NP-MRD: Showing NP-Card for (1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid (NP0203481)

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Record Information

Version

2.0

Created at

2022-09-04 22:56:56 UTC

Updated at

2022-09-04 22:56:56 UTC

NP-MRD ID

NP0203481

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

Description

Moriniafungin F belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid is found in Curvularia hawaiiensis. Based on a literature review very few articles have been published on Moriniafungin F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052200562D          

 50 55  0  0  1  0            999 V2000
   -3.8950   -6.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2305   -6.8541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0510   -6.9403    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3866   -7.6940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9016   -8.3614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2070   -7.7802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6920   -7.1128    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5125   -7.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8613   -7.9827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7500   -8.3262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.7645   -7.4538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5589   -7.1990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.0030   -6.5037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.7512   -5.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8015   -6.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8509   -7.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0829   -7.8362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.4024   -8.4200    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.9349   -9.2171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9899   -9.3855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9266   -9.2618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2961   -8.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1946   -9.0507    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.4839   -9.8199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2991   -9.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7749  -10.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6300  -10.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5917  -11.4076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4517   -8.9881    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.4377   -8.9523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0549   -8.2682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8004   -9.9078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3564   -6.3591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8413   -5.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5359   -6.2729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9484   -5.5584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3964   -4.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5679   -4.1384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6427   -5.2809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9283   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2138   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0704   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3586   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0730   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875   -4.8684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0730   -6.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7290   -6.1014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 18 22  1  0  0  0  0
 23 22  1  6  0  0  0
 10 23  1  0  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
 26 28  1  0  0  0  0
 25 29  1  0  0  0  0
 10 29  1  0  0  0  0
 18 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  7 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
  3 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 39 50  1  0  0  0  0
 35 50  1  0  0  0  0
M  END

     RDKit          3D

104109  0  0  0  0  0  0  0  0999 V2000
    2.7988    2.7133   -2.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5099    2.6415   -1.0355 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4897    1.7202   -0.8344 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3145    2.4476   -0.2418 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7900    2.5557   -1.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151    1.9707    0.9564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3534    0.6454    1.0552 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5138    0.1780    0.4311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3940   -0.3673    1.3495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6630   -0.9133    0.8012 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3593   -1.9883   -0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5388   -2.7412   -0.6120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4806   -3.5613   -1.8332 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6370   -3.0828   -2.9540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9600   -3.6720   -2.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7057   -2.7065   -1.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5924   -1.7049   -1.0323 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8639   -0.7630    0.0443 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0920   -0.0084   -0.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0611   -0.0997    0.5674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1816    0.7983   -1.3204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9488   -1.4770    1.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5756   -1.3905    1.9492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5647   -0.0358    2.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9991    0.7874    1.6297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7491    2.0264    1.9738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9002    3.2381    1.6978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0118    2.0921    3.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6571    0.1352    0.3268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2118    0.9335   -0.7505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972    2.1544   -0.6754 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9595    0.4238   -2.0349 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8537   -0.1493    0.7251 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4122   -1.2951    0.0241 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470    0.5551   -0.0114 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6073   -0.4429   -0.8042 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8608   -0.6072   -0.2411 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.6152   -0.2859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1317    0.6834    0.4041 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1787    0.6926    1.4498 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5207    0.3431    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0271    1.2641   -0.1734 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3732    0.8305   -0.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3702    0.8563    0.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7533    0.4456   -0.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7513   -0.9286   -0.5697 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3716   -2.0053    0.3505 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0944   -1.8358    1.5492 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3060   -3.3257   -0.1144 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8680    1.0100    0.9185 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6275    3.4728   -2.5110 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2631    1.7466   -2.7535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9223    2.9474   -3.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120    1.3210   -1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5787    3.5361   -0.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2083    1.5318   -1.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3425    2.8296   -2.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5427    3.3193   -1.0056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5577    0.4488    2.1627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5420    0.3648    2.1746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8324   -1.2139    1.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6256   -2.6708    0.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8162   -1.5158   -1.0189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9296   -3.3843    0.2035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0849   -4.5749   -1.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7069   -3.7122   -3.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1669   -3.2128   -3.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2999   -2.0537   -2.9352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2869   -4.6895   -1.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1101   -3.4586   -3.2925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4630   -2.1805   -1.9218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0895   -3.2003   -0.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3528   -1.2829   -1.9923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5487    0.4695   -2.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3751   -2.4808    1.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7033   -0.8771    1.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1824   -2.1896    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3017    0.2365    3.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7364    2.0718    1.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2510    3.8001    0.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1052    3.9700    2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8221    3.0674    1.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0468    2.3149    3.9979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6704    2.9625    3.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4574    1.1406    3.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1136    0.6803   -2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2813   -0.5607    1.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8792   -2.1024    0.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4227    1.3927   -0.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9234    0.1108    2.3575 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2627    1.7584    1.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2443    0.2473    1.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5423   -0.6890    0.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0253    2.3243    0.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2854    1.1905   -1.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7278    1.5359   -1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3324   -0.1621   -1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4870    1.8810    0.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1378    0.1940    1.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4176    0.4792    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1087    1.1385   -0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8068   -1.1542   -0.8903 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1372   -1.0143   -1.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4169   -3.7236   -0.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 49104  1  0
M  END


