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[PDF][PDF] The spectrum of phytoestrogens in nature: our knowledge is expanding
P Moutsatsou - HORMONES-ATHENS-, 2007 - researchgate.net
The classical phytoestrogens, so far known, constitute a group of plant-derived compounds
which include mainly isoflavones, lignans, coumestanes, stilbenes and the flavonoids …
which include mainly isoflavones, lignans, coumestanes, stilbenes and the flavonoids …
Genotoxicity of phytoestrogens
H Stopper, E Schmitt, K Kobras - Mutation Research/Fundamental and …, 2005 - Elsevier
Plant extracts containing phytohormones are very popular as 'alternative'medicine for many
kinds of diseases. They are especially favored by women who enter menopause and are …
kinds of diseases. They are especially favored by women who enter menopause and are …
Density functional theory study of the structure–antioxidant activity of polyphenolic deoxybenzoins
Quantum chemical calculations based on the density functional theory (DFT) have been
employed to study the relationship between the structure and the antioxidant activity of four …
employed to study the relationship between the structure and the antioxidant activity of four …
New concepts, experimental approaches, and dereplication strategies for the discovery of novel phytoestrogens from natural sources
Phytoestrogens constitute an attractive research topic due to their estrogenic profile and
their biological involvement in womanʼs health. Therefore, numerous studies are currently …
their biological involvement in womanʼs health. Therefore, numerous studies are currently …
Bis 1, 2, 3‐Triazoles Linked Deoxybenzoin Hybrids as Antimicrobial Agents: Synthesis, In Vitro and In Silico Screening
S Aitha, V Thumma, S Ambala, R Matta… - …, 2023 - Wiley Online Library
A series of new deoxybenzoin based bis 1, 2, 3‐triazole analogues were synthesized and
reported in the present communication. Synthesis of analogues were accomplished by a …
reported in the present communication. Synthesis of analogues were accomplished by a …
[HTML][HTML] Estrogen receptor α and β in uterine fibroids: a basis for altered estrogen responsiveness
OBJECTIVE: To investigate the relative expression and the DNA-binding status of estrogen
receptors α and β in fibroids and normal myometrial tissue to explore the molecular basis of …
receptors α and β in fibroids and normal myometrial tissue to explore the molecular basis of …
Novel dehydroepiandrosterone derivatives with antiapoptotic, neuroprotective activity
DHEA analogues with modifications at positions C3 or C17 were synthesized and evaluated
for neuroprotective activity against the neural-crest-derived PC12 cell model of serum …
for neuroprotective activity against the neural-crest-derived PC12 cell model of serum …
Can antioxidants reduce the toxicity of bisphenol?
W Mączka, M Grabarczyk, K Wińska - Antioxidants, 2022 - mdpi.com
BPA is still the subject of extensive research due to its widespread use, despite its significant
toxicity resulting not only from its negative impact on the endocrine system but also from …
toxicity resulting not only from its negative impact on the endocrine system but also from …
Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors
A Vontzalidou, G Zoidis, E Chaita… - Bioorganic & medicinal …, 2012 - Elsevier
The synthesis, molecular modeling and biological evaluation of substituted deoxybenzoins
and optimized dihydrostilbenes are reported. Preliminary structure–activity relationship data …
and optimized dihydrostilbenes are reported. Preliminary structure–activity relationship data …
Transition Metal‐Free Aroylation of Diarylmethanes with N‐Bn‐N‐Boc Arylamides and N‐Acylpyrroles
F Yang, D Zou, S Chen, H Wang, Y Zhao… - Advanced Synthesis …, 2020 - Wiley Online Library
In the last 20 years, efficient transition metal catalysts for the α‐arylation of enolates have
been introduced. Despite the popularity and utility of these reactions, there remains room for …
been introduced. Despite the popularity and utility of these reactions, there remains room for …