NP-MRD: Showing NP-Card for (2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate (NP0258610)

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Record Information

Version

2.0

Created at

2022-09-08 00:09:08 UTC

Updated at

2022-09-08 00:09:09 UTC

NP-MRD ID

NP0258610

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082202092D          

 51 55  0  0  1  0            999 V2000
    3.8518   -1.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6556   -0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 39 84  1  0
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 41 86  1  0
 41 87  1  0
 35 79  1  0
 29 75  1  1
 32 76  1  0
 32 77  1  0
 32 78  1  0
 24 71  1  6
 27 72  1  0
 27 73  1  0
 27 74  1  0
 22 68  1  0
 22 69  1  0
 23 70  1  0
M  END


  Mrv1652309082202092D          

 51 55  0  0  1  0            999 V2000
    3.8518   -1.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8028   -0.8132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -0.3590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2292   -0.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9179   -0.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6556   -0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8689    0.5494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5576    1.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5086    1.8272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7708    2.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7218    3.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4105    3.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1483    3.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1973    2.2814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4424    0.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7047    0.8339    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6557    1.6574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3444    2.1116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2954    2.9352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0821    1.7423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0160    0.3797    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0907    1.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790    2.0262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3986    0.9715    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7114    1.7349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2067    2.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3892    2.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195    3.1509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.9830    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2440    1.7499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4277    1.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0843    1.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1235    2.6367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8946    0.3507    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1227    0.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9720   -0.6057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6814   -1.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1733   -0.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2826    0.3435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3244    0.4808    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8533    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1457    0.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7691    0.7971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2450   -0.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6647   -1.0900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5217   -1.1309    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8634   -1.8819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3839   -2.5532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7255   -3.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5627   -2.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650   -0.4439    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
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  1  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  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 34 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 45 44  1  6  0  0  0
 36 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 46 51  1  0  0  0  0
 51  2  1  1  0  0  0
 21 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258610

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)C(=C)[C@H]2[C@H](OC(C)=O)[C@@H]3CC(=O)[C@@]4(C)OCC3(C)[C@@]4(O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@]12CO

> <INCHI_IDENTIFIER>
InChI=1S/C37H44O14/c1-19-26(51-29(44)14-13-24-11-9-8-10-12-24)16-28(47-20(2)39)36(17-38)30(19)31(48-21(3)40)25-15-27(43)35(7)37(45,34(25,6)18-46-35)33(50-23(5)42)32(36)49-22(4)41/h8-14,25-26,28,30-33,38,45H,1,15-18H2,2-7H3/b14-13+/t25-,26-,28-,30-,31+,32-,33-,34?,35-,36+,37+/m0/s1

> <INCHI_KEY>
MQEGHHBOQKLTGK-RSKDIHLYSA-N

> <FORMULA>
C37H44O14

> <MOLECULAR_WEIGHT>
712.745

> <EXACT_MASS>
712.273106097

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
71.23604740428249

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4R,5R,6S,8S,10R,11R,12R,15S)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0^{2,15}.0^{5,10}]heptadecan-8-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
1.1117905689999976

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.901804121857214

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.149187824155101

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8334940514367446

> <JCHEM_POLAR_SURFACE_AREA>
198.25999999999996

> <JCHEM_REFRACTIVITY>
174.37780000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4R,5R,6S,8S,10R,11R,12R,15S)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0^{2,15}.0^{5,10}]heptadecan-8-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       7.190  -3.055   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.098  -1.518   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.384  -0.670   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.761  -1.360   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.047  -0.512   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.424  -1.201   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.955   1.026   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.241   1.873   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.149   3.411   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.772   4.100   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.681   5.637   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.966   6.485   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.343   5.796   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.435   4.259   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.293   0.867   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.916   1.557   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.824   3.094   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.110   3.942   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.018   5.479   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.487   3.252   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.630   0.709   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.769   2.242   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.748   3.782   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.477   1.813   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.061   3.238   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.119   4.457   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.593   4.250   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.703   5.882   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.890   1.835   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.322   3.266   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.798   3.490   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.157   2.283   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.231   4.922   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.670   0.655   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.229   1.198   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       1.814  -1.131   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.272  -2.572   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.324  -0.966   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       0.528   0.641   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.472   0.897   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.460   2.079   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.005   0.479   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.169   1.488   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.191  -1.010   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.107  -2.035   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.707  -2.111   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       5.345  -3.513   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       4.450  -4.766   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.088  -6.168   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       2.917  -4.617   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       5.721  -0.829   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   51                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    3   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22   24   51                                             
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35   36   40                                             
CONECT   35   34                                                            
CONECT   36   34   37   38   45                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   34   41   42                                             
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   36   46                                                  
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
CONECT   51   46    2   21                                                  
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₄O₁₄

Average Mass

712.7450 Da

Monoisotopic Mass

712.27311 Da

IUPAC Name

(2R,3S,4R,5R,6S,8S,10R,11R,12R,15S)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0^{2,15}.0^{5,10}]heptadecan-8-yl (2E)-3-phenylprop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)C(=C)[C@H]2[C@H](OC(C)=O)[C@@H]3CC(=O)[C@@]4(C)OCC3(C)[C@@]4(O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@]12CO

InChI Identifier

InChI=1S/C37H44O14/c1-19-26(51-29(44)14-13-24-11-9-8-10-12-24)16-28(47-20(2)39)36(17-38)30(19)31(48-21(3)40)25-15-27(43)35(7)37(45,34(25,6)18-46-35)33(50-23(5)42)32(36)49-22(4)41/h8-14,25-26,28,30-33,38,45H,1,15-18H2,2-7H3/b14-13+/t25-,26-,28-,30-,31+,32-,33-,34?,35-,36+,37+/m0/s1

InChI Key

MQEGHHBOQKLTGK-RSKDIHLYSA-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
Taxus cuspidata	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	1.11	ChemAxon
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	198.26 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	174.38 m³·mol⁻¹	ChemAxon
Polarizability	71.24 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate (NP0258610)

MOL for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0258610 ((2r,3s,4r,5r,6s,8s,10r,11r,12r,15s)-3,4,6,11-tetrakis(acetyloxy)-2-hydroxy-5-(hydroxymethyl)-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0²,¹⁵.0⁵,¹⁰]heptadecan-8-yl (2e)-3-phenylprop-2-enoate)