  Mrv1652309052200562D          

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   -8.4839   -9.8199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2991   -9.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7749  -10.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6300  -10.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.4377   -8.9523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0549   -8.2682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8004   -9.9078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9484   -5.5584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5679   -4.1384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6427   -5.2809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9283   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2138   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0704   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3586   -4.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0730   -5.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875   -4.8684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0730   -6.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7290   -6.1014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
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 10 23  1  0  0  0  0
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 18 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  2  0  0  0  0
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  7 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
  3 35  1  0  0  0  0
 35 36  1  1  0  0  0
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 37 38  2  0  0  0  0
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 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 39 50  1  0  0  0  0
 35 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0203481

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@@H](C)O[C@@H](OC[C@@]23C[C@@H]4[C@H](C)CC[C@H]4[C@]4(C[C@@H]2C=C(C(C)C)[C@@]34C(O)=O)C(O)=O)[C@@H](O)[C@]11O[C@@H](CCCCCCCC(O)=O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C37H54O13/c1-19(2)25-15-22-16-35(32(42)43)24-14-13-20(3)23(24)17-34(22,36(25,35)33(44)45)18-47-31-28(40)37(29(46-5)21(4)48-31)49-26(30(41)50-37)11-9-7-6-8-10-12-27(38)39/h15,19-24,26,28-29,31,40H,6-14,16-18H2,1-5H3,(H,38,39)(H,42,43)(H,44,45)/t20-,21-,22+,23-,24-,26+,28-,29-,31-,34+,35-,36-,37-/m1/s1

> <INCHI_KEY>
APMMEDCBRAXORN-LNXQFXEOSA-N

> <FORMULA>
C37H54O13

> <MOLECULAR_WEIGHT>
706.826

> <EXACT_MASS>
706.356441799

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
76.00941790363797

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,4R,5R,8R,9S,11R)-2-({[(2S,5R,6R,7R,9R,10R)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-5-methyl-13-(propan-2-yl)tetracyclo[7.4.0.0^{2,11}.0^{4,8}]tridec-12-ene-1,9-dicarboxylic acid

> <JCHEM_LOGP>
5.299273980999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.771002112568364

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.187023876402864

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7255062525337928

> <JCHEM_POLAR_SURFACE_AREA>
195.34999999999997

> <JCHEM_REFRACTIVITY>
174.54420000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4R,5R,8R,9S,11R)-2-({[(2S,5R,6R,7R,9R,10R)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0^{2,11}.0^{4,8}]tridec-12-ene-1,9-dicarboxylic acid

