NP-MRD: Showing NP-Card for (1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate (NP0240131)

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Record Information

Version

2.0

Created at

2022-09-06 23:52:07 UTC

Updated at

2022-09-06 23:52:07 UTC

NP-MRD ID

NP0240131

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate

Description

(1S,3S,4R,8R,9R,10S,13S,14R)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]Hexadecan-3-yl 2-methylprop-2-enoate belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. Based on a literature review very few articles have been published on (1S,3S,4R,8R,9R,10S,13S,14R)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]Hexadecan-3-yl 2-methylprop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201522D          

 32 36  0  0  1  0            999 V2000
    2.0790    3.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3237    3.0769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7636    2.4711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1283    2.8948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    3.5006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3730    2.1069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8129    1.5011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0083    1.6832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4483    1.0774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7050    0.7194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0898    1.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4325   -0.0593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7904   -0.8026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691   -1.0751    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6153   -1.8988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3518   -2.2706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3980   -3.0943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7078   -3.5462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9713   -3.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9251   -2.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3124   -0.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6861   -0.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2270    0.8049    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9399    1.2200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6929    0.2895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4976    0.1074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9007   -0.6124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7098   -0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3156   -1.0115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8068    0.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5266    0.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0576    0.7132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  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  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  6  0  0  0
 14 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 32 30  1  1  0  0  0
  7 32  1  0  0  0  0
 26 32  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
    5.6733   -0.3230   -0.6280 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4700   -0.7688    0.5958 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6069   -1.2861    1.3760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0985   -0.7400    1.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8672   -1.1547    2.2726 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0387   -0.2967    0.3702 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6745   -0.2580    0.8007 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2742    1.2003    0.8415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0652    1.5373    0.3138 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6141    2.7362    1.1195 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2492    3.7936    1.1604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8280    3.1403    0.5682 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8030    2.1482    0.6085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3913    0.8642   -0.0815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4159   -0.1889    0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8932   -0.4531    1.3752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8351   -1.4499    1.5387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3097   -2.1849    0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8337   -1.9229   -0.7930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8928   -0.9297   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.0501   -1.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2095    2.1785   -1.8625 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455    2.0710   -1.0739 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5124    3.4100   -0.9548 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0884    0.4640    0.5592 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6213   -0.9099    0.3728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2500   -1.6882   -0.6099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4180   -2.7839   -0.7781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6694   -3.8846   -1.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8959   -2.4610   -0.1319 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7472   -3.3513    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8135   -0.9801   -0.1130 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6881   -0.3461   -1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8976    0.0676   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0614   -0.4435    1.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3874   -1.7291    0.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2158   -2.0755    2.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786   -0.6901    1.8363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4251    1.5687    1.8944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0589    1.7646    0.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7530    2.3535    2.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0632    3.6466    1.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8844    1.8987    1.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7214    2.5870    0.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5366    0.1064    2.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2046   -1.6497    2.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0551   -2.9777    0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2159   -2.5136   -1.6080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5101   -0.7239   -1.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1327    1.2529   -2.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6790    0.1423   -1.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6923    3.1794   -1.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9787    2.0546   -2.9654 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136    1.5912   -1.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3100    3.5901   -1.4692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3103    0.5504    1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6514   -1.5301    1.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6793   -3.1019    0.7009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5903   -4.4372    0.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8996   -0.7133   -1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  9  8  1  1
  9 23  1  0
 23 24  1  0
 23 22  1  0
 22 21  1  0
 21 14  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  0
 14 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28 30  1  0
 30 31  2  3
 30 32  1  0
 14 15  1  6
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 32  7  1  0
 20 15  1  0
 10  9  1  0
 32 26  1  0
 25  9  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  1 33  1  0
  1 34  1  0
  7 38  1  1
  8 39  1  0
  8 40  1  0
 23 54  1  6
 24 55  1  0
 22 52  1  0
 22 53  1  0
 21 50  1  0
 21 51  1  0
 13 43  1  0
 13 44  1  0
 10 41  1  1
 11 42  1  0
 25 56  1  1
 26 57  1  1
 31 58  1  0
 31 59  1  0
 32 60  1  6
 16 45  1  0
 17 46  1  0
 18 47  1  0
 19 48  1  0
 20 49  1  0
M  END


