NP-MRD: Showing NP-Card for methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate (NP0321423)

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Record Information

Version

2.0

Created at

2022-09-11 23:37:28 UTC

Updated at

2022-09-11 23:37:28 UTC

NP-MRD ID

NP0321423

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate

Description

Methyl (2S)-2-(acetyloxy)-2-[(1S,2R,4S,5S,6R,10R,11S,12R,13S,14R,15R,17S,18S)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]Octadecan-18-yl]acetate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate is found in Xylocarpus granatum. Based on a literature review very few articles have been published on methyl (2S)-2-(acetyloxy)-2-[(1S,2R,4S,5S,6R,10R,11S,12R,13S,14R,15R,17S,18S)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]Octadecan-18-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122201372D          

 50 55  0  0  1  0            999 V2000
   -2.8099    1.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086    1.7977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1509    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5029    0.8909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    1.8752    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4685    2.7641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9472    3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7618    3.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6755    4.3210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4629    1.3189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5436    1.4179    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5286    2.3002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4173    1.4227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7102    2.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5246    2.3258    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3214    3.1811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0460    1.6865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4573    2.5003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8604    1.8184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1534    2.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    3.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186    3.9229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9898    3.6300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9495    2.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3818    1.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0889    0.4078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8116   -0.0878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745    0.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5215    0.8868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9387    0.7834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0209   -0.2506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297   -0.0235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9461   -1.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5570   -1.8683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8811   -2.6755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8654   -2.4105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.0922    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9633   -0.2896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3561   -0.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3395   -1.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -2.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1916   -1.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5429    0.4860    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819    0.4221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9608    1.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5422    0.6788    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4259    0.6444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3707    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0584    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -0.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 10  5  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 17 29  1  0  0  0  0
 29 30  1  0  0  0  0
 13 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 38 43  1  0  0  0  0
 10 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 37 46  1  0  0  0  0
 11 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
M  END

     RDKit          3D

 94 99  0  0  0  0  0  0  0  0999 V2000
   -1.6264    4.9268    0.7488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0333    3.5839    0.9178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8537    2.9986   -0.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    3.6582   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2779    1.5772    0.1937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1308    1.2753   -0.8584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4909    1.2629   -0.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4269    0.9301   -1.8197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0499    1.5224    0.4085 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1421    0.6218    0.4642 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1335    0.4977   -0.6650 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4916    1.2567   -1.9084 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3306    0.6796   -0.3632 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6792    1.8709    0.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1253    2.2093    0.5472 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4861    3.2534   -0.3332 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1073    1.1099    0.3234 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6379    1.1580   -1.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2560    1.2706    1.2941 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5490    1.6081    0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4393    0.7086    0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5196    1.4484   -0.4599 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2875    2.6990   -0.1695 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1500    2.8406    0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5430    0.1127    2.0572 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216   -0.5248    2.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6381   -1.2524    3.7244 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1867   -0.1903    2.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4219   -0.2250    0.6518 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2585   -0.4916   -0.2596 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8270   -0.8712   -1.4861 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6212   -1.7865    0.2729 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6760   -2.8446   -0.6630 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2769   -4.0608   -0.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2786   -5.1247   -1.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8365   -4.2617    0.6439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6934   -1.3732    0.5837 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8294   -1.8208    1.2375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8650   -1.8172    2.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2721   -2.9083    3.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3083   -2.8999    4.9020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6239   -3.9439    2.8146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7984   -0.7184    0.6969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0695   -0.7769    1.4003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7477   -1.3175   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2525   -0.9741   -0.8253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6631   -1.6607   -1.8149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263   -1.8056   -3.1404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069   -2.6176   -4.0825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9180   -1.2182   -3.5861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6508    5.2352   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5806    5.0330    1.0842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2712    5.5519    1.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848    1.6622    1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8859    1.9129   -2.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2638    0.3187   -1.4035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8987    0.4450   -2.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7204    1.0833    1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1414    2.3286   -1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4395    1.1162   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7092    0.8983   -2.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7139    1.1071   -1.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2367    2.7658   -0.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1577    1.9049    1.4542 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2998    2.6607    1.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9301    4.0539   -0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5857    1.7738   -1.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9575    1.7419   -1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9137    0.1751   -1.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0635    2.1515    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2714   -0.3503   -0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3623    0.9996   -0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7393    3.7714    0.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4404   -0.7884    2.5726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451    0.8628    2.4981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2004   -0.9934    0.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540   -0.2291   -2.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1686   -2.1933    1.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8311   -4.6573   -2.3961 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2397   -5.3543   -1.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8501   -5.9844   -1.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4892   -0.4675    1.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1802   -2.8131    0.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6851   -3.7219    5.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3568   -3.1315    5.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0289   -1.9101    5.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3641   -0.8520   -1.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -2.4072   -0.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3458   -2.3822   -5.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4174   -3.6863   -3.9059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9839   -2.5489   -3.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  5 10  1  0
 10 43  1  0
 43 44  1  1
 43 45  1  0
 45 46  1  0
 46 47  1  6
 47 48  1  0
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 48 50  2  0
 46 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 37 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  2  0
 32 30  1  0
 30 31  1  6
 30 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  6
 17 19  1  0
 19 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 19 20  1  0
 20 24  2  0
 24 23  1  0
 23 22  1  0
 22 21  2  0
 13 11  1  0
 11 12  1  6
 11 10  1  0
 38 43  1  0
 29 30  1  0
 21 20  1  0
 11 46  1  0
 29 17  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  5 54  1  1
  8 55  1  0
  8 56  1  0
  8 57  1  0
 10 58  1  1
 44 87  1  0
 44 88  1  0
 44 89  1  0
 45 90  1  0
 45 91  1  0
 49 92  1  0
 49 93  1  0
 49 94  1  0
 37 82  1  1
 38 83  1  6
 41 84  1  0
 41 85  1  0
 41 86  1  0
 32 78  1  1
 35 79  1  0
 35 80  1  0
 35 81  1  0
 31 77  1  0
 13 62  1  6
 14 63  1  0
 14 64  1  0
 15 65  1  1
 16 66  1  0
 18 67  1  0
 18 68  1  0
 18 69  1  0
 19 70  1  1
 28 74  1  0
 28 75  1  0
 29 76  1  1
 24 73  1  0
 22 72  1  0
 21 71  1  0
 12 59  1  0
 12 60  1  0
 12 61  1  0
M  END


