3691-71-2 Usage
Description
α-ETHYL-4,4′-STILBENEDIOL, also known as (E)-2-ethyl-4,4′-dihydroxystilbene, is a chemical compound with the molecular formula C16H16O2. It is a derivative of stilbene, a polyphenolic compound found in various plants, and is used in the production of pharmaceuticals and organic synthesis. α-ETHYL-4,4′-STILBENEDIOL has been studied for its potential therapeutic applications, including its antioxidant and anti-inflammatory properties. It is also being investigated for its potential role in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Additionally, it has been identified as a potential chemopreventive and chemotherapeutic agent, with research indicating its ability to inhibit the growth of cancer cells. Overall, α-ETHYL-4,4′-STILBENEDIOL shows promise in various areas of medicinal and pharmaceutical research due to its diverse biological activities.
Uses
Used in Pharmaceutical Industry:
α-ETHYL-4,4′-STILBENEDIOL is used as a key compound in the production of pharmaceuticals for its potential therapeutic applications. Its antioxidant and anti-inflammatory properties make it a candidate for the development of treatments targeting a range of conditions.
Used in Organic Synthesis:
In the field of organic synthesis, α-ETHYL-4,4′-STILBENEDIOL serves as a valuable intermediate for the synthesis of other complex organic molecules, contributing to the advancement of chemical research and the creation of new compounds with potential applications.
Used in Neurodegenerative Disease Research:
α-ETHYL-4,4′-STILBENEDIOL is used as a research compound in the study of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its potential role in the treatment of these conditions is being explored, with the aim of developing new therapeutic strategies to combat these debilitating disorders.
Used in Cancer Research and Treatment:
α-ETHYL-4,4′-STILBENEDIOL is used as a chemopreventive and chemotherapeutic agent in cancer research. Its ability to inhibit the growth of cancer cells is being investigated, with the potential to contribute to the development of new cancer treatments and prevention strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 3691-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3691-71:
(6*3)+(5*6)+(4*9)+(3*1)+(2*7)+(1*1)=102
102 % 10 = 2
So 3691-71-2 is a valid CAS Registry Number.
3691-71-2Relevant articles and documents
Bibenzyl- and stilbene-core compounds with non-polar linker atom substituents as selective ligands for estrogen receptor beta
Waibel, Michael,De Angelis, Meri,Stossi, Fabio,Kieser, Karen J.,Carlson, Kathryn E.,Katzenellenbogen, Benita S.,Katzenellenbogen, John A.
experimental part, p. 3412 - 3424 (2009/10/23)
A series of structurally simple bibenzyl-diol and stilbene-diol core molecules, structural analogs of the well-known hexestrol and diethylstilbestrol non-steroidal estrogens, were prepared and evaluated as estrogen receptor (ER) subtype-selective ligands. Analysis of their ERα and ERβ binding showed that certain substitution patterns engendered binding affinities that were >100-fold selective for ERβ. When further investigated in cell-based gene transcription assays, some molecules showed similarly high relative transcriptional potency selectivity in favor of ERβ. Interestingly, the most ERβ-selective molecules were those bearing non-polar substituents on one of the internal carbon atoms. These compounds should be useful probes for determining the physiological roles of ERβ, and they might lead to the development of more selective and thus safer pharmaceuticals.
