NP-MRD: Showing NP-Card for methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate (NP0280758)

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Record Information

Version

2.0

Created at

2022-09-09 06:43:43 UTC

Updated at

2022-09-09 06:43:43 UTC

NP-MRD ID

NP0280758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate

Description

Methyl (1S,5R,10S,14R)-10-[(2S)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]Heptadeca-2(17),7,11-triene-11-carboxylate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate is found in Sinularia maxima. Based on a literature review very few articles have been published on methyl (1S,5R,10S,14R)-10-[(2S)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]Heptadeca-2(17),7,11-triene-11-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208432D          

 32 34  0  0  1  0            999 V2000
   -0.0227   -3.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1409   -2.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9071   -2.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5071   -1.8511    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3889   -1.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0369   -0.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0320    0.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484    0.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802    1.4905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3669    0.1333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1505    0.3915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5257    1.0857    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0151    1.7336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210    2.4999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1375    2.6181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8104    3.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1162    3.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2838    1.4112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1656    2.2276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    1.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7640    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4120    1.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0895    0.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9924   -0.7571    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1680   -0.7893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9439   -1.5833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6298   -2.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6620   -2.8661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2778   -1.5311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9213   -1.6464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2733   -2.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8031   -0.8299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  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  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 18  1  4  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 24 29  1  1  0  0  0
 30 26  1  6  0  0  0
 30 31  1  0  0  0  0
  4 31  1  0  0  0  0
 30 32  1  0  0  0  0
  6 32  1  0  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
   -3.5257   -2.2153   -1.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8790   -1.3990   -0.0366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2089   -0.7016   -0.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0441   -1.1249    1.1348 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.8322   -1.2524    0.1236 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4619   -1.5616   -0.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8738   -2.8329    0.5801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053   -3.1714    0.4775 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838   -3.7281    1.2367 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5039   -4.9466    1.7874 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4633   -0.7037   -0.6722 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8591    0.3087    0.1888 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1374    0.1835    0.6782 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0635    1.2603    0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2688    0.2540    2.1596 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4206   -0.7436    2.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848   -0.2903   -2.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2557   -1.0724   -2.6231 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099    0.8731   -2.7789 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3189    2.1467   -2.4883 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5307    3.0517   -2.4921 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0522    2.8240   -2.1754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0321    3.4819   -0.8499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4671    2.4908    0.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6096    2.0808   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2183    3.2385   -0.9875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3199    3.2769   -1.5892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2557    4.2659   -0.8434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490    0.7473   -0.1612 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6872    0.3598    1.2413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4105   -0.2911   -0.7076 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1687   -2.4028   -1.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5892   -2.7458   -1.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3561   -0.3160   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2624    0.1454    0.5924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0188   -1.4533    0.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -1.4313    2.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0098   -2.9280    0.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3202   -1.7792    2.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3915   -4.8592    2.4457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3667   -5.3917    2.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7037   -5.6421    0.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3988   -1.3566   -0.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5946   -0.7751    0.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1023    1.0666    0.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8032    2.2676    0.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380    1.1747   -0.9966 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9550    1.2783    2.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3371    0.1852    2.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4421   -0.5169    3.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3730   -0.6281    2.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8313   -1.7431    2.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0714    0.6829   -3.7428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3862    2.6315   -3.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2789    4.0158   -2.9904 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7210    3.3077   -1.4314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8405    2.1843   -2.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0588    3.6386   -2.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8322    4.0635   -0.5993 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2090    2.3778    1.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1702    0.6485   -0.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5236    0.9533    1.6009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7823    0.4161    1.8868 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 14  1  0
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  4  5  1  0
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  6 32  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  7 12  1  0
 25 24  1  0
 32 30  1  0
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 30 62  1  6
 31 63  1  0
 31 64  1  0
  4 38  1  1
  5 39  1  0
  5 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  1 33  1  0
  1 34  1  0
M  END