  Mrv1652309122201372D          

 50 55  0  0  1  0            999 V2000
   -2.8099    1.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086    1.7977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1509    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5029    0.8909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    1.8752    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4685    2.7641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9472    3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7618    3.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6755    4.3210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4629    1.3189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5436    1.4179    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5286    2.3002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4173    1.4227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7102    2.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5246    2.3258    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3214    3.1811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0460    1.6865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4573    2.5003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8604    1.8184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1534    2.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    3.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186    3.9229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9898    3.6300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9495    2.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3818    1.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0889    0.4078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8116   -0.0878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745    0.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5215    0.8868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9387    0.7834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0209   -0.2506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297   -0.0235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9461   -1.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5570   -1.8683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8811   -2.6755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8654   -2.4105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.0922    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9633   -0.2896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3561   -0.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3395   -1.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -2.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1916   -1.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5429    0.4860    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819    0.4221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9608    1.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5422    0.6788    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4259    0.6444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3707    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0584    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -0.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 10  5  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 17 29  1  0  0  0  0
 29 30  1  0  0  0  0
 13 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 38 43  1  0  0  0  0
 10 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 37 46  1  0  0  0  0
 11 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0321423

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](OC(C)=O)[C@H]1[C@@]2(C)C[C@]3(OC(C)=O)[C@@H]([C@H]2OC(C)=O)[C@@H](OC(C)=O)[C@@]2(O)[C@H](C[C@H](O)[C@@]4(C)[C@@H](OC(=O)C[C@@H]24)C2=COC=C2)[C@]13C

> <INCHI_IDENTIFIER>
InChI=1S/C35H44O15/c1-15(36)46-25(30(42)44-8)26-31(5)14-34(50-18(4)39)24(28(31)47-16(2)37)29(48-17(3)38)35(43)20-12-23(41)49-27(19-9-10-45-13-19)32(20,6)22(40)11-21(35)33(26,34)7/h9-10,13,20-22,24-29,40,43H,11-12,14H2,1-8H3/t20-,21-,22+,24+,25+,26+,27+,28-,29-,31-,32+,33-,34+,35+/m1/s1

> <INCHI_KEY>
KRYOGVYVKJASNO-DQGCNJLYSA-N

> <FORMULA>
C35H44O15

> <MOLECULAR_WEIGHT>
704.722

> <EXACT_MASS>
704.268020717

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
69.50242586295315

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S)-2-(acetyloxy)-2-[(1S,2R,4S,5S,6R,10R,11S,12R,13S,14R,15R,17S,18S)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0^{2,11}.0^{5,10}.0^{13,17}]octadecan-18-yl]acetate

