NP-MRD: Showing NP-Card for methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate (NP0201815)

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Record Information

Version

2.0

Created at

2022-09-04 20:55:18 UTC

Updated at

2022-09-04 20:55:18 UTC

NP-MRD ID

NP0201815

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate

Description

Lipidyl Pseudopterane F belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate is found in Antillogorgia acerosa. Based on a literature review very few articles have been published on Lipidyl Pseudopterane F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222552D          

 46 50  0  0  1  0            999 V2000
   -3.6490    3.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2971    2.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    2.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7674    2.0023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3648    1.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111    0.8587    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8966    1.2712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1822    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1822    0.0337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4677    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2468    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9612    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6757    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3902    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1047    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8191    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5336    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2481    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9625    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6770    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3915    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1059    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8204    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5349    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6974    0.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5043   -0.1333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0662   -0.8399    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1827   -1.2053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4883   -0.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7197   -1.0597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8867   -0.7537    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3716   -1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1921   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0361   -2.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2222    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8897   -0.4849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9759    0.3356    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8897    1.1561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6966    1.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2487    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9516    2.1122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7585    2.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6347    1.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0729    1.4211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5879    2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7373    0.6674    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  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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
 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 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  1  0  0  0  0
 37 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 38 43  1  0  0  0  0
 43 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
  4 45  1  0  0  0  0
 44 46  1  1  0  0  0
 35 46  1  1  0  0  0
M  END

     RDKit          2D

100104  0  0  0  0  0  0  0  0999 V2000
    2.3250    4.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3755    3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9064    1.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1049    3.6097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1192    4.7148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5699    5.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2909   25.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1257   26.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 34 94  1  0
 33 90  1  0
 33 91  1  0
 42 96  1  0
 42 97  1  0
 42 98  1  0
  3 49  1  0
  3 50  1  0
  3 51  1  0
  1 47  1  0
  1 48  1  0
M  END


  Mrv1652309042222552D          

 46 50  0  0  1  0            999 V2000
   -3.6490    3.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2971    2.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    2.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7674    2.0023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3648    1.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111    0.8587    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8966    1.2712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1822    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1822    0.0337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4677    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2468    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9612    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6757    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3902    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1047    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8191    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5336    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2481    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9625    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6770    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3915    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1059    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8204    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5349    1.2712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6974    0.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5043   -0.1333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0662   -0.8399    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1827   -1.2053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4883   -0.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7197   -1.0597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8867   -0.7537    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3716   -1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1921   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0361   -2.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2222    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8897   -0.4849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9759    0.3356    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8897    1.1561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6966    1.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2487    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9516    2.1122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7585    2.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6347    1.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0729    1.4211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5879    2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7373    0.6674    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  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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
 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 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  1  0  0  0  0
 37 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 38 43  1  0  0  0  0
 43 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
  4 45  1  0  0  0  0
 44 46  1  1  0  0  0
 35 46  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0201815

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@H]1C[C@H](C[C@@]23O[C@]2([C@H]2O[C@@]2(O3)[C@@H]([C@@H]2OC(=O)C1=C2)C(C)=C)C(=O)OC)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C37H54O9/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-30(38)42-28-21-26(24(2)3)23-35-36(45-35,34(40)41-6)33-37(44-33,46-35)31(25(4)5)29-22-27(28)32(39)43-29/h22,26,28-29,31,33H,2,4,7-21,23H2,1,3,5-6H3/t26-,28+,29-,31-,33-,35+,36-,37-/m1/s1

> <INCHI_KEY>
QVTVESXGEJHBTQ-JNWNXVASSA-N

> <FORMULA>
C37H54O9

> <MOLECULAR_WEIGHT>
642.83

> <EXACT_MASS>
642.376783319

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
67.76904521204543

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1R,2R,3R,7S,9R,11S,13S,14R)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

> <JCHEM_LOGP>
9.449432994666669

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.554049860286499

> <JCHEM_PKA_STRONGEST_BASIC>
-4.04275509260025

> <JCHEM_POLAR_SURFACE_AREA>
113.19

> <JCHEM_REFRACTIVITY>
171.189

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2R,3R,7S,9R,11S,13S,14R)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.811   6.396   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.155   5.003   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.620   4.875   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.033   3.738   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.281   2.229   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.874   1.603   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.540   2.373   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.207   1.603   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.207   0.063   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.873   2.373   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.461   1.603   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.794   2.373   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.128   1.603   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.462   2.373   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.795   1.603   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.129   2.373   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.463   1.603   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.796   2.373   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.130   1.603   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.464   2.373   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.797   1.603   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.131   2.373   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.465   1.603   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.798   2.373   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.035   0.071   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.541  -0.249   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -7.590  -1.568   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.941  -2.250   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.645  -1.418   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.210  -1.978   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -9.122  -1.407   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -10.027  -2.653   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -11.559  -2.492   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.401  -4.060   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -9.748   0.000   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -10.994  -0.905   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -11.155   0.626   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -10.994   2.158   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -12.500   2.478   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0     -13.531   1.334   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0     -12.976   3.943   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0     -14.483   4.263   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0     -10.518   3.623   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -9.469   2.653   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -8.564   3.899   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -8.843   1.246   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   45                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   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   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25    6   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   37   46                                             
CONECT   36   35   37                                                       
CONECT   37   36   35   38                                                  
CONECT   38   37   39   43   44                                             
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41                                                            
CONECT   43   38   44                                                       
CONECT   44   43   38   45   46                                             
CONECT   45   44    4                                                       
CONECT   46   44   35                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₄O₉

Average Mass

642.8300 Da

Monoisotopic Mass

642.37678 Da

IUPAC Name

methyl (1R,2R,3R,7S,9R,11S,13S,14R)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

Traditional Name

methyl (1R,2R,3R,7S,9R,11S,13S,14R)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1C[C@H](C[C@@]23O[C@]2([C@H]2O[C@@]2(O3)[C@@H]([C@@H]2OC(=O)C1=C2)C(C)=C)C(=O)OC)C(C)=C

InChI Identifier

InChI=1S/C37H54O9/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-30(38)42-28-21-26(24(2)3)23-35-36(45-35,34(40)41-6)33-37(44-33,46-35)31(25(4)5)29-22-27(28)32(39)43-29/h22,26,28-29,31,33H,2,4,7-21,23H2,1,3,5-6H3/t26-,28+,29-,31-,33-,35+,36-,37-/m1/s1

InChI Key

QVTVESXGEJHBTQ-JNWNXVASSA-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 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

Diterpene lactone
Pseudopterane diterpenoid
Diterpenoid
Ileabethane, pseudopterane or nor-sandresane diterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Meta-dioxane
2-furanone
Monosaccharide
Oxirane carboxylic acid
Oxirane carboxylic acid or derivatives
Fatty acyl
Oxolane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Lactone
Carboxylic acid ester
Carboxylic acid derivative
Organoheterocyclic compound
Oxirane
Oxacycle
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	9.45	ChemAxon
pKa (Strongest Acidic)	11.55	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	113.19 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	171.19 m³·mol⁻¹	ChemAxon
Polarizability	67.77 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102279562

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate (NP0201815)

MOL for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D MOL for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D SDF for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D-SDF for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

PDB for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D PDB for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

SMILES for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

INCHI for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

Structure for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D Structure for NP0201815 (methyl (1r,2r,3r,7s,9r,11s,13s,14r)-7-(hexadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)