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    Technical details about Sterculic Acid, learn more about the structure, uses, toxicity, action, side effects and more

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    Sterculic Acid

    PharmaCompass

    Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.

    One Pharma aims to be one of the leading generic companies in Europe.

    2D Structure
    1. Also known as: 738-87-4, Sterculinic acid, 8-(2-octylcyclopropen-1-yl)octanoic acid, 9,10-methylene-9-octadecenoic acid, Mxv06g5rok, 1-cyclopropene-1-octanoicacid, 2-octyl-
    Molecular Formula
    C19H34O2
    Molecular Weight
    294.5  g/mol
    InChI Key
    PQRKPYLNZGDCFH-UHFFFAOYSA-N
    FDA UNII
    MXV06G5ROK
    sterculic acid is a natural product found in Hibiscus syriacus, Amaranthus cruentus, and other organisms with data available.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    8-(2-octylcyclopropen-1-yl)octanoic acid
    2.1.2 InChI
    InChI=1S/C19H34O2/c1-2-3-4-5-7-10-13-17-16-18(17)14-11-8-6-9-12-15-19(20)21/h2-16H2,1H3,(H,20,21)
    2.1.3 InChI Key
    PQRKPYLNZGDCFH-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCCCCCCCC1=C(C1)CCCCCCCC(=O)O
    2.2 Other Identifiers
    2.2.1 UNII
    MXV06G5ROK
    2.3 Synonyms
    2.3.1 Depositor-Supplied Synonyms

    1. 738-87-4

    2. Sterculinic Acid

    3. 8-(2-octylcyclopropen-1-yl)octanoic Acid

    4. 9,10-methylene-9-octadecenoic Acid

    5. Mxv06g5rok

    6. 1-cyclopropene-1-octanoicacid, 2-octyl-

    7. 1-cyclopropene-1-octanoic Acid, 2-octyl-

    8. Omega-(2-n-octylcycloprop-1-enyl)octanoic Acid

    9. 2-octyl-1-cyclopropene-1-octanoic Acid

    10. Sterculia-saeure

    11. Unii-mxv06g5rok

    12. Sterculinsaeure

    13. Stearculic Acid

    14. Ster-culic Acid

    15. Stearculinic Acid

    16. Hsdb 3904

    17. Schembl31295

    18. 2-octyl-1-cyclopropene-1-octanoic Acid Homopolymer

    19. 55088-60-3

    20. Sterculic Acid [hsdb]

    21. Chebi:9261

    22. Us8962837, Sterculic Acid

    23. 1-cyclopropene-1-octanoic Acid, 2-octyl-, Homopolymer

    24. Chembl3677268

    25. Dtxsid90970445

    26. Bdbm149345

    27. Zinc8221051

    28. Lmfa01140018

    29. 9,10-mt 9c-18:1

    30. 1-cyclopropene-1-octanoic Acid 2-octyl-

    31. Da-03178

    32. Fa(19:2)

    33. 8-(2-octyl-1-cyclopropenyl)octanoic Acid

    34. 8-(2-octyl-cycloprop-1-enyl)-octansaeure

    35. Hy-127143

    36. Cs-0093556

    37. Ft-0724977

    38. 8-(2-octylcycloprop-1-en-1-yl)octanoic Acid

    39. C08366

    40. 738s874

    41. A837950

    42. Q2345401

    2.4 Create Date
    2005-06-24
    3 Chemical and Physical Properties
    Molecular Weight 294.5 g/mol
    Molecular Formula C19H34O2
    XLogP35.8
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count15
    Exact Mass294.255880323 g/mol
    Monoisotopic Mass294.255880323 g/mol
    Topological Polar Surface Area37.3 Ų
    Heavy Atom Count21
    Formal Charge0
    Complexity318
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 Absorption, Distribution and Excretion

    STERCULIC ACID IS A NATURALLY OCCURRING CYCLOPROPENOID FATTY ACID. THE DISTRIBUTION OF RADIOACTIVITY FROM STERCULIC ACID, LABELED ON 9,10-METHYLENE C OF THE CYCLOPROPENE RING, WAS INVESTIGATED IN TROUT, S GAIRDNERI. OF THE ADMIN DOSE, 50% WAS EXCRETED IN FECES & URINE BY 168 HR, BUT LESS THAN 1% OF THE DOSE WAS EXPIRED AS CO2 DURING THE SAME TIME PERIOD. INCORPORATION OF RADIOACTIVITY INTO MOST ORGANS PEAKED AT 119 HR & THE MAJORITY OF THE LABEL IN THE LIVER WAS IN THE FATTY ACID PORTION OF THE LIPID FRACTION. RAINBOW TROUT READILY ABSORB, TRANSPORT & INCORPORATE STERCULIC ACID INTO TISSUE LIPID, INCL MEMBRANE LIPID, BUT CANNOT OXIDIZE THE METHYLENE C OF THE CYCLOPROPENOID TO CO2.

    EISELE TA ET AL; INCORPORATION OF LABEL FROM (9,10-METHYLENE-14C) STERCULIC ACID IN RAINBOW TROUT, SALMO GAIRDNERI; LIPIDS 14(6) 523 (1979)

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