2304-89-4 Usage
Description
4-(7,12-dihydroxy-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid is a complex organic compound with a unique molecular structure. It is characterized by its pentanoic acid backbone and a tetradecahydrocyclopenta[a]phenanthren-17-yl group, which is further modified with hydroxy and methyl groups. 4-(7,12-dihydroxy-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-te tradecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid belongs to the class of steroidal compounds, specifically keto bile acid derivatives, and exhibits a variety of biological activities.
Uses
Used in Pharmaceutical Industry:
4-(7,12-dihydroxy-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid is used as a pharmaceutical agent for its potential therapeutic applications. The compound's unique structure and functional groups allow it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Drug Delivery Systems:
In the field of drug delivery, this compound can be utilized as a carrier or a component in the design of novel drug delivery systems. Its structural features enable it to encapsulate or conjugate with other therapeutic agents, improving their solubility, stability, and targeted delivery to specific tissues or cells.
Used in Cosmetic Industry:
Due to its steroidal nature and potential biological activities, 4-(7,12-dihydroxy-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid may also find applications in the cosmetic industry. It could be used as an active ingredient in anti-aging, skin care, or hair care products, where its properties may contribute to improved skin hydration, elasticity, and overall health.
Used in Research and Development:
The complex structure and potential biological activities of this compound make it an interesting subject for research and development. It can be used as a starting material or a model compound in the synthesis of new steroidal compounds, as well as in the study of their biological effects and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 2304-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2304-89:
(6*2)+(5*3)+(4*0)+(3*4)+(2*8)+(1*9)=64
64 % 10 = 4
So 2304-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H38O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-14,16-20,22,26-27H,4-12H2,1-3H3,(H,28,29)/t13-,14+,16+,17+,18+,19-,20+,22+,23+,24-/m1/s1
2304-89-4Relevant articles and documents
A new non-enzymatic route to chenodeoxycholic acid
Bortolini, Olga,Cova, Umberto,Fantin, Giancarlo,Medici, Alessandro
, p. 335 - 336 (1996)
A novel route for the production of the chenodeoxycholic acid is described, based on the selective non-enzymatic reduction of dehydrocholic acid. The relative reactivity scale was established to be in the order: 12-keto (1), 7-keto (2), 3-keto (17.5).
Radical-mediated dehydrogenation of bile acids by means of hydrogen atom transfer to triplet carbonyls
Miro,Marin,Miranda
, p. 2679 - 2683 (2016/03/05)
The aim of the present paper is to explore the potential of radical-mediated dehydrogenation of bile salts (BSs), which is reminiscent of the enzymatic action of hydroxysteroid dehydrogenase enzymes (HSDH). The concept has been demonstrated using triplet carbonyls that can be efficiently generated upon selective UVA-excitation. Hydrogen atom transfer (HAT) from BSs to triplet benzophenone (BP) derivatives gave rise to radicals, ultimately leading to reduction of the BP chromophore with concomitant formation of the oxo-analogs of the corresponding BSs. The direct reactivity of triplet BP with BSs in the initial step was evaluated by determining the kinetic rate constants using laser flash photolysis (LFP). The BP triplet decay was monitored (λmax = 520 nm) upon addition of increasing BS concentrations, and the obtained rate constant values indicated a reactivity of the methine hydrogen atoms in the order of C-3 2 than under O2, also supporting the role of the oxygen-quenchable triplet in the dehydrogenation process. Furthermore, irradiation of deaerated aqueous solutions of sodium cholate in the presence of KPMe provided the oxo-analogs, 3[O],7[O]-CA, 3[O]-CA and 7[O]-CA, arising from the HAT process.
