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(6beta,15beta,20xi)-hetisan-15-ol is a chemical compound belonging to the class of organic compounds known as hetisanes, which are a type of triterpenoid derived from squalene. This specific form of hetisan features a hydroxyl group (OH) at the 15th position of the molecule. It may possess pharmacological or biological activities, as many triterpenoids have been found to exhibit anti-inflammatory, anti-cancer, and other health-promoting properties. However, research on its specific properties and potential uses is ongoing, and further studies are required to fully understand its effects and applications.

79808-87-0

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79808-87-0 Usage

Uses

Used in Pharmaceutical Applications:
(6beta,15beta,20xi)-hetisan-15-ol is used as a potential therapeutic agent for various health conditions due to its possible anti-inflammatory and anti-cancer properties, which are common among triterpenoids. Its exact role and efficacy in pharmaceutical applications are still under investigation.
Used in Research and Development:
In the field of research and development, (6beta,15beta,20xi)-hetisan-15-ol serves as a subject of study to explore its potential pharmacological and biological activities. This may lead to the discovery of new treatments and applications in the medical and healthcare industries.

Check Digit Verification of cas no

The CAS Registry Mumber 79808-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,0 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79808-87:
(7*7)+(6*9)+(5*8)+(4*0)+(3*8)+(2*8)+(1*7)=190
190 % 10 = 0
So 79808-87-0 is a valid CAS Registry Number.

79808-87-0Downstream Products

79808-87-0Relevant academic research and scientific papers

Asymmetric synthetic access to the hetisine alkaloids: Total synthesis of (+)-nominine

Peese, Kevin M.,Gin, David Y.

supporting information; experimental part, p. 1654 - 1665 (2009/04/04)

A dual cycloaddition strategy for the synthesis of the hetisine alkaloids has been developed, illustrated by a concise asymmetric total synthesis of (+)-nominine (7). The approach relies on an early-stage intramolecular 1,3-dipolar cyclo-addition of a 4-o

THE STRUCTURE OF THE NEW DITERPENE ALKALOID NOMININE AND THE ABSOLUTE CONFIGURATION OF KOBUSINE

Sakai, Shin-ichiro,Yamamoto, Ichiro,Yamaguchi, Keiichi,Takayama, Hiromitsu,Ito, Miyuki,Okamoto, Toshihiko

, p. 4579 - 4582 (2007/10/02)

The structure of nominine (II), a minor diterpene alkaloid isolated from Aconitum sanyoense Nakai ( native of Nomi, Kyoto prefecture) was established as 11-deoxykobusine by chemical transformation of kobusine (Ia); their absolute configurations have been

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