Genistin (BioDeep_00000285152)

Main id: BioDeep_00000000023

 

natural product PANOMIX_OTCML-2023


代谢物信息卡片


5-hydroxy-3-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

化学式: C21H20O10 (432.105642)
中文名称: 染料木苷, 染料木苷, 染料木甙
谱图信息: 最多检出来源 Viridiplantae(plant) 1.14%

分子结构信息

SMILES: C1(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)=CC2OC=C(C3=CC=C(O)C=C3)C(=O)C=2C(O)=C1
InChI: InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-5-13(24)16-14(6-11)29-8-12(17(16)25)9-1-3-10(23)4-2-9/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20+,21+/m0/s1

描述信息

Genistein 7-O-beta-D-glucoside is a 7-hydroxyisoflavones 7-O-beta-D-glucoside. It is functionally related to a genistein. It is a conjugate acid of a genistein 7-O-beta-D-glucoside(1-).
Genistin is a natural product found in Ficus septica, Dalbergia sissoo, and other organisms with data available.
Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3].
Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3].

同义名列表

57 个代谢物同义名

5-hydroxy-3-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-7-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)-; 5-hydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside; Genistin, United States Pharmacopeia (USP) Reference Standard; 5,4-DI-HYDROXYISOFLAVONE-7-O-.BETA.-D-GLUCOPYRANOSIDE; 4,5,7-Trihydroxyisoflavone 7-.beta.-D-glucopyranoside; Genistin, primary pharmaceutical reference standard; Genistin, from Glycine max (soybean), >=95\\% (HPLC); GENISTIN (CONSTITUENT OF SOY ISOFLAVONES) [DSC]; 4-18-00-02732 (Beilstein Handbook Reference); 4,5,7-trihydroxyisoflavone 7-D-glucoside; GENISTEIN 7-O-.BETA.-D-GLUCOPYRANOSIDE; Glucopyranoside, genistein-7, beta-D-; 7-O-.beta.-D-glucopyranosyl genistein; Genistein, 7-beta-D-glucopyranoside; Genistein 7-O-b-D-glucopyranoside; Genistein, 7-O-beta-D-glucoside; Genistein 7-O-beta-D-glucoside; Genistin, analytical standard; Genisteol 7-monoglucoside; Genistin, >=97.5\\% (TLC); GENISTEIN GENISTIN [MI]; genistein 7-O-glucoside; Genistein 7-glucoside; Glucosyl-7-genistein; Genistein glucoside; GENISTIN [USP-RS]; UNII-1POG3SCN5T; MEGxp0_000436; Genistin,(S); ACon1_001495; Genistoside; 1POG3SCN5T; Genistine; Genistin; 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone; 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone; 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-chromen-4-one; 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)- (9CI); 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-; Prevention 10 (soy isoflavone concentrate); 4′,5,7-Trihydroxyisoflavone 7-glucoside; Genistein-7-O-beta-D-glucopyranoside; NCGC00163559-01; Genistin (8ci); CHEBI:27514; 48756_FLUKA; G0897_SIGMA; BRN 0064479; 529-59-9; NSC 5112; C09126; Genistein 7-O-β-D-glucopyranoside



数据库引用编号

47 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

20 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(20)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

