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Interactions between thrombin and natural products of
Millettia nitita var. hirsutissima using capillary zone electrophoresis. Shuyu Zhang, Jun Cheng, Wenjing Chen, Xiaomei Ling, Yuying Zhao, Jie Feng, Cheng Xiang and Hong Liang, Journal of Chromatography B, Volume 877, Issue 32, 15 December 2009,
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Microsomal metabolism of calycosin, formononetin and drug–drug interactions by dynamic microdialysis sampling and HPLC–DAD–MS analysis. Xiao-Dong Wen, Lian-Wen Qi, Bin Lia, Ping Li, Ling Yia, Ya-Qiong Wang, E-Hu Liu and Xiao-Lin Yang, Journal of
Pharmaceutical and Biomedical Analysis, Volume 50,
463:
Isoflavonoid production by callus cultures of
Maackia amurensis. S.A Fedoreyev, T.V Pokushalov, M.V Veselova, L.I Glebko, N.I Kulesh, T.I Muzarok, L.D Seletskaya, V.P Bulgakov and Yu.N Zhuravlev, Fitoterapia, 1 August 2000, Volume 71, Issue 4, Pages 365–372,
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Isoflavones from
Dipteryx odorata. Teruo Hayashi and Ronald H. Thomson, Phytochemistry, Volume 13, Issue 9, September 1974, Pages 1943-1946
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InChI=1S/C16H12O5/c1-20-10-4-2-9(3-5-10)12-8-21-16-11(14(12)18)6-7-13(17)15(16)19/h2-8,17,19H,1H3
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InChI=1/C16H12O5/c1-20-10-4-2-9(3-5-10)12-8-21-16-11(14(12)18)6-7-13(17)15(16)19/h2-8,17,19H,1H3
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Except where otherwise noted, data are given for materials in their
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253:Key: DLXIJJURUIXRFK-UHFFFAOYAG
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67:7,8-Dihydroxy-3-(4-methoxyphenyl)-4
810:. You can help Knowledge (XXG) by
56:7,8-Dihydroxy-4′-methoxyisoflavone
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331:
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327:(at 25 °C , 100 kPa).
1:
470:10.1016/S0367-326X(00)00129-5
453:10.1016/j.jchromb.2009.10.033
723:Di-O-methylalpinumisoflavone
728:4'-methyl-alpinumisoflavone
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390:. It can also be found in
317:284.26 g/mol
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867:4-Methoxyphenyl compounds
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857:O-methylated isoflavones
548:O-methylated isoflavones
16:Not to be confused with
872:Aromatic compound stubs
370:O-methylated isoflavone
802:This article about an
511:Isoflavones and their
744:Anagyroidisoflavone A
63:Systematic IUPAC name
580:5-O-methylgenistein
71:-1-benzopyran-4-one
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354:Infobox references
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18:retusin (flavonol)
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713:Alpinumisoflavone
706:Pyranoisoflavones
692:7-O-Methylluteone
447:pages 4107-4114,
393:Maackia amurensis
362:Chemical compound
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196:CompTox Dashboard
119:Interactive image
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812:expanding it
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605:Tectorigenin
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565:Formononetin
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78:Identifiers
68:
779:Ipriflavone
737:Derivatives
718:Barbigerone
677:Bidwillol A
670:isoflavones
555:Biochanin A
521:Isoflavones
283:Properties
851:Categories
668:Prenylated
658:Tectoridin
615:Glycosides
585:Pratensein
513:glycosides
400:References
313:Molar mass
150:ChemSpider
106:3D model (
95:37816-19-6
85:CAS Number
53:IUPAC name
862:Catechols
772:Synthetic
763:Rotenoids
697:Wighteone
682:Derrubone
638:Mirificin
570:Glycitein
560:Calycosin
534:Genistein
804:aromatic
648:Puerarin
628:Genistin
590:Prunetin
575:Irigenin
529:Daidzein
24:Retusin
753:Irilone
687:Luteone
623:Daidzin
600:Retusin
384:and in
366:Retusin
347:what is
345: (
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184:5481240
171:PubChem
159:4587189
643:Ononin
633:Iridin
539:Orobol
368:is an
342:verify
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267:SMILES
130:ChEMBL
47:Names
378:, in
232:InChI
108:JSmol
808:stub
746:and
466:doi
449:doi
201:EPA
174:CID
853::
301:12
297:16
839:e
832:t
825:v
814:.
748:B
504:e
497:t
490:v
468::
451::
337:N
305:5
303:O
299:H
295:C
203:)
199:(
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69:H
20:.
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