NP-MRD: Showing NP-Card for (1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate (NP0303154)

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Record Information

Version

2.0

Created at

2022-09-10 17:15:39 UTC

Updated at

2022-09-10 17:15:40 UTC

NP-MRD ID

NP0303154

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate

Description

(1S,2S,3S,4R,7S,8Z,10R,12S,13S,14R,15S)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-10-yl (2R)-2-methylbutanoate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate is found in Junceella juncea. Based on a literature review very few articles have been published on (1S,2S,3S,4R,7S,8Z,10R,12S,13S,14R,15S)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-10-yl (2R)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102219152D          

 48 50  0  0  1  0            999 V2000
    2.0313    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    2.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    2.3842    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8892    2.7967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    3.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    4.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    4.0342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    1.5592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0481    0.8349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    2.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3181    1.1467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    1.1467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1747    0.7342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    0.1628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1747   -0.0908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    1.1467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3181    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    0.3217    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0313   -0.5033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -1.7408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603   -0.5033    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4603    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747   -1.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    1.1467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0107    1.6988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3248    2.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0877    3.1669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493    2.4192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6974    2.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    1.5592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9843    2.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    1.1467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2863    1.9314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342    2.5444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273    2.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9892    3.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    1.5592    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
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 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  2  0  0  0  0
 43 48  1  0  0  0  0
 48  2  1  1  0  0  0
 14 48  1  0  0  0  0
M  END

     RDKit          3D

 98100  0  0  0  0  0  0  0  0999 V2000
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    2.2807   -0.1611   -0.4168 C   0  0  1  0  0  0  0  0  0  0  0  0
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 31 30  1  0
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 28 29  1  0
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 26 25  1  0
 25 24  1  0
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 35 34  1  0
 34 32  2  0
 32 33  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
 32 24  1  0
 48 14  1  0
 35 41  1  0
 31 81  1  0
 31 82  1  0
 31 83  1  0
 30 79  1  0
 30 80  1  0
 28 75  1  1
 29 76  1  0
 29 77  1  0
 29 78  1  0
 24 74  1  6
 23 72  1  0
 23 73  1  0
 16 64  1  6
 20 65  1  0
 21 66  1  0
 21 67  1  0
 21 68  1  0
 22 69  1  0
 22 70  1  0
 22 71  1  0
 15 61  1  0
 15 62  1  0
 15 63  1  0
  9 57  1  1
 12 58  1  0
 12 59  1  0
 12 60  1  0
  4 53  1  1
  3 51  1  0
  3 52  1  0
  1 49  1  0
  1 50  1  0
 48 98  1  6
 43 94  1  6
 46 95  1  0
 46 96  1  0
 46 97  1  0
 42 93  1  0
 39 89  1  1
 40 90  1  0
 40 91  1  0
 40 92  1  0
 35 88  1  1
 34 87  1  0
 33 84  1  0
 33 85  1  0
 33 86  1  0
  7 54  1  0
  7 55  1  0
  7 56  1  0
M  END


  Mrv1652309102219152D          

 48 50  0  0  1  0            999 V2000
    2.0313    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    2.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    2.3842    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8892    2.7967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    3.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    4.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    4.0342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747    1.5592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0481    0.8349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037    2.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3181    1.1467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    1.1467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1747    0.7342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    0.1628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1747   -0.0908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    1.1467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3181    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6037   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    0.3217    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0313   -0.5033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -1.7408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603   -0.5033    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4603    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1747   -1.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168   -0.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168   -0.9158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    1.1467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0107    1.6988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3248    2.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0877    3.1669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493    2.4192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6974    2.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    1.5592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9843    2.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    1.1467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2863    1.9314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342    2.5444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273    2.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9892    3.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    1.5592    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  2  0  0  0  0
 43 48  1  0  0  0  0
 48  2  1  1  0  0  0
 14 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303154

