NP-MRD: Showing NP-Card for ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate (NP0204771)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 00:31:29 UTC

Updated at

2022-09-05 00:31:29 UTC

NP-MRD ID

NP0204771

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate

Description

Trijugin C belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate is found in Heynea trijuga. ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate was first documented in 2008 (PMID: 18280524). Based on a literature review very few articles have been published on Trijugin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202312D          

 37 42  0  0  1  0            999 V2000
    7.1973    1.5931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4041    1.8200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8109    1.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0178    1.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8178    2.2740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    0.9003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5398    0.0833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7985   -0.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6557   -1.0912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2251    0.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9165   -0.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4006    0.2853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8707   -0.3470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1056   -0.0383    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6790   -0.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4520   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0254   -2.0178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6516   -1.6246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0782   -1.0315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7222   -1.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0309   -1.9966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8539   -1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0539   -1.1390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3545   -0.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3052   -0.2383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5117   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1323    0.4611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3976    1.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1627    0.7847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2198    1.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9631    0.9847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3501    1.7133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9125    2.4127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1745    1.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0026    2.5494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9393    2.0520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6121    1.0431    0.0000 C   0  0  2  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  1  0  0  0  0
  4  5  2  0  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  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
 14 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37  6  1  6  0  0  0
 10 37  1  0  0  0  0
M  END

     RDKit          3D

 69 74  0  0  0  0  0  0  0  0999 V2000
    4.8472   -3.4102    1.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5355   -2.8943    0.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8025   -1.9012   -0.0498 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4228   -0.6965    0.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7537   -0.4298    1.6471 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542    0.2584   -0.3243 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4349   -0.3069   -1.6254 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2347    0.1512   -2.1580 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7207   -0.1485   -3.2516 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6724    1.0736   -1.1723 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2065    2.4612   -1.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1984    1.1491   -1.1058 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4859   -0.0153   -0.9208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5445    0.2017   -0.0734 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3675   -0.7085    1.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -2.0367    0.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650   -2.8718    1.6190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2160   -2.2719   -0.6389 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9432   -1.3227   -1.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2937   -1.8566   -1.6181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1168   -2.4381   -0.6850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2779   -2.7816   -1.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1497   -2.4228   -2.5762 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9886   -1.8661   -2.8091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8993   -0.0150   -0.7277 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9662    0.1263    0.3348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0065    1.1749   -1.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5030    2.2911   -0.7346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5983    1.6489    0.2821 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9812    1.8958    1.5942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1598    2.0836    0.0318 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6145    1.8660    1.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1174    2.1840    2.3165 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9983    1.2744    1.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9910    0.3683    2.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9579    2.3899    1.6141 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2468    0.5003    0.1150 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8070   -3.6854    1.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3301   -4.3648    2.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8713   -2.6426    2.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5893   -2.6064    0.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5936   -3.7768   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2426    1.1757   -0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    2.4877   -1.7173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6594    2.7946   -2.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9027    3.2019   -0.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1465    1.6836   -2.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3023   -0.9263    1.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8225   -0.3225    2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3843   -1.2116   -2.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8953   -2.6003    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1458   -3.2530   -0.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6780   -1.4947   -3.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7793   -0.4718    1.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9673   -0.0542   -0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972    1.1992    0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3951    1.0423   -2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0763    1.3563   -1.9233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3143    2.8816   -0.2853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9243    2.9810   -1.3890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4035    2.7882    1.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1688    3.1425   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7965    0.6216    3.2546 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260    0.4123    3.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0774   -0.6818    2.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6711    2.6112    0.8223 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5793    2.1907    2.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4182    3.3316    1.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7718   -0.5142    0.2157 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 14 13  1  6
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 24  2  0
 24 23  1  0
 23 22  1  0
 22 21  2  0
 19 25  1  0
 25 26  1  1
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  1
 29 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 34 37  1  0
 37  6  1  0
 37 10  1  0
 31 12  1  0
 25 14  1  0
 29 14  1  0
 21 20  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  2 41  1  0
  2 42  1  0
  6 43  1  6
 11 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  6
 15 48  1  0
 15 49  1  0
 19 50  1  6
 24 53  1  0
 22 52  1  0
 21 51  1  0
 26 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 30 61  1  0
 31 62  1  6
 35 63  1  0
 35 64  1  0
 35 65  1  0
 36 66  1  0
 36 67  1  0
 36 68  1  0
 37 69  1  1
M  END


  Mrv1652309052202312D          

 37 42  0  0  1  0            999 V2000
    7.1973    1.5931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4041    1.8200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8109    1.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0178    1.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8178    2.2740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    0.9003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5398    0.0833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7985   -0.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6557   -1.0912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2251    0.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9165   -0.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4006    0.2853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8707   -0.3470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1056   -0.0383    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6790   -0.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4520   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0254   -2.0178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6516   -1.6246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0782   -1.0315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7222   -1.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0309   -1.9966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8539   -1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0539   -1.1390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3545   -0.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3052   -0.2383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5117   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1323    0.4611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3976    1.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1627    0.7847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2198    1.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9631    0.9847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3501    1.7133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9125    2.4127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1745    1.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0026    2.5494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9393    2.0520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6121    1.0431    0.0000 C   0  0  2  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  1  0  0  0  0
  4  5  2  0  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  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
 14 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37  6  1  6  0  0  0
 10 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0204771

