NP-MRD: Showing NP-Card for methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate (NP0323651)

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Record Information

Version

2.0

Created at

2022-09-12 03:12:59 UTC

Updated at

2022-09-12 03:13:00 UTC

NP-MRD ID

NP0323651

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate

Description

Methyl (2S)-2-(acetyloxy)-2-[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]Docosan-16-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-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate is found in Xylocarpus granatum. Based on a literature review very few articles have been published on methyl (2S)-2-(acetyloxy)-2-[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]Docosan-16-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122205132D          

 54 61  0  0  1  0            999 V2000
   -1.2729    1.2599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4481    1.2758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0219    0.5694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4206   -0.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029    0.5853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2016    1.3076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7754    2.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0494    1.9981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1741    2.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291   -0.1211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0531   -0.2804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0586    0.5446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1118   -0.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6606    0.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5046    0.6653    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9119    1.3827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4942    2.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6692    2.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9015    2.8116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9235   -0.0600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3193    0.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7476   -0.0219    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1267    0.7109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566    1.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3436    2.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0763    1.6490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9423    0.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1927   -0.7166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8137   -1.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2588   -2.1440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9896   -1.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5445   -0.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6740   -0.8411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9075   -0.0298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0224    0.3122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1301    1.1301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9925   -0.7823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1220    0.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0035   -0.9106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1728   -1.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742   -0.9628    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1541   -1.0528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5109   -1.9162    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2004   -2.6805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495   -1.6694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4975   -2.4810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8686   -3.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0166   -3.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0439   -2.9910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2375   -1.6032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6776   -2.3010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2932   -3.0310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332   -3.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4688   -3.0631    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  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
 22 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 32 31  1  1  0  0  0
 20 32  1  0  0  0  0
 32 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 13 37  1  6  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 10 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 39 45  1  0  0  0  0
 45 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 45 50  1  0  0  0  0
 33 50  1  0  0  0  0
 50 51  1  6  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  2  0  0  0  0
M  END

     RDKit          3D

 98105  0  0  0  0  0  0  0  0999 V2000
    3.3725    3.7165   -3.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1999    3.3566   -2.3659 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0449    2.0085   -1.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0753    1.1935   -2.8938 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8655    1.6759   -0.5353 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5605    2.8369    0.1343 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3868    3.5969    0.8887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9742    4.8604    1.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5878    3.2338    1.0199 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437    0.3920   -0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6027    0.0247    0.9720 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2444    0.7317    2.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1379    0.0511    1.1572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4448    1.3237    0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6670    1.1551   -0.2481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9698    2.4463   -0.6643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6459    2.9216   -1.9552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765    4.3034   -2.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0652    2.1125   -2.7164 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6608    0.4191    0.5425 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9712    1.2588    1.7878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9716    0.3356   -0.1708 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7439    1.5901   -0.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8701    2.4200   -1.3438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6937    3.4826   -1.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0529    3.3023    0.2185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5210    2.2088    0.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8763   -0.5747    0.4655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3453   -1.7496    0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9605   -2.4833    1.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9806   -2.0413    0.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0991   -0.9442    0.9025 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6529   -1.1720    0.7547 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3820   -2.1416    1.7834 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3708   -1.4952    2.7162 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0026   -1.9944    4.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0243   -0.1734    2.5675 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729   -1.8082    2.3926 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9483   -1.4748    1.1020 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3849   -1.4068    0.7559 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.7736   -0.6798 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3539   -0.6864   -1.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2018   -1.9242   -1.1539 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5421   -1.4104   -2.2627 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776   -2.3084    0.0063 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2363   -3.5587    0.4257 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -4.6512    0.8833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9840   -5.8799    1.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0054   -4.5948    1.0255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0884   -1.8847   -0.4011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7783   -3.1417   -0.5600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2350   -3.6397   -1.7467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9460   -4.9596   -1.8398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0591   -2.9858   -2.7780 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0696    4.7500   -3.8900 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4219    3.6019   -4.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755    3.0623   -4.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0219    1.5730   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8568    4.9068    1.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4568    4.8115    2.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3665    5.7439    1.0551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3345    0.3350   -1.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2838    0.9892    2.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1555    0.1377    3.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5805    1.6268    2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6676    2.0746    1.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2290    1.8532    0.0052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2190    0.6297   -1.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0480    4.5398   -2.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3649    5.0669   -1.9049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9516    4.3448   -3.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1831    1.2624    2.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2443    2.2604    1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8079    0.6757    2.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7760   -0.0731   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4203    2.2929   -2.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9815    4.3051   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7100    1.8980    1.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1382   -1.9163   -0.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7441   -3.0357    0.6859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -1.0135    2.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8281   -1.8840    4.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9104   -1.4686    4.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2024   -3.0811    3.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0132   -0.7029    1.3091 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9542   -2.2838    0.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0960   -1.4957   -0.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8404    0.2673   -1.3387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2629   -1.0373   -2.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8982   -2.6765   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9461   -1.6761   -3.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6224   -6.7874    1.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5398   -5.8123    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1426   -5.9493    0.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1040   -1.4537   -1.3787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9815   -4.7218   -2.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4919   -5.5692   -2.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9911   -5.4704   -0.8801 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 41  1  0
 41 42  1  6
 41 40  1  0
 40 39  1  0
 39 38  1  1
 38 35  1  0
 35 36  1  1
 35 37  1  0
 37 13  1  0
 13 14  1  1
 14 15  1  0
 15 16  1  0
 16 17  1  0
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 17 19  2  0
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 20 21  1  1
 20 32  1  0
 32 31  1  0
 31 29  1  0
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 29 28  1  0
 28 22  1  0
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 32 33  1  0
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 51 52  1  0
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 45 46  1  1
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 45 43  1  0
 43 44  1  0
 13 11  1  0
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 43 41  1  0
 45 39  1  0
 11 39  1  0
 34 35  1  0
 33 13  1  0
 22 20  1  0
 24 23  1  0
  1 55  1  0
  1 56  1  0
  1 57  1  0
  5 58  1  1
  8 59  1  0
  8 60  1  0
  8 61  1  0
 10 62  1  6
 42 87  1  0
 42 88  1  0
 42 89  1  0
 40 85  1  0
 40 86  1  0
 36 82  1  0
 36 83  1  0
 36 84  1  0
 14 66  1  0
 14 67  1  0
 15 68  1  6
 18 69  1  0
 18 70  1  0
 18 71  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 32 81  1  1
 31 79  1  0
 31 80  1  0
 22 75  1  6
 27 78  1  0
 25 77  1  0
 24 76  1  0
 50 95  1  6
 53 96  1  0
 53 97  1  0
 53 98  1  0
 48 92  1  0
 48 93  1  0
 48 94  1  0
 43 90  1  6
 44 91  1  0
 12 63  1  0
 12 64  1  0
 12 65  1  0
M  END


