27832-84-4 Usage
Uses
Used in Pharmaceutical Industry:
Serratenediol diacetate is used as a pharmaceutical candidate for its potential anti-tumor properties, making it a promising agent for the development of new cancer treatments. Its anti-inflammatory and anti-angiogenic activities also contribute to its potential use in treating other inflammatory disorders.
Used in Drug Development:
Serratenediol diacetate is utilized in drug development for its potential to target and treat various types of cancer by inhibiting tumor growth and progression. Its unique chemical structure allows for further investigation and optimization to enhance its therapeutic efficacy and selectivity.
Used in Scientific Research:
Serratenediol diacetate serves as a subject of scientific research to explore its pharmacological properties and potential applications in medicine. Studies aim to understand its mechanism of action, optimize its chemical structure, and evaluate its safety and efficacy in preclinical and clinical settings.
Check Digit Verification of cas no
The CAS Registry Mumber 27832-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27832-84:
(7*2)+(6*7)+(5*8)+(4*3)+(3*2)+(2*8)+(1*4)=134
134 % 10 = 4
So 27832-84-4 is a valid CAS Registry Number.
27832-84-4Relevant academic research and scientific papers
Saga, Yusuke,Araki, Takeshi,Araya, Hiroshi,Saito, Kazuki,Yamazaki, Mami,Suzuki, Hideyuki,Kushiro, Tetsuo
, p. 496 - 499 (2017)
Ferns are known to produce onoceroids including onoceranes and serratanes having unusual structures among triterpenes. From the fern Lycopodium clavatum, a novel onoceroid synthase gene was cloned that showed high sequence identity with a previously identified α-onocerin synthase. Functional analysis by coexpression with pre-α-onocerin synthase in yeast led to the production of tohogenol and serratenediol. The result suggested that serratanes are directly biosynthesized from pre-α-onocerin and not from α-onocerin as previously assumed.
