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CAS 5488-51-7

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Pregna-5,7-diene-3,20-dione, cyclic 3,20-bis(1,2-ethanediyl acetal), (9β,10α)-

Description:
Pregna-5,7-diene-3,20-dione, cyclic 3,20-bis(1,2-ethanediyl acetal), (9β,10α)-, commonly referred to in the context of steroid chemistry, is a synthetic derivative of progesterone. This compound features a steroid backbone characterized by a fused four-ring structure typical of steroids, with specific functional groups that contribute to its biological activity. The presence of the diene and ketone functionalities indicates potential reactivity and interaction with biological systems, particularly in hormone signaling pathways. The cyclic acetal formation suggests enhanced stability and solubility, which can influence its pharmacokinetic properties. This compound is often studied for its potential applications in reproductive health and hormonal therapies. Its structural configuration, particularly the stereochemistry at the 9β and 10α positions, plays a crucial role in determining its biological activity and receptor binding affinity. As with many steroid derivatives, understanding its characteristics is essential for exploring its therapeutic potential and safety profile in clinical applications.
Formula:C25H36O4
InChI:InChI=1S/C25H36O4/c1-22-10-11-25(28-14-15-29-25)16-17(22)4-5-18-19-6-7-21(24(3)26-12-13-27-24)23(19,2)9-8-20(18)22/h4-5,19-21H,6-16H2,1-3H3/t19-,20+,21-,22+,23-/m0/s1
InChI key:InChIKey=CFZNXPSHLNMZGD-BFRACDOUSA-N
SMILES:C[C@@]12[C@](C=3[C@@](CC1)([C@@]4(C)C(=CC3)CC5(CC4)OCCO5)[H])(CC[C@@H]2[C@@]6(C)OCCO6)[H]
Synonyms:
  • Pregna-5,7-diene-3,20-dione, cyclic 3,20-bis(1,2-ethanediyl acetal), (9β,10α)-
  • Dydrogesterone bis(Ethylene Acetal)
  • 9β,10α-Pregna-5,6-diene-3,20-dione bis(cyclic ethylene acetal)
  • 9β,10α-3,20-Bis(ethylenedioxy)-5,7-pregnadiene
  • Pregna-5,7-diene-3,20-dione, cyclic bis(1,2-ethanediyl acetal), (9β,10α)-
  • 9β,10α-Pregna-5,7-diene-3,20-dione, cyclic bis(ethylene acetal)
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