NP-MRD: Showing NP-Card for (1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate (NP0283751)

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Record Information

Version

2.0

Created at

2022-09-09 11:08:59 UTC

Updated at

2022-09-09 11:09:00 UTC

NP-MRD ID

NP0283751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate

Description

(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-5,7,9,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]Hexadecan-2-yl acetate belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. (1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate is found in Euphorbia esula. Based on a literature review very few articles have been published on (1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-5,7,9,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]Hexadecan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092213092D          

 47 49  0  0  1  0            999 V2000
    3.3429    2.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9495    2.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    3.0972    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1154    3.8547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2960    3.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8033    3.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9692    4.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2616    3.0014    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7397    3.6737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    4.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5753    4.5019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8748    5.0962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6548    2.1887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2322    2.7779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0312    2.5725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4474    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6087    3.1617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4045    1.8444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2094    1.6635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1920    2.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3087    1.0250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4998    0.8629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9298    0.1628    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7176   -0.6344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8090   -0.2128    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8729   -1.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5085    0.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2735   -0.0843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1103    0.2586    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3561   -0.5289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7970   -1.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9921   -0.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0428   -1.9231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4909   -0.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812    0.1345    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0237   -0.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0635    2.0163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7836    1.0161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2762    1.6779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4568    1.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    2.5312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106    2.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6227    3.1929    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
  3  4  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
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 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
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 35 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
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 42 37  1  6  0  0  0
 29 42  1  0  0  0  0
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  2 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
M  END

     RDKit          3D

 91 93  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309092213092D          

 47 49  0  0  1  0            999 V2000
    3.3429    2.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9495    2.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    3.0972    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1154    3.8547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2960    3.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8033    3.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9692    4.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2616    3.0014    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7397    3.6737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    4.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5753    4.5019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8748    5.0962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6548    2.1887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2322    2.7779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0312    2.5725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4474    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6087    3.1617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4045    1.8444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2094    1.6635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1920    2.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3087    1.0250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4998    0.8629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9298    0.1628    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7176   -0.6344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8090   -0.2128    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8729   -1.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5085    0.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2735   -0.0843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1103    0.2586    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3561   -0.5289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7970   -1.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9921   -0.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0428   -1.9231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4909   -0.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812    0.1345    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0237   -0.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9622    0.9395    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    1.5589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6084    1.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3443    0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0635    2.0163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7836    1.0161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2762    1.6779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4568    1.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    2.5312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106    2.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6227    3.1929    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
  3  4  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 42 37  1  6  0  0  0
 29 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 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
M  END
> <DATABASE_ID>
NP0283751

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O15/c1-13-12-31(46-21(9)38)22(24(13)41-16(4)33)25(42-17(5)34)14(2)26(43-18(6)35)27(44-19(7)36)29(45-20(8)37)30(10,11)28-23(39)15(3)32(31,40)47-28/h13,15,22,24-29,40H,2,12H2,1,3-11H3/t13-,15-,22+,24-,25-,26+,27+,28-,29+,31+,32+/m0/s1

> <INCHI_KEY>
YBKKAGOLXZOIRX-ICPRFOGGSA-N

> <FORMULA>
C32H44O15

> <MOLECULAR_WEIGHT>
668.689

> <EXACT_MASS>
668.268020717

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
65.0240665292934

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0^{2,6}]hexadecan-9-yl acetate

> <JCHEM_LOGP>
1.3526451689999992

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.655809681535874

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.583550800044282

> <JCHEM_PKA_STRONGEST_BASIC>
-4.432571727697257

> <JCHEM_POLAR_SURFACE_AREA>
204.32999999999996

> <JCHEM_REFRACTIVITY>
153.97220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0^{2,6}]hexadecan-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.240   5.590   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.372   4.546   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.292   5.781   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.682   7.195   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.152   7.374   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.233   6.139   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.542   8.788   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.822   5.603   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.714   6.858   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.074   8.258   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.541   8.404   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.966   9.513   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.556   4.086   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.634   5.185   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.125   4.802   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.902   3.643   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      14.203   5.902   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      11.955   3.443   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.458   3.105   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.425   3.902   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.776   1.913   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.266   1.611   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.202   0.304   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.806  -1.184   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.843  -0.397   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.963  -1.933   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.149   0.419   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.577  -0.157   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.673   0.483   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.131  -0.987   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.088  -2.120   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.585  -1.782   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.547  -3.590   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.516  -0.534   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.192   0.251   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.778  -0.359   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.529   1.754   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.512   2.910   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       3.002   2.607   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.509   1.148   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.985   3.764   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.063   1.897   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.982   3.132   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       6.453   3.311   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.843   4.725   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.313   4.904   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       6.762   5.960   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    3    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25   29                                             
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   21   28                                                  
CONECT   28   27                                                            
CONECT   29   23   30   34   42                                             
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   37   29   43                                                  
CONECT   43   42    2   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   98    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-5,7,9,10,11-Pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0,]hexadecan-2-yl acetic acid	Generator

Chemical Formula

C₃₂H₄₄O₁₅

Average Mass

668.6890 Da

Monoisotopic Mass

668.26802 Da

IUPAC Name

(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0^{2,6}]hexadecan-9-yl acetate

Traditional Name

(1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15S)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0^{2,6}]hexadecan-9-yl acetate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C32H44O15/c1-13-12-31(46-21(9)38)22(24(13)41-16(4)33)25(42-17(5)34)14(2)26(43-18(6)35)27(44-19(7)36)29(45-20(8)37)30(10,11)28-23(39)15(3)32(31,40)47-28/h13,15,22,24-29,40H,2,12H2,1,3-11H3/t13-,15-,22+,24-,25-,26+,27+,28-,29+,31+,32+/m0/s1

InChI Key

YBKKAGOLXZOIRX-ICPRFOGGSA-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
Euphorbia esula	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
3-furanone
Cyclitol or derivatives
Tetrahydrofuran
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	1.35	ChemAxon
pKa (Strongest Acidic)	10.58	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	204.33 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	153.97 m³·mol⁻¹	ChemAxon
Polarizability	65.02 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

163087274

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate (NP0283751)

MOL for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

3D MOL for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

3D SDF for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

3D-SDF for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

PDB for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

3D PDB for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

SMILES for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

INCHI for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

Structure for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)

3D Structure for NP0283751 ((1r,2r,4s,5s,6r,7r,9r,10s,11s,13r,15s)-2,5,7,10,11-pentakis(acetyloxy)-1-hydroxy-4,12,12,15-tetramethyl-8-methylidene-14-oxo-16-oxatricyclo[11.2.1.0²,⁶]hexadecan-9-yl acetate)