NP-MRD: Showing NP-Card for (+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene (NP0038169)

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Record Information

Version

2.0

Created at

2021-06-20 20:55:48 UTC

Updated at

2021-06-30 00:10:48 UTC

NP-MRD ID

NP0038169

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene

Provided By

JEOL Database JEOL Logo

Description

(+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene is found in Chandonanthus hirtellus. (+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene was first documented in 2009 (Wang, Y., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122553D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306202122553D          

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M  END
> <DATABASE_ID>
NP0038169

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O2/c1-11-6-8-14-15(17(14,4)5)10-12(2)16(9-7-11)19-13(3)18/h7,10,14-16H,6,8-9H2,1-5H3/b11-7-,12-10-/t14-,15+,16+/m1/s1

> <INCHI_KEY>
NHDCQMVLIJWKMN-OBKVTZAQSA-N

> <FORMULA>
C17H26O2

> <MOLECULAR_WEIGHT>
262.393

> <EXACT_MASS>
262.193280077

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.253896318454725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2Z,4S,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-dien-4-yl acetate

> <ALOGPS_LOGP>
5.01

> <JCHEM_LOGP>
3.671690064666667

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.014517490075339

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
79.1919

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.35e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2Z,4S,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-dien-4-yl acetate

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    2.7862   -0.6583   -4.3760 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3594   -0.9418   -2.9684 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -1.9246   -2.3283 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487    0.0538   -2.5230 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0435   -0.0906   -1.1744 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1274    0.3757   -0.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2431    1.8757   -0.0516 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9944    2.6197    1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892    4.1221    0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6138    2.0552    2.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    1.8215    2.5737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2832    0.3686    2.4492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8982   -0.2567    1.2117 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1159    0.5387   -0.0019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2915    0.6496   -1.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6807    1.5415   -2.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7422   -0.0689    2.4667 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8422    0.9648    2.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0752   -1.3171    3.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3584    0.2722   -4.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4228   -1.4730   -4.7329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9084   -0.5942   -5.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8364   -1.1559   -1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    0.0019   -0.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9276   -0.0834    0.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5221    2.3782   -0.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8653    4.4818    1.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1341    4.5739    1.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3371    4.4828   -0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9397    2.7740    3.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1901    1.1476    2.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1653    2.1307    3.5919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4660    2.4656    1.8961 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4034   -0.2525    3.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6058   -1.2825    0.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0543    1.0879   -0.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    2.2987   -2.3950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8152    0.9521   -3.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6199    2.0741   -2.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6084    1.8925    2.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7630    0.5605    2.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0465    1.2284    3.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2711   -2.0597    3.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9842   -1.7831    2.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2419   -1.0694    4.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
 13 12  1  0
 17 13  1  0
 12 17  1  0
  6  5  1  0
  6  7  1  0
  5 15  1  0
 17 18  1  6
  8 10  1  0
 12 34  1  1
 14 13  1  0
 13 35  1  6
 12 11  1  0
 17 19  1  0
 11 10  1  0
  5  4  1  0
 15 14  2  0
  4  2  1  0
  8  9  1  0
  2  1  1  0
  8  7  2  0
  2  3  2  0
  6 24  1  0
  6 25  1  0
  5 23  1  1
  7 26  1  0
 14 36  1  0
 11 32  1  0
 11 33  1  0
 10 30  1  0
 10 31  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       2.786  -0.658  -4.376  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.359  -0.942  -2.968  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.704  -1.925  -2.328  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.549   0.054  -2.523  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.044  -0.091  -1.174  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.127   0.376  -0.170  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.243   1.876  -0.052  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.994   2.620   1.044  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.089   4.122   0.983  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.614   2.055   2.398  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.104   1.821   2.574  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.283   0.369   2.449  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.898  -0.257   1.212  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.116   0.539  -0.002  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.292   0.650  -1.066  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.681   1.542  -2.218  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.742  -0.069   2.467  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.842   0.965   2.533  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.075  -1.317   3.254  0.00  0.00           C+0
HETATM   20  H   UNK     0       3.358   0.272  -4.409  0.00  0.00           H+0
HETATM   21  H   UNK     0       3.423  -1.473  -4.733  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.908  -0.594  -5.024  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.836  -1.156  -1.004  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.111   0.002  -0.479  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.928  -0.083   0.802  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.522   2.378  -0.977  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.865   4.482   1.667  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.134   4.574   1.271  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.337   4.483  -0.020  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.940   2.774   3.163  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.190   1.148   2.613  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.165   2.131   3.592  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.466   2.466   1.896  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.403  -0.253   3.020  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.606  -1.283   0.994  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.054   1.088  -0.045  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.090   2.299  -2.395  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.815   0.952  -3.131  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.620   2.074  -2.033  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.608   1.893   2.005  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.763   0.561   2.099  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.046   1.228   3.576  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.271  -2.060   3.208  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.984  -1.783   2.859  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.242  -1.069   4.307  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    6   15    4   23                                             
CONECT    6    5    7   24   25                                             
CONECT    7    6    8   26                                                  
CONECT    8   10    9    7                                                  
CONECT    9    8   27   28   29                                             
CONECT   10    8   11   30   31                                             
CONECT   11   12   10   32   33                                             
CONECT   12   13   17   34   11                                             
CONECT   13   12   17   14   35                                             
CONECT   14   13   15   36                                                  
CONECT   15   16    5   14                                                  
CONECT   16   15   37   38   39                                             
CONECT   17   13   12   18   19                                             
CONECT   18   17   40   41   42                                             
CONECT   19   17   43   44   45                                             
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    6                                                            
CONECT   26    7                                                            
CONECT   27    9                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   11                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   18                                                            
CONECT   41   18                                                            
CONECT   42   18                                                            
CONECT   43   19                                                            
CONECT   44   19                                                            
CONECT   45   19                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   92    0
END

