24480-44-2 Usage
Uses
Used in Pharmaceutical Industry:
(20R)-3-Oxo-D:C-friedoolean-8-en-29-oic acid is used as a potential drug candidate for the treatment of various diseases due to its pharmacological properties. Its anti-inflammatory effects make it a promising candidate for treating inflammatory conditions, while its anti-cancer properties suggest its potential use in cancer therapy.
Used in Cancer Research:
(20R)-3-Oxo-D:C-friedoolean-8-en-29-oic acid is used as a cytotoxic agent against cancer cells, exhibiting significant cytotoxicity and providing a basis for further research into its potential as a novel drug candidate for cancer treatment.
Used in Inflammation Research:
(20R)-3-Oxo-D:C-friedoolean-8-en-29-oic acid is used as an anti-inflammatory agent, with its ability to inhibit the production of inflammatory mediators making it a valuable compound for studying and potentially treating inflammatory diseases.
Further research is needed to fully understand the pharmacological properties and potential therapeutic uses of (20R)-3-Oxo-D:C-friedoolean-8-en-29-oic acid, as well as to explore its applications in various industries and therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 24480-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,8 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24480-44:
(7*2)+(6*4)+(5*4)+(4*8)+(3*0)+(2*4)+(1*4)=102
102 % 10 = 2
So 24480-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O3/c1-25(2)21-9-8-20-19(28(21,5)12-11-23(25)31)10-13-30(7)22-18-27(4,24(32)33)15-14-26(22,3)16-17-29(20,30)6/h21-23,31H,8-18H2,1-7H3,(H,32,33)/t21-,22+,23-,26+,27+,28+,29+,30-/m0/s1
24480-44-2Relevant academic research and scientific papers
7-Oxodihydrokarounidiol [7-oxo-D:C-friedo-olean-8-ene-3α,29-diol], novel triterpene from Trichosanthes kirilowii
Akihisa,Kokke,Tamura,Nambara
, p. 1199 - 1202 (2007/10/02)
The structure of 7-oxodihydrokarounidiol [7-oxo-D:C-friedo-olean-8-ene-3α,29-diol], isolated from the seeds of Trichosanthes kirilowii (Cucurbitaceae), was determined by chemical correlation with karounidiol [D:C-friedo-oleana-7,9(11)-diene-3α,29-diol] from the same source. Two other natural products, viz. bryonolic acid (3β-hydroxy-D:C-friedo-olean-8-en-29-oic acid) and bryononic acid (3-oxo-D:C-friedo-olean-8-en-29-oic acid), were also correlated with karounidiol.
Bryocoumaric acid, a new triterpene from Bryonia dioica
Hylands, Peter J.,Mansour, El-Sayed S.,Oskoui, Moosa T.
, p. 2933 - 2936 (2007/10/02)
Bryocoumaric acid, from the roots of Bryonia dioica, is shown on the basis of chemical and spectroscopic evidence to have the structure 3α-p-hydroxycinnamyloxymultiflora-7,9(11)-dien-29α-oic acid. The structure of the new terpenoid portion, 3α-hydroxymultiflora-7,9(11)-dien- 29α-oic acid, is confirmed by correlation with bryonolic acid, 3β-hydroxymultiflor-8-en-29α-oic acid, isolated from the same plant.