  Mrv1652309122205132D          

 54 61  0  0  1  0            999 V2000
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   -0.4481    1.2758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4206   -0.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029    0.5853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2016    1.3076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7754    2.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0494    1.9981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1741    2.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291   -0.1211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0531   -0.2804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0586    0.5446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1118   -0.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6606    0.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5046    0.6653    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9119    1.3827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4942    2.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6692    2.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9015    2.8116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9235   -0.0600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3193    0.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7476   -0.0219    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1267    0.7109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566    1.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3436    2.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0763    1.6490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9423    0.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1927   -0.7166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8137   -1.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2588   -2.1440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9896   -1.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5445   -0.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6740   -0.8411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9075   -0.0298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0224    0.3122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1301    1.1301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9925   -0.7823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1220    0.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0035   -0.9106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1728   -1.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742   -0.9628    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1541   -1.0528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5109   -1.9162    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2004   -2.6805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495   -1.6694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4975   -2.4810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8686   -3.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0166   -3.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0439   -2.9910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2375   -1.6032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6776   -2.3010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2932   -3.0310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332   -3.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4688   -3.0631    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  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
 22 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 32 31  1  1  0  0  0
 20 32  1  0  0  0  0
 32 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 13 37  1  6  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 10 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 39 45  1  0  0  0  0
 45 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 45 50  1  0  0  0  0
 33 50  1  0  0  0  0
 50 51  1  6  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0323651

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](OC(C)=O)[C@H]1[C@@]2(C)C[C@]34O[C@@]5(C)O[C@@]6(C[C@H](OC(C)=O)[C@]7(C)[C@@H](CC(=O)O[C@H]7C7=COC=C7)[C@@]6(O5)[C@H](OC(C)=O)[C@@]3(OC(C)=O)[C@H]2O)[C@]14C

> <INCHI_IDENTIFIER>
InChI=1S/C37H44O17/c1-16(38)47-22-13-34-32(7)25(24(27(43)45-9)48-17(2)39)30(5)15-35(32)37(28(30)44,51-19(4)41)29(49-18(3)40)36(34,54-33(8,52-34)53-35)21-12-23(42)50-26(31(21,22)6)20-10-11-46-14-20/h10-11,14,21-22,24-26,28-29,44H,12-13,15H2,1-9H3/t21-,22+,24+,25+,26+,28+,29+,30-,31+,32+,33-,34+,35-,36-,37+/m1/s1

> <INCHI_KEY>
KVKWJIYJUPHQFZ-CPWJCNHSSA-N

> <FORMULA>
C37H44O17

> <MOLECULAR_WEIGHT>
760.742

> <EXACT_MASS>
760.257849957

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
73.28482189689677

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S)-2-(acetyloxy)-2-[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1^{14,17}.0^{1,10}.0^{2,7}.0^{10,15}.0^{14,19}]docosan-16-yl]acetate

> <JCHEM_LOGP>
0.639511575333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.400362646480865

