30891-88-4 Usage
Uses
Used in Pharmaceutical Industry:
(+/-)-Isoelaeocarpin is used as a therapeutic agent for various conditions due to its potential health benefits. It is particularly promising for the treatment of cardiovascular disease, diabetes, and cancer, as studies have shown its potential to positively impact these conditions.
Used in Nutraceutical Industry:
(+/-)-Isoelaeocarpin is used as a dietary supplement or functional food ingredient for its antioxidant and anti-inflammatory properties. These benefits can contribute to overall health and well-being, making it a valuable addition to nutraceutical products.
Used in Cosmetic Industry:
(+/-)-Isoelaeocarpin is used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. It can help protect the skin from environmental damage and promote a healthier, more youthful appearance.
Further research is needed to fully understand the potential benefits and mechanisms of action of (+/-)-Isoelaeocarpin, but its natural origin and promising biological activities make it a compound of interest in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 30891-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30891-88:
(7*3)+(6*0)+(5*8)+(4*9)+(3*1)+(2*8)+(1*8)=124
124 % 10 = 4
So 30891-88-4 is a valid CAS Registry Number.
30891-88-4Relevant academic research and scientific papers
Zhou, Chang-Xin,Wang, Xue-Yao,Mo, Jian-Xia,Zhang, Jian,Gan, Li-She
, p. 347 - 354 (2011)
Two new indolizidine alkaloids, (±)-3-oxoisoelaeocarpine (1) and (±)-elaeocarpine N-oxide (2), along with three known alkaloids, (±)-isoelaeocarpine (3), (±)-elaeocarpine (4), and (-)-isoelaeocarpiline (5), were isolated from an EtOH extract of the branches and leaves of Elaeocarpus sphaericus. The structures of these compounds were determined by spectroscopic and chemical methods. Furthermore, enantiomers of compounds 1 and 3 were separated on a chiral CD-Ph column, and their absolute configurations were determined by TD-DFT (=time-dependent density-functional theory) quantumchemical calculations of their electronic circular dichroism (ECD) spectra.
