NP-MRD: Showing NP-Card for (1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate (NP0259138)

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Record Information

Version

2.0

Created at

2022-09-08 00:54:07 UTC

Updated at

2022-09-08 00:54:07 UTC

NP-MRD ID

NP0259138

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate

Description

(1'S,3R,3'S,3aS,6'S,7'R,8'S,9aS,9bS,10'R,12'S)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-3a,4,5,7,9a,9b-hexahydro-2H-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]Pentadecan]-2'(11')-en-8'-yl acetate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate is found in Achillea collina. Based on a literature review very few articles have been published on (1'S,3R,3'S,3aS,6'S,7'R,8'S,9aS,9bS,10'R,12'S)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-3a,4,5,7,9a,9b-hexahydro-2H-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]Pentadecan]-2'(11')-en-8'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082202542D          

 40 46  0  0  1  0            999 V2000
   11.8982    2.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.9398    0.7788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3896    0.1641    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1113   -0.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1606   -0.6285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5659    0.2110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.2143    3.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8992    3.7700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0164    2.8144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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 40 39  1  1  0  0  0
 28 40  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082202542D          

 40 46  0  0  1  0            999 V2000
   11.8982    2.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2250    1.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.6441    3.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0805    1.9919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2676    0.8078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0221    1.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9128    0.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2214   -0.5386    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3999   -0.6150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9230    0.0582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5020   -0.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8285   -1.4090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6971   -0.4701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6207    0.3513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8931    0.7401    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1678    0.3470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0594   -0.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5697    0.9153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255    1.6597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    2.3850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    1.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2843    2.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9578    2.9319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1086    2.1397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5955    1.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3784    0.6778    0.0000 C   0  0  1  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  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  1  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 16  1  6  0  0  0
  5 18  1  0  0  0  0
 12 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 22 21  1  1  0  0  0
 10 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  1  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 39  1  1  0  0  0
 28 40  1  0  0  0  0
 24 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259138

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](OC1=O)C1=C([C@H]3C[C@]1(C)[C@@]1(C3)[C@@H]3CCC(C)=C4[C@@H]([C@H]3OC1=O)C(C)=CC4=O)[C@](C)(O)C[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H38O8/c1-13-7-8-18-26(22-14(2)9-19(34)21(13)22)40-29(36)32(18)11-17-10-30(32,5)25-24(17)31(6,37)12-20(38-16(4)33)23-15(3)28(35)39-27(23)25/h9,15,17-18,20,22-23,26-27,37H,7-8,10-12H2,1-6H3/t15-,17-,18+,20-,22-,23+,26-,27-,30-,31+,32-/m0/s1

> <INCHI_KEY>
NFDTXVLEKTXJLR-AHIAIQFDSA-N

> <FORMULA>
C32H38O8

> <MOLECULAR_WEIGHT>
550.648

> <EXACT_MASS>
550.256668184

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
59.77644741836225

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,3R,3'S,3aS,6'S,7'R,8'S,9aS,9bS,10'R,12'S)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-3a,4,5,7,9a,9b-hexahydro-2H-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0^{2,11}.0^{3,7}]pentadecan]-2'(11')-en-8'-yl acetate

> <JCHEM_LOGP>
2.3919845190000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.3991871165344

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.291617155357173

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0917008252893368

> <JCHEM_POLAR_SURFACE_AREA>
116.20000000000002

> <JCHEM_REFRACTIVITY>
144.23669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,3R,3'S,3aS,6'S,7'R,8'S,9aS,9bS,10'R,12'S)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3aH-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0^{2,11}.0^{3,7}]pentadecan]-2'(11')-en-8'-yl acetate

> <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      22.210   4.109   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.953   3.219   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      21.096   1.686   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      19.554   3.862   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      18.297   2.972   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.554   1.454   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.527   0.306   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.875  -0.440   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      17.100  -1.173   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      15.990   0.394   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.100   1.650   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.527   3.130   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      14.528   4.302   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      15.333   5.614   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.745   7.037   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.831   5.254   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.002   6.253   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.950   3.718   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.566   1.508   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.108   2.978   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.771   0.474   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.347  -1.005   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.813  -1.148   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.923   0.109   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.137  -1.216   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.747  -2.630   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      10.635  -0.878   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.492   0.656   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.134   1.382   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.780   0.648   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.578  -0.879   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.664   1.709   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.328   3.098   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.594   4.452   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.854   2.896   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.864   4.059   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.255   5.473   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.403   3.994   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.312   2.751   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.906   1.265   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   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   22                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    5   12                                                  
CONECT   19   11   20   21   24                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   10   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   19   25   40                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   40                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   29   36                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   28   24                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Value	Source
(1's,3R,3's,3AS,6's,7'r,8's,9as,9BS,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-3a,4,5,7,9a,9b-hexahydro-2H-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0,.0,]pentadecan]-2'(11')-en-8'-yl acetic acid	Generator

Chemical Formula

C₃₂H₃₈O₈

Average Mass

550.6480 Da

Monoisotopic Mass

550.25667 Da

IUPAC Name

Traditional Name

(1'S,3R,3'S,3aS,6'S,7'R,8'S,9aS,9bS,10'R,12'S)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3aH-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0^{2,11}.0^{3,7}]pentadecan]-2'(11')-en-8'-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](OC1=O)C1=C([C@H]3C[C@]1(C)[C@@]1(C3)[C@@H]3CCC(C)=C4[C@@H]([C@H]3OC1=O)C(C)=CC4=O)[C@](C)(O)C[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C32H38O8/c1-13-7-8-18-26(22-14(2)9-19(34)21(13)22)40-29(36)32(18)11-17-10-30(32,5)25-24(17)31(6,37)12-20(38-16(4)33)23-15(3)28(35)39-27(23)25/h9,15,17-18,20,22-23,26-27,37H,7-8,10-12H2,1-6H3/t15-,17-,18+,20-,22-,23+,26-,27-,30-,31+,32-/m0/s1

InChI Key

NFDTXVLEKTXJLR-AHIAIQFDSA-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
Achillea collina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Gamma butyrolactone
Tertiary alcohol
Tetrahydrofuran
Lactone
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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	2.39	ChemAxon
pKa (Strongest Acidic)	14.29	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	116.2 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	144.24 m³·mol⁻¹	ChemAxon
Polarizability	59.78 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	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

163077754

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate (NP0259138)

MOL for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

3D MOL for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

3D SDF for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

3D-SDF for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

PDB for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

3D PDB for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

SMILES for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

INCHI for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

Structure for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)

3D Structure for NP0259138 ((1's,3r,3's,3as,6's,7'r,8's,9as,9bs,10'r,12's)-10'-hydroxy-1',6,6',9,10'-pentamethyl-2,5',7-trioxo-4,5,9a,9b-tetrahydro-3ah-4'-oxaspiro[azuleno[4,5-b]furan-3,14'-tetracyclo[10.2.1.0²,¹¹.0³,⁷]pentadecan]-2'(11')-en-8'-yl acetate)