Studies on the synthesis and antitumor activities of soybean isoflavones and their derivatives

Yaoxue Xuebao

Volumn 35, Issue 8, 2000, Pages 583-586

  Liu, Peng ^a   Chang, Jun Biao ^a   Chen, Rong Feng ^a   Xie, Jing Xi ^b   Wang, Qiang ^a  

^a HENAN INSTITUTE OF CHEMISTRY   (China)

^b INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Daidzein; Genistein; Soybean isoflavone

Indexed keywords

EID: 0042724402     PISSN: 05134870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Christine G. The Joy of Soy[N]. Time Weekly, 1999, June 7:68-69.
2. Barnes S, Grubbs C, Setchell KDR, et al. Soybeans inhibit mammary tumors in models of breast cancer [A]. In: Mutagens and Carcinogens in the Diet [M], New York: Wiley-Liss, 1984.239-253.
3. Anderson RL, Wolf WJ. Compositional changes in trypsin inhibitors, phytic acid, saponins and isoflavones related to soybean processing [J]. J Nutr, 1995, 125 (35):581s-588s.
4. Coward L, Barnes NC, Setchell KDR, et al. Genistein, daidzein and their β-glycoside conjugates: antitumor isoflavones in soybean foods from American and Asian diet [J]. Agric Food Chem, 1993,41:1961-1967.
5. Wei HC, Bowen R, Cai QY, et al. Antioxident and antipromotional effects of the soybean isoflavone genistein [J]. Proc Soc Exp Biol Med, 1995,208(1):124-130.
6. Wähälä K, Hase TA. An expedient synthesis of polyhydroxy isoflavones[J]. J Chem Soc Perkin Trans 1, 1991,(22):3005-3008.
7. Devi N, Jain N, Krishnamurty HG. A new synthesis of deoxybenzoins[J]. Indian J Chem, 1993,32B:874.
8. Gulati. 2, 4, 6-Trihydroxyacetophenone [A]. In: Org Syn (Coll vol 2) [M]. London and New York: John Wiley & Sons, Inc. 1963.522-523.
9. Spoerri PE, DuBois AS. The hoesch reaction [A]. Adams G. Organic Reactions (V) [M]. London and New York: Chapman and Hall, 1952.407-430.
10. Bass RJ. Synthesis of chromones by cyclization of 2-hydroxyphenyl kefornes with boron trifluoride-diethyl ether and methanesulphonyl chloride [J]. J Chem Soc Chem Comm, 1976,(2):78-79.
11. Kagal SA, Nair PM, Venkataraman K. A synthesis of isoflavones by a modified Vilsmeier-Haack Reaction[J]. Tetrahedron Lett, 1962,14:593-596.
12. Singh OV, Kapil RS. A general method for the synthesis of isoflavones by oxidative rearrangement of isoflavones using thallium (III) perchlorate [J]. Indian J Chem, 1993,32B:911-915.
13. Sheng WC. Improved synthesis of p-hydroxyphenylacetic acid[J]. Chin J Pharm(in Chinese), 1993,24(6):276-277.