NP-MRD: Showing NP-Card for (1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate (NP0240830)

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Record Information

Version

2.0

Created at

2022-09-07 00:44:40 UTC

Updated at

2022-09-07 00:44:40 UTC

NP-MRD ID

NP0240830

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate

Description

(1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]Hexadec-5-en-8-yl benzoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate is found in Taxus wallichiana. Based on a literature review very few articles have been published on (1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]Hexadec-5-en-8-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202442D          

 45 49  0  0  1  0            999 V2000
    6.3662   -1.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5882   -0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0111    0.0464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5764    0.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8797   -0.0745    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309072202442D          

 45 49  0  0  1  0            999 V2000
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    7.3873   -0.3382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0111    0.0464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2120   -0.1586    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5764    0.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8797   -0.0745    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8207    0.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7617    1.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2893    1.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6436    0.8074    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0847   -0.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9081   -0.9256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3500   -1.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5878   -1.5321    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9654   -2.2656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7631   -1.5542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4251   -2.3068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9079   -2.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7286   -2.8921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0527   -4.3973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7147   -5.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8939   -5.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4112   -4.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7491   -3.8119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2316   -0.9231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9754   -1.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3876   -1.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1667   -1.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3679   -2.1300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1471   -2.9249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2101   -1.5413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8017   -0.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119    0.2498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4260    0.8306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    0.4667    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2859    1.1056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5783    1.8771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0563    2.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3925    2.0096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1792    1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9946    1.0778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1271    0.2635    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3937   -0.1142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 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  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 37 42  1  0  0  0  0
 42 43  1  0  0  0  0
 44 43  1  6  0  0  0
  7 44  1  0  0  0  0
 45 44  1  1  0  0  0
 27 45  1  0  0  0  0
 37 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240830

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@]2([C@H]3OC[C@]4(OC(C)=O)[C@@H]3[C@@](C)([C@@H](C[C@H]4O)OC(C)=O)[C@@H](OC(=O)C3=CC=CC=C3)[C@H](O)C2=C1C)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C33H42O12/c1-16-21(42-17(2)34)14-32(30(5,6)40)24(16)25(38)27(44-29(39)20-11-9-8-10-12-20)31(7)23(43-18(3)35)13-22(37)33(45-19(4)36)15-41-28(32)26(31)33/h8-12,21-23,25-28,37-38,40H,13-15H2,1-7H3/t21-,22+,23+,25+,26-,27-,28-,31+,32-,33+/m0/s1

> <INCHI_KEY>
DLRXNNIHKMPBBR-JZIDVVRGSA-N

> <FORMULA>
C33H42O12

> <MOLECULAR_WEIGHT>
630.687

> <EXACT_MASS>
630.267626792

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
64.76292729618498

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0^{2,6}.0^{13,16}]hexadec-5-en-8-yl benzoate

> <JCHEM_LOGP>
0.4774680523333331

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.91970052723703

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.317259571297207

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9519346146390344

> <JCHEM_POLAR_SURFACE_AREA>
175.11999999999998

> <JCHEM_REFRACTIVITY>
155.54330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0^{2,6}.0^{13,16}]hexadec-5-en-8-yl benzoate

> <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      11.883  -2.497   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.298  -1.014   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.790  -0.631   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.221   0.087   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.729  -0.296   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.543   0.686   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.242  -0.139   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.132   1.397   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.022   2.933   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.140   2.575   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.668   1.507   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.625  -1.631   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.162  -1.728   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.987  -3.028   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.697  -2.860   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.402  -4.229   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.158  -2.901   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.527  -4.306   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.428  -5.555   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.960  -5.399   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.797  -6.960   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.698  -8.208   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.067  -9.613   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.535  -9.769   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.634  -8.520   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.265  -7.116   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.166  -1.723   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.687  -3.187   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.590  -2.107   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.178  -3.591   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.687  -3.976   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.275  -5.460   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.392  -2.877   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.497  -1.023   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.889   0.466   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.795   1.550   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.375   0.871   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.400   2.064   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.946   3.504   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.972   4.697   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.466   3.751   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.068   2.246   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.590   2.012   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       5.837   0.492   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.468  -0.213   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12   44                                             
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12    7   13   15                                                  
CONECT   13   12    5   14                                                  
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   27                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
CONECT   27   17   28   29   45                                             
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
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   45                                             
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   37   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43    7   45                                                  
CONECT   45   44   27   37                                                  
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-Tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0,.0,]hexadec-5-en-8-yl benzoic acid	Generator

Chemical Formula

C₃₃H₄₂O₁₂

Average Mass

630.6870 Da

Monoisotopic Mass

630.26763 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@]2([C@H]3OC[C@]4(OC(C)=O)[C@@H]3[C@@](C)([C@@H](C[C@H]4O)OC(C)=O)[C@@H](OC(=O)C3=CC=CC=C3)[C@H](O)C2=C1C)C(C)(C)O

InChI Identifier

InChI=1S/C33H42O12/c1-16-21(42-17(2)34)14-32(30(5,6)40)24(16)25(38)27(44-29(39)20-11-9-8-10-12-20)31(7)23(43-18(3)35)13-22(37)33(45-19(4)36)15-41-28(32)26(31)33/h8-12,21-23,25-28,37-38,40H,13-15H2,1-7H3/t21-,22+,23+,25+,26-,27-,28-,31+,32-,33+/m0/s1

InChI Key

DLRXNNIHKMPBBR-JZIDVVRGSA-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 wallichiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Monocyclic benzene moiety
Benzenoid
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Alcohol
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

8162070

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9986483

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,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate (NP0240830)

MOL for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

3D MOL for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

3D SDF for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

3D-SDF for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

PDB for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

3D PDB for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

SMILES for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

INCHI for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

Structure for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)

3D Structure for NP0240830 ((1s,2s,4s,7r,8r,9s,10r,12r,13r,16r)-4,10,13-tris(acetyloxy)-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.0²,⁶.0¹³,¹⁶]hexadec-5-en-8-yl benzoate)