CAS 152-62-5: Dydrogesterone
Formula:C21H28O2
InChI:InChI=1S/C21H28O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h4-5,12,16-19H,6-11H2,1-3H3/t16-,17+,18-,19+,20+,21+/m0/s1
InChI key:InChIKey=JGMOKGBVKVMRFX-HQZYFCCVSA-N
SMILES:C[C@]12[C@]3([C@]([C@]4([C@](C)(CC3)[C@@H](C(C)=O)CC4)[H])(C=CC1=CC(=O)CC2)[H])[H]
Synonyms:- (9Beta,10Xi)-Pregna-4,6-Diene-3,20-Dione
- (9b,10a)-Pregna-4,6-diene-3,20-dione
- (9beta,10alpha)-Pregna-4,6-diene-3,20-dione
- .DELTA.6-Retroprogesterone
- 10a-Isopregnenone
- 6-Dehydro-9.beta.,10.alpha.-progesterone
- 6-Dehydro-9b,10a-progesterone
- 6-Dehydroretroprogesterone
- 6α-Dehydro-retro-Δ4-pregnene-3,20-dione
- 6α-Dehydro-retro-Δ<sup>4</sup>-pregnene-3,20-dione
- 9beta,10alpha-Pregna-4,6-diene-3,20-dione (8CI)
- See more synonyms
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Found 12 products.
Dydrogesterone-d6 (Major)
CAS:Controlled ProductApplications Labelled Dydrogesterone. A synthetic progestin largely used in hormone therapy, on the central nervous system by studying two markers of the neuroendocrine function: the neurosteroid allopregnanolone and the opioid .beta.-endorphin. Progestogen. References Bernardi, F., et al.: Eur. J. Endocrinol., 138, 316 (1998), Rupprecht, R., et al.: Steroids, 64, 83 (1999), Uzunova, V., et al.: Brain Res., 976, 1 (2003), Pluchino, N., et al.: J. Steroid Biochem. Mol. Biol., 102, 205 (2006),Formula:C21H22D6O2Color and Shape:NeatMolecular weight:318.48Dydrogesterone
CAS:Dydrogesterone is a potent progestogen which can be used in progesterone deficiency studies.Formula:C21H28O2Purity:98.26% - 99.78%Color and Shape:Crystals From Acetone + Hexane SolidMolecular weight:312.45Dydrogesterone
CAS:Estrogens and progestinsFormula:C21H28O2Color and Shape:White Off-White SolidMolecular weight:312.20893Dydrogesterone
CAS:Controlled ProductDydrogesterone is a progestin medication that is used to treat symptoms of endometriosis in women. It can be used alone or in combination with estradiol benzoate. Dydrogesterone is not active against bacteria. High-sensitivity C-reactive protein (hsCRP) levels are an indicator of inflammation and have been shown to be elevated in untreated women with endometriosis. Histological analysis of tissue from these patients has revealed increased levels of dydrogesterone. Dydrogesterone binds to the progesterone receptor, which regulates the expression of genes that play a role in cell proliferation and differentiation. This regulation is mediated by nuclear DNA, which is transcribed into messenger RNA and translated into protein by ribosomes. Coumarin derivatives inhibit the production of mRNA by binding to the enzyme RNA polymerase II, which catalyzes the transcription process. Studies have shown that coumarin derivatives can reduceFormula:C21H28O2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:312.45 g/molDydrogesterone
CAS:Controlled ProductApplications A synthetic progestin largely used in hormone therapy, on the central nervous system by studying two markers of the neuroendocrine function: the neurosteroid allopregnanolone and the opioid .beta.-endorphin. Progestogen. References Bernardi, F., et al.: Eur. J. Endocrinol., 138, 316 (1998), Rupprecht, R., et al.: Steroids, 64, 83 (1999), Uzunova, V., et al.: Brain Res., 976, 1 (2003), Pluchino, N., et al.: J. Steroid Biochem. Mol. Biol., 102, 205 (2006),Formula:C21H28O2Color and Shape:WhiteMolecular weight:312.45Dydrogesterone
CAS:Formula:C21H28O2Purity:>98.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:312.45
