NP-MRD: Showing NP-Card for (1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate (NP0146627)

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Record Information

Version

2.0

Created at

2022-09-02 02:03:44 UTC

Updated at

2022-09-02 02:03:44 UTC

NP-MRD ID

NP0146627

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

Description

CASEARLUCIN D belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. (1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate is found in Casearia lucida. Based on a literature review very few articles have been published on CASEARLUCIN D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204032D          

 40 42  0  0  1  0            999 V2000
    2.9944   -1.4965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6019   -0.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7595   -0.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107   -0.8066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0886   -0.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088   -0.2329    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4744   -1.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4247   -0.7818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3830   -1.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2080   -0.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3888    0.0520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3565    0.2801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1758   -0.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4435   -1.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8877    0.3309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7595    0.8339    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9269    1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3110    2.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5277    1.9316    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0286    2.6494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8676    2.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4114    2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6902    3.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6567    4.1290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5138    2.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2683    3.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    1.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9762    0.5749    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7469    1.7321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1943    2.5020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9611    2.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7749    2.6728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1524    3.7539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0863    0.9802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4761    0.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9274   -0.4800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7777   -0.9246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6279   -1.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -0.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 28  1  0  0  0  0
 29 28  1  6  0  0  0
  7 29  1  0  0  0  0
 17 29  1  0  0  0  0
 18 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 17 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
M  END

     RDKit          3D

 84 86  0  0  0  0  0  0  0  0999 V2000
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   -5.9941   -2.2849    0.7190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9195   -1.3078    0.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -0.0784    0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6739   -1.7184    1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.1002    1.3360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4959   -1.1515    0.1725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9351   -2.6693    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8307   -1.0390   -1.2348 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0091   -0.3564   -1.7829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6282   -0.5443   -2.0808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0989    0.7721   -1.6470 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8985    1.7668   -2.2574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    2.6081   -3.2326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2125    3.6283   -3.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8347    2.4748   -3.5601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0831    0.9804   -0.1432 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2759    1.5218    0.2814 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495    0.8135    0.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2618   -0.5792   -0.1887 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.0746   -1.8741   -1.7359 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4118   -2.7416    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3642   -1.8369    0.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9044   -3.8598    0.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0248   -4.7237    1.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0078   -1.2243    0.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1916   -0.3399    0.5011 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0213    2.9786    0.6882 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9265    3.4383    1.6243 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435    4.6133    1.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5987    5.0403    2.6068 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4749    5.3521    0.5691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2000    2.6935    1.3735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539    2.1418    0.2134 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1970    2.2662    0.3139 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9081    3.2819   -0.2648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3798    3.4106   -0.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2874    4.1622   -0.9295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1567   -4.0185    1.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8560   -4.1551    0.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9192   -1.9230    0.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1032    0.1475    0.0314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340    0.7124    0.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6104   -2.8630    1.5253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9188   -1.5829    2.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7463   -1.5690    2.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5389   -0.0042    1.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6694   -3.0034   -0.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3097   -2.7887    1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8656   -3.2913    0.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9439   -2.1048   -1.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2311    0.6566   -1.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9240   -1.0367   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7931   -0.2490   -2.9111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0775   -0.4069   -3.1145 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0952   -1.3515   -2.2275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9065    0.8943   -2.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0545    3.6179   -4.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9780    4.6048   -3.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2933    3.4278   -3.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.3054    0.5492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3522   -0.6722   -1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9530   -3.1985   -0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3848   -2.2650    0.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0931   -1.6589    1.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3433   -0.8509    0.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2017   -4.5062    0.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3194   -3.4244    1.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8119   -4.7527    0.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4230   -4.3397    2.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6021   -5.7340    1.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9342   -2.1231   -0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3207   -1.6207    1.4104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3142   -0.1281    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8931    3.6311   -0.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7993    4.2581    3.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5413    5.4504    2.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1271    5.8858    3.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5570    2.9666   -0.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6453    4.4709   -0.2877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7582    3.0693    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8140    2.8454   -1.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 28  1  0
 28 29  1  0
 29 17  1  0
 17 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 38 40  2  0
 36 35  1  0
 35 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 32 34  2  0
 30 18  1  0
 18 19  2  0
 17 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  3
  3  2  1  0
  2  1  2  3
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 19 20  1  0
  7 29  1  0
 17 18  1  1
 27 71  1  0
 27 72  1  0
 27 73  1  0
 26 69  1  0
 26 70  1  0
 24 65  1  6
 25 66  1  0
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 20 64  1  6
 28 74  1  0
 28 75  1  0
 29 76  1  1
 36 81  1  6
 39 82  1  0
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 39 84  1  0
 30 77  1  6
 33 78  1  0
 33 79  1  0
 33 80  1  0
 19 63  1  0
 12 59  1  6
 11 57  1  0
 11 58  1  0
  9 53  1  6
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  8 50  1  0
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  8 52  1  0
  6 48  1  0
  6 49  1  0
  5 46  1  0
  5 47  1  0
  4 44  1  0
  4 45  1  0
  2 43  1  0
  1 41  1  0
  1 42  1  0
 15 60  1  0
 15 61  1  0
 15 62  1  0
M  END


