32884-36-9 Usage
Uses
Used in Pharmaceutical Industry:
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is used as a pharmaceutical agent for its anti-cancer properties. It has been studied for its potential to inhibit the growth and progression of various types of cancer, including breast, prostate, and lung cancer. Genistein modulates multiple oncological signaling pathways, exerting inhibitory effects on tumor growth and progression.
Used in Nutraceutical Industry:
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is used as a nutraceutical ingredient for its anti-inflammatory and anti-aging properties. It has been investigated for its potential to reduce inflammation and oxidative stress, promoting overall health and well-being.
Used in Bone Health Applications:
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is used as a bone health supplement for its potential to improve bone density and reduce the risk of osteoporosis. It has been studied for its ability to promote bone formation and inhibit bone resorption, contributing to better bone health.
Used in Cardiovascular Health Applications:
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is used as a cardiovascular health supplement for its potential to reduce the risk of cardiovascular diseases. It has been investigated for its ability to lower cholesterol levels, improve blood vessel function, and reduce inflammation, contributing to better cardiovascular health.
Used in Menopause Management:
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is used as a natural remedy for menopause management due to its estrogen-like effects. It has been studied for its potential to alleviate symptoms of menopause, such as hot flashes and mood swings, providing relief and improving the quality of life for menopausal women.
Check Digit Verification of cas no
The CAS Registry Mumber 32884-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32884-36:
(7*3)+(6*2)+(5*8)+(4*8)+(3*4)+(2*3)+(1*6)=129
129 % 10 = 9
So 32884-36-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O6/c1-21-9-5-13(19)15-14(6-9)22-7-11(16(15)20)10-3-2-8(17)4-12(10)18/h2-7,17-19H,1H3
32884-36-9Relevant academic research and scientific papers
Total synthesis of apios isoflavones and investigation of their tyrosinase inhibitory activity
Asebi, Nana,Nihei, Ken-ichi
, (2019/09/12)
Apios isoflavone glucosides 1 and 2 were synthesized for the first time via Friedel–Crafts reaction, Bischler–Napieralski-type cyclization, and phase-transfer catalyzed glycosylation as the key steps. In addition, aglycones 4 and 5 and related natural iso
Constrained phytoestrogens and analogues as ERβ selective ligands
Miller, Chris P.,Collini, Michael D.,Harris, Heather A.
, p. 2399 - 2403 (2007/10/03)
A new series of ERbeta (ERβ) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERβ over ERα of over 40-fold. In addition to its binding selectivity, 6 was a
Substituted 10,11-benzo[b]fluoren-10-ones as estrogenic agents
-
, (2008/06/13)
This invention provides estrogen receptor modulators of formula 1, having the structure wherein X, Y1, Y2, Y3, Y4, Z1, Z2, Z3, and Z4 are as defined in the specificati