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8620305789549496

> <JCHEM_POLAR_SURFACE_AREA>
218.85999999999996

> <JCHEM_REFRACTIVITY>
171.03070000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(S)-(methyl (acetyloxy)[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1^{14,17}.0^{1,10}.0^{2,7}.0^{10,15}.0^{14,19}]docosan-16-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      -2.376   2.352   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.836   2.381   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.041   1.063   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.785  -0.285   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.499   1.093   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.243   2.441   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.447   3.759   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.092   3.730   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.192   5.108   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.294  -0.226   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.832  -0.523   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.843   1.017   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.809  -0.169   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.833   1.219   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.409   1.242   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.169   2.581   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.389   3.909   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.849   3.898   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.149   5.248   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.191  -0.112   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.929   1.239   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.729  -0.041   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.436   1.327   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.746   2.703   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.841   3.786   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.209   3.078   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.959   1.559   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.560  -1.338   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      10.852  -2.705   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.683  -4.002   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.314  -2.777   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.483  -1.480   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.858  -1.570   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.294  -0.056   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.642   0.583   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.843   2.110   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.586  -1.460   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       3.961   0.402   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       3.740  -1.700   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.189  -2.797   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.819  -1.797   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.288  -1.965   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.820  -3.577   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       2.241  -5.004   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       4.386  -3.116   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       4.662  -4.631   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       3.488  -5.628   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       3.764  -7.143   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       1.949  -5.583   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       6.043  -2.993   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       6.865  -4.295   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       6.147  -5.658   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       6.969  -6.961   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       4.608  -5.718   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   41                                                  
CONECT   11   10   12   13   39                                             
CONECT   12   11                                                            
CONECT   13   11   14   33   37                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   22   32                                             
CONECT   21   20                                                            
CONECT   22   20   23   28                                                  
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23                                                       
CONECT   28   22   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   20   33                                                  
CONECT   33   32   13   34   50                                             
CONECT   34   33   35                                                       
CONECT   35   34   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35   13                                                       
CONECT   38   35   39                                                       
CONECT   39   38   11   40   45                                             
CONECT   40   39   41                                                       
CONECT   41   40   10   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   39   46   50                                             
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   45   33   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  122    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-2-(acetyloxy)-2-[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1,.0,.0,.0,.0,]docosan-16-yl]acetic acid	Generator

Chemical Formula

C₃₇H₄₄O₁₇

Average Mass

760.7420 Da

Monoisotopic Mass

760.25785 Da

IUPAC Name

methyl (2S)-2-(acetyloxy)-2-[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1^{14,17}.0^{1,10}.0^{2,7}.0^{10,15}.0^{14,19}]docosan-16-yl]acetate

Traditional Name

(S)-(methyl (acetyloxy)[(1R,2R,6R,7S,8S,10S,12R,14R,15S,16S,17R,18S,19S,20S)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1^{14,17}.0^{1,10}.0^{2,7}.0^{10,15}.0^{14,19}]docosan-16-yl]acetate)

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](OC(C)=O)[C@H]1[C@@]2(C)C[C@]34O[C@@]5(C)O[C@@]6(C[C@H](OC(C)=O)[C@]7(C)[C@@H](CC(=O)O[C@H]7C7=COC=C7)[C@@]6(O5)[C@H](OC(C)=O)[C@@]3(OC(C)=O)[C@H]2O)[C@]14C

InChI Identifier

InChI=1S/C37H44O17/c1-16(38)47-22-13-34-32(7)25(24(27(43)45-9)48-17(2)39)30(5)15-35(32)37(28(30)44,51-19(4)41)29(49-18(3)40)36(34,54-33(8,52-34)53-35)21-12-23(42)50-26(31(21,22)6)20-10-11-46-14-20/h10-11,14,21-22,24-26,28-29,44H,12-13,15H2,1-9H3/t21-,22+,24+,25+,26+,28+,29+,30-,31+,32+,33-,34+,35-,36-,37+/m1/s1

InChI Key

KVKWJIYJUPHQFZ-CPWJCNHSSA-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

Mexicanolide
Limonoid skeleton
Prostaglandin skeleton
Eicosanoid
Hexacarboxylic acid or derivatives
Naphthopyran
Naphthalene
1,3-dioxepane
Carboxylic acid orthoester
Ortho ester
Delta valerolactone
Delta_valerolactone
Dioxepane
Meta-dioxane
Pyran
Oxane
Fatty acyl
Meta-dioxolane
Cyclic alcohol
Heteroaromatic compound
Furan
Methyl ester
Carboxylic acid ester
Secondary alcohol
Lactone
Orthocarboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
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
logP	0.64	ChemAxon
pKa (Strongest Acidic)	13.4	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	218.86 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	171.03 m³·mol⁻¹	ChemAxon
Polarizability	73.28 Å³	ChemAxon
Number of Rings	8	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

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

163004703

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

MOL for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

3D MOL for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

3D SDF for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

3D-SDF for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

PDB for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

3D PDB for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

SMILES for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)

INCHI for NP0323651 (methyl (2s)-2-(acetyloxy)-2-[(1r,2r,6s,7s,8s,10s,12r,14r,15s,16s,17r,18s,19s,20s)-8,19,20-tris(acetyloxy)-6-(furan-3-yl)-18-hydroxy-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁴,¹⁷.0¹,¹⁰.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁹]docosan-16-yl]acetate)