NP-MRD: Showing NP-Card for (1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate (NP0187162)

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Record Information

Version

2.0

Created at

2022-09-04 03:14:11 UTC

Updated at

2022-09-04 03:14:12 UTC

NP-MRD ID

NP0187162

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate

Description

[(1R,2S,4S,4aR,5S,6R,8S,8aR)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl (3R)-3-hydroxy-2-methylidenebutanoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. (1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate is found in Ajuga decumbens. Based on a literature review very few articles have been published on [(1R,2S,4S,4aR,5S,6R,8S,8aR)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl (3R)-3-hydroxy-2-methylidenebutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042205142D          

 43 46  0  0  1  0            999 V2000
    3.4099    0.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4099   -0.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2499   -2.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9143   -2.8564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -2.2752    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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  5  6  1  0  0  0  0
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  2 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  1  0  0  0
M  END

     RDKit          3D

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 11 51  1  0
M  END


  Mrv1652309042205142D          

 43 46  0  0  1  0            999 V2000
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    1.7649   -1.4353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2499   -2.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0703   -2.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9143   -2.8564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -2.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2116   -2.3614    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5471   -3.1151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6965   -1.6940    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3805   -1.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2696   -2.2874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0701   -2.0878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6432   -2.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4999   -3.4938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2284   -3.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3432   -4.6981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8218   -3.3080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4602   -2.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3609   -0.9403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8459   -0.2729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6664   -0.3591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1513    0.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9718    0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8157    1.0620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103    0.4808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3102    0.5670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6457    1.3207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1608    1.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6597    1.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964    2.7418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7951   -0.1004    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4625    0.3845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5488   -0.4360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -1.0256    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8389   -0.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -1.8506    0.0000 O   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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 26 16  1  1  0  0  0
  7 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 33 38  1  0  0  0  0
  7 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 40  1  1  0  0  0
  2 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0187162

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](O)C(=C)C(=O)OC[C@@]12[C@H](C[C@@H](C)[C@](C)(CCC3=CC(=O)OC3)[C@H]1[C@H](C[C@H](OC(C)=O)[C@]21CO1)OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H42O12/c1-16-10-24(42-20(5)34)30(14-39-28(37)17(2)18(3)32)27(29(16,7)9-8-22-11-26(36)38-13-22)23(41-19(4)33)12-25(43-21(6)35)31(30)15-40-31/h11,16,18,23-25,27,32H,2,8-10,12-15H2,1,3-7H3/t16-,18-,23+,24+,25+,27-,29+,30-,31-/m1/s1

> <INCHI_KEY>
PIIQPVTUGULYTD-ITVHRRKTSA-N

> <FORMULA>
C31H42O12

> <MOLECULAR_WEIGHT>
606.665

> <EXACT_MASS>
606.267626792

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
62.693366866664974

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,2S,4S,4aR,5S,6R,8S,8aR)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl (3R)-3-hydroxy-2-methylidenebutanoate

> <JCHEM_LOGP>
1.6392419126666653

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.669771618832154

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.471525035531811

> <JCHEM_PKA_STRONGEST_BASIC>
-2.943241905956998

> <JCHEM_POLAR_SURFACE_AREA>
164.26000000000002

> <JCHEM_REFRACTIVITY>
148.06980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4S,4aR,5S,6R,8S,8aR)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2H-furan-3-yl)ethyl]-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-ylmethyl (3R)-3-hydroxy-2-methylidenebutanoate

> <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       6.365   0.396   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.365  -1.144   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.031  -1.914   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.031  -3.454   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       3.698  -1.144   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.364  -1.914   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.858  -1.594   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.763  -2.840   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.295  -2.679   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.200  -3.925   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.731  -3.764   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.573  -5.332   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.137  -4.247   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.395  -4.408   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.021  -5.815   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.300  -3.162   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.577  -2.301   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.370  -4.270   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.864  -3.897   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.934  -5.005   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.667  -6.522   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.026  -7.245   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -6.241  -8.770   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -7.134  -6.175   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -6.459  -4.791   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.674  -1.755   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.579  -0.509   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.111  -0.670   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.016   0.576   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.547   0.415   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -3.389   1.982   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.953   0.898   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.579   1.058   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.205   2.465   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.300   3.711   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.231   3.550   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.927   5.118   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.484  -0.187   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.730   0.718   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.891  -0.814   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.699  -1.914   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.033  -1.144   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       7.699  -3.454   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   41                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   26   38                                             
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   26                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   20                                                       
CONECT   26   16    7   27                                                  
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   33    7   39   40                                             
CONECT   39   38   40                                                       
CONECT   40   39   38                                                       
CONECT   41    2   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Value	Source
[(1R,2S,4S,4AR,5S,6R,8S,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl (3R)-3-hydroxy-2-methylidenebutanoic acid	Generator

Chemical Formula

C₃₁H₄₂O₁₂

Average Mass

606.6650 Da

Monoisotopic Mass

606.26763 Da

IUPAC Name

Traditional Name

(1R,2S,4S,4aR,5S,6R,8S,8aR)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2H-furan-3-yl)ethyl]-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-ylmethyl (3R)-3-hydroxy-2-methylidenebutanoate

CAS Registry Number

Not Available

SMILES

C[C@@H](O)C(=C)C(=O)OC[C@@]12[C@H](C[C@@H](C)[C@](C)(CCC3=CC(=O)OC3)[C@H]1[C@H](C[C@H](OC(C)=O)[C@]21CO1)OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C31H42O12/c1-16-10-24(42-20(5)34)30(14-39-28(37)17(2)18(3)32)27(29(16,7)9-8-22-11-26(36)38-13-22)23(41-19(4)33)12-25(43-21(6)35)31(30)15-40-31/h11,16,18,23-25,27,32H,2,8-10,12-15H2,1,3-7H3/t16-,18-,23+,24+,25+,27-,29+,30-,31-/m1/s1

InChI Key

PIIQPVTUGULYTD-ITVHRRKTSA-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
Ajuga decumbens	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Beta-hydroxy acid
Fatty acid ester
2-furanone
Fatty acyl
Hydroxy acid
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Lactone
Dialkyl ether
Oxacycle
Oxirane
Ether
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen 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	1.64	ChemAxon
pKa (Strongest Acidic)	7.47	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	164.26 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	148.07 m³·mol⁻¹	ChemAxon
Polarizability	62.69 Å³	ChemAxon
Number of Rings	4	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

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

162850046

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate (NP0187162)

MOL for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

3D MOL for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

3D SDF for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

3D-SDF for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

PDB for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

3D PDB for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

SMILES for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

INCHI for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

Structure for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)

3D Structure for NP0187162 ((1r,2s,4s,4ar,5s,6r,8s,8ar)-2,4,8-tris(acetyloxy)-5,6-dimethyl-5-[2-(5-oxo-2h-furan-3-yl)ethyl]-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl (3r)-3-hydroxy-2-methylidenebutanoate)