NP-MRD: Showing NP-Card for methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate (NP0330626)

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Record Information

Version

2.0

Created at

2022-09-12 16:09:25 UTC

Updated at

2022-09-12 16:09:25 UTC

NP-MRD ID

NP0330626

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate

Description

Methyl 2-[(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]Heptadec-2-en-8-yl]acetate belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate is found in Ekebergia capensis. Based on a literature review very few articles have been published on methyl 2-[(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]Heptadec-2-en-8-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122218092D          

 33 37  0  0  1  0            999 V2000
   -1.0715   -3.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746   -3.6735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0609   -2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -2.2932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360   -2.6632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9496   -1.8663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3902   -1.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1152   -1.8412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3567   -0.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5714   -0.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0970    0.1135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2784    0.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242   -0.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2763   -1.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2385   -1.2735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3091   -0.5167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4649   -0.6040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8662   -1.5249    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5557   -1.9779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1410   -2.0692    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6162   -2.7468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4342   -2.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7818   -1.8668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3171   -2.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896   -1.6370    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1790   -2.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9925   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3747   -2.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7976   -3.3972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0586   -3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8001   -0.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3483    0.5323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 14  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 26 30  2  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 16 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END

     RDKit          3D

 65 69  0  0  0  0  0  0  0  0999 V2000
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   -5.3155   -0.5188   -1.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0472    0.9901   -0.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0361    0.0269   -0.9850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0801    0.7485   -0.1141 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3456    0.7526    1.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1148    2.0420    1.7073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2762   -0.3612    1.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1589    0.8010    2.2281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230    1.8646    2.1937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -0.0909    3.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7478   -0.6933    2.5452 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7702   -0.6197    1.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6987   -0.1722    0.3445 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5356    1.2196   -0.1653 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1284    1.4178   -0.2513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6457    0.3344   -0.5231 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7352    0.2446   -2.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3012   -1.0088    0.0335 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3799   -1.9949   -0.8088 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807   -1.9316   -1.2505 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6858   -1.0233   -0.3161 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5713   -1.9414    0.4202 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5887   -0.2933   -1.2684 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6866    0.4589   -0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    1.2294   -1.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1124    0.5998    0.6505 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1261    1.8273   -0.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4285    2.6104    2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2087    2.7207    0.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0103    1.8670    2.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5821   -1.0589    1.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1769   -0.0055    2.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7553   -1.0040    2.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6435   -0.3449    3.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2760   -0.6265   -2.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1066    1.2125   -2.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9170   -1.5932   -2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3335   -3.0321    0.2115 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6 18  1  0
 18 19  1  6
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 31 25  1  0
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 10  7  1  0
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 27 26  1  0
 15 23  1  0
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  8 40  1  0
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  8 42  1  0
  9 43  1  0
  9 44  1  0
  9 45  1  0
M  END


  Mrv1652309122218092D          

 33 37  0  0  1  0            999 V2000
   -1.0715   -3.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746   -3.6735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0609   -2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -2.2932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360   -2.6632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9496   -1.8663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3902   -1.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1152   -1.8412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0970    0.1135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2385   -1.2735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3091   -0.5167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4649   -0.6040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8662   -1.5249    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.1410   -2.0692    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6162   -2.7468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4342   -2.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7818   -1.8668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3171   -2.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896   -1.6370    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    5.9925   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3747   -2.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7976   -3.3972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0586   -3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8001   -0.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3483    0.5323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
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  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
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  6 18  1  0  0  0  0
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 18 20  1  0  0  0  0
 20 14  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 15 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
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 29 30  1  0  0  0  0
 26 30  2  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 16 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0330626

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@@H]1[C@@]2(C)O[C@@H]3C(=O)O[C@@H](C4=COC=C4)[C@]4(C)CC[C@H]2C(CCC(=O)C1(C)C)=C34

