
Dydrogesterone
CAS No. 152-62-5
Dydrogesterone( —— )
Catalog No. M27963 CAS No. 152-62-5
Dydrogesterone is a potent progestogen which can be used in progesterone deficiency studies.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 47 | Get Quote |
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5MG | 76 | Get Quote |
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10MG | 125 | Get Quote |
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25MG | 260 | Get Quote |
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50MG | 417 | Get Quote |
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100MG | 615 | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameDydrogesterone
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NoteResearch use only, not for human use.
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Brief DescriptionDydrogesterone is a potent progestogen which can be used in progesterone deficiency studies.
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DescriptionDydrogesterone is a potent progestogen which can be used in progesterone deficiency studies.(In Vitro):Dydrogesterone is orally active at far lower doses. Its freedom from estrogenic, androgenic, anabolic, corticoid and other undesirable hormonal effects gives it additional benefits over most other synthetic progestogens.
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In VitroDydrogesterone is a potent, orally active progestogen indicated in a wide variety of gynaecological conditions related to progesterone deficiency. Although similar in molecular structure and pharmacological effects to endogenous progesterone. It is orally active at far lower doses. Its freedom from estrogenic, androgenic, anabolic, corticoid and other undesirable hormonal effects gives it additional benefits over most other synthetic progestogens. Dydrogesterone has also been registered as hormone replacement therapy (HRT) to counteract the negative effects of unopposed estrogen on the endometrium in women with an intact uterus. Dydrogesterone is relatively safe and well tolerated, and does not exhibit the androgenic side effects that are common with some other progestins, like medroxyprogesterone.
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In Vivo——
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Synonyms——
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PathwayMicrobiology/Virology
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TargetFilovirus
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RecptorTHR-β
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Research Area——
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Indication——
Chemical Information
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CAS Number152-62-5
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Formula Weight312.45
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Molecular FormulaC21H28O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 33.33 mg/mL (106.67 mM)
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SMILESC[C@](CC[C@H]1[C@]2(C)CC3)([C@@H](CC4)[C@@H]1C=CC2=CC3=O)[C@H]4C(C)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Cable EE, et al. Reduction of hepatic steatosis in rats and mice after treatment with aliver-targeted thyroidhormone receptor agonist. Hepatology. 2009 Feb;49(2):407-17.
molnova catalog



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