93 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。



文献列表

  • Xiaoqin Tang, Rui Liao, Ling Zhou, Taian Yi, Mei Ran, Jiesi Luo, Feihong Huang, Anguo Wu, Qibing Mei, Long Wang, Xinwu Huang, Jianming Wu. Genistin: A Novel Estrogen Analogue Targeting ERβ to Alleviate Thrombocytopenia. International journal of biological sciences. 2024; 20(6):2236-2260. doi: 10.7150/ijbs.90483. [PMID: 38617546]
  • Jie Chen, Yishu Ni, Pingjing Zhang, Xianrui Liang, Sheng Fang. Acidic natural deep eutectic solvents as dual solvents and catalysts for the solubilization and deglycosylation of soybean isoflavone extracts: Genistin as a model compound. Food chemistry. 2023 Apr; 406(?):134999. doi: 10.1016/j.foodchem.2022.134999. [PMID: 36459802]
  • Zhe Li, Weichao Dong, Yanan Li, Xin Liu, Hong Wang, Long Dai, Jiayu Zhang, Shaoping Wang. The Metabolites and Mechanism Analysis of Genistin against Hyperlipidemia via the UHPLC-Q-Exactive Orbitrap Mass Spectrometer and Metabolomics. Molecules (Basel, Switzerland). 2023 Feb; 28(5):. doi: 10.3390/molecules28052242. [PMID: 36903488]
  • Zhe Wang, Xiaonan Li, Yiqiang Dai, Liqing Yin, Fidelis Azi, Jianzhong Zhou, Mingsheng Dong, Xiudong Xia. Sustainable production of genistin from glycerol by constructing and optimizing Escherichia coli. Metabolic engineering. 2022 11; 74(?):206-219. doi: 10.1016/j.ymben.2022.10.015. [PMID: 36336175]
  • Dong Meng, Biying Dong, Lili Niu, Zhihua Song, Litao Wang, Rohul Amin, Hongyan Cao, Hanghang Li, Qing Yang, Yujie Fu. The pigeon pea CcCIPK14-CcCBL1 pair positively modulates drought tolerance by enhancing flavonoid biosynthesis. The Plant journal : for cell and molecular biology. 2021 06; 106(5):1278-1297. doi: 10.1111/tpj.15234. [PMID: 33733535]
  • Miwako Toyofuku, Fuki Okutani, Masaru Nakayasu, Shoichiro Hamamoto, Hisabumi Takase, Kazufumi Yazaki, Akifumi Sugiyama. Enhancement of developmentally regulated daidzein secretion from soybean roots in field conditions as compared with hydroponic culture. Bioscience, biotechnology, and biochemistry. 2021 Apr; 85(5):1165-1169. doi: 10.1093/bbb/zbab017. [PMID: 33784734]
  • Yae Rim Choi, Jaewon Shim, Min Jung Kim. Genistin: A Novel Potent Anti-Adipogenic and Anti-Lipogenic Agent. Molecules (Basel, Switzerland). 2020 Apr; 25(9):. doi: 10.3390/molecules25092042. [PMID: 32349444]
  • Anowarul Islam, Md Sadikul Islam, Md Nazim Uddin, Mir Md Iqbal Hasan, Md Rashedunnabi Akanda. The potential health benefits of the isoflavone glycoside genistin. Archives of pharmacal research. 2020 Apr; 43(4):395-408. doi: 10.1007/s12272-020-01233-2. [PMID: 32253713]
  • You Jin Lim, Ho Young Jeong, Chan Saem Gil, Soon-Jae Kwon, Jong Kuk Na, Chanhui Lee, Seok Hyun Eom. Isoflavone accumulation and the metabolic gene expression in response to persistent UV-B irradiation in soybean sprouts. Food chemistry. 2020 Jan; 303(?):125376. doi: 10.1016/j.foodchem.2019.125376. [PMID: 31442900]
  • Feng Qiu, Linyi Shi, Siqi Wang, Sha Wu, Manyuan Wang. Simultaneous high-performance liquid chromatography with diode array detection and time-of-flight mass spectrometric confirmation of the ten bioactive compounds in Semen Sojae Preparatum. Journal of separation science. 2018 Sep; 41(17):3360-3371. doi: 10.1002/jssc.201800504. [PMID: 30016573]
  • Young Hye Seo, Ju-Hyun Jeon, Miran Jeong, Seung Mok Ryu, Won Kyung Jeon, Dae Sik Jang, Sang Hee Shim, Dongho Lee, Jung-Hye Choi, Jun Lee. Chemical Constituents of Apios americana Tubers and Their Inhibitory Activities on Nitric Oxide Production in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages. Journal of natural products. 2018 07; 81(7):1598-1603. doi: 10.1021/acs.jnatprod.8b00182. [PMID: 29932657]
