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26:
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Lipase-catalyzed regioselective protection/deprotection of hydroxyl groups of the isoflavone irilone isolated from Iris germanica. Nighat Nazir, Surrinder Koul, Mushtaq Ahmad
Qurishi, Subhash Chandra Taneja and Ghulam Nabi Qazi, Biocatalysis and Biotransformation, 2 December 2008, 1029–2446, Volume
437:
New and Known
Constituents from Iris unguicularis and Their Antioxidant Activity. Atta-ur-Rahman, Sumaira Hareem, M. Iqbal Choudhary, Bilge Sener, Ahmed Abbaskhan, Hina Siddiqui, Shazia Anjum, Ilkay Orhan, Ilhan Gurbuz and Filiz Ayanoglu, HeteroCycles, 2010, Special issue, Vol 82, No. 1, pages
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The red clover isoflavone irilone is largely resistant to degradation by the human gut microbiota. Annett Braune, Ronald Maul, Nils Helge Schebb, Sabine E. Kulling and
Michael Blaut, Molecular Nutrition & Food Research, 8 Dec
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InChI=1S/C16H10O6/c17-9-3-1-8(2-4-9)10-6-20-11-5-12-16(22-7-21-12)15(19)13(11)14(10)18/h1-6,17,19H,7H2
485:
269:
InChI=1/C16H10O6/c17-9-3-1-8(2-4-9)10-6-20-11-5-12-16(22-7-21-12)15(19)13(11)14(10)18/h1-6,17,19H,7H2
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Except where otherwise noted, data are given for materials in their
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293:C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=C(C=C4)O)O
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391:, a type of flavonoid. It can be found in
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262:Key: NUGRQNBDTZWXTP-UHFFFAOYSA-N
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272:Key: NUGRQNBDTZWXTP-UHFFFAOYAV
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176:
13:
14:
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346:(at 25 °C , 100 kPa).
62:9-Hydroxy-7-(4-hydroxyphenyl)-2
448:
431:
419:
1:
412:
51:4′,9-Dihydroxy-6,7-isoflavone
803:. You can help Knowledge by
713:Di-O-methylalpinumisoflavone
455:27, Issue 2, Pages 118–123,
7:
718:4'-methyl-alpinumisoflavone
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336:298.24 g/mol
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538:O-methylated isoflavones
70:-dioxolobenzopyran-8-one
855:Aromatic compound stubs
795:This article about an
501:Isoflavones and their
734:Anagyroidisoflavone A
58:Systematic IUPAC name
444:10.3987/COM-10-S(E)6
570:5-O-methylgenistein
20:
394:Trifolium pratense
373:Infobox references
18:
812:
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777:
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703:Alpinumisoflavone
696:Pyranoisoflavones
682:7-O-Methylluteone
400:Iris unguicularis
397:(red clover), in
381:Chemical compound
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215:CompTox Dashboard
118:Interactive image
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748:Pseudobaptigenin
585:Psi-tectorigenin
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805:expanding it
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595:Tectorigenin
555:Formononetin
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77:Identifiers
67:
63:
15:
850:Isoflavones
769:Ipriflavone
727:Derivatives
708:Barbigerone
667:Bidwillol A
660:isoflavones
545:Biochanin A
511:Isoflavones
302:Properties
844:Categories
658:Prenylated
648:Tectoridin
605:Glycosides
575:Pratensein
503:glycosides
413:References
389:isoflavone
332:Molar mass
149:ChemSpider
138:CHEBI:5970
105:3D model (
94:41653-81-0
84:CAS Number
48:IUPAC name
762:Synthetic
753:Rotenoids
687:Wighteone
672:Derrubone
628:Mirificin
560:Glycitein
550:Calycosin
524:Genistein
438:813–824,
797:aromatic
638:Puerarin
618:Genistin
580:Prunetin
565:Irigenin
519:Daidzein
463:21235726
19:Irilone
743:Irilone
677:Luteone
613:Daidzin
590:Retusin
403:and in
385:Irilone
366:what is
364: (
326:
203:5281779
190:PubChem
158:4445092
633:Ononin
623:Iridin
529:Orobol
460:
387:is an
361:verify
358:
286:SMILES
178:C10467
42:Names
457:INIST
251:InChI
129:ChEBI
107:JSmol
801:stub
736:and
427:2009
169:KEGG
440:doi
220:EPA
193:CID
846::
409:.
320:10
316:16
66:,8
832:e
825:t
818:v
807:.
738:B
494:e
487:t
480:v
442::
356:N
324:6
322:O
318:H
314:C
222:)
218:(
109:)
68:H
64:H
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