CymitQuimica logo

CAS 7690-08-6

:

16-Methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione

Description:
16-Methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione, commonly known as a synthetic steroid, is characterized by its structural modifications that enhance its biological activity compared to natural steroids. This compound features a methylene group at the 16 position and a hydroxyl group at the 17α position, which contribute to its unique pharmacological properties. The presence of the 19-nor configuration indicates the absence of a carbon atom at the 19 position, which is significant in altering the compound's interaction with steroid receptors. This compound is often studied for its potential applications in medicine, particularly in hormone replacement therapies and as an anabolic agent. Its chemical stability and solubility characteristics are influenced by the presence of the ketone groups at the 3 and 20 positions, which are crucial for its biological activity. Overall, 16-Methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione is an important compound in the field of steroid chemistry, with implications for both therapeutic and research applications.
Formula:C21H28O3
InChI:InChI=1S/C21H28O3/c1-12-10-19-18-6-4-14-11-15(23)5-7-16(14)17(18)8-9-20(19,3)21(12,24)13(2)22/h11,16-19,24H,1,4-10H2,2-3H3/t16-,17+,18+,19-,20-,21-/m0/s1
InChI key:InChIKey=SFLXYFZGKSGFKA-XUDSTZEESA-N
SMILES:C[C@@]12[C@]([C@]3([C@](CC1)([C@@]4(C(CC3)=CC(=O)CC4)[H])[H])[H])(CC(=C)[C@@]2(C(C)=O)O)[H]
Synonyms:
  • 17-Hydroxy-16-methylene-19-norpregn-4-ene-3,20-dione
  • 19-Norpregn-4-ene-3,20-dione, 17-hydroxy-16-methylene-
  • 17α-Deacetylnestorone
  • 16-Methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione
  • Segesterone
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
  • Segesterone
    Biosynth
    + Info

    Segesterone

    Controlled Product
    CAS:
    <p>Segesterone is a synthetic progestin, which is a chemically engineered hormone analogue. It is synthesized from steroid precursors, specifically designed to mimic the naturally occurring hormone progesterone. Segesterone acts primarily through binding to progesterone receptors, exerting its effects by modulating gene expression related to reproductive processes. This mechanism inhibits ovulation, alters cervical mucus to prevent sperm penetration, and modifies the endometrial lining to reduce the likelihood of implantation.</p>
    Formula:C21H28O3
    Purity:Min. 95%
    Molecular weight:328.4 g/mol

    Ref: 3D-XS182941

    ne
    To inquire