300px
| IUPACName = 7-(β-<small>D</small>-Glucopyranosyloxy)-3′,5-dihydroxy-4′,5′,6-trimethoxyisoflavone
| IUPACName = <nowiki>5-hydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-7-oxychromen-4-one</nowiki> | SystematicName = 5-Hydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-7-{oxy}-4''H''-1-benzopyran-4-one
| OtherNames = Irisin<ref></ref><!-- <br> --> | OtherNames = Irisin<ref></ref><!-- <br> -->
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 491-74-7 | CASNo = 491-74-7
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 6NTS007OHQ
| PubChem = 5281777 | PubChem = 5281777
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 487014
| Beilstein = | Beilstein =
| SMILES = COC1=CC(=CC(=C1OC)O)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O | SMILES = COC1=CC(=CC(=C1OC)O)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 4445090
| InChI = 1/C24H26O13/c1-32-13-5-9(4-11(26)22(13)33-2)10-8-35-12-6-14(23(34-3)19(29)16(12)17(10)27)36-24-21(31)20(30)18(28)15(7-25)37-24/h4-6,8,15,18,20-21,24-26,28-31H,7H2,1-3H3/t15-,18-,20+,21-,24-/m1/s1
| InChIKey = LNQCUTNLHUQZLR-OZJWLQQPBX
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C24H26O13/c1-32-13-5-9(4-11(26)22(13)33-2)10-8-35-12-6-14(23(34-3)19(29)16(12)17(10)27)36-24-21(31)20(30)18(28)15(7-25)37-24/h4-6,8,15,18,20-21,24-26,28-31H,7H2,1-3H3/t15-,18-,20+,21-,24-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = LNQCUTNLHUQZLR-OZJWLQQPSA-N
| RTECS =
| MeSHName =
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 5963
| KEGG_Ref = {{keggcite|changed|kegg}}
| KEGG = C10465
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| Formula = C<sub>24</sub>H<sub>26</sub>O<sub>13</sub> | Formula = C<sub>24</sub>H<sub>26</sub>O<sub>13</sub>
| MolarMass = 522.45 g/mol | MolarMass = 522.45 g/mol
| ExactMass = 522.137341
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = 208 °C | MeltingPtC = 208
| BoilingPt = | BoilingPt =
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt =
}}
}} }}
'''Iridin''' is an ], a type of flavonoid. It is the 7-] of ] and can be isolated from several species of ] like orris root, '']''<ref></ref> or '']'', also commonly known as the larger blue flag. '''Iridin''' is an ], a type of flavonoid. It is the 7-] of ] and can be isolated from several species of ] like orris root, '']''<ref></ref> or '']'', also commonly known as the larger blue flag. It can also be found in '']''.<ref>{{cite journal |last1=Agarwal |first1=V.K. |last2=Thappa |first2=R.K. |last3=Agarwal |first3=S.G. |last4=Mehraa |first4=M.S. |last5= Dhar |first5=K.L. |date=1984 |title=Isoflavones of two Iris species |journal= Phytochemistry|volume=23 |issue=11 |pages=2703–2704 |doi=10.1016/S0031-9422(00)84141-2 |bibcode=1984PChem..23.2703A }}</ref><ref> J. B. Harborne {{Google books|snL1BwAAQBAJ|The Flavonoids: Advances in Research since 1980|page=133}}</ref>


The compound is toxic and these plants have been mentioned as causing poisoning in humans and animals.<ref></ref> The compound is toxic and these plants have been mentioned as causing poisoning in humans and animals.<ref> {{webarchive|url=https://web.archive.org/web/20110610084858/http://www.cbif.gc.ca/pls/pp/ppack.info?p_psn=228&p_type=all&p_sci=comm |date=2011-06-10 }}</ref>


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


{{isoflavone}} {{isoflavone}}


]
] ]
] ]
{{Aromatic-stub}}

{{Natural phenol-stub}}

]