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CAS 72064-79-0

:

(11β)-21-(Acetyloxy)-11-hydroxy-17-[(1-oxopentyl)oxy]pregna-1,4-diene-3,20-dione

Description:
The chemical substance known as "(11β)-21-(Acetyloxy)-11-hydroxy-17-[(1-oxopentyl)oxy]pregna-1,4-diene-3,20-dione," with the CAS number 72064-79-0, is a synthetic steroid compound. It is characterized by its complex structure, which includes multiple functional groups such as acetoxy and hydroxy groups, contributing to its biological activity. This compound is derived from the steroid nucleus, specifically the pregnane structure, and features a diene system that may influence its reactivity and interaction with biological targets. The presence of the oxopentyl group suggests potential lipophilicity, which can affect its pharmacokinetics and bioavailability. Such compounds are often studied for their potential therapeutic applications, particularly in fields like endocrinology and oncology, due to their ability to modulate hormonal pathways. Additionally, the specific stereochemistry at various positions on the steroid framework can significantly impact the compound's efficacy and safety profile. Overall, this substance exemplifies the intricate relationship between chemical structure and biological function in steroid chemistry.
Formula:C28H38O7
InChI:InChI=1S/C28H38O7/c1-5-6-7-24(33)35-28(23(32)16-34-17(2)29)13-11-21-20-9-8-18-14-19(30)10-12-26(18,3)25(20)22(31)15-27(21,28)4/h10,12,14,20-22,25,31H,5-9,11,13,15-16H2,1-4H3/t20-,21-,22-,25+,26-,27-,28-/m0/s1
InChI key:InChIKey=DGYSDXLCLKPUBR-SLPNHVECSA-N
SMILES:C(COC(C)=O)(=O)[C@]1(OC(CCCC)=O)[C@]2(C)[C@@](CC1)([C@]3([C@]([C@@H](O)C2)([C@]4(C)C(CC3)=CC(=O)C=C4)[H])[H])[H]
Synonyms:
  • (11Beta)-21-(Acetyloxy)-11-Hydroxy-3,20-Dioxopregna-1,4-Dien-17-Yl Pentanoate
  • (11β)-21-(Acetyloxy)-11-hydroxy-17-[(1-oxopentyl)oxy]pregna-1,4-diene-3,20-dione
  • 11-beta,17-alpha,21-Trihydroxy-1,4-pregnadiene-3,20-dione 21-acetate 17-valerate
  • 11beta,17,21-Trihydroxypregna-1,4-diene-3,20-dione 21-acetate 17-valerate
  • 11beta,17alpha,21-Trihydroxy-1,4-pregnadiene-3,20-dione 21-acetate 17-valerate
  • 17-(Acetyloxy)-11-Hydroxy-3,20-Dioxopregna-1,4-Dien-21-Yl Pentanoate
  • 21-(Acetyloxy)-11-beta-hydroxy-17-((1-oxopentyl)oxy)pregna-1,4-diene-3,20-dione
  • Acepreval
  • Brn 2713941
  • Lidomex
  • See more synonyms
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Found 5 products.
  • CymitQuimica logo
    Apollo Scientific
    + Info

    Prednisolone valerate acetate

    CAS:
    Prednisolone valerate acetate
    Purity:≥98%
    Molecular weight:486.6g/mol

    Ref: 54-BUP20995

    5mg
    1,161.00€
    10mg
    1,627.00€
    25mg
    2,318.00€
    50mg
    3,254.00€
    100mg
    3,658.00€
    200mg
    4,821.00€
  • Prednival Acetate (Prednisolone 17-Valerate 21-Acetate)
    Mikromol
    + Info

    Prednival Acetate (Prednisolone 17-Valerate 21-Acetate)

    Controlled Product
    CAS:
    Formula:C28H38O7
    Color and Shape:Neat
    Molecular weight:486.60

    Ref: 86-MM0195.00

    250mg
    1,479.00€
  • Prednisolone valerate acetate
    Targetmol
    + Info

    Prednisolone valerate acetate

    CAS:
    <p>Prednisolone valerate acetate is a prodrug anti-inflammatory and immunosuppressive,converted to the active form of Prednisolone and glucocorticoid receptor.</p>
    Formula:C28H38O7
    Purity:99.93%
    Color and Shape:Solid
    Molecular weight:486.6

    Ref: TM-T20734

  • Prednisolone 21-Acetate 17-Valerate
    Standalix
    + Info

    Prednisolone 21-Acetate 17-Valerate

    CAS:
    Formula:C28H38O7
    Molecular weight:486.6

    Ref: ST-EA-CP-P20066

    10mg
    To inquire
    25mg
    To inquire
    50mg
    To inquire
    100mg
    To inquire
  • Prednisolone valeroacetate
    Biosynth
    + Info

    Prednisolone valeroacetate

    Controlled Product
    CAS:
    <p>Prednisolone valeroacetate is a synthetic corticosteroid, which is a chemically modified derivative of prednisolone. It originates from chemical synthesis processes designed to enhance specific therapeutic effects and mitigate side effects. This compound acts primarily by modulating the immune system and exerting anti-inflammatory effects. Its mechanism of action involves the inhibition of phospholipase A2, leading to a reduction in the synthesis of proinflammatory mediators like prostaglandins and leukotrienes. Additionally, it suppresses the migration of immune cells to sites of inflammation, thereby reducing immune responses.</p>
    Formula:C28H38O7
    Purity:Min. 97 Area-%
    Color and Shape:Powder
    Molecular weight:486.6 g/mol

    Ref: 3D-FP42750

    1g
    264.00€
    2g
    458.00€
    5g
    885.00€