15051-81-7 Usage
General Description
10-epi-γ-eudesmol is a sesquiterpene alcohol compound found in essential oils of various plants, including eucalyptus and turmeric. It has been reported to exhibit anti-inflammatory and anti-cancer properties, making it a potential candidate for pharmaceutical and cosmetic applications. Studies have shown that 10-epi-γ-eudesmol can inhibit the growth of cancer cells, reduce inflammation, and modulate immune responses. Additionally, it has been identified as a potential candidate for the treatment of inflammatory diseases and as an ingredient in skincare products due to its anti-inflammatory and antioxidant properties. Overall, 10-epi-γ-eudesmol has shown promising therapeutic potential and merits further research and development for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 15051-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,5 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15051-81:
(7*1)+(6*5)+(5*0)+(4*5)+(3*1)+(2*8)+(1*1)=77
77 % 10 = 7
So 15051-81-7 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/h12,16H,5-10H2,1-4H3/t12-,15+/m1/s1
15051-81-7Relevant articles and documents
Marshall,Pike
, p. 435 (1968)
First enantioselective total syntheses and absolute configurations of 4,5-dioxo-seco-γ-eudesmol and 5β,11-dihydroxyiphionan-4-one, two aglycones of naturally occurring sesquiterpenes with new skeletons
Gao,Xiong,Zhou,Li
, p. 37 - 39 (2007/10/03)
A facile synthetic route to two new carbon skeleton sesquiterpenes 4,5-dioxo-seco-γ-eudesmol and 5β,11-dihydroxyiphionan-4-one from (+)-dihydrocarvone has been described. The configuration of the 5β,11-dihydroxyipbionan-4-one was confirmed by stereospecific synthesis.
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.
