Please Wait
Applying Filters...
menu
    • menu
    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

    Virtual Booth

    Contact Supplier

    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    With Fermion, start the journey of your innovative API.

    Virtual Booth

    Contact Supplier

    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    Menu

    Desoxycorticosterone Acetate

    FINISHED DOSAGE FORMULATIONS

    REF. STANDARDS & IMPURITIES

    PharmaCompass
    Xls

    Filters

    clear-filterReset all filters
    2D Structure
    Also known as: 56-47-3, Desoxycorticosterone acetate, Desoxycortone acetate, Doca, Cortexone acetate, Percotol
    Molecular Formula
    C23H32O4
    Molecular Weight
    372.5  g/mol
    InChI Key
    VPGRYOFKCNULNK-ACXQXYJUSA-N
    FDA UNII
    6E0A168OB8
    The 21-acetate derivative of desoxycorticosterone.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    [2-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate
    2.1.2 InChI
    InChI=1S/C23H32O4/c1-14(24)27-13-21(26)20-7-6-18-17-5-4-15-12-16(25)8-10-22(15,2)19(17)9-11-23(18,20)3/h12,17-20H,4-11,13H2,1-3H3/t17-,18-,19-,20+,22-,23-/m0/s1
    2.1.3 InChI Key
    VPGRYOFKCNULNK-ACXQXYJUSA-N
    2.1.4 Canonical SMILES
    CC(=O)OCC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C
    2.1.5 Isomeric SMILES
    CC(=O)OCC(=O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C
    2.2 Other Identifiers
    2.2.1 UNII
    6E0A168OB8
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Acetate, Desoxycortone

