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(20R)-20,25-Epoxy-5α-dammarane-3,6,12-trione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66007-90-7

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66007-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66007-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66007-90:
(7*6)+(6*6)+(5*0)+(4*0)+(3*7)+(2*9)+(1*0)=117
117 % 10 = 7
So 66007-90-7 is a valid CAS Registry Number.

66007-90-7Downstream Products

66007-90-7Relevant academic research and scientific papers

Synthesis and evaluation of panaxatriol derivatives as Na+, K+-ATPase inhibitors

Wu, Qiong,Chen, Peng,Tu, Guangzhong,Li, Meng,Pan, Bowen,Guo, Yan,Zhai, Jinbi,Fu, Hongzheng

, p. 2885 - 2889 (2018)

Panaxatriol, a triterpene bearing a steroid-like structure similar to cardiac glycosides, was presumed to share the same bioactivity with cardiac glycosides, and may be a potential Na+, K+-ATPase inhibitor. In this paper, a series of panaxatriol derivatives were synthesized and evaluated for Na+, K+-ATPase inhibitory activities. The results of biological tests showed that more than half of the synthesized derivatives presented increased inhibitory activities compared with panaxatriol. Of these compounds, 13a with a 3, 4-seco skeleton showed the most potent inhibitory activity, which was equal to that of the standard drug digoxin. To understand the binding mode of the most active compound, molecular docking study of 13a with Na+, K+-ATPase was conducted. Therefore, 13a may serve as a new lead compound for the development of novel Na+, K+-ATPase inhibitors.

Synthesis of dammarane-type triterpene derivatives and their ability to inhibit HIV and HCV proteases

Wei, Ying,Ma, Chao-Mei,Hattori, Masao

experimental part, p. 3003 - 3010 (2009/09/05)

We synthesized dammarane-type triterpene derivatives and evaluated their ability to inhibit HIV-1 and HCV proteases to understand their structure-activity relationships. All of the mono- and di-succinyl derivatives (5a-5f) were powerful inhibitors of HIV-

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