NP-MRD: Showing NP-Card for 6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one (NP0201556)

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Record Information

Version

2.0

Created at

2022-09-04 20:37:44 UTC

Updated at

2022-09-04 20:37:44 UTC

NP-MRD ID

NP0201556

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one

Description

Agardhilactone belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. 6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one is found in Agardhiella subulata. Based on a literature review very few articles have been published on Agardhilactone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    7.9139    0.9750    1.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7565    1.2482    0.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4391    0.7387    0.8302 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5643   -0.6499    1.0212 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3921    1.0276   -0.1853 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    0.1445   -0.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5203    0.4365   -1.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6995   -0.4951   -2.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6325   -0.2208   -3.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012   -0.4978   -2.5341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200   -0.9231   -1.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1594   -1.2022   -0.7447 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4104   -0.3219    0.4630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8867   -0.0553    0.5255 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2923    0.8136    1.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8244    0.7874    1.7324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4122    1.1069    0.3809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3596    1.4580   -0.6079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4566    2.4498   -1.3770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2386    0.6405   -0.6603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8691   -1.1185    1.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8705   -2.5526    1.1572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0880   -3.0246    0.7018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1893   -2.6177   -0.2630 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7389    0.1132    1.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8123    0.8297    0.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1151    1.8486    1.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8943    0.8484   -0.7848 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6759    2.3561    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2278    1.2641    1.7684 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2329   -0.9937    0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3318    2.0369   -0.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6206   -0.8638   -0.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4153    1.4278   -2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8067   -1.4833   -1.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7028    0.8237   -3.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   -0.8934   -3.9471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5633   -0.3482   -3.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0358   -1.0822   -0.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9603   -0.9923   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8419    0.6249    0.3787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4561   -0.9871    0.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9473    0.4623    2.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9792    1.8612    1.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1025   -0.2821    1.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2283    1.4737    2.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0969    1.9816    0.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0086    0.2653   -0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8087   -0.8072    1.7816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3981   -1.0025    2.5457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1054   -3.2521    1.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253   -3.3767   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 13 12  1  0
 20 14  1  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  1
  4 31  1  0
  5 32  1  0
  6 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  6
 24 52  1  6
 22 51  1  6
 21 49  1  0
 21 50  1  0
 13 41  1  6
 14 42  1  1
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
M  END


  Mrv1652309042222372D          

 24 26  0  0  1  0            999 V2000
    0.2518    4.9108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8038    4.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5489    3.5131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2581    3.3416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1009    2.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8460    2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3980    1.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1431    0.7177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6951    0.1046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4402   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9922   -1.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7372   -2.0778    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2222   -2.7452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0472   -2.7452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4597   -2.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2847   -2.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6972   -2.7452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2847   -3.4597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6972   -4.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4597   -3.4597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7372   -3.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526   -3.1577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2382   -2.7452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526   -2.3327    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 24 23  1  1  0  0  0
 22 24  1  0  0  0  0
 12 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201556

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](O)\C=C\C=C\C\C=C\[C@H]1[C@@H]2O[C@@H]2C[C@@H]1C1CCCC(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-2-14(21)9-6-4-3-5-7-10-15-16(13-18-20(15)24-18)17-11-8-12-19(22)23-17/h3-4,6-7,9-10,14-18,20-21H,2,5,8,11-13H2,1H3/b4-3+,9-6+,10-7+/t14-,15+,16-,17?,18+,20-/m0/s1

> <INCHI_KEY>
YFHYWHWBWQBXAP-IBURHQOWSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.790824152212124

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(1S,2R,3S,5R)-2-[(1E,4E,6E,8S)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one

> <JCHEM_LOGP>
3.073197856666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.606923431588807

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6573034349272686

> <JCHEM_POLAR_SURFACE_AREA>
59.06

> <JCHEM_REFRACTIVITY>
95.99009999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
6-[(1S,2R,3S,5R)-2-[(1E,4E,6E,8S)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one

> <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       0.470   9.167   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.500   8.022   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.025   6.558   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.482   6.238   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.055   5.413   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.579   3.949   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.610   2.804   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.134   1.340   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.164   0.195   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.688  -1.269   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.719  -2.414   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.243  -3.878   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.148  -5.124   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.688  -5.124   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.458  -3.791   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.998  -3.791   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.768  -5.124   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.998  -6.458   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.768  -7.792   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       6.458  -6.458   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.243  -6.370   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.778  -5.894   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.445  -5.124   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.778  -4.354   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   24                                                  
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14                                                       
CONECT   21   13   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   24                                                       
CONECT   24   23   22   12                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

6-[(1S,2R,3S,5R)-2-[(1E,4E,6E,8S)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one

Traditional Name

6-[(1S,2R,3S,5R)-2-[(1E,4E,6E,8S)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one

CAS Registry Number

Not Available

SMILES

CC[C@H](O)\C=C\C=C\C\C=C\[C@H]1[C@@H]2O[C@@H]2C[C@@H]1C1CCCC(=O)O1

InChI Identifier

InChI=1S/C20H28O4/c1-2-14(21)9-6-4-3-5-7-10-15-16(13-18-20(15)24-18)17-11-8-12-19(22)23-17/h3-4,6-7,9-10,14-18,20-21H,2,5,8,11-13H2,1H3/b4-3+,9-6+,10-7+/t14-,15+,16-,17?,18+,20-/m0/s1

InChI Key

YFHYWHWBWQBXAP-IBURHQOWSA-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
Agardhiella subulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Delta valerolactone
Delta_valerolactone
Oxane
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Dialkyl ether
Ether
Oxirane
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen 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	3.07	ChemAxon
pKa (Strongest Acidic)	17.61	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	95.99 m³·mol⁻¹	ChemAxon
Polarizability	37.79 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00000421

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

101759352

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one (NP0201556)

MOL for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

3D MOL for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

3D SDF for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

3D-SDF for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

PDB for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

3D PDB for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

SMILES for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

INCHI for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

Structure for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)

3D Structure for NP0201556 (6-[(1s,2r,3s,5r)-2-[(1e,4e,6e,8s)-8-hydroxydeca-1,4,6-trien-1-yl]-6-oxabicyclo[3.1.0]hexan-3-yl]oxan-2-one)