    2. Deoxycorticosterone 21 Acetate

    3. Deoxycorticosterone-21-acetate

    4. Desoxycorticosterone 21 Acetate

    5. Desoxycorticosterone Acetate

    6. Desoxycorticosterone-21-acetate

    7. Desoxycortone Acetate

    8. Doc 21 Acetate

    9. Doc-21-acetate

    10. Doca

    11. Syncortyl

    2.3.2 Depositor-Supplied Synonyms

    1. 56-47-3

    2. Desoxycorticosterone Acetate

    3. Desoxycortone Acetate

    4. Doca

    5. Cortexone Acetate

    6. Percotol

    7. Doc Acetate

    8. 11-deoxycorticosterone Acetate

    9. Decosteron

    10. Decosterone

    11. Sincortex

    12. Syncortyl

    13. Deoxycortone Acetate

    14. Descorterone

    15. Pregn-4-ene-3,20-dione, 21-(acetyloxy)-

    16. Cortacet

    17. Cortenil

    18. Cortesan

    19. Cortifar

    20. Cortigen

    21. Cortinaq

    22. Cortiron

    23. Cortivis

    24. Cortixyl

    25. Decorten

    26. Decorton

    27. Decostrate

    28. Descornaq

    29. Desocort

    30. Docaquosum

    31. Dorcostrin

    32. Doxatone

    33. Doxycamon

    34. Krinocorts

    35. Mincortid

    36. Ocritena

    37. Primocort

    38. Primocortan

    39. Syncorta

    40. Unidocan

    41. Arcort

    42. Cortate

    43. Ocriten

    44. Steraq

    45. Doca Acetate

    46. Bio-corten

    47. 3,20-dioxopregn-4-en-21-yl Acetate

    48. Doc-ac

    49. 21-(acetyloxy)-pregn-4-ene-3,20-dione

    50. Organon's Doca Acetate

    51. 21-acetoxypregn-4-ene-3,20-dione

    52. Percorten

    53. Syncort

    54. Deoxycorticosterone 21-acetate

    55. 11-desoxycorticosterone Acetate

    56. Desoxycorticosterone-21-acetate

    57. Corticosterone, Deoxy-, Acetate

    58. 4-pregnene-3,20-dione-21-ol Acetate

    59. 11-deoxycorticosterone 21-acetate

    60. 4-pregnene-3,20-dione 21-acetate

    61. Doxo

    62. 21-acetoxy-3,20-diketopregn-4-ene

    63. 21-hydroxypregn-4-ene-3,20-dione 21-acetate

    64. Pregn-4-ene-3,20-dione, 21-hydroxy-, Acetate

    65. Mls000028509

    66. Chebi:34671

    67. 6e0a168ob8

    68. Desoxycorticosterone Acetate [usp]

    69. Nsc-9567

    70. Ncgc00022043-04

    71. Desoxykorton

    72. Cortormon

    73. Percortene

    74. Smr000058339

    75. Dsstox_cid_2894

    76. Dsstox_rid_76777

    77. Dsstox_gsid_22894

    78. Descotone

    79. 2-((8s,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl Acetate

    80. 11-deoxycorticosterone, Acetate

    81. Desoxycorticosterone Acetate (usp)

    82. Cas-56-47-3

    83. Ccris 7517

    84. Nsc 9567

    85. Einecs 200-275-9

    86. Brn 2570798

    87. Unii-6e0a168ob8

    88. 21-acetoxypregn-4-en-3,20-dione

    89. 21-acetoxy-4-pregnene-3,20-dione

    90. 21-acetyloxypregn-4-ene-3,20-dione

    91. Doca (tn)

    92. Opera_id_47

    93. St075186

    94. Schembl4169

    95. Deoxy Corticosterone Acetate

    96. 4-08-00-02195 (beilstein Handbook Reference)

    97. Mls001074065

    98. Megxm0_000470

    99. Chembl1200542

    100. Dtxsid6022894

    101. Niosh/tu5076000

    102. Acon1_002189

    103. 11-deoxycorticosterone21-acetate

    104. Deoxycorticosterone Acetate, 98%

    105. Hms2230b14

    106. Hy-b1472

    107. Zinc4428527

    108. Tox21_110876

    109. Mfcd00003660

    110. S4243

    111. Desoxycortone Acetate [mart.]

    112. Akos004910359

    113. Akos015837895

    114. Desoxycortone Acetate [who-dd]

    115. Tox21_110876_1

    116. Ccg-268330

    117. Cs-5159

    118. Db06780

    119. Deoxycorticosterone Acetate [mi]

    120. Ncgc00022043-05

    121. Ncgc00022043-06

    122. [2-[(8s,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxo-ethyl] Acetate

    123. [2-[(8s,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] Acetate

    124. 2-((1s,10s,11s,14s,15s,2r)-2,15-dimethyl-5-oxotetracyclo[8.7.0.0<2,7>.0<11,15> ]heptadec-6-en-14-yl)-2-oxoethyl Acetate

    125. As-11731

    126. 3,20-dioxopregn-4-en-21-yl Acetate #

    127. Desoxycortone Acetate [ep Impurity]

    128. 21-hydroxypregn-4-ene-3,20-dione Acetate

    129. Desoxycorticosterone Acetate [vandf]

    130. D0047

    131. Desoxycorticosterone Acetate [usp-rs]

    132. Tu50760000

    133. D03698

    134. D81855

    135. Ab00383000_10

    136. 003d660

    137. A831058

    138. Desoxycorticosterone Acetate [orange Book]

    139. Desoxycorticosterone Acetate [usp Impurity]

    140. Sr-01000000097

    141. 21-hydroxypregn-4-ene-3,20-dione Acetate (ester)

    142. Sr-01000000097-3

    143. W-105514

    144. Brd-k24556098-001-01-9

    145. Brd-k24556098-001-19-1

    146. Q27116214

    147. Pregn-4-ene-3,20-dione, 21-hydroxy-, Acetate (ester)

    148. Desoxycortone Acetate, European Pharmacopoeia (ep) Reference Standard

    149. Deoxycorticosterone Acetate, United States Pharmacopeia (usp) Reference Standard

    150. 2-((8s,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl)-2-oxoethylacetate

    151. Acetic Acid [2-keto-2-[(8s,9s,10r,13s,14s,17s)-3-keto-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethyl] Ester

    2.4 Create Date
    2005-06-29
    3 Chemical and Physical Properties
    Molecular Weight 372.5 g/mol
    Molecular Formula C23H32O4
    XLogP33.1
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count4
    Rotatable Bond Count4
    Exact Mass372.23005950 g/mol
    Monoisotopic Mass372.23005950 g/mol
    Topological Polar Surface Area60.4 Ų
    Heavy Atom Count27
    Formal Charge0
    Complexity707
    Isotope Atom Count0
    Defined Atom Stereocenter Count6
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Mineralocorticoids

    A group of CORTICOSTEROIDS primarily associated with water and electrolyte balance. This is accomplished through the effect on ION TRANSPORT in renal tubules, resulting in retention of sodium and loss of potassium. Mineralocorticoid secretion is itself regulated by PLASMA VOLUME, serum potassium, and ANGIOTENSIN II. (See all compounds classified as Mineralocorticoids.)