NP-MRD: Showing NP-Card for methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate (NP0159392)

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Record Information

Version

2.0

Created at

2022-09-02 17:08:32 UTC

Updated at

2022-09-02 17:08:32 UTC

NP-MRD ID

NP0159392

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate

Description

Lipidyl Pseudopterane E belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid. methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate is found in Antillogorgia acerosa. Based on a literature review very few articles have been published on Lipidyl Pseudopterane E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022219082D          

 44 46  0  0  1  0            999 V2000
    0.7722    3.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6929    2.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6105    2.4779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4692    2.6978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1283    2.1200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2482    1.2446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7560    2.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4202    2.1726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0844    2.6902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7733    2.2003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4503    2.7075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1681    2.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8634    2.7424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5927    2.3109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2953    2.7853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0320    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7457    2.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4993    2.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2306    2.8702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9870    2.4779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7179    2.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0113    2.0440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6968    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6128    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1399    0.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8087    0.8088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5614    0.4712    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2941   -0.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4734   -0.4288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2078   -1.2586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2302    0.9543    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0534    0.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7748    1.0831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3447   -0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1462    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4080    1.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8295    1.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0799    1.5293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8425    2.1318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566    0.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0862    0.3362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0058    2.9345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3393    2.1799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.8505    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22  2  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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  1  1  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
 29 30  2  0  0  0  0
 27 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
 31 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 37 42  2  0  0  0  0
 42 43  1  0  0  0  0
 35 43  1  0  0  0  0
 42 44  1  0  0  0  0
 22 44  1  0  0  0  0
M  END

     RDKit          3D

 96 98  0  0  0  0  0  0  0  0999 V2000
   -1.6462   -1.1418   -2.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4086   -0.3712   -2.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8298    1.0008   -1.8079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7806    1.0283   -0.3667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9503    0.1736    0.3089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2445   -0.6100   -0.3706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8130    0.1011    1.8008 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7253   -0.0199    1.9965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.2275    1.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8464    1.2679    1.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4315    0.1132    0.7378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9798    0.1189    0.7216 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4918    1.3312    0.0510 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9431    1.4818   -0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.5841   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.7242   -0.5144    1.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0493   -0.7733    0.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3402   -0.3506   -0.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8325   -0.7002   -0.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7176   -0.7191   -1.6000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9937   -2.1059   -1.9627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1168   -2.4709   -1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6929   -2.6177   -0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.6886   -2.8440    0.8919 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8298   -2.4504    2.0156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9179   -1.8145    1.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2998   -0.7974    1.2993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3206   -1.7686    0.2144 C   0  0  1  0  0  0  0  0  0  0  0  0
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  -10.5975   -1.3607    1.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.9992    0.8138   -0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9246    1.4141   -1.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7980    3.2778   -2.0590 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3245   -0.0207    1.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
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 34 88  1  0
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 33 86  1  0
 33 87  1  0
 41 92  1  0
 41 93  1  0
 41 94  1  0
M  END


  Mrv1652309022219082D          

 44 46  0  0  1  0            999 V2000
    0.7722    3.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6929    2.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6105    2.4779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4692    2.6978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1283    2.1200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2482    1.2446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7560    2.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4202    2.1726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0844    2.6902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7733    2.2003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4503    2.7075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1681    2.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8634    2.7424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5927    2.3109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2953    2.7853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0320    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7457    2.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4993    2.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2306    2.8702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9870    2.4779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7179    2.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0113    2.0440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6968    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6128    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1399    0.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8087    0.8088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5614    0.4712    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2941   -0.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4734   -0.4288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2078   -1.2586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2302    0.9543    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0534    0.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7748    1.0831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3447   -0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1462    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4080    1.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8295    1.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0799    1.5293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8425    2.1318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566    0.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0862    0.3362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0058    2.9345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3393    2.1799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.8505    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22  2  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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  1  1  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
 29 30  2  0  0  0  0
 27 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
 31 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 37 42  2  0  0  0  0
 42 43  1  0  0  0  0
 35 43  1  0  0  0  0
 42 44  1  0  0  0  0
 22 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0159392