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  • Michaela Kopečná-Zapletalová, Kristýna Krasulová, Pavel Anzenbacher, Petr Hodek, Eva Anzenbacherová. Interaction of isoflavonoids with human liver microsomal cytochromes P450: inhibition of CYP enzyme activities. Xenobiotica; the fate of foreign compounds in biological systems. 2017 Apr; 47(4):324-331. doi: 10.1080/00498254.2016.1195028. [PMID: 27312150]
  • Alírica I Suárez, Zaw Min Thu, Jorge Ramírez, Diana León, Luis Cartuche, Chabaco Armijos, Geovanni Vidari. Main Constituents and Antidiabetic Properties of Otholobium mexicanum. Natural product communications. 2017 Apr; 12(4):533-535. doi: . [PMID: 30520590]
  • Hee Rae Kang, Dahae Lee, René Benndorf, Won Hee Jung, Christine Beemelmanns, Ki Sung Kang, Ki Hyun Kim. Termisoflavones A-C, Isoflavonoid Glycosides from Termite-Associated Streptomyces sp. RB1. Journal of natural products. 2016 Dec; 79(12):3072-3078. doi: 10.1021/acs.jnatprod.6b00738. [PMID: 28006913]
  • Liangliang Liu, Juan Leng, Xiai Yang, Liping Liao, Yin Cen, Aiping Xiao, Lei Ma. Rapid Screening and Identification of BSA Bound Ligands from Radix astragali Using BSA Immobilized Magnetic Nanoparticles Coupled with HPLC-MS. Molecules (Basel, Switzerland). 2016 Nov; 21(11):. doi: 10.3390/molecules21111471. [PMID: 27827956]
  • José P da Graça, Tatiana E Ueda, Tatiani Janegitz, Simone S Vieira, Mariana C Salvador, Maria C N de Oliveira, Sonia M Zingaretti, Stephen J Powers, John A Pickett, Michael A Birkett, Clara B Hoffmann-Campo. The natural plant stress elicitor cis-jasmone causes cultivar-dependent reduction in growth of the stink bug, Euschistus heros and associated changes in flavonoid concentrations in soybean, Glycine max. Phytochemistry. 2016 Nov; 131(?):84-91. doi: 10.1016/j.phytochem.2016.08.013. [PMID: 27659594]
  • Heung Joo Yuk, Yeong Hun Song, Marcus J Curtis-Long, Dae Wook Kim, Su Gyeong Woo, Yong Bok Lee, Zia Uddin, Cha Young Kim, Ki Hun Park. Ethylene Induced a High Accumulation of Dietary Isoflavones and Expression of Isoflavonoid Biosynthetic Genes in Soybean (Glycine max) Leaves. Journal of agricultural and food chemistry. 2016 Oct; 64(39):7315-7324. doi: 10.1021/acs.jafc.6b02543. [PMID: 27626287]
  • Yan Zhang, Sam K C Chang. Isoflavone Profiles and Kinetic Changes during Ultra-High Temperature Processing of Soymilk. Journal of food science. 2016 Mar; 81(3):C593-9. doi: 10.1111/1750-3841.13236. [PMID: 26814612]
  • Huihua Qu, Baoping Qu, Xueqian Wang, Yue Zhang, Jinjun Cheng, Wenhao Zeng, Shuchen Liu, Qingguo Wang, Yan Zhao. Rapid, sensitive separation of the three main isoflavones in soybean using immunoaffinity chromatography. Journal of separation science. 2016 Mar; 39(6):1195-201. doi: 10.1002/jssc.201501052. [PMID: 26813984]
  • S Persiani, F Sala, C Manzotti, M Colovic, M Zangarini, Y Donazzolo, B Barbetta, C Vitalini, G Giacovelli, C Benvenuti, L C Rovati. Evaluation of Levothyroxine Bioavailability after Oral Administration of a Fixed Combination of Soy Isoflavones in Post-menopausal Female Volunteers. Drug research. 2016 Mar; 66(3):136-40. doi: 10.1055/s-0035-1555784. [PMID: 26125285]
  • Bingrui Liu, Kenneth T Kongstad, Sun Qinglei, Nils T Nyberg, Anna K Jäger, Dan Staerk. Dual high-resolution α-glucosidase and radical scavenging profiling combined with HPLC-HRMS-SPE-NMR for identification of minor and major constituents directly from the crude extract of Pueraria lobata. Journal of natural products. 2015 Feb; 78(2):294-300. doi: 10.1021/np5009416. [PMID: 25679337]
