NP-MRD: Showing NP-Card for 13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate (NP0195914)

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Record Information

Version

2.0

Created at

2022-09-04 13:52:35 UTC

Updated at

2022-09-04 13:52:35 UTC

NP-MRD ID

NP0195914

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate

Description

13-(Acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]Pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate belongs to the class of organic compounds known as phorbol esters. These are tigliane diterpenoids which are esters of phorbol. 13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate is found in Euphorbia tirucalli. 13-(Acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]Pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171508452D          

 40 43  0  0  0  0            999 V2000
    5.1609   -5.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3575   -5.7684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7936   -5.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9901   -5.3534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4263   -4.7511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6228   -4.9383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0589   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2554   -4.5233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3084   -3.9210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0688   -3.1316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7347   -2.9444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6326   -2.5294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3930   -1.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4105   -1.5527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9743   -2.1550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9742   -3.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
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 13 36  1  0  0  0  0
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 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
M  END

     RDKit          3D

 82 85  0  0  0  0  0  0  0  0999 V2000
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   -0.5011   -0.7165    2.8017 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004171508452D          

 40 43  0  0  0  0            999 V2000
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    0.2055    0.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9181    1.0710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8528    1.8934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1079    2.2480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6875    0.7730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9342   -0.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5105    0.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4725   -0.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -1.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555   -1.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4392   -1.5282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7271   -0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775    0.2656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172   -0.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -0.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8446    0.2233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2117   -0.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9569   -1.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5591   -1.7016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3719   -2.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6952   -2.9769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -3.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 18 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 13 36  1  0  0  0  0
 32 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195914

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC=CC=CC=CC(=O)OC1C(C)C2(O)C3C=C(C)C(=O)C3(O)CC(CO)=CC2C2C(C)(C)C12OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H42O8/c1-7-8-9-10-11-12-13-14-25(35)39-28-20(3)31(38)23(26-29(5,6)32(26,28)40-21(4)34)16-22(18-33)17-30(37)24(31)15-19(2)27(30)36/h9-16,20,23-24,26,28,33,37-38H,7-8,17-18H2,1-6H3

> <INCHI_KEY>
UUDRJPRIBMGADE-UHFFFAOYSA-N

> <FORMULA>
C32H42O8

> <MOLECULAR_WEIGHT>
554.68

> <EXACT_MASS>
554.287968312

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
61.78914808955179

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate

> <ALOGPS_LOGP>
4.05

> <JCHEM_LOGP>
3.4211980879999997

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.933210788161254

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.57036933080439

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7316135464905127

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
154.24080000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.06e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.634 -10.418   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.134 -10.768   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.081  -9.644   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.582  -9.993   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.529  -8.869   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.029  -9.218   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.977  -8.094   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.477  -8.443   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.576  -7.319   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.128  -5.846   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.371  -5.496   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.181  -4.721   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.734  -3.248   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.766  -2.898   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.819  -4.023   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.214  -1.425   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.179  -2.625   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.161  -0.301   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.384   1.223   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.714   1.999   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.592   3.534   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.201   4.196   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.150   1.443   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.610  -0.027   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.686   1.075   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.749  -1.303   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.696  -2.517   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.144  -1.991   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.420  -2.853   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.091  -0.452   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.305   0.496   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -1.339  -0.650   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.839  -1.000   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.443   0.417   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.129  -1.841   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.786  -2.124   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.910  -3.176   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -2.561  -4.676   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.298  -5.557   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -3.685  -5.729   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   36                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   26                                             
CONECT   17   16                                                            
CONECT   18   16   19   32                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25   26   30                                             
CONECT   25   24                                                            
CONECT   26   24   16   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   24   31                                                  
CONECT   31   30                                                            
CONECT   32   18   33   36                                                  
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   13   32   37                                             
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Value	Source
13-(Acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0,.0,]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoic acid	Generator
13-(Acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoic acid	Generator

Chemical Formula

C₃₂H₄₂O₈

Average Mass

554.6800 Da

Monoisotopic Mass

554.28797 Da

IUPAC Name

13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate

Traditional Name

13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate

CAS Registry Number

Not Available

SMILES

CCCC=CC=CC=CC(=O)OC1C(C)C2(O)C3C=C(C)C(=O)C3(O)CC(CO)=CC2C2C(C)(C)C12OC(C)=O

InChI Identifier

InChI=1S/C32H42O8/c1-7-8-9-10-11-12-13-14-25(35)39-28-20(3)31(38)23(26-29(5,6)32(26,28)40-21(4)34)16-22(18-33)17-30(37)24(31)15-19(2)27(30)36/h9-16,20,23-24,26,28,33,37-38H,7-8,17-18H2,1-6H3

InChI Key

UUDRJPRIBMGADE-UHFFFAOYSA-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 tirucalli	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phorbol esters. These are tigliane diterpenoids which are esters of phorbol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Phorbol esters

Alternative Parents

Substituents

Phorbol ester
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.05	ALOGPS
logP	3.42	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	12.57	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	154.24 m³·mol⁻¹	ChemAxon
Polarizability	61.79 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

5129522

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate (NP0195914)

MOL for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

3D MOL for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

3D SDF for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

3D-SDF for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

PDB for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

3D PDB for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

SMILES for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

INCHI for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

Structure for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)

3D Structure for NP0195914 (13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl deca-2,4,6-trienoate)