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)OCC(=C)[C@H]1CC2=C(C=C(O2)[C@@H]([C@@H]2OC(=O)C(=C2)\C=C/1)C(C)=C)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C37H52O7/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-34(38)42-25-27(4)28-20-21-29-23-32(44-36(29)39)35(26(2)3)33-24-30(37(40)41-5)31(22-28)43-33/h20-21,23-24,28,32,35H,2,4,6-19,22,25H2,1,3,5H3/b21-20-/t28-,32-,35-/m1/s1

> <INCHI_KEY>
BGGBFMRIJOTUOF-OYFUMOLQSA-N

> <FORMULA>
C37H52O7

> <MOLECULAR_WEIGHT>
608.816

> <EXACT_MASS>
608.371304014

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
72.20463220443517

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2R,3R,7Z,9S)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate

> <ALOGPS_LOGP>
7.68

> <JCHEM_LOGP>
9.355603738

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.066700875561391

> <JCHEM_PKA_STRONGEST_BASIC>
-3.046373928935664

> <JCHEM_POLAR_SURFACE_AREA>
92.04

> <JCHEM_REFRACTIVITY>
174.94330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
21

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.00e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R,3R,7Z,9S)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.441   6.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.293   5.084   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.006   4.625   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.609   5.036   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.839   3.957   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.063   2.323   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.011   5.036   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.251   4.055   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.491   5.022   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.777   4.107   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.041   5.054   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.381   4.217   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.678   5.119   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.040   4.314   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.351   5.199   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.726   4.414   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.059   5.272   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.465   4.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.830   5.358   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.242   4.625   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      25.607   5.407   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.021   3.815   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.301   2.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.144   1.238   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.261   0.608   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.510   1.510   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.915   0.880   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.416  -0.644   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.884  -0.801   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.388  -2.349   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.163   1.781   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.700   1.186   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -7.046   2.022   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.243  -0.315   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.006   3.313   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.628   2.626   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.548   3.724   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.149   2.855   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       1.573   3.979   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       0.292   1.317   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.028   0.628   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.877   5.478   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -2.500   4.069   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.345   5.321   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22    2   23   44                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   25   30                                                  
CONECT   30   29                                                            
CONECT   31   27   32   35                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   31   36   43                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   42                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40                                                            
CONECT   42   37   43   44                                                  
CONECT   43   42   35                                                       
CONECT   44   42   22                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₂O₇

Average Mass

608.8160 Da

Monoisotopic Mass

608.37130 Da

IUPAC Name

methyl (2R,3R,7Z,9S)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate

Traditional Name

methyl (2R,3R,7Z,9S)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)OCC(=C)[C@H]1CC2=C(C=C(O2)[C@@H]([C@@H]2OC(=O)C(=C2)\C=C/1)C(C)=C)C(=O)OC

InChI Identifier

InChI=1S/C37H52O7/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-34(38)42-25-27(4)28-20-21-29-23-32(44-36(29)39)35(26(2)3)33-24-30(37(40)41-5)31(22-28)43-33/h20-21,23-24,28,32,35H,2,4,6-19,22,25H2,1,3,5H3/b21-20-/t28-,32-,35-/m1/s1

InChI Key

BGGBFMRIJOTUOF-OYFUMOLQSA-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
Antillogorgia acerosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furans

Sub Class

Furoic acid and derivatives

Direct Parent

Furoic acid esters

Alternative Parents

Substituents

Furoic acid ester
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Fatty acid ester
2-furanone
Dicarboxylic acid or derivatives
Fatty acyl
Dihydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Heteroaromatic compound
Lactone
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	7.68	ALOGPS
logP	9.36	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	13.07	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	92.04 Å²	ChemAxon
Rotatable Bond Count	21	ChemAxon
Refractivity	174.94 m³·mol⁻¹	ChemAxon
Polarizability	72.2 Å³	ChemAxon
Number of Rings	3	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

27023889

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102279561

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate (NP0159392)

MOL for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

3D MOL for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

3D SDF for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

3D-SDF for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

PDB for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

3D PDB for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

SMILES for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

INCHI for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

Structure for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)

3D Structure for NP0159392 (methyl (2r,3r,7z,9s)-9-[3-(hexadecanoyloxy)prop-1-en-2-yl]-5-oxo-2-(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate)