NP-MRD: Showing NP-Card for (1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate (NP0271546)

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Record Information

Version

2.0

Created at

2022-09-08 17:52:57 UTC

Updated at

2022-09-08 17:52:57 UTC

NP-MRD ID

NP0271546

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate

Description

(1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate is found in Taxus sumatrana.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219522D          

 46 48  0  0  1  0            999 V2000
    6.1691    1.5950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4688    2.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7409    1.6429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7133    0.8183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5026    0.5782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9388    1.2785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0661   -0.0243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082219522D          

 46 48  0  0  1  0            999 V2000
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    5.9388    1.2785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0661   -0.0243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7940    0.3640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2528   -0.8279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0127   -1.6172    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7130   -2.0534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4409   -1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4685   -0.8405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1411   -2.1013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8690   -1.7129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5693   -2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2971   -1.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974   -2.1970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9698   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2419   -3.4098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5416   -2.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4101   -2.1807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7985   -2.9086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3623   -3.6089    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6066   -2.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8173   -2.1273    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3811   -2.8276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2538   -1.5248    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4292   -1.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0409   -0.7693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2163   -0.7416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7801   -1.4419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1685   -2.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0444   -1.4143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4771   -0.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    0.6589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3016   -0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9097    0.6316    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4773    1.3342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8696    2.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4372    2.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6942    2.0832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6900   -0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4309   -0.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4050   -1.2360    0.0000 C   0  0  0  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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  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  2  0  0  0  0
 17 22  1  0  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 38 44  1  0  0  0  0
 29 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0271546

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@@H]2[C@H](O)\C=C(CO)/[C@@H](C[C@H](O)\C(C)=C(OC(C)=O)/[C@@H](OC(C)=O)C(=C1C)C2(C)C)OC(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C35H44O11/c1-19-27(40)17-30(46-31(42)14-13-24-11-9-8-10-12-24)25(18-36)15-28(41)26-16-29(43-21(3)37)20(2)32(35(26,6)7)34(45-23(5)39)33(19)44-22(4)38/h8-15,26-30,34,36,40-41H,16-18H2,1-7H3/b14-13+,25-15-,33-19+/t26-,27+,28-,29-,30-,34+/m1/s1

> <INCHI_KEY>
QLIOXOVTRYEVGV-YDSKHBNCSA-N

> <FORMULA>
C35H44O11

> <MOLECULAR_WEIGHT>
640.726

> <EXACT_MASS>
640.288362237

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
66.45552160500304

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3E,5R,7S,8E,10S,13R)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
1.9597937996666674

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.639603799072994

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.101400532761286

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7663803184562603

> <JCHEM_POLAR_SURFACE_AREA>
165.89000000000001

> <JCHEM_REFRACTIVITY>
170.05300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3E,5R,7S,8E,10S,13R)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-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      11.516   2.977   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.208   3.792   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.260   5.331   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.850   3.067   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.798   1.528   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.271   1.079   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.086   2.387   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.323  -0.045   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.682   0.680   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.672  -1.545   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.224  -3.019   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.531  -3.833   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.890  -3.108   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.941  -1.569   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      15.197  -3.922   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.555  -3.197   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.863  -4.012   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.221  -3.287   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.528  -4.101   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.477  -5.640   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.118  -6.365   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.811  -5.551   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.099  -4.071   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.824  -5.429   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.010  -6.737   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.599  -4.419   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.126  -3.971   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.311  -5.278   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.074  -2.846   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.535  -2.795   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.810  -1.436   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.271  -1.384   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.456  -2.692   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.181  -4.050   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -0.083  -2.640   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.624  -0.129   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.899   1.230   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.163  -0.180   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.298   1.179   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       6.491   2.491   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.223   3.845   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.416   5.157   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       8.763   3.889   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       6.888  -1.539   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       8.271  -0.862   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.223  -2.307   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   39                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   11   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   44                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   44                                                  
CONECT   39   38    5   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   38   29   45   46                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₄₄O₁₁

Average Mass

640.7260 Da

Monoisotopic Mass

640.28836 Da

IUPAC Name

(1S,2R,3E,5R,7S,8E,10S,13R)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2E)-3-phenylprop-2-enoate

Traditional Name

(1S,2R,3E,5R,7S,8E,10S,13R)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2E)-3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@H]2[C@H](O)\C=C(CO)/[C@@H](C[C@H](O)\C(C)=C(OC(C)=O)/[C@@H](OC(C)=O)C(=C1C)C2(C)C)OC(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C35H44O11/c1-19-27(40)17-30(46-31(42)14-13-24-11-9-8-10-12-24)25(18-36)15-28(41)26-16-29(43-21(3)37)20(2)32(35(26,6)7)34(45-23(5)39)33(19)44-22(4)38/h8-15,26-30,34,36,40-41H,16-18H2,1-7H3/b14-13+,25-15-,33-19+/t26-,27+,28-,29-,30-,34+/m1/s1

InChI Key

QLIOXOVTRYEVGV-YDSKHBNCSA-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 sumatrana	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	1.96	ChemAxon
pKa (Strongest Acidic)	14.1	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	165.89 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	170.05 m³·mol⁻¹	ChemAxon
Polarizability	66.46 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate (NP0271546)

MOL for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0271546 ((1s,2r,3e,5r,7s,8e,10s,13r)-9,10,13-tris(acetyloxy)-2,7-dihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,8,11-trien-5-yl (2e)-3-phenylprop-2-enoate)