7,8-二羥基-4'-甲氧基異黃酮

Retusin
	IUPAC名; 7,8-Dihydroxy-4′-methoxyisoflavone
識別
CAS號	37816-19-6
PubChem	5481240
ChemSpider	4587189
SMILES	COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3O)O;
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;
InChIKey	DLXIJJURUIXRFK-UHFFFAOYAG
性質
化學式	C16H12O5
摩爾質量	284.26 g/mol g·mol⁻¹
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

7,8-二羥基-4'-甲氧基異黃酮（英語：Retusin，7,8-Dihydroxy-4′-methoxyisoflavone）是一種O-甲基化黃酮類化合物，分子式C₁₆H₁₂O₅，存在於香豆樹（Dipteryx odorata）^[1]^[2]、微凹黃檀（Dalbergia retusa）^[3]、亮葉崖豆藤（Millettia nitida）^[4]等植物乃至朝鮮槐（Maackia amurensis）的細胞培養物中^[5]。

參考文獻[編輯]

^ Isoflavones from Dipteryx odorata. Teruo Hayashi and Ronald H. Thomson, Phytochemistry, Volume 13, Issue 9, September 1974, Pages 1943-1946
^ 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, Issue 1, 15 August 2009, Pages 100-105
^ Retusin (Dalbergia) on kanaya.naist.jp/. [2023-02-21]. （原始內容存檔於2014-08-12）.
^ 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, pages 4107-4114, doi:10.1016/j.jchromb.2009.10.033
^ 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, doi:10.1016/S0367-326X(00)00129-5

外部連結[編輯]

Template:異黃酮

[1] Isoflavones from Dipteryx odorata. Teruo Hayashi and Ronald H. Thomson, Phytochemistry, Volume 13, Issue 9, September 1974, Pages 1943-1946

[2] 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, Issue 1, 15 August 2009, Pages 100-105

[3] Retusin (Dalbergia) on kanaya.naist.jp/. [2023-02-21]. （原始內容存檔於2014-08-12）.

[4] 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, pages 4107-4114, doi:10.1016/j.jchromb.2009.10.033

[5] 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, doi:10.1016/S0367-326X(00)00129-5

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