NP-MRD: Showing NP-Card for (1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate (NP0144136)

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Record Information

Version

2.0

Created at

2022-09-01 23:01:44 UTC

Updated at

2022-09-01 23:01:45 UTC

NP-MRD ID

NP0144136

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate

Description

CHEMBL3609768 belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). (1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate is found in Celastrus flagellaris. Based on a literature review very few articles have been published on CHEMBL3609768.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201012D          

 46 50  0  0  1  0            999 V2000
    5.6683   -2.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5838   -0.9369    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


  Mrv1652309022201012D          

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    4.0331   -0.2371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7887    0.2693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5407    0.7508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3286    1.5865    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4188    0.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8901    1.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7131    1.2480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1739    1.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9969    1.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3592    1.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8984    0.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0753    0.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7597    1.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484    0.6415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0299   -0.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4374   -2.6677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0167   -3.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1832   -3.9434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5312   -4.3699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0951   -5.1060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4996   -5.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3246   -5.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7290   -6.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3085   -7.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4836   -7.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0791   -6.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3740   -1.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9236   -1.3292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3370   -2.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411   -2.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3824   -1.9151    0.0000 O   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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 28 40  1  0  0  0  0
  5 40  1  0  0  0  0
 21 40  1  0  0  0  0
 40 41  1  6  0  0  0
 26 42  1  0  0  0  0
 21 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0144136

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)[C@@H](OC(C)=O)[C@@]2(C)[C@H](C[C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)OC(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H42O9/c1-23-21-29(44-31(40)19-17-26-13-9-7-10-14-26)34(43-25(3)39)36(6)30(45-32(41)20-18-27-15-11-8-12-16-27)22-28-33(42-24(2)38)37(23,36)46-35(28,4)5/h7-20,23,28-30,33-34H,21-22H2,1-6H3/b19-17+,20-18+/t23-,28-,29+,30+,33-,34-,36-,37-/m1/s1

> <INCHI_KEY>
JUCKRBRETJEQNN-IQBZRUAFSA-N

> <FORMULA>
C37H42O9

> <MOLECULAR_WEIGHT>
630.734

> <EXACT_MASS>
630.282882932

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
68.3335917360723

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4S,5S,6R,7S,9R,12R)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2E)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl (2E)-3-phenylprop-2-enoate

> <ALOGPS_LOGP>
5.82

> <JCHEM_LOGP>
6.339890902000002

> <ALOGPS_LOGS>
-6.39

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.230453882922728

> <JCHEM_POLAR_SURFACE_AREA>
114.43

> <JCHEM_REFRACTIVITY>
169.61859999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.57e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,5S,6R,7S,9R,12R)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2E)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      10.581  -4.783   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.953  -3.309   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.565  -3.203   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.296  -2.680   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.939   0.503   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.343   1.402   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.947   2.961   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.982   1.129   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.861   2.436   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.398   2.330   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.258   3.607   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.794   3.501   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.470   2.117   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.610   0.840   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.074   0.946   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.151   2.629   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.464   1.198   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.056  -0.280   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.550  -4.980   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.765  -6.720   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.209  -7.361   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.725  -8.157   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.911  -9.531   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.666 -10.873   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.206 -10.891   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.961 -12.233   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.176 -13.558   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.636 -13.541   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.881 -12.198   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.298  -2.856   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       3.591  -2.481   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       2.496  -3.926   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.250  -5.351   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       0.714  -3.575   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   40                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    6   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   40   42                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27   42                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   40                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
CONECT   40   28    5   21   41                                             
CONECT   41   40                                                            
CONECT   42   26   21   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₂O₉

Average Mass

630.7340 Da

Monoisotopic Mass

630.28288 Da

IUPAC Name

(1S,2R,4S,5S,6R,7S,9R,12R)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2E)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl (2E)-3-phenylprop-2-enoate

Traditional Name

(1S,2R,4S,5S,6R,7S,9R,12R)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2E)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl (2E)-3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)[C@@H](OC(C)=O)[C@@]2(C)[C@H](C[C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)OC(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C37H42O9/c1-23-21-29(44-31(40)19-17-26-13-9-7-10-14-26)34(43-25(3)39)36(6)30(45-32(41)20-18-27-15-11-8-12-16-27)22-28-33(42-24(2)38)37(23,36)46-35(28,4)5/h7-20,23,28-30,33-34H,21-22H2,1-6H3/b19-17+,20-18+/t23-,28-,29+,30+,33-,34-,36-,37-/m1/s1

InChI Key

JUCKRBRETJEQNN-IQBZRUAFSA-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
Celastrus flagellaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Cinnamic acid or derivatives
Cinnamic acid ester
Styrene
Fatty acid ester
Oxepane
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Ether
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen 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
logP	5.82	ALOGPS
logP	6.34	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.43 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	169.62 m³·mol⁻¹	ChemAxon
Polarizability	68.33 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

59002459

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122187810

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate (NP0144136)

MOL for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0144136 ((1s,2r,4s,5s,6r,7s,9r,12r)-5,12-bis(acetyloxy)-2,6,10,10-tetramethyl-7-{[(2e)-3-phenylprop-2-enoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl (2e)-3-phenylprop-2-enoate)