> <JCHEM_LOGP>
-0.15172784166666653

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.626700961286527

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.32095755064378

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8886981341021243

> <JCHEM_POLAR_SURFACE_AREA>
211.39999999999995

> <JCHEM_REFRACTIVITY>
163.07800000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(S)-(methyl (acetyloxy)[(1S,2R,4S,5S,6R,10R,11S,12R,13S,14R,15R,17S,18S)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0^{2,11}.0^{5,10}.0^{13,17}]octadecan-18-yl]acetate)

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.245   2.780   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.749   3.356   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.148   3.098   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.805   1.663   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.553   3.500   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.874   5.160   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.768   6.544   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.289   7.039   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.261   8.066   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.864   2.462   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.881   2.647   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.853   4.294   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.512   2.656   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.059   4.095   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.579   4.342   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.200   5.938   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.553   3.148   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.320   4.667   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.073   3.394   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.620   4.834   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.776   6.123   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.741   7.323   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.181   6.776   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.106   5.238   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.046   2.201   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.499   0.761   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.848  -0.164   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.979   0.515   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.573   1.655   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.486   1.462   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.639  -0.468   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.909  -0.044   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.499  -1.897   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.773  -3.487   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.378  -4.994   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.482  -4.500   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.322  -0.172   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.798  -0.541   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       0.665  -1.752   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -0.634  -2.759   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.036  -4.297   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -2.224  -2.566   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       1.013   0.907   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.526   0.788   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.793   2.446   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.879   1.267   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       4.528   1.203   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       6.292   0.413   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       7.576   1.482   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       6.778  -1.219   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   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   43                                                  
CONECT   11   10   12   13   46                                             
CONECT   12   11                                                            
CONECT   13   11   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   29                                             
CONECT   18   17                                                            
CONECT   19   17   20   25                                                  
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20                                                       
CONECT   25   19   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   17   30                                                  
CONECT   30   29   13   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   38   46                                                  
CONECT   38   37   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   38   10   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   37   11   47                                             
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  110    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-2-(acetyloxy)-2-[(1S,2R,4S,5S,6R,10R,11S,12R,13S,14R,15R,17S,18S)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0,.0,.0,]octadecan-18-yl]acetic acid	Generator

Chemical Formula

C₃₅H₄₄O₁₅

Average Mass

704.7220 Da

Monoisotopic Mass

704.26802 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](OC(C)=O)[C@H]1[C@@]2(C)C[C@]3(OC(C)=O)[C@@H]([C@H]2OC(C)=O)[C@@H](OC(C)=O)[C@@]2(O)[C@H](C[C@H](O)[C@@]4(C)[C@@H](OC(=O)C[C@@H]24)C2=COC=C2)[C@]13C

InChI Identifier

InChI=1S/C35H44O15/c1-15(36)46-25(30(42)44-8)26-31(5)14-34(50-18(4)39)24(28(31)47-16(2)37)29(48-17(3)38)35(43)20-12-23(41)49-27(19-9-10-45-13-19)32(20,6)22(40)11-21(35)33(26,34)7/h9-10,13,20-22,24-29,40,43H,11-12,14H2,1-8H3/t20-,21-,22+,24+,25+,26+,27+,28-,29-,31-,32+,33-,34+,35+/m1/s1

InChI Key

KRYOGVYVKJASNO-DQGCNJLYSA-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
Xylocarpus granatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Mexicanolide
Prostaglandin skeleton
Steroid lactone
Eicosanoid
Hexacarboxylic acid or derivatives
6-hydroxysteroid
Hydroxysteroid
Oxosteroid
2-oxosteroid
3-oxasteroid
Steroid
Naphthopyran
Naphthalene
Delta valerolactone
Delta_valerolactone
Fatty acyl
Oxane
Pyran
Methyl ester
Cyclic alcohol
Furan
Heteroaromatic compound
Tertiary alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

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

27023528

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162850779

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate (NP0321423)

MOL for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

3D MOL for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

3D SDF for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

3D-SDF for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

PDB for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

3D PDB for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

SMILES for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

INCHI for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

Structure for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)

3D Structure for NP0321423 (methyl (2s)-2-(acetyloxy)-2-[(1s,2r,4s,5s,6s,10r,11s,12r,13s,14r,15r,17s,18s)-12,14,17-tris(acetyloxy)-6-(furan-3-yl)-4,11-dihydroxy-1,5,15-trimethyl-8-oxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadecan-18-yl]acetate)