52230-62-3 Usage
Chemical structure
A synthetic derivative of the natural hormone 17beta-estradiol, which is a steroid hormone responsible for the development and maintenance of female reproductive tissues.
Esterification
The compound is a palmitic acid ester, which means it has a palmitic acid group attached to the 17beta-hydroxyestr-4-en-3-one molecule.
Stability
The palmitate ester is added to improve the stability of the hormone, making it more resistant to degradation and breakdown.
Bioavailability
The addition of the palmitic acid ester also enhances the bioavailability of the hormone, allowing it to be more easily absorbed and utilized by the body.
Pharmaceutical use
17beta-hydroxyestr-4-en-3-one 17-palmitate is suitable for use in pharmaceutical preparations due to its improved stability and bioavailability.
Menopausal symptoms
It is effective in the prevention and treatment of menopausal symptoms, such as hot flashes, night sweats, and vaginal dryness.
Osteoporosis prevention
17beta-hydroxyestr-4-en-3-one 17-palmitate can help prevent and treat osteoporosis by maintaining bone density and reducing the risk of fractures.
Potential cancer treatment
The compound is being studied for its potential use in the treatment of hormone-related cancers and other conditions.
Synthetic origin
As a synthetic derivative, 17beta-hydroxyestr-4-en-3-one 17-palmitate is not naturally occurring and is produced through chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 52230-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,3 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52230-62:
(7*5)+(6*2)+(5*2)+(4*3)+(3*0)+(2*6)+(1*2)=83
83 % 10 = 3
So 52230-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H36O3/c1-3-4-5-6-23(26)27-22-12-11-21-20-9-7-16-15-17(25)8-10-18(16)19(20)13-14-24(21,22)2/h15,18-22H,3-14H2,1-2H3/t18-,19+,20+,21-,22-,24-/m0/s1