  • Seiichi Sakamoto, Gorawit Yusakul, Benyakan Pongkitwitoon, Madan Kumar Paudel, Hiroyuki Tanaka, Satoshi Morimoto. Simultaneous determination of soy isoflavone glycosides, daidzin and genistin by monoclonal antibody-based highly sensitive indirect competitive enzyme-linked immunosorbent assay. Food chemistry. 2015 Feb; 169(?):127-33. doi: 10.1016/j.foodchem.2014.08.004. [PMID: 25236207]
  • Evgeny G Chulkov, Ludmila V Schagina, Olga S Ostroumova. Membrane dipole modifiers modulate single-length nystatin channels via reducing elastic stress in the vicinity of the lipid mouth of a pore. Biochimica et biophysica acta. 2015 Jan; 1848(1 Pt A):192-9. doi: 10.1016/j.bbamem.2014.09.004. [PMID: 25223717]
  • Vera van der Velpen, Anouk Geelen, Peter C H Hollman, Evert G Schouten, Pieter van 't Veer, Lydia A Afman. Isoflavone supplement composition and equol producer status affect gene expression in adipose tissue: a double-blind, randomized, placebo-controlled crossover trial in postmenopausal women. The American journal of clinical nutrition. 2014 Nov; 100(5):1269-77. doi: 10.3945/ajcn.114.088484. [PMID: 25332325]
  • Jose Manuel Silvan, Chou Srey, Jennifer M Ames, Maria Dolores del Castillo. Glycation is regulated by isoflavones. Food & function. 2014 Sep; 5(9):2036-42. doi: 10.1039/c4fo00260a. [PMID: 25051420]
  • Abubaker M A Morgan, Hyun Woo Lee, Sang-Hyun Lee, Chi-Hwan Lim, Hae-Dong Jang, Young Ho Kim. Anti-osteoporotic and antioxidant activities of chemical constituents of the aerial parts of Ducrosia ismaelis. Bioorganic & medicinal chemistry letters. 2014 Aug; 24(15):3434-9. doi: 10.1016/j.bmcl.2014.05.077. [PMID: 24953601]
  • Liqin Du, Zilong Wang, Yingli Zhao, Jinqun Huang, Hao Pang, Yutuo Wei, Lihua Lin, Ribo Huang. A β-glucosidase from Novosphingobium sp. GX9 with high catalytic efficiency toward isoflavonoid glycoside hydrolysis and (+)-catechin transglycosylation. Applied microbiology and biotechnology. 2014 Aug; 98(16):7069-79. doi: 10.1007/s00253-014-5661-3. [PMID: 24682446]
  • Jia Li, Zhaobo Li, Changfu Li, Junbo Gou, Yansheng Zhang. Molecular cloning and characterization of an isoflavone 7-O-glucosyltransferase from Pueraria lobata. Plant cell reports. 2014 Jul; 33(7):1173-85. doi: 10.1007/s00299-014-1606-7. [PMID: 24700248]
  • Vamsidhar Yerramsetty, Daniel D Gallaher, Baraem Ismail. Malonylglucoside conjugates of isoflavones are much less bioavailable compared with unconjugated β-glucosidic forms in rats. The Journal of nutrition. 2014 May; 144(5):631-7. doi: 10.3945/jn.114.190801. [PMID: 24647389]
  • Hyeon-Jeong Oh, Young-Gyu Kang, Tae-Young Na, Hyeon-Ji Kim, Jun Seong Park, Won-Jea Cho, Mi-Ock Lee. Identification of daidzein as a ligand of retinoic acid receptor that suppresses expression of matrix metalloproteinase-9 in HaCaT cells. Molecular and cellular endocrinology. 2013 Aug; 376(1-2):107-13. doi: 10.1016/j.mce.2013.06.015. [PMID: 23791815]
  • P Bontempo, D Rigano, A Doto, C Formisano, M Conte, A Nebbioso, V Carafa, G Caserta, V Sica, A M Molinari, L Altucci. Genista sessilifolia DC. extracts induce apoptosis across a range of cancer cell lines. Cell proliferation. 2013 Apr; 46(2):183-92. doi: 10.1111/cpr.12022. [PMID: 23510473]
  • Xin Dong, Wenqing Xu, Robert A Sikes, Changqing Wu. Apoptotic effects of cooked and in vitro digested soy on human prostate cancer cells. Food chemistry. 2012 Dec; 135(3):1643-52. doi: 10.1016/j.foodchem.2012.06.023. [PMID: 22953905]
  • Soha M Hamdy, Abdel Karim M Abdel Latif, Ehab A Drees, Sahar M Soliman. Prevention of rat breast cancer by genistin and selenium. Toxicology and industrial health. 2012 Sep; 28(8):746-57. doi: 10.1177/0748233711422732. [PMID: 22089659]
