113558-03-5 Usage
Uses
Used in Pharmaceutical Applications:
1,2,3,19-Tetrahydroxy-12-ursen-28-oic acid is used as a therapeutic agent for its potential in treating conditions like diabetes, cancer, and cardiovascular diseases. Its antioxidant and anti-inflammatory properties contribute to its potential health benefits in these areas.
Used in Cancer Treatment:
In the field of oncology, 1,2,3,19-Tetrahydroxy-12-ursen-28-oic acid is used as an anti-cancer agent, with studies indicating its potential to target and treat various types of cancer. Its specific mechanisms of action and synergistic effects with other treatments are under investigation to enhance its efficacy in cancer therapy.
Used in Skincare Products:
1,2,3,19-Tetrahydroxy-12-ursen-28-oic acid is used as an ingredient in skincare products for its antioxidant and anti-aging properties. Its potential to protect the skin from oxidative stress and promote a youthful appearance makes it a valuable component in cosmetic formulations.
Used in Nutraceuticals:
Given its wide range of health benefits, 1,2,3,19-Tetrahydroxy-12-ursen-28-oic acid is also used in the development of nutraceutical products, which aim to provide additional health support through dietary supplements and functional foods.
Check Digit Verification of cas no
The CAS Registry Mumber 113558-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113558-03:
(8*1)+(7*1)+(6*3)+(5*5)+(4*5)+(3*8)+(2*0)+(1*3)=105
105 % 10 = 5
So 113558-03-5 is a valid CAS Registry Number.
113558-03-5Relevant academic research and scientific papers
Triterpenoid saponins from Acorus calamus
Rai, Renu,Siddiqui,Singh
, p. 473 - 476 (2007/10/03)
Two new triterpenoid saponins have been isolated from the rhizome of plant Acorus calamus. They are characterized as 1β, 2α, 3β, 19α-tetrahydroxyurs-12-en-28-oic acid-28-O{-β-D-glucopyranosyl (1→2)}-β-D-galactopyranoside 1 and 3β, 22α, 24, 29-tetrahydroxyolean-12-en-3-O-{-β-D-arabinosyl (1→3)}-β-D-arabinopyranoside 2 and their structures elucidated by spectral and chemical studies.