RDKit          3D

45 46  0  0  0  0  0  0  0  0999 V2000
    2.7862   -0.6583   -4.3760 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3594   -0.9418   -2.9684 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -1.9246   -2.3283 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487    0.0538   -2.5230 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0435   -0.0906   -1.1744 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1274    0.3757   -0.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2431    1.8757   -0.0516 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9944    2.6197    1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892    4.1221    0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6138    2.0552    2.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    1.8215    2.5737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2832    0.3686    2.4492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8982   -0.2567    1.2117 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1159    0.5387   -0.0019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2915    0.6496   -1.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6807    1.5415   -2.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7422   -0.0689    2.4667 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8422    0.9648    2.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0752   -1.3171    3.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3584    0.2722   -4.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4228   -1.4730   -4.7329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9084   -0.5942   -5.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8364   -1.1559   -1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    0.0019   -0.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9276   -0.0834    0.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5221    2.3782   -0.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8653    4.4818    1.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1341    4.5739    1.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3371    4.4828   -0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9397    2.7740    3.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1901    1.1476    2.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1653    2.1307    3.5919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4660    2.4656    1.8961 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4034   -0.2525    3.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6058   -1.2825    0.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0543    1.0879   -0.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    2.2987   -2.3950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8152    0.9521   -3.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6199    2.0741   -2.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6084    1.8925    2.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7630    0.5605    2.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0465    1.2284    3.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2711   -2.0597    3.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9842   -1.7831    2.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2419   -1.0694    4.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
 13 12  1  0
 17 13  1  0
 12 17  1  0
  6  5  1  0
  6  7  1  0
  5 15  1  0
 17 18  1  6
  8 10  1  0
 12 34  1  1
 14 13  1  0
 13 35  1  6
 12 11  1  0
 17 19  1  0
 11 10  1  0
  5  4  1  0
 15 14  2  0
  4  2  1  0
  8  9  1  0
  2  1  1  0
  8  7  2  0
  2  3  2  0
  6 24  1  0
  6 25  1  0
  5 23  1  1
  7 26  1  0
 14 36  1  0
 11 32  1  0
 11 33  1  0
 10 30  1  0
 10 31  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆O₂

Average Mass

262.3930 Da

Monoisotopic Mass

262.19328 Da

IUPAC Name

(1S,2Z,4S,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-dien-4-yl acetate

Traditional Name

(1S,2Z,4S,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-dien-4-yl acetate

CAS Registry Number

Not Available

SMILES

[H]\C1=C(C([H])([H])[H])\C([H])([H])C([H])([H])[C@]2([H])[C@]([H])(\C([H])=C(C([H])([H])[H])/[C@@]([H])(OC(=O)C([H])([H])[H])C1([H])[H])C2(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C17H26O2/c1-11-6-8-14-15(17(14,4)5)10-12(2)16(9-7-11)19-13(3)18/h7,10,14-16H,6,8-9H2,1-5H3/b11-7-,12-10-/t14-,15+,16+/m1/s1

InChI Key

NHDCQMVLIJWKMN-OBKVTZAQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Plicanthus hirtellus	JEOL database	Wang, Y., et al, Tetrahedron 65, 4035 (2009)

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	5.01	ALOGPS
logP	3.67	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.19 m³·mol⁻¹	ChemAxon
Polarizability	31.25 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Wang, Y., et al. (2009). Wang, Y., et al, Tetrahedron 65, 4035 (2009). Tetrahedron.

Showing NP-Card for (+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene (NP0038169)

MOL for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

3D MOL for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

3D SDF for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

3D-SDF for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

PDB for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

3D PDB for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

SMILES for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

INCHI for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

Structure for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )

3D Structure for NP0038169 ((+)-3beta-acetoxybicyclogermacra-1(10)(E),4(E)-diene )