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    Osaterone acetate

    ACTIVE PHARMA INGREDIENTS

    PharmaCompass
    Xls

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    2D Structure
    Also known as: Osaterone acetate ester, 105149-00-6, Tzp-4238, Fr26fsv5ez, 2-oxapregna-4,6-diene-3,20-dione, 17-(acetyloxy)-6-chloro-, Osaterone acetate (jan)
    Molecular Formula
    C22H27ClO5
    Molecular Weight
    406.9  g/mol
    InChI Key
    KKTIOMQDFOYCEN-OFUYBIASSA-N
    FDA UNII
    FR26FSV5EZ
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    [(1R,3aS,3bR,9aR,9bS,11aS)-1-acetyl-5-chloro-9a,11a-dimethyl-7-oxo-2,3,3a,3b,9,9b,10,11-octahydroindeno[4,5-h]isochromen-1-yl] acetate
    2.1.2 InChI
    InChI=1S/C22H27ClO5/c1-12(24)22(28-13(2)25)8-6-16-14-9-18(23)17-10-19(26)27-11-20(17,3)15(14)5-7-21(16,22)4/h9-10,14-16H,5-8,11H2,1-4H3/t14-,15+,16+,20-,21+,22+/m1/s1
    2.1.3 InChI Key
    KKTIOMQDFOYCEN-OFUYBIASSA-N
    2.1.4 Canonical SMILES
    CC(=O)C1(CCC2C1(CCC3C2C=C(C4=CC(=O)OCC34C)Cl)C)OC(=O)C
    2.1.5 Isomeric SMILES
    CC(=O)[C@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C=C(C4=CC(=O)OC[C@]34C)Cl)C)OC(=O)C
    2.2 Other Identifiers
    2.2.1 UNII
    FR26FSV5EZ
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 17-acetoxy-6-chloro-2-oxa-4,6 Pregnadiene-3,20-dione

    2. 2-oxachloromadinone Acetate

    3. Tzp 4238

    4. Tzp-4238

    2.3.2 Depositor-Supplied Synonyms

    1. Osaterone Acetate Ester

    2. 105149-00-6

    3. Tzp-4238

    4. Fr26fsv5ez

    5. 2-oxapregna-4,6-diene-3,20-dione, 17-(acetyloxy)-6-chloro-

    6. Osaterone Acetate (jan)

    7. Osaterone Acetate [jan]

    8. Ypozane

    9. Tzp 4238

    10. Ccris 6738

    11. Unii-fr26fsv5ez

    12. Hipros

    13. 17-(acetyloxy)-6-chloro-2-oxapregna-4,6-diene-3,20-dione

    14. 17-alpha-acetoxy-6-chloro-2-oxa-4,6-pregnadiene-3,20-dione

    15. [(1r,3as,3br,9ar,9bs,11as)-1-acetyl-5-chloro-9a,11a-dimethyl-7-oxo-2,3,3a,3b,9,9b,10,11-octahydroindeno[4,5-h]isochromen-1-yl] Acetate

    16. 7-acetyl-7-(acetyloxy)-11-chloro-4ar,4b,5,6,6as,7r,8,9,9as,9br-decahydro-4a,6a-dimethylcyclopenta(5,6)naphtho(1,2-c)pyran-2(4h)-one

    17. Schembl528987

    18. Chebi:81713

    19. 2-oxochlormadinone Acetate

    20. Dtxsid501030455

    21. Osaterone Acetate Ester [mi]

    22. Cyclopenta(5,6)naphtho(1,2-c)pyran-2(4h)-one, 7-acetyl-7-(acetyloxy)-11-chloro-4a,4b,5,6,6a,7,8,9,9a,9b-decahydro-4a,6a-dimethyl-, (4ar,4bs,6as,7r,9as,9br)-

    23. C18375

    24. D11105

    25. Osaterone Acetate [ema Epar Veterinary]

    26. Q27155575

    27. 17alpha-acetoxy-6-chloro-2-oxapregna-4,6-diene-3,20-dione

    2.4 Create Date
    2005-08-08
    3 Chemical and Physical Properties
    Molecular Weight 406.9 g/mol
    Molecular Formula C22H27ClO5
    XLogP33.4
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count5
    Rotatable Bond Count3
    Exact Mass406.1547017 g/mol
    Monoisotopic Mass406.1547017 g/mol
    Topological Polar Surface Area69.7 Ų
    Heavy Atom Count28
    Formal Charge0
    Complexity829
    Isotope Atom Count0
    Defined Atom Stereocenter Count6
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Drug and Medication Information
    4.1 Drug Indication

    Treatment of benign prostatic hypertrophy (BPH) in male dogs.

    5 Pharmacology and Biochemistry
    5.1 MeSH Pharmacological Classification

    Androgen Antagonists

    Compounds which inhibit or antagonize the biosynthesis or actions of androgens. (See all compounds classified as Androgen Antagonists.)

    5.2 ATC Code

    QG04CX90