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CAS 25908-76-3

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(17beta)-16-ethyl-17-(fluoroacetyl)estr-4-en-3-one

Description:
The chemical substance known as (17beta)-16-ethyl-17-(fluoroacetyl)estr-4-en-3-one, with the CAS number 25908-76-3, is a synthetic steroid derivative. It belongs to the class of compounds known as estrogens, which are primarily involved in the regulation of various biological processes, including reproductive functions. This compound features a modified steroid structure, characterized by the presence of an ethyl group at the 16-position and a fluoroacetyl group at the 17-position, which can influence its biological activity and receptor binding affinity. The presence of the double bond at the 4-position contributes to its stability and reactivity. Such modifications can enhance the compound's potency and selectivity as a pharmaceutical agent. Additionally, the fluorine atom in the fluoroacetyl group may impart unique properties, such as increased lipophilicity or altered metabolic pathways. Overall, this compound's structural characteristics suggest potential applications in medicinal chemistry, particularly in the development of hormone-related therapies.
Formula:C22H31FO2
InChI:InChI=1/C22H31FO2/c1-3-13-11-19-18-6-4-14-10-15(24)5-7-16(14)17(18)8-9-22(19,2)21(13)20(25)12-23/h10,13,16-19,21H,3-9,11-12H2,1-2H3/t13?,16-,17+,18+,19-,21+,22-/m0/s1
Synonyms:
  • Estr-4-En-3-One, 16-Ethyl-17-(2-Fluoroacetyl)-, (17Beta)-
  • (17beta)-16-Ethyl-17-(fluoroacetyl)estr-4-en-3-one
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Found 1 products.
  • 21-Fluoro-16-Ethyl-19-Norprogesterone

    Controlled Product
    CAS:
    21-Fluoro-16-Ethyl-19-Norprogesterone is a glycol ether that has a molecular weight of 462.5 Da. It is an inhibitor of the enzyme activities that cause infectious diseases, such as glycol esterase and protein kinase. 21-Fluoro-16-Ethyl-19-Norprogesterone is used to treat wastewater and magnetic particles. The molecule can be adsorbed onto nanoparticles with a size range of 5 nm to 100 nm, which are then used for drug delivery or targeted cancer therapy. 21-Fluoro-16-Ethyl-19-Norprogesterone has been shown to inhibit fatty acid biosynthesis in Escherichia coli cells by inhibiting the activity of 3 enzymes: acetyl CoA carboxylase, thiolase, and enoyl CoA hydratase.
    Formula:C22H31FO2
    Purity:Min. 95%
    Molecular weight:346.48 g/mol

    Ref: 3D-FF83449

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