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Zedoarofuran is a natural sesquiterpene compound derived from the rhizome of the Zedoary plant, a member of the ginger family. It is known for its anti-inflammatory, antibacterial, and antifungal properties, making it a promising candidate for the development of new drugs and natural products for various medical and cosmetic purposes.

213833-34-2

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213833-34-2 Usage

Uses

Used in Pharmaceutical Industry:
Zedoarofuran is used as a therapeutic agent for the treatment of skin diseases, inflammatory conditions, and infectious diseases due to its anti-inflammatory, antibacterial, and antifungal properties.
Used in Cosmetic Industry:
Zedoarofuran is used as an active ingredient in cosmetic products for its potential skin health benefits, including anti-inflammatory and antimicrobial effects, contributing to the development of natural skincare solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 213833-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,8,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 213833-34:
(8*2)+(7*1)+(6*3)+(5*8)+(4*3)+(3*3)+(2*3)+(1*4)=112
112 % 10 = 2
So 213833-34-2 is a valid CAS Registry Number.

213833-34-2Relevant 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)

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.

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