Results 1 - 10 of 218

<

1

2

3

...

21

22

>

Application of Mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents. Mykhaylo S. Frasinyuk, Galyna P. Mrug, Svitlana P. Bondarenko, Vitaliy M. Sviripa, Wen Zhang, Xianfeng Cai, Michael V. Fiandalo, James L. Mohler, Chunming Liu, David S. Watt , Org. Biomol. Chem. , 2015 , 13 , 11292

Synthesis and tautomerization of hydroxylated isoflavones bearing heterocyclic hemi-aminals. Mykhaylo S. Frasinyuk, Svitlana P. Bondarenko, Volodymyr P. Khilya, Chunming Liu, David S. Watt, Vitaliy M. Sviripa , Org. Biomol. Chem. , 2015 , 13 , 1053

Isoflavonoids of the Leguminosae. Nigel C. Veitch , Nat. Prod. Rep. , 2009 , 26 , 776

Isoflavonoids of the Leguminosae. Nigel C. Veitch , Nat. Prod. Rep. , 2013 , 30 , 988

Isoflavonoids of the Leguminosae. Nigel C. Veitch , Nat. Prod. Rep. , 2007 , 24 , 417

Biologically guided isolation and ADMET profile of new factor Xa inhibitors from Glycyrrhiza glabra roots using in vitro and in silico approaches. Reham S. Ibrahim, Rahma S. R. Mahrous, Rasha M. Abu EL-Khair, Samir A. Ross, Abdallah A. Omar, Hoda M. Fathy , RSC Adv. , 2021 , 11 , 9995

Natural isoflavone formononetin inhibits IgE-mediated mast cell activation and allergic inflammation by increasing IgE receptor degradation. Zi-Wen Zhou, Kunmei Ji, Xue-Yan Zhu, Xin-Ying Wu, Ruo-Tong Lin, Chu-Chu Xie, Ze-Lang Cai, Jia-Jie Chen , Food Funct. , 2023 , 14 , 2857

An updated review of fatty acid residue-tethered heterocyclic compounds: synthetic strategies and biological significance. Taghreed A. Majrashi, Ahmed Sabt, Hayam A. Abd El Salam, Ghada H. Al-Ansary, Mohamed Farouk Hamissa, Wagdy M. Eldehna , RSC Adv. , 2023 , 13 , 13655

Formononetin inhibits human bladder cancer cell proliferation and invasiveness via regulation of miR-21 and PTEN. Yiying Wu, Xing Zhang, Zhengzhao Li, Haibiao Yan, Jian Qin, Tianyu Li , Food Funct. , 2017 , 8 , 1061

381. A new synthesis of isoflavones. Part I. Wilson Baker, J. Chadderton, J. B. Harborne, W. D. Ollis , J. Chem. Soc. , 1953 , 1852