NP-MRD: Showing NP-Card for (1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate (NP0186665)

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Record Information

Version

2.0

Created at

2022-09-04 02:36:13 UTC

Updated at

2022-09-04 02:36:13 UTC

NP-MRD ID

NP0186665

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate

Description

(1S,3S,4S,5R,7R,8S,9S,10S)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2Z)-2-methylbut-2-enoyl]oxy}-8-{[(2R)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]Undecan-3-yl (2Z)-2-methylbut-2-enoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on (1S,3S,4S,5R,7R,8S,9S,10S)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2Z)-2-methylbut-2-enoyl]oxy}-8-{[(2R)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]Undecan-3-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204362D          

 42 43  0  0  1  0            999 V2000
    1.3120   -1.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6445   -1.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042204362D          

 42 43  0  0  1  0            999 V2000
    1.3120   -1.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4793   -3.5914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7764   -2.1936    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5048   -1.8063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2843   -2.8438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013   -2.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6092   -3.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4103   -1.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5214   -1.4090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3284   -1.5806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8804   -0.9675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6255   -0.1828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6874   -1.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9424   -1.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2395   -0.5259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9845    0.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0735   -0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8185   -0.0113    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5636    0.7733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116    0.1602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3985    0.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595   -0.4529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3474   -0.2814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    0.5033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0503    1.1164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094    0.6748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9614    0.0617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6643    1.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1123    2.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 27 35  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186665

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C32H48O10/c1-12-18(6)28(35)38-24-16-25-32(11,42-25)27(40-30(37)20(8)14-3)26(39-29(36)19(7)13-2)22(17(4)5)15-23(34)31(24,10)41-21(9)33/h12,14,19,22-27,34H,4,13,15-16H2,1-3,5-11H3/b18-12-,20-14-/t19-,22-,23-,24+,25+,26+,27+,31+,32+/m1/s1

> <INCHI_KEY>
GGLLZIOOCOASQA-YWPCKLFWSA-N

> <FORMULA>
C32H48O10

> <MOLECULAR_WEIGHT>
592.726

> <EXACT_MASS>
592.324747746

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
64.09911970879614

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,4S,5R,7R,8S,9S,10S)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2Z)-2-methylbut-2-enoyl]oxy}-8-{[(2R)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
5.692925320999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.87330472411378

> <JCHEM_PKA_STRONGEST_BASIC>
-3.291616513672632

> <JCHEM_POLAR_SURFACE_AREA>
137.96000000000004

> <JCHEM_REFRACTIVITY>
155.04290000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4S,5R,7R,8S,9S,10S)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2Z)-2-methylbut-2-enoyl]oxy}-8-{[(2R)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       2.449  -2.229   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.203  -3.134   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.234  -4.279   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.303  -3.454   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.779  -4.919   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.285  -5.239   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.761  -6.704   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.316  -4.095   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.676  -3.372   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.264  -5.308   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.789  -5.094   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.737  -6.308   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.366  -3.666   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.840  -2.630   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.346  -2.950   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -5.377  -1.806   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.901  -0.341   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.883  -2.126   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.359  -3.591   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -7.914  -0.982   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -7.438   0.483   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.870  -1.486   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.395  -0.021   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.919   1.444   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.888   0.299   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.744   1.330   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.858  -0.845   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.649  -0.525   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.124   0.939   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.094   2.084   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.631   1.260   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.661   0.115   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.107   2.724   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.076   3.869   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.000  -1.540   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       1.334  -3.850   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   35                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   14                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   14   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23   25                                                       
CONECT   25   24   23   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33                                                            
CONECT   35   27    4   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

View in JSmol

Synonyms

Value	Source
(1S,3S,4S,5R,7R,8S,9S,10S)-4-(Acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2Z)-2-methylbut-2-enoyl]oxy}-8-{[(2R)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₂H₄₈O₁₀

Average Mass

592.7260 Da

Monoisotopic Mass

592.32475 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@H]1[C@H](C[C@@H](O)[C@](C)(OC(C)=O)[C@H](C[C@@H]2O[C@]2(C)[C@H]1OC(=O)C(\C)=C/C)OC(=O)C(\C)=C/C)C(C)=C

InChI Identifier

InChI=1S/C32H48O10/c1-12-18(6)28(35)38-24-16-25-32(11,42-25)27(40-30(37)20(8)14-3)26(39-29(36)19(7)13-2)22(17(4)5)15-23(34)31(24,10)41-21(9)33/h12,14,19,22-27,34H,4,13,15-16H2,1-3,5-11H3/b18-12-,20-14-/t19-,22-,23-,24+,25+,26+,27+,31+,32+/m1/s1

InChI Key

GGLLZIOOCOASQA-YWPCKLFWSA-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

Not Available

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
Fatty acid ester
Cyclitol or derivatives
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Secondary alcohol
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	5.69	ChemAxon
pKa (Strongest Acidic)	13.87	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	137.96 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	155.04 m³·mol⁻¹	ChemAxon
Polarizability	64.1 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

162927811

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate (NP0186665)

MOL for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

PDB for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

Structure for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0186665 ((1s,3s,4s,5r,7r,8s,9s,10s)-4-(acetyloxy)-5-hydroxy-4,10-dimethyl-9-{[(2z)-2-methylbut-2-enoyl]oxy}-8-{[(2r)-2-methylbutanoyl]oxy}-7-(prop-1-en-2-yl)-11-oxabicyclo[8.1.0]undecan-3-yl (2z)-2-methylbut-2-enoate)