  Mrv1652309022204032D          

 40 42  0  0  1  0            999 V2000
    2.9944   -1.4965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6019   -0.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7595   -0.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107   -0.8066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0886   -0.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088   -0.2329    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4744   -1.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4247   -0.7818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3830   -1.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2080   -0.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3888    0.0520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3565    0.2801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1758   -0.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4435   -1.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8877    0.3309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7595    0.8339    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9269    1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3110    2.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5277    1.9316    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0286    2.6494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8676    2.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4114    2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6902    3.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6567    4.1290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5138    2.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2683    3.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    1.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9762    0.5749    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7469    1.7321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1943    2.5020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9611    2.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7749    2.6728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1524    3.7539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0863    0.9802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4761    0.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9274   -0.4800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7777   -0.9246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6279   -1.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -0.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 28  1  0  0  0  0
 29 28  1  6  0  0  0
  7 29  1  0  0  0  0
 17 29  1  0  0  0  0
 18 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 17 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0146627

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)O[C@H]1C[C@H]2[C@]3([C@@H](OC(C)=O)O[C@@H](OC(C)=O)C3=C1)[C@@H](C[C@H](C)[C@]2(C)CCC(=C)C=C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H44O9/c1-10-17(3)12-13-30(9)19(5)14-26(36-20(6)32)31-24(28(37-21(7)33)40-29(31)38-22(8)34)15-23(16-25(30)31)39-27(35)18(4)11-2/h10,15,18-19,23,25-26,28-29H,1,3,11-14,16H2,2,4-9H3/t18?,19-,23+,25+,26+,28+,29-,30-,31-/m0/s1

> <INCHI_KEY>
SVSGAQXPAAFAGR-VPPCHDCASA-N

> <FORMULA>
C31H44O9

> <MOLECULAR_WEIGHT>
560.684

> <EXACT_MASS>
560.298532997

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
60.85434250035617

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,5S,6aR,7S,8S,10R,10aR)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

> <ALOGPS_LOGP>
3.71

> <JCHEM_LOGP>
4.998777290000001

> <ALOGPS_LOGS>
-5.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.548199558188874

> <JCHEM_POLAR_SURFACE_AREA>
114.43

> <JCHEM_REFRACTIVITY>
145.8617

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.70e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,5S,6aR,7S,8S,10R,10aR)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       5.590  -2.794   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.857  -1.402   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.284  -1.117   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.692   0.398   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.700  -1.506   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.165  -0.784   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.510  -0.435   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.886  -1.987   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.659  -1.459   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.582  -3.116   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.122  -0.976   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.459   0.097   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.265   0.523   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -7.795  -0.404   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.295  -2.159   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -9.124   0.618   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.284   1.557   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.597   3.064   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.447   4.089   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.985   3.606   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.053   4.946   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.620   5.544   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.635   4.332   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.155   6.134   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.092   7.707   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.692   5.544   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.101   6.255   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.673   2.098   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.822   1.073   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.128   3.233   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.963   4.670   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -7.394   5.458   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -8.913   4.989   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -7.751   7.007   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -5.761   1.830   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -4.622   0.793   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -5.464  -0.896   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -7.052  -1.726   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -6.772  -3.388   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -8.834  -1.231   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   29                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   29   36                                             
CONECT   18   17   19   30                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   20   29                                                       
CONECT   29   28    7   17                                                  
CONECT   30   18   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30   36                                                       
CONECT   36   35   17   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₄O₉

Average Mass

560.6840 Da

Monoisotopic Mass

560.29853 Da

IUPAC Name

(1R,3S,5S,6aR,7S,8S,10R,10aR)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

Traditional Name

(1R,3S,5S,6aR,7S,8S,10R,10aR)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)O[C@H]1C[C@H]2[C@]3([C@@H](OC(C)=O)O[C@@H](OC(C)=O)C3=C1)[C@@H](C[C@H](C)[C@]2(C)CCC(=C)C=C)OC(C)=O

InChI Identifier

InChI=1S/C31H44O9/c1-10-17(3)12-13-30(9)19(5)14-26(36-20(6)32)31-24(28(37-21(7)33)40-29(31)38-22(8)34)15-23(16-25(30)31)39-27(35)18(4)11-2/h10,15,18-19,23,25-26,28-29H,1,3,11-14,16H2,2,4-9H3/t18?,19-,23+,25+,26+,28+,29-,30-,31-/m0/s1

InChI Key

SVSGAQXPAAFAGR-VPPCHDCASA-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
Casearia lucida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Naphthofuran
Tetracarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Tetrahydrofuran
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.71	ALOGPS
logP	5	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.43 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	145.86 m³·mol⁻¹	ChemAxon
Polarizability	60.85 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00045722

Chemspider ID

24691584

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44584137

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate (NP0146627)

MOL for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D MOL for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D SDF for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D-SDF for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

PDB for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D PDB for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

SMILES for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

INCHI for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

Structure for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D Structure for NP0146627 ((1r,3s,5s,6ar,7s,8s,10r,10ar)-1,3,10-tris(acetyloxy)-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)