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O7/c1-24(2)17(12-19(28)30-5)26(4)16-8-10-25(3)20(15(16)6-7-18(24)27)21(33-26)23(29)32-22(25)14-9-11-31-13-14/h9,11,13,16-17,21-22H,6-8,10,12H2,1-5H3/t16-,17-,21-,22-,25+,26-/m0/s1

> <INCHI_KEY>
SAKHPJFLERYVSP-SLGBOPGLSA-N

> <FORMULA>
C26H32O7

> <MOLECULAR_WEIGHT>
456.535

> <EXACT_MASS>
456.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.600129191963596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0^{2,13}.0^{3,10}]heptadec-2-en-8-yl]acetate

> <JCHEM_LOGP>
3.3866931426666653

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8720881061851444

> <JCHEM_POLAR_SURFACE_AREA>
92.04000000000002

> <JCHEM_REFRACTIVITY>
118.08860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0^{2,13}.0^{3,10}]heptadec-2-en-8-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.000  -7.256   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.513  -6.857   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.114  -5.370   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.203  -4.281   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.374  -4.971   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.773  -3.484   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.728  -2.220   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.215  -3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.666  -1.566   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.067  -0.691   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.181   0.212   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.386   0.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.779  -0.545   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.249  -2.371   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.045  -2.377   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.177  -0.964   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.601  -1.127   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.484  -2.847   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.771  -3.692   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.996  -3.862   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.884  -5.127   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.411  -4.878   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.059  -3.485   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.059  -4.657   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.567  -3.056   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.668  -4.133   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.186  -3.876   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.900  -5.241   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.822  -6.341   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.443  -5.657   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.960  -1.555   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.776  -0.508   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.117   0.994   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17   32                                                  
CONECT   17   16   18                                                       
CONECT   18   17    6   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   14   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   15   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26   31                                                  
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   26                                                       
CONECT   31   25   32                                                       
CONECT   32   31   16   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0,.0,]heptadec-2-en-8-yl]acetic acid	Generator

Chemical Formula

C₂₆H₃₂O₇

Average Mass

456.5350 Da

Monoisotopic Mass

456.21480 Da

IUPAC Name

methyl 2-[(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0^{2,13}.0^{3,10}]heptadec-2-en-8-yl]acetate

Traditional Name

methyl [(1S,8S,9S,10S,13R,14R)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0^{2,13}.0^{3,10}]heptadec-2-en-8-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@@H]1[C@@]2(C)O[C@@H]3C(=O)O[C@@H](C4=COC=C4)[C@]4(C)CC[C@H]2C(CCC(=O)C1(C)C)=C34

InChI Identifier

InChI=1S/C26H32O7/c1-24(2)17(12-19(28)30-5)26(4)16-8-10-25(3)20(15(16)6-7-18(24)27)21(33-26)23(29)32-22(25)14-9-11-31-13-14/h9,11,13,16-17,21-22H,6-8,10,12H2,1-5H3/t16-,17-,21-,22-,25+,26-/m0/s1

InChI Key

SAKHPJFLERYVSP-SLGBOPGLSA-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
Ekebergia capensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta valerolactone
Delta_valerolactone
Dicarboxylic acid or derivatives
Oxane
Pyran
Furan
Heteroaromatic compound
Methyl ester
Carboxylic acid ester
Ketone
Cyclic ketone
Ether
Dialkyl ether
Oxacycle
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
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	3.39	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	92.04 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.09 m³·mol⁻¹	ChemAxon
Polarizability	47.6 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162883219

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate (NP0330626)

MOL for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

3D MOL for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

3D SDF for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

3D-SDF for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

PDB for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

3D PDB for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

SMILES for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

INCHI for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

Structure for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)

3D Structure for NP0330626 (methyl 2-[(1s,8s,9s,10s,13r,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-6,16-dioxo-15,17-dioxatetracyclo[7.7.1.0²,¹³.0³,¹⁰]heptadec-2-en-8-yl]acetate)