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)O[C@@H]1C[C@H](OC(=O)C(C)C)[C@@]2(C)[C@@H](OC(C)=O)[C@H](CC(=C)[C@@H]2[C@H](OC(C)=O)[C@]2(O)[C@@H](C)C(=O)O[C@H]2\C=C1\C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H50O13/c1-12-17(4)32(40)46-24-15-26(47-31(39)16(2)3)34(11)28(19(6)13-25(43-21(8)36)29(34)44-22(9)37)30(45-23(10)38)35(42)20(7)33(41)48-27(35)14-18(24)5/h14,16-17,20,24-30,42H,6,12-13,15H2,1-5,7-11H3/b18-14-/t17-,20+,24-,25+,26+,27+,28-,29+,30+,34-,35+/m1/s1

> <INCHI_KEY>
BBSAIKIEESIWEO-PRLAGJRCSA-N

> <FORMULA>
C35H50O13

> <MOLECULAR_WEIGHT>
678.772

> <EXACT_MASS>
678.32514167

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
69.86290086166002

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,4R,7S,8Z,10R,12S,13S,14R,15S)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-10-yl (2R)-2-methylbutanoate

> <JCHEM_LOGP>
3.406663053999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.34986179571624

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9579704505537157

> <JCHEM_POLAR_SURFACE_AREA>
178.03

> <JCHEM_REFRACTIVITY>
167.24990000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,4R,7S,8Z,10R,12S,13S,14R,15S)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-8-en-10-yl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.792   5.221   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.125   4.451   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.459   5.221   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.793   4.451   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.127   5.221   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.127   6.761   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.460   7.531   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.793   7.531   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.793   2.911   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.423   1.558   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.460   2.911   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.460   4.451   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.794   2.141   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.459   2.141   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.793   1.371   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.877   0.304   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.793  -0.169   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.127   0.601   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.127   2.141   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.460  -0.169   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.794   0.601   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.460  -1.709   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.125  -0.169   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.792   0.601   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.792  -0.939   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.125  -1.709   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.125  -3.249   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.459  -0.939   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.459   0.601   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.793  -1.709   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.793  -3.249   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.458  -0.169   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.458  -1.709   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.124   0.601   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.124   2.141   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.020   3.171   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.606   4.578   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -0.164   5.912   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.332   4.516   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.168   5.561   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.458   2.911   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       3.704   3.816   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.792   2.141   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.268   3.605   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       3.237   4.750   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       1.731   4.429   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       3.713   6.214   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       5.125   2.911   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16   48                                             
CONECT   15   14                                                            
CONECT   16   14   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   16   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30                                                            
CONECT   32   24   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   41                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   35   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48   43    2   14                                                  
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,3S,4R,7S,8Z,10R,12S,13S,14R,15S)-2,14,15-Tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0,]heptadec-8-en-10-yl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₃₅H₅₀O₁₃

Average Mass

678.7720 Da

Monoisotopic Mass

678.32514 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@@H]1C[C@H](OC(=O)C(C)C)[C@@]2(C)[C@@H](OC(C)=O)[C@H](CC(=C)[C@@H]2[C@H](OC(C)=O)[C@]2(O)[C@@H](C)C(=O)O[C@H]2\C=C1\C)OC(C)=O

InChI Identifier

InChI=1S/C35H50O13/c1-12-17(4)32(40)46-24-15-26(47-31(39)16(2)3)34(11)28(19(6)13-25(43-21(8)36)29(34)44-22(9)37)30(45-23(10)38)35(42)20(7)33(41)48-27(35)14-18(24)5/h14,16-17,20,24-30,42H,6,12-13,15H2,1-5,7-11H3/b18-14-/t17-,20+,24-,25+,26+,27+,28-,29+,30+,34-,35+/m1/s1

InChI Key

BBSAIKIEESIWEO-PRLAGJRCSA-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
Junceella juncea	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

Briarane diterpenoid
Hexacarboxylic acid or derivatives
Diterpenoid
Diterpene lactone
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.41	ChemAxon
pKa (Strongest Acidic)	12.35	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	178.03 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	167.25 m³·mol⁻¹	ChemAxon
Polarizability	69.86 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

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

163103470

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate (NP0303154)

MOL for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

3D MOL for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

3D SDF for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

3D-SDF for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

PDB for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

3D PDB for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

SMILES for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

INCHI for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

Structure for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)

3D Structure for NP0303154 ((1s,2s,3s,4r,7s,8z,10r,12s,13s,14r,15s)-2,14,15-tris(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-12-[(2-methylpropanoyl)oxy]-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-10-yl (2r)-2-methylbutanoate)