473-15-4 Usage
Description
Beta-Eudesmol, a carbobicyclic compound, is a sesquiterpenoid molecule that significantly impacts the central nervous system (CNS). It is characterized by its unique structure, featuring trans-decalin substituted at positions 2, 4a, and 8 by 2-hydroxypropan-2-yl, methyl, and methylidene groups, respectively (the 2R,4aR,8aS-diastereoisomer). beta-Eudesmol is known for its ability to induce neurite outgrowth and possesses antiangiogenic activity.
Uses
Used in Pharmaceutical Industry:
Beta-Eudesmol is used as a neuroactive agent for its ability to influence the central nervous system. Its neurite outgrowth induction property makes it a potential candidate for the development of treatments targeting neurological disorders and conditions related to neuronal growth and regeneration.
Used in Oncology:
In the field of oncology, beta-Eudesmol is utilized for its antiangiogenic activity. It plays a crucial role in inhibiting the formation of new blood vessels, which is a critical process for tumor growth and metastasis. By targeting angiogenesis, beta-Eudesmol can potentially be employed in the development of novel cancer therapies and treatments.
Used in Cosmetic Industry:
Due to its impact on the central nervous system and neurite outgrowth, beta-Eudesmol can also be used as an active ingredient in the cosmetic industry. It may be incorporated into skincare products and formulations aimed at promoting skin health, regeneration, and overall well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 473-15-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 473-15:
(5*4)+(4*7)+(3*3)+(2*1)+(1*5)=64
64 % 10 = 4
So 473-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-11-6-5-8-15(4)9-7-12(10-13(11)15)14(2,3)16/h12-13,16H,1,5-10H2,2-4H3/t12-,13+,15-/m1/s1
473-15-4Relevant articles and documents
Biotransformation of (+/-)-4,8-dimethylcyclodeca-3(E),7(E)-dien-1β-ol and (+)-Hedycaryol by Cichorium intybus
Piet, Dennis P.,Minnaard, Adriaan J.,Heyden, Karel A. van der,Franssen, Maurice C. R.,Wijnberg, Joannes B. P. A.,Groot, Aede de
, p. 243 - 254 (2007/10/02)
The biotransformation of the synthetic (E,E)-1,5-cyclodecadienol 5 and (+)-hedycaryol (11) by a root suspension of fresh chicory has been investigated.Incubation of 5 with a root suspension gave a 2:1 mixture of epimeric eudesmanediols 7a and 7b whereas 11 was selectively converted into cryptomeridiol (12).An explanation for the obtained results is proposed.
