NP-MRD: Showing NP-Card for (1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate (NP0251175)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 14:17:38 UTC

Updated at

2022-09-07 14:17:38 UTC

NP-MRD ID

NP0251175

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate

Description

(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-2-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate is found in Junceella fragilis. Based on a literature review very few articles have been published on (1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216172D          

 33 35  0  0  1  0            999 V2000
    1.2443    5.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9407    4.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6719    5.3483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9060    4.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6025    3.6997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3337    4.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0302    3.6396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    4.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7961    4.8459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4578    3.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4231    2.7551    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0124    2.1778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6454    1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275    0.7077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7232    1.5111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2519    0.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6919    2.3731    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0046    1.9167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9954    2.8153    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7077    2.0421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2334    1.4063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0469    1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9457    0.6331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2642    2.4332    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2295    1.6090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9551    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4788    0.8225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    1.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8018    1.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8365    2.4934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1401    2.9356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5677    2.8755    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8713    3.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  6  0  0  0
 25 27  1  1  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
  5 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  1  0  0  0
M  END

     RDKit          3D

 69 71  0  0  0  0  0  0  0  0999 V2000
    4.4521    0.9651    1.7864 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1153    1.1626    1.1785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2232    1.7451    1.8036 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8636    0.7012   -0.0763 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6222    0.8257   -0.7755 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6898    1.8074   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    2.7662   -1.9774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1226    3.0595   -0.6910 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4903    4.0243    0.2662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2676    2.4805   -0.3422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9991    1.5207   -1.1484 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3875    1.8607   -1.3668 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1140    0.6826   -1.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9996    0.1703   -1.9143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4759    0.1766    0.0567 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8342    1.2602    0.9993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0824    0.1328   -0.4932 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1963   -0.8362   -1.5259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9978   -0.2466    0.3744 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5102   -0.9721    1.5123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4692   -0.5555    2.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0465   -1.4325    3.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9566    0.5362    3.0843 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1480   -1.0767   -0.1038 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0376   -2.5500   -0.1697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0564   -3.1639    0.7362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3644   -3.0700   -1.4203 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2828   -3.2403    0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4372   -2.2663    0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3233   -1.4952   -1.0539 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4833   -0.8331   -1.4461 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.5524   -1.1104 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7442   -0.5891   -2.5559 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2346    1.2790    1.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6537   -0.0968    2.0435 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5690    1.5400    2.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823    1.3744   -0.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8482    1.4135   -2.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435    2.3971   -1.7046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9815    3.7590   -2.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717    2.5818   -2.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    5.0543    0.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2914    3.6608    1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5909    3.9600    0.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6751    2.7561    0.6212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6477    1.3634   -2.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8838   -0.7916    0.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2427    1.4498    1.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0204    2.2679    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8663    0.9856    1.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -0.3829   -2.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6245    0.6976    0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3535   -1.5866    4.7016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3800   -2.4049    3.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9913   -0.9221    4.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8007   -0.9964    0.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1032   -2.9578    0.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886   -3.1647    1.8084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9757   -4.2811    0.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4180   -4.0347   -1.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178   -4.0878   -0.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2432   -3.6544    1.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6445   -1.7358    1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3581   -2.9126    0.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2155   -2.3083   -1.8441 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0899   -1.3658   -1.9816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2043    0.2454   -2.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2715   -1.5017   -2.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7187   -0.5972   -3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  2  0
  8  9  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 32  1  0
 32 33  1  6
 32 30  1  0
 30 31  1  0
 30 29  1  0
 29 28  1  0
 28 25  1  0
 25 26  1  0
 25 27  1  6
 25 24  1  0
 24 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 19 17  1  0
 17 18  1  6
 17 15  1  0
 17 11  1  0
 24 32  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 15 47  1  1
 11 46  1  6
 10 45  1  0
  9 42  1  0
  9 43  1  0
  9 44  1  0
  7 40  1  0
  7 41  1  0
  6 38  1  0
  6 39  1  0
  5 37  1  1
  1 34  1  0
  1 35  1  0
  1 36  1  0
 33 67  1  0
 33 68  1  0
 33 69  1  0
 30 65  1  6
 31 66  1  0
 29 63  1  0
 29 64  1  0
 28 61  1  0
 28 62  1  0
 26 57  1  0
 26 58  1  0
 26 59  1  0
 27 60  1  0
 24 56  1  1
 19 52  1  1
 22 53  1  0
 22 54  1  0
 22 55  1  0
 18 51  1  0
M  END