  Mrv1652309092208432D          

 32 34  0  0  1  0            999 V2000
   -0.0227   -3.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1409   -2.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9071   -2.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5071   -1.8511    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3889   -1.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0369   -0.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0320    0.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484    0.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802    1.4905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3669    0.1333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1505    0.3915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5257    1.0857    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0151    1.7336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210    2.4999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1375    2.6181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8104    3.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1162    3.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2838    1.4112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1656    2.2276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    1.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7640    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4120    1.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0895    0.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9924   -0.7571    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1680   -0.7893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9439   -1.5833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6298   -2.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6620   -2.8661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2778   -1.5311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9213   -1.6464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2733   -2.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8031   -0.8299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  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  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 18  1  4  0  0  0
 20 21  2  0  0  0  0
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 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
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 27 29  1  0  0  0  0
 24 29  1  1  0  0  0
 30 26  1  6  0  0  0
 30 31  1  0  0  0  0
  4 31  1  0  0  0  0
 30 32  1  0  0  0  0
  6 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)O[C@@H]1C(=O)C=C(C)C[C@H]2OC(=O)C(=C2)[C@@H]2C[C@H](CC(O2)=C1C(=O)OC)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O7/c1-7-15(5)30-23-19(26)9-14(4)8-17-12-18(24(27)31-17)20-10-16(13(2)3)11-21(32-20)22(23)25(28)29-6/h9,12,15-17,20,23H,2,7-8,10-11H2,1,3-6H3/t15-,16+,17+,20-,23+/m0/s1

> <INCHI_KEY>
MFAOJWKVAMAJML-LHXOAYRSSA-N

> <FORMULA>
C25H32O7

> <MOLECULAR_WEIGHT>
444.524

> <EXACT_MASS>
444.21480337

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
46.52051124485335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,5R,10S,14R)-10-[(2S)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1^{2,5}]heptadeca-2(17),7,11-triene-11-carboxylate

> <JCHEM_LOGP>
3.9470870503333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.898455468971338

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.036680282185308

> <JCHEM_PKA_STRONGEST_BASIC>
-4.141176367285608

> <JCHEM_POLAR_SURFACE_AREA>
88.13000000000001

> <JCHEM_REFRACTIVITY>
120.76289999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,5R,10S,14R)-10-[(2S)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1^{2,5}]heptadeca-2(17),7,11-triene-11-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.042  -5.933   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.263  -4.409   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.693  -3.838   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.947  -3.455   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.726  -1.931   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.935  -0.978   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.926   0.793   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.464   1.275   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.150   2.782   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -0.685   0.249   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.148   0.731   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.848   2.027   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.895   3.236   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.466   4.666   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.990   4.887   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.513   5.876   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.084   7.306   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.263   2.634   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.042   4.158   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.792   2.453   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.026   1.531   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.236   2.484   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.634   0.116   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.452  -1.413   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.914  -1.473   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.495  -2.955   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.776  -3.811   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.836  -5.350   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       7.985  -2.858   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.586  -3.073   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.377  -4.026   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.366  -1.549   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   31                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   12   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   30                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   24                                                       
CONECT   30   26   31   32                                                  
CONECT   31   30    4                                                       
CONECT   32   30    6                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,5R,10S,14R)-10-[(2S)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1,]heptadeca-2(17),7,11-triene-11-carboxylic acid	Generator

Chemical Formula

C₂₅H₃₂O₇

Average Mass

444.5240 Da

Monoisotopic Mass

444.21480 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@H](C)O[C@@H]1C(=O)C=C(C)C[C@H]2OC(=O)C(=C2)[C@@H]2C[C@H](CC(O2)=C1C(=O)OC)C(C)=C

InChI Identifier

InChI=1S/C25H32O7/c1-7-15(5)30-23-19(26)9-14(4)8-17-12-18(24(27)31-17)20-10-16(13(2)3)11-21(32-20)22(23)25(28)29-6/h9,12,15-17,20,23H,2,7-8,10-11H2,1,3-6H3/t15-,16+,17+,20-,23+/m0/s1

InChI Key

MFAOJWKVAMAJML-LHXOAYRSSA-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
Sinularia maxima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpenoid
Diterpene lactone
Macrolide
Oxane
Dicarboxylic acid or derivatives
2-furanone
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Cyclic ketone
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

162870368

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate (NP0280758)

MOL for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

3D MOL for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

3D SDF for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

3D-SDF for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

PDB for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

3D PDB for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

SMILES for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

INCHI for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

Structure for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)

3D Structure for NP0280758 (methyl (1s,5r,10s,14r)-10-[(2s)-butan-2-yloxy]-7-methyl-3,9-dioxo-14-(prop-1-en-2-yl)-4,16-dioxatricyclo[10.3.1.1²,⁵]heptadeca-2(17),7,11-triene-11-carboxylate)