> <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      -7.271 -11.387   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -7.897 -12.794   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -9.429 -12.955   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.055 -14.362   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.150 -15.608   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0     -11.586 -14.523   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0     -12.492 -13.277   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0     -14.023 -13.438   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0     -14.674 -14.901   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -16.333 -15.542   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.360 -13.914   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -17.843 -13.438   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -18.672 -12.140   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -18.202 -10.614   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -20.163 -12.528   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -20.255 -14.065   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -18.821 -14.628   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -17.551 -15.717   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -18.545 -17.205   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -16.781 -17.520   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0     -20.396 -17.289   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -15.486 -15.489   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -15.297 -16.895   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -15.837 -18.330   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -17.358 -18.225   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -18.246 -19.726   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -19.843 -19.879   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -17.905 -21.294   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -17.643 -16.778   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -19.484 -16.711   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -20.636 -15.434   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0     -20.161 -18.495   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0     -11.865 -11.870   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0     -12.770 -10.624   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0     -10.334 -11.709   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -11.104 -10.376   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -10.073  -9.231   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -10.393  -7.725   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -8.666  -9.858   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -7.333  -9.088   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -5.999  -9.858   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -4.665  -9.088   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -3.332  -9.858   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.998  -9.088   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.664  -9.858   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.669  -9.088   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.003  -9.858   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       3.337  -9.088   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       2.003 -11.398   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -8.827 -11.389   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   35                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   33                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   23   29                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17   19   22   29                                             
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   18   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   25   10   18   30                                             
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33    7   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    3   36   50                                             
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   50                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   39   35                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₄O₁₃

Average Mass

706.8260 Da

Monoisotopic Mass

706.35644 Da

IUPAC Name

(1R,2S,4R,5R,8R,9S,11R)-2-({[(2S,5R,6R,7R,9R,10R)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-5-methyl-13-(propan-2-yl)tetracyclo[7.4.0.0^{2,11}.0^{4,8}]tridec-12-ene-1,9-dicarboxylic acid

Traditional Name

(1R,2S,4R,5R,8R,9S,11R)-2-({[(2S,5R,6R,7R,9R,10R)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0^{2,11}.0^{4,8}]tridec-12-ene-1,9-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@@H](C)O[C@@H](OC[C@@]23C[C@@H]4[C@H](C)CC[C@H]4[C@]4(C[C@@H]2C=C(C(C)C)[C@@]34C(O)=O)C(O)=O)[C@@H](O)[C@]11O[C@@H](CCCCCCCC(O)=O)C(=O)O1

InChI Identifier

InChI=1S/C37H54O13/c1-19(2)25-15-22-16-35(32(42)43)24-14-13-20(3)23(24)17-34(22,36(25,35)33(44)45)18-47-31-28(40)37(29(46-5)21(4)48-31)49-26(30(41)50-37)11-9-7-6-8-10-12-27(38)39/h15,19-24,26,28-29,31,40H,6-14,16-18H2,1-5H3,(H,38,39)(H,42,43)(H,44,45)/t20-,21-,22+,23-,24-,26+,28-,29-,31-,34+,35-,36-,37-/m1/s1

InChI Key

APMMEDCBRAXORN-LNXQFXEOSA-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
Curvularia hawaiiensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Tetracarboxylic acid or derivatives
O-glycosyl compound
Glycosyl compound
Ketal
Oxane
Monosaccharide
Meta-dioxolane
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.3	ChemAxon
pKa (Strongest Acidic)	4.19	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	195.35 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	174.54 m³·mol⁻¹	ChemAxon
Polarizability	76.01 Å³	ChemAxon
Number of Rings	6	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

81360767

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145721231

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid (NP0203481)

MOL for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

3D MOL for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

3D SDF for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

3D-SDF for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

PDB for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

3D PDB for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

SMILES for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

INCHI for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

Structure for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)

3D Structure for NP0203481 ((1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid)