217817-09-9 Usage
Uses
Used in Pharmaceutical Industry:
Curcolonol is used as an active pharmaceutical ingredient for its various therapeutic properties, including anti-inflammatory, antioxidant, and anticancer activities. Its potential use in the treatment of neurological disorders is also being studied due to its neuroprotective effects.
Used in Medical Industry:
Curcolonol is used as a potential treatment for neurological disorders, given its neuroprotective effects. Additionally, its antimicrobial and antifungal properties make it a candidate for use in medical applications to combat infections.
Used in Cosmetics Industry:
Curcolonol is used as a fragrance ingredient in cosmetics due to its pleasant, woody odor. Its antioxidant properties may also contribute to the development of skincare products with added benefits.
Used in Food and Beverage Industry:
Curcolonol can be used as a natural flavoring agent in the food and beverage industry, adding a unique taste and aroma to various products. Its antimicrobial properties may also have potential applications in food preservation.
Used in Agriculture:
Curcolonol's antimicrobial and antifungal properties can be utilized in agriculture as a natural pesticide or fungicide, helping to protect crops from diseases and pests while reducing the need for synthetic chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 217817-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,8,1 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 217817-09:
(8*2)+(7*1)+(6*7)+(5*8)+(4*1)+(3*7)+(2*0)+(1*9)=139
139 % 10 = 9
So 217817-09-9 is a valid CAS Registry Number.
217817-09-9Relevant academic research and scientific papers
Seven pairs of new enantiomeric sesquiterpenoids from Curcuma phaeocaulis
Chen, Jin-Feng,Guo, Li,Liu, Fei,Peng, Cheng,Qiao, Ming-Ming,Xiong, Liang,Zhao, Hao-Yu,Zhou, Qin-Mei
, (2020/04/17)
Seven pairs of new enantiomeric sesquiterpenoids, (+)/(?)-phaeocauline A ? G [(+)/(?)-1–7], were isolated from the rhizomes of Curcuma phaeocaulis by chiral HPLC separation. Their structures, including absolute configurations, were determined by spectroscopic analyses and ECD data. The isolates were assessed for vasorelaxant, anti-platelet aggregative, and neuroprotective activities. Enantiomers (+)-1 and (?)-1 showed similar activity against abnormal platelet aggregation induced by arachidonic acid, while their C-4 epimers (+)-2 and (?)-2 were inactive, which indicated that those effects were stereoselective, but not enantioselective. Compounds (+)/(?)-3–5 exhibited vasorelaxant effects against KCl-induced contraction of rat aortic rings.
