10092-04-3 Usage
Uses
Used in Pharmaceutical Industry:
(3R)-4β-Acetoxy-3,3aα,4,4a,7aα,8,9,9aβ-octahydro-3,4aβ,8α-trimethylazuleno[6,5-b]furan-2,5-dione is used as a potential therapeutic agent for its anti-inflammatory properties, helping to reduce inflammation and alleviate symptoms associated with various inflammatory conditions.
Used in Antioxidant Applications:
(3R)-4β-Acetoxy-3,3aα,4,4a,7aα,8,9,9aβ-octahydro-3,4aβ,8α-trimethylazuleno[6,5-b]furan-2,5-dione is utilized as an antioxidant, protecting cells from oxidative stress and damage caused by reactive oxygen species. Its antioxidant activity can contribute to the prevention of various diseases and promote overall health.
Used in Anticancer Research:
(3R)-4β-Acetoxy-3,3aα,4,4a,7aα,8,9,9aβ-octahydro-3,4aβ,8α-trimethylazuleno[6,5-b]furan-2,5-dione is being studied for its anticancer properties, as it may exhibit inhibitory effects on tumor growth and progression. Further research is needed to understand its potential as a cancer treatment option.
Used in Medicinal Chemistry Research:
As a complex and biologically active compound, (3R)-4β-Acetoxy-3,3aα,4,4a,7aα,8,9,9aβ-octahydro-3,4aβ,8α-trimethylazuleno[6,5-b]furan-2,5-dione serves as an interesting subject for research in medicinal chemistry. Its unique structure and potential applications provide opportunities for the development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 10092-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,9 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10092-04:
(7*1)+(6*0)+(5*0)+(4*9)+(3*2)+(2*0)+(1*4)=53
53 % 10 = 3
So 10092-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H22O5/c1-8-7-12-14(9(2)16(20)22-12)15(21-10(3)18)17(4)11(8)5-6-13(17)19/h5-6,8-9,11-12,14-15H,7H2,1-4H3/t8-,9-,11+,12+,14-,15-,17+/m1/s1
10092-04-3Relevant academic research and scientific papers
Waddell,Gebert,Tait
, p. 1474 - 1476 (1983)
The antitumor pseudoguainolide tenulin has been exposed to a wide variety of biological and model nucleophilic reagents and has been shown to react exclusively with sulfur nucleophiles in a Michael-like fashion. The biological implications of these results are discussed.