  Mrv1652309072201522D          

 32 36  0  0  1  0            999 V2000
    2.0790    3.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3237    3.0769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7636    2.4711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1283    2.8948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    3.5006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3730    2.1069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8129    1.5011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0083    1.6832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4483    1.0774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7050    0.7194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0898    1.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4325   -0.0593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7904   -0.8026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691   -1.0751    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6153   -1.8988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3518   -2.2706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3980   -3.0943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7078   -3.5462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9713   -3.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9251   -2.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3124   -0.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6861   -0.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2270    0.8049    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9399    1.2200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6929    0.2895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4976    0.1074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9007   -0.6124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7098   -0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3156   -1.0115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8068    0.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5266    0.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0576    0.7132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  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  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  6  0  0  0
 14 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 32 30  1  1  0  0  0
  7 32  1  0  0  0  0
 26 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240131

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C(=O)O[C@H]1C[C@]23[C@H](O)CC[C@](CO[C@@H]2O)([C@H]3[C@H]2OC(=O)C(=C)[C@H]12)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O7/c1-13(2)21(27)31-16-11-25-17(26)9-10-24(12-30-23(25)29,15-7-5-4-6-8-15)20(25)19-18(16)14(3)22(28)32-19/h4-8,16-20,23,26,29H,1,3,9-12H2,2H3/t16-,17+,18+,19-,20+,23-,24+,25+/m0/s1

> <INCHI_KEY>
ZIRJPOSBPXPZIL-YTMYDONJSA-N

> <FORMULA>
C25H28O7

> <MOLECULAR_WEIGHT>
440.492

> <EXACT_MASS>
440.183503242

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.98559346096877

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3S,4R,8R,9R,10S,13S,14R)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0^{1,9}.0^{4,8}]hexadecan-3-yl 2-methylprop-2-enoate

> <JCHEM_LOGP>
2.7036926460000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.629702453204295

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.864264860277162

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0049942486266703

> <JCHEM_POLAR_SURFACE_AREA>
102.29000000000002

> <JCHEM_REFRACTIVITY>
113.22470000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4R,8R,9R,10S,13S,14R)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0^{1,9}.0^{4,8}]hexadecan-3-yl 2-methylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       3.881   7.214   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.337   5.744   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.292   4.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.840   5.404   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.885   6.534   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       6.296   3.933   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.251   2.802   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.749   3.142   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.703   2.011   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.316   1.343   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.168   2.369   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.807  -0.111   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.475  -1.498   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.929  -2.007   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.015  -3.544   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.390  -4.238   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.476  -5.776   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.188  -6.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.813  -5.925   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.727  -4.388   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.316  -1.339   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.014  -0.278   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.157   1.502   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.488   2.277   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.160   0.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.662   0.200   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.415  -1.143   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.925  -0.843   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.056  -1.888   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.106   0.687   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.450   1.439   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.707   1.331   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   23   25                                             
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21   25                                             
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   14   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    9   24                                                  
CONECT   24   23                                                            
CONECT   25   14    9   26                                                  
CONECT   26   25   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    7   26                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Value	Source
(1S,3S,4R,8R,9R,10S,13S,14R)-13,14-Dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0,.0,]hexadecan-3-yl 2-methylprop-2-enoic acid	Generator

Chemical Formula

C₂₅H₂₈O₇

Average Mass

440.4920 Da

Monoisotopic Mass

440.18350 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=C)C(=O)O[C@H]1C[C@]23[C@H](O)CC[C@](CO[C@@H]2O)([C@H]3[C@H]2OC(=O)C(=C)[C@H]12)C1=CC=CC=C1

InChI Identifier

InChI=1S/C25H28O7/c1-13(2)21(27)31-16-11-25-17(26)9-10-24(12-30-23(25)29,15-7-5-4-6-8-15)20(25)19-18(16)14(3)22(28)32-19/h4-8,16-20,23,26,29H,1,3,9-12H2,2H3/t16-,17+,18+,19-,20+,23-,24+,25+/m0/s1

InChI Key

ZIRJPOSBPXPZIL-YTMYDONJSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Gamma butyrolactone
Benzenoid
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Hemiacetal
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
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

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

162892660

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate (NP0240131)

MOL for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

3D MOL for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

3D SDF for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

3D-SDF for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

PDB for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

3D PDB for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

SMILES for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

INCHI for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

Structure for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)

3D Structure for NP0240131 ((1s,3s,4r,8r,9r,10s,13s,14r)-13,14-dihydroxy-5-methylidene-6-oxo-10-phenyl-7,12-dioxatetracyclo[8.3.3.0¹,⁹.0⁴,⁸]hexadecan-3-yl 2-methylprop-2-enoate)