  • Lu Chang, Yanping Ren, Liang Cao, Yingguang Sun, Qian Sun, Ning Sheng, Lin Yuan, Xuran Zhi, Lantong Zhang. Simultaneous determination and pharmacokinetic study of six flavonoids from Fructus Sophorae extract in rat plasma by LC-MS/MS. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2012 Sep; 904(?):59-64. doi: 10.1016/j.jchromb.2012.07.015. [PMID: 22867839]
  • Venkata K Yellepeddi, Kiran K Vangara, Ajay Kumar, Srinath Palakurthi. Comparative evaluation of small-molecule chemosensitizers in reversal of cisplatin resistance in ovarian cancer cells. Anticancer research. 2012 Sep; 32(9):3651-8. doi: . [PMID: 22993302]
  • Ann-Cathrin Hellström, Jonas Muntzing. The pollen extract Femal--a nonestrogenic alternative to hormone therapy in women with menopausal symptoms. Menopause (New York, N.Y.). 2012 Jul; 19(7):825-9. doi: 10.1097/gme.0b013e31824017bc. [PMID: 22334059]
  • Sarawoot Gomuttapong, Rangsima Pewphong, Sucha Choeisiri, Sukanya Jaroenporn, Suchinda Malaivijitnond. Testing of the estrogenic activity and toxicity of Stephania venosa herb in ovariectomized rats. Toxicology mechanisms and methods. 2012 Jul; 22(6):445-57. doi: 10.3109/15376516.2012.668573. [PMID: 22394346]
  • Jing Luo, Liying Zhang, Danjun Chen, Peng Wang, Jiawei Zhao, Yan Peng, Shuhu Du, Zhongping Zhang. Molecularly imprinted layer-coated monodisperse spherical silica microparticles toward affinity-enrichment of isoflavonoid glycosides from Radix puerariae. The Analyst. 2012 Jun; 137(12):2891-902. doi: 10.1039/c2an35049a. [PMID: 22553769]
  • Seong Eun Jin, You Kyung Son, Byung-Sun Min, Hyun Ah Jung, Jae Sue Choi. Anti-inflammatory and antioxidant activities of constituents isolated from Pueraria lobata roots. Archives of pharmacal research. 2012 May; 35(5):823-37. doi: 10.1007/s12272-012-0508-x. [PMID: 22644850]
  • Samara A Brito, Fabíola F G Rodrigues, Adriana R Campos, José G M da Costa. Evaluation of the antifungal activity and modulation between Cajanus cajan (L.) Millsp. leaves and roots ethanolic extracts and conventional antifungals. Pharmacognosy magazine. 2012 Apr; 8(30):103-6. doi: 10.4103/0973-1296.96550. [PMID: 22701281]
  • Sachiko Arase, Megumi Kasai, Akira Kanazawa. In planta assays involving epigenetically silenced genes reveal inhibition of cytosine methylation by genistein. Plant methods. 2012 Mar; 8(?):10. doi: 10.1186/1746-4811-8-10. [PMID: 22424588]
  • Bo Yuan, Huijuan Zhen, Yi Jin, Li Xu, Xue Jiang, Shuaiting Sun, Chibing Li, Haiyan Xu. Absorption and plasma disposition of genistin differ from those of genistein in healthy women. Journal of agricultural and food chemistry. 2012 Feb; 60(6):1428-36. doi: 10.1021/jf204421c. [PMID: 22256777]
  • Preety Dixit, Raju Chillara, Vikram Khedgikar, Jyoti Gautam, Priyanka Kushwaha, Avinash Kumar, Divya Singh, Ritu Trivedi, Rakesh Maurya. Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(2):890-7. doi: 10.1016/j.bmcl.2011.12.036. [PMID: 22212722]
  • MinHee Park, Min Kyu Jeong, MiJa Kim, JaeHwan Lee. Modification of isoflavone profiles in a fermented soy food with almond powder. Journal of food science. 2012 Jan; 77(1):C128-34. doi: 10.1111/j.1750-3841.2011.02504.x. [PMID: 22182181]
  • Qing Miao, Jing-Ge Li, Shan Miao, Nan Hu, Jin Zhang, Song Zhang, Yan-Hua Xie, Jian-Bo Wang, Si-Wang Wang. The bone-protective effect of genistein in the animal model of bilateral ovariectomy: roles of phytoestrogens and PTH/PTHR1 against post-menopausal osteoporosis. International journal of molecular sciences. 2012; 13(1):56-70. doi: 10.3390/ijms13010056. [PMID: 22312238]
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