  Mrv1652309072216172D          

 33 35  0  0  1  0            999 V2000
    1.2443    5.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9407    4.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6719    5.3483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9060    4.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6025    3.6997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3337    4.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0302    3.6396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    4.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7961    4.8459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4578    3.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4231    2.7551    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0124    2.1778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6454    1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275    0.7077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7232    1.5111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2519    0.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6919    2.3731    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0046    1.9167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9954    2.8153    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7077    2.0421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2334    1.4063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0469    1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9457    0.6331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2642    2.4332    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2295    1.6090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9551    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4788    0.8225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    1.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8018    1.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8365    2.4934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1401    2.9356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5677    2.8755    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8713    3.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  6  0  0  0
 25 27  1  1  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
  5 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0251175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C(=O)O[C@H]2\C=C(C)/CC[C@H](OC(C)=O)[C@@]3(C)[C@@H](O)CC[C@](C)(O)[C@@H]3[C@H](OC(C)=O)[C@@]12O

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O9/c1-12-7-8-17(31-14(3)25)23(6)16(27)9-10-22(5,29)19(23)20(32-15(4)26)24(30)13(2)21(28)33-18(24)11-12/h11,13,16-20,27,29-30H,7-10H2,1-6H3/b12-11-/t13-,16-,17-,18-,19-,20-,22-,23+,24+/m0/s1

> <INCHI_KEY>
UOAWVEYDWZRBSY-CWHLLGMTSA-N

> <FORMULA>
C24H36O9

> <MOLECULAR_WEIGHT>
468.543

> <EXACT_MASS>
468.235932739

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.06665503224427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-2-yl acetate

> <JCHEM_LOGP>
0.5262241703333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.34437209492815

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.351133796171226

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9424960638940396

> <JCHEM_POLAR_SURFACE_AREA>
139.59

> <JCHEM_REFRACTIVITY>
115.841

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       2.323  10.096   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.623   9.270   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.988   9.983   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.558   7.732   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.858   6.906   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.223   7.619   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.523   6.794   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.888   7.507   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.953   9.046   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.188   6.682   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.123   5.143   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.223   4.065   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.538   2.686   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.251   1.321   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.817   2.821   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.937   1.811   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.758   4.430   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.475   3.578   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.458   5.255   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.921   3.812   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.902   2.625   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.421   2.882   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.365   1.182   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.093   4.542   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.028   3.003   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.383   2.271   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.494   1.535   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.663   2.290   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.363   3.116   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.428   4.654   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.128   5.480   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.793   5.368   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.493   6.193   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   32                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   32                                                  
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    5   24   33                                             
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(Acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0,]heptadec-8-en-2-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₆O₉

Average Mass

468.5430 Da

Monoisotopic Mass

468.23593 Da

IUPAC Name

(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-2-yl acetate

Traditional Name

(1S,2S,3R,4R,7S,8Z,12S,13R,14S,17S)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1C(=O)O[C@H]2\C=C(C)/CC[C@H](OC(C)=O)[C@@]3(C)[C@@H](O)CC[C@](C)(O)[C@@H]3[C@H](OC(C)=O)[C@@]12O

InChI Identifier

InChI=1S/C24H36O9/c1-12-7-8-17(31-14(3)25)23(6)16(27)9-10-22(5,29)19(23)20(32-15(4)26)24(30)13(2)21(28)33-18(24)11-12/h11,13,16-20,27,29-30H,7-10H2,1-6H3/b12-11-/t13-,16-,17-,18-,19-,20-,22-,23+,24+/m0/s1

InChI Key

UOAWVEYDWZRBSY-CWHLLGMTSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Junceella fragilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Briarane diterpenoid
Diterpenoid
Diterpene lactone
Tricarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.53	ChemAxon
pKa (Strongest Acidic)	12.35	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	115.84 m³·mol⁻¹	ChemAxon
Polarizability	49.07 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162959581

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate (NP0251175)

MOL for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

3D MOL for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

3D SDF for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

3D-SDF for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

PDB for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

3D PDB for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

SMILES for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

INCHI for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

Structure for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)

3D Structure for NP0251175 ((1s,2s,3r,4r,7s,8z,12s,13r,14s,17s)-12-(acetyloxy)-3,14,17-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate)