33282-87-0 Usage
Description
(20S)-3β,16β-Dihydroxypregn-5-ene-20-carboxylic acid γ-lactone, also known as 20-hydroxyecdysone, is a naturally occurring steroid hormone that is found in both plants and insects. It is known for its crucial role in regulating growth and development in insects, where it acts as a molting hormone and controls the timing of metamorphosis. In plants, it functions as a phytoecdysteroid and has potential beneficial effects on human health, such as anti-inflammatory and antioxidant properties. Furthermore, it has been studied for its potential use in agriculture as a biopesticide, due to its ability to disrupt insect development and reproduction. This chemical compound has diverse and significant roles in both the insect and plant kingdoms, with potential applications in various fields, including medicine and agriculture.
Uses
Used in Pharmaceutical Industry:
(20S)-3β,16β-Dihydroxypregn-5-ene-20-carboxylic acid γ-lactone is used as a pharmaceutical agent for its potential beneficial effects on human health. Its anti-inflammatory and antioxidant properties make it a promising candidate for the development of new drugs to treat various conditions.
Used in Agricultural Industry:
(20S)-3β,16β-Dihydroxypregn-5-ene-20-carboxylic acid γ-lactone is used as a biopesticide in agriculture. Its ability to disrupt insect development and reproduction makes it a potential alternative to traditional chemical pesticides, offering a more environmentally friendly and sustainable solution for pest control.
Used in Research Applications:
(20S)-3β,16β-Dihydroxypregn-5-ene-20-carboxylic acid γ-lactone is used as a research tool in the study of insect growth and development, as well as in the investigation of its potential health benefits in humans. (20S)-3β,16β-Dihydroxypregn-5-ene-20-carboxylic acid γ-lactone can help scientists better understand the mechanisms of action and develop new strategies for pest control and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33282-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,8 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33282-87:
(7*3)+(6*3)+(5*2)+(4*8)+(3*2)+(2*8)+(1*7)=110
110 % 10 = 0
So 33282-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H32O3/c1-12-19-18(25-20(12)24)11-17-15-5-4-13-10-14(23)6-8-21(13,2)16(15)7-9-22(17,19)3/h4,12,14-19,23H,5-11H2,1-3H3/t12-,14-,15+,16-,17-,18-,19-,21-,22-/m0/s1
33282-87-0Relevant articles and documents
Conversion of spirostane and solanidane into pregnane (1) introduction of oxygen function into C-23
Nakata, Nodoka,Tokudome, Asami,Yanai, Hiroyuki,Nohara, Toshihiro
, p. 150 - 153 (2012)
A spirosolane derivative possessing a hydroxyl group at C-23, esculeogenin A, a sapogenol of tomato saponin, was found to be easily converted into the corresponding pregnane derivative by refluxing with aqueous pyridine. Therefore, introduction of a hydroxyl group into the C-23 of diosgenin (as representative of spirostane derivatives) and solasodine (as representative of spirosolane derivatives) was attempted by the reaction of NaNO2-BF3 · Et2O. In diosgenin, the objective compound was obtained by the reaction in AcOH. However, in solasodine, we obtained a 23-nitroso derivative by the reaction in AcOH and 23,24-bisnorcholanic acid 22-16 lactone, or vespertilin, in AcOH and CHCl3.
Peculiar side-chain fission of steroidal glycosides
Nafady, Alaa Mohamed,El-Shanawany, Mohamed Ahmed,Mohamed, Mahmoud Hamed,Hassanean, Hashim Abdel-Halim,Zhu, Xing-Hua,Yoshihara, Tsutomu,Okawa, Masafumi,Ikeda, Tsuyoshi,Nohara, Toshihiro
, p. 3509 - 3511 (2003)
The characteristic novel steroidal glycosides of the 23,26-oxygenated spirostanol-type and 16,22-dicarbonyl cholestanol-type obtained in our laboratory underwent the peculiar reactions of side-chain fission between C-22 and C-23 of the steroidal skeleton