55497-79-5 Usage
Uses
Used in Pharmaceutical Industry:
Myriceric acid B is used as a potential drug candidate for its anti-inflammatory and anti-tumor properties, making it suitable for the development of new therapeutics to treat various diseases.
Used in Cancer Treatment:
Myriceric acid B is used as an anti-tumor agent, targeting the inhibition of tumor growth and progression. Its anti-tumor properties are being explored for potential applications in cancer treatment.
Used in Inflammation Management:
Myriceric acid B is used as an anti-inflammatory agent, which could be beneficial in managing inflammatory conditions and diseases.
Research on Myriceric acid B is ongoing to further understand its full potential for therapeutic use and to develop novel drug delivery systems that can enhance its efficacy and bioavailability.
Check Digit Verification of cas no
The CAS Registry Mumber 55497-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,9 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55497-79:
(7*5)+(6*5)+(5*4)+(4*9)+(3*7)+(2*7)+(1*9)=165
165 % 10 = 5
So 55497-79-5 is a valid CAS Registry Number.
55497-79-5Relevant academic research and scientific papers
Endothelin receptor antagonist triterpenoid, myriceric acid A, isolated from Myrica cerifera, and structure activity relationships of its derivatives
Sakurawi, Kensuke,Yasuda, Fumio,Tozyo, Takehiko,Nakamura, Miharu,Sato, Tomohiro,Kikuchi, Junko,Terui, Yoshihiro,Ikenishi, Yuji,Iwata, Tsuyoshi,Takahashi, Kazuhiro,Konoike, Toshiro,Mihara, Shin-Ichi,Fujimoto, Masafumi
, p. 343 - 351 (2007/10/03)
As the first non-peptide endothelin receptor antagonist from a higher plant, a new triterpenoid, myriceric acid A (50-235) (1) was isolated from the bayberry, Myrica cerifera. Myriceric acid A (1) inhibited not only an endothelin-1-induced increase in cytosolic free Ca2+ concentration (IC50 = 11 ± 2 nM) but [125I]endothelin-1 binding in rat aortic smooth muscle cells (K(i)=66 ±15 nM). Two new related triterpenoids, myriceric acid C (6), and myriceric acid D (8), were also isolated. Furthermore, the chemical modification of these natural products led to the synthesis of sulfated derivatives (13, 14, 15) which showed 1.5 to 20 times higher affinity for endothelin receptors. The structure activity relationships of myriceric acids and their derivatives are discussed.