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)[C@H]1OC(=O)[C@@]2(C)[C@H]3O[C@]45CC(=O)O[C@@H](C6=COC=C6)[C@]4(C)CC[C@]5(O)[C@H]3C(=O)C(C)(C)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O10/c1-6-34-21(30)16-17-23(2,3)18(29)15-20(25(17,5)22(31)36-16)37-27-11-14(28)35-19(13-7-10-33-12-13)24(27,4)8-9-26(15,27)32/h7,10,12,15-17,19-20,32H,6,8-9,11H2,1-5H3/t15-,16-,17-,19-,20-,24-,25+,26-,27+/m0/s1

> <INCHI_KEY>
VHCAGQBZLHICLC-QWQLQPSYSA-N

> <FORMULA>
C27H32O10

> <MOLECULAR_WEIGHT>
516.543

> <EXACT_MASS>
516.19954723

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
51.42770920475317

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl (1R,3S,4R,7S,8S,11S,12S,15S,16R)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0^{1,15}.0^{3,11}.0^{4,8}]nonadecane-7-carboxylate

> <JCHEM_LOGP>
2.393866771999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.67829593479506

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.638219261768892

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8694509642854262

> <JCHEM_POLAR_SURFACE_AREA>
138.57000000000002

> <JCHEM_REFRACTIVITY>
122.8064

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
ethyl (1R,3S,4R,7S,8S,11S,12S,15S,16R)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0^{1,15}.0^{3,11}.0^{4,8}]nonadecane-7-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      13.435   2.974   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.954   3.397   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.847   2.327   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       9.367   2.751   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.993   4.245   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.259   1.680   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.474   0.156   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.091  -0.520   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.824  -2.037   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.020   0.587   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.444  -0.841   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.481   0.532   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.492  -0.648   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.064  -0.072   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.134  -1.179   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.710  -2.659   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.781  -3.767   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       1.216  -3.033   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.146  -1.925   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.348  -2.299   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.924  -3.727   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.461  -3.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.834  -2.126   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.528  -1.309   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.570  -0.445   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.955  -0.660   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.247   0.861   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.742   2.041   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.170   1.465   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.277   3.001   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.664   1.838   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.387   3.198   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.570   4.504   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.926   3.253   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.605   4.759   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.353   3.830   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.743   1.947   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12   37                                             
CONECT   11   10                                                            
CONECT   12   10   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   25   29                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   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   14   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   14   30   31                                             
CONECT   30   29                                                            
CONECT   31   29   12   32                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34    6   10                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₂O₁₀

Average Mass

516.5430 Da

Monoisotopic Mass

516.19955 Da

IUPAC Name

ethyl (1R,3S,4R,7S,8S,11S,12S,15S,16R)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0^{1,15}.0^{3,11}.0^{4,8}]nonadecane-7-carboxylate

Traditional Name

ethyl (1R,3S,4R,7S,8S,11S,12S,15S,16R)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0^{1,15}.0^{3,11}.0^{4,8}]nonadecane-7-carboxylate

CAS Registry Number

Not Available

SMILES

CCOC(=O)[C@H]1OC(=O)[C@@]2(C)[C@H]3O[C@]45CC(=O)O[C@@H](C6=COC=C6)[C@]4(C)CC[C@]5(O)[C@H]3C(=O)C(C)(C)[C@H]12

InChI Identifier

InChI=1S/C27H32O10/c1-6-34-21(30)16-17-23(2,3)18(29)15-20(25(17,5)22(31)36-16)37-27-11-14(28)35-19(13-7-10-33-12-13)24(27,4)8-9-26(15,27)32/h7,10,12,15-17,19-20,32H,6,8-9,11H2,1-5H3/t15-,16-,17-,19-,20-,24-,25+,26-,27+/m0/s1

InChI Key

VHCAGQBZLHICLC-QWQLQPSYSA-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
Heynea trijuga	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Delta_valerolactone
Delta valerolactone
Oxane
Gamma butyrolactone
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Furan
Cyclic alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.39	ChemAxon
pKa (Strongest Acidic)	12.64	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	138.57 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	122.81 m³·mol⁻¹	ChemAxon
Polarizability	51.43 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101241141

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wang XN, Fan CQ, Yin S, Gan LS, Yue JM: Structural elucidation of limonoids and steroids from Trichilia connaroides. Phytochemistry. 2008 Apr;69(6):1319-27. doi: 10.1016/j.phytochem.2008.01.018. Epub 2008 Feb 15. [PubMed:18280524 ]
LOTUS database [Link]

Showing NP-Card for ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate (NP0204771)

MOL for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

3D MOL for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

3D SDF for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

3D-SDF for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

PDB for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

3D PDB for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

SMILES for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

INCHI for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

Structure for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)

3D Structure for NP0204771 (ethyl (1r,3s,4r,7s,8s,11s,12s,15s,16s)-16-(furan-3-yl)-12-hydroxy-4,9,9,15-tetramethyl-5,10,18-trioxo-2,6,17-trioxapentacyclo[10.7.0.0¹,¹⁵.0³,¹¹.0⁴,⁸]nonadecane-7-carboxylate)