7,8-二羟基-4'-甲氧基异黄酮

Retusin
	IUPAC名; 7,8-Dihydroxy-4′-methoxyisoflavone
识别
CAS号	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
性质
化学式	C16H12O5
摩尔质量	284.26 g/mol g·mol⁻¹
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

7,8-二羟基-4'-甲氧基异黄酮（英语：Retusin，7,8-Dihydroxy-4′-methoxyisoflavone）是一种O-甲基化黄酮类化合物，分子式C₁₆H₁₂O₅，存在于香豆树（Dipteryx odorata）^[1]^[2]、微凹黄檀（Dalbergia retusa）^[3]、亮叶崖豆藤（Millettia nitida）^[4]等植物乃至朝鲜槐（Maackia amurensis）的细胞培养物中^[5]。

参考文献

^ 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]. （原始内容存档于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

外部链接

Template:异黄酮

[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]. （原始内容存档于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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Retusin


IUPAC名 7,8-Dihydroxy-4′-methoxyisoflavone
识别
CAS号	37816-19-6 ^Y
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
性质
化学式	C₁₆H₁₂O₅
摩尔质量	284.26 g/mol g·mol⁻¹
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。