55930-44-4 Usage
Uses
Used in Pharmaceutical Industry:
Eucommiol is used as a therapeutic agent for various diseases due to its diverse pharmacological effects, including its anti-inflammatory, antioxidant, and anti-microbial properties.
Used in Cancer Treatment:
Eucommiol is used as a potential anti-cancer agent, exhibiting potential efficacy against various types of cancer through its multi-targeting capabilities and synergistic effects with conventional treatments.
Used in Diabetes Management:
Eucommiol is used as a potential treatment for diabetes, leveraging its anti-inflammatory and antioxidant properties to help manage and mitigate the disease's complications.
Used in Cardiovascular Disorders:
Eucommiol is used as a protective agent in cardiovascular health, potentially reducing inflammation and oxidative stress associated with heart diseases.
Used in Anti-Microbial Applications:
Eucommiol is used as an anti-microbial agent, effective against various pathogens, making it a candidate for new drug development in the fight against resistant infections.
Used in Anti-Fungal Applications:
Eucommiol is used as an anti-fungal agent, demonstrating potential in treating fungal infections and contributing to the development of new anti-fungal drugs.
Used in Anti-Aging Research:
Eucommiol is used in anti-aging studies for its potential to extend lifespan and improve healthspan by combating age-related inflammation and oxidative stress.
Used in Skin Care Industry:
Eucommiol is used as a protective agent against UV-induced skin damage, offering potential benefits in skincare products for sun protection and skin health preservation.
Check Digit Verification of cas no
The CAS Registry Mumber 55930-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55930-44:
(7*5)+(6*5)+(5*9)+(4*3)+(3*0)+(2*4)+(1*4)=134
134 % 10 = 4
So 55930-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O4/c10-2-1-7-8(5-12)6(4-11)3-9(7)13/h7,9-13H,1-5H2/t7-,9-/m1/s1
55930-44-4Relevant academic research and scientific papers
Bernini, Romolo,Iavarone, Carlo,Trogolo, Corrado
, p. 1431 - 1434 (1984)
Eucommiol and a new eucommiol glucoside (eucommioside II) were isolated from Aucuba japonica, besides known aucubin.The structure of eucommioside II was determined, by 1H and 13CNMR spectroscopy and some chemical transformations, as 1-O-β-D-glucopyranosyl eucommiol.Similarities between components of A. japonica and Eucommia ulmoides (aucubin, eucommiol, eucommioside I) are discussed briefly. - Keywords: Aucuba japonica; Cornaceae; eucommiol; eucommioside II; 1-O-β-D-glucopyranosyl eucommiol; Birch reduction; 1H and 13C NMR; eucommioside I.
Davini, Enrico,Iavarone, Carlo,Trogolo, Corrado
, p. 1449 - 1452 (1987)
Key Word Index - Eucommia ulmoides; Eucommiaceae; aucubin; aucubigenin; iridoid aglycones; eucommial; eucommiol; 1H NMR and 13C NMR.Aucubigenin, which exists only in the closed hemiacetal form, has been transformed into a stable conjugated 1,5-dialdehyde form, 'eucommial', by a base-catalysed Δ7 -> Δ8 double-bond shift.Further reduction of eucommial leads to eucommiol, which co-occurs with aucubin in the autumn in Eucommia ulmoides and Aucuba japonica.The successful transformation of aucubin to eucommiol seems to support an in vivo relationship between these compounds.
