NP-MRD: Showing NP-Card for (2,4-trans)-10R-annonacin-A-one (NP0083660)

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Record Information

Version

2.0

Created at

2022-04-29 04:37:51 UTC

Updated at

2022-04-29 04:37:51 UTC

NP-MRD ID

NP0083660

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2,4-trans)-10R-annonacin-A-one

Description

Isoannonacin A, also known as annonacin-a-one, belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. Thus, isoannonacin a is considered to be a fatty alcohol lipid molecule. Isoannonacin A is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, Isoannonacin A has been detected, but not quantified in, fruits. (2,4-trans)-10R-annonacin-A-one is found in Annona muricata , Annona reticulata, Asimina longifolia, Asimina triloba and Goniothalamus gardneri. This could make isoannonacin a a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061312462D          

 42 43  0  0  0  0            999 V2000
   -2.3357   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2366   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3801   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.0383   20.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3  1  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
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M  END

     RDKit          3D

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 24 85  1  0
 25 86  1  6
 26 87  1  0
 27 88  1  0
 27 89  1  0
 28 90  1  0
 28 91  1  0
 29 92  1  0
 29 93  1  0
 30 94  1  0
 30 95  1  0
 31 96  1  0
 31 97  1  0
 32 98  1  6
 33 99  1  0
 33100  1  0
 34101  1  1
 35102  1  0
 35103  1  0
 37104  1  0
 37105  1  0
 37106  1  0
M  END


  Mrv0541 05061312462D          

 42 43  0  0  0  0            999 V2000
   -2.3357   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2310   23.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9068   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1923   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5222   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2366   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9511   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3801   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0945   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7027   20.2344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8823   20.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0383   20.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8090   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5702   18.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2346   17.7147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5467   19.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3907   18.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8588   21.0743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5235   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4142   17.6284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0386   16.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8456   16.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8020   23.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0013   21.9995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5165   22.8200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0876   22.8200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7262   19.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1943   21.8280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2379   17.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0786   16.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9524   17.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2581   16.7885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3339   23.1556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5165   21.9950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2413   19.9757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2379   18.3036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5635   16.2073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1624   23.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7818   22.5425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7061   17.4016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 13 12  1  0  0  0  0
 14 12  1  0  0  0  0
 15 11  1  0  0  0  0
 17 16  1  0  0  0  0
 18 13  1  0  0  0  0
 19 16  1  0  0  0  0
 20 14  1  0  0  0  0
 21 15  1  0  0  0  0
 22 17  1  0  0  0  0
 24 23  1  0  0  0  0
 27  2  1  0  0  0  0
 27 25  1  0  0  0  0
 28 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 18  1  0  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 30 26  1  0  0  0  0
 31 21  1  0  0  0  0
 32 22  1  0  0  0  0
 33 23  1  0  0  0  0
 33 31  1  0  0  0  0
 34 24  1  0  0  0  0
 34 32  1  0  0  0  0
 35 28  1  0  0  0  0
 36 27  2  0  0  0  0
 37 29  1  0  0  0  0
 38 31  1  0  0  0  0
 39 32  1  0  0  0  0
 40 35  2  0  0  0  0
 41 30  1  0  0  0  0
 41 35  1  0  0  0  0
 42 33  1  0  0  0  0
 42 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083660

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC(O)C1CCC(O1)C(O)CCCCC(O)CCCCCC1CC(CC(C)=O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C35H64O7/c1-3-4-5-6-7-8-9-10-11-15-21-31(38)33-23-24-34(42-33)32(39)22-17-16-19-29(37)18-13-12-14-20-30-26-28(25-27(2)36)35(40)41-30/h28-34,37-39H,3-26H2,1-2H3

> <INCHI_KEY>
DGQPZGGOYKKJLX-UHFFFAOYSA-N

> <FORMULA>
C35H64O7

> <MOLECULAR_WEIGHT>
596.8785

> <EXACT_MASS>
596.465204402

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
74.71722503388193

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-{6,11-dihydroxy-11-[5-(1-hydroxytridecyl)oxolan-2-yl]undecyl}-3-(2-oxopropyl)oxolan-2-one

> <ALOGPS_LOGP>
6.61

> <JCHEM_LOGP>
7.496113493666664

> <ALOGPS_LOGS>
-5.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.501062459706915

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.898977669929621

> <JCHEM_PKA_STRONGEST_BASIC>
-1.27430907683708

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
167.49029999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.97e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{6,11-dihydroxy-11-[5-(1-hydroxytridecyl)oxolan-2-yl]undecyl}-3-(2-oxopropyl)oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -4.360  32.627   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      34.031  43.367   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.026  31.857   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.693  32.627   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.359  31.857   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.975  32.627   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.308  31.857   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.642  32.627   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.976  31.857   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.310  32.627   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.643  31.857   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      25.578  37.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.047  37.610   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.205  39.178   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.977  32.627   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.731  34.474   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.105  33.067   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.421  36.203   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.263  34.635   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      27.736  39.339   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.311  31.857   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.573  32.906   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.139  30.325   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.645  30.005   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      31.364  43.367   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      29.869  41.066   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      32.697  42.597   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      30.030  42.597   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      21.889  36.042   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      28.363  40.746   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.644  32.627   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.947  31.500   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.978  31.857   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.415  31.339   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      28.623  43.224   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      32.697  41.057   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      20.984  37.288   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      11.644  34.167   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      17.852  30.254   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      28.303  44.730   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      27.593  42.079   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      14.385  32.483   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2   27                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   15                                                       
CONECT   12   13   14                                                       
CONECT   13   12   18                                                       
CONECT   14   12   20                                                       
CONECT   15   11   21                                                       
CONECT   16   17   19                                                       
CONECT   17   16   22                                                       
CONECT   18   13   29                                                       
CONECT   19   16   29                                                       
CONECT   20   14   30                                                       
CONECT   21   15   31                                                       
CONECT   22   17   32                                                       
CONECT   23   24   33                                                       
CONECT   24   23   34                                                       
CONECT   25   27   28                                                       
CONECT   26   28   30                                                       
CONECT   27    2   25   36                                                  
CONECT   28   25   26   35                                                  
CONECT   29   18   19   37                                                  
CONECT   30   20   26   41                                                  
CONECT   31   21   33   38                                                  
CONECT   32   22   34   39                                                  
CONECT   33   23   31   42                                                  
CONECT   34   24   32   42                                                  
CONECT   35   28   40   41                                                  
CONECT   36   27                                                            
CONECT   37   29                                                            
CONECT   38   31                                                            
CONECT   39   32                                                            
CONECT   40   35                                                            
CONECT   41   30   35                                                       
CONECT   42   33   34                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

View in JSmol

Synonyms

Value	Source
Annonacin-a-one	HMDB
Annonacin-a-one, ((2,4-cis)-10R)-isomer	MeSH

Chemical Formula

C₃₅H₆₄O₇

Average Mass

596.8785 Da

Monoisotopic Mass

596.46520 Da

IUPAC Name

5-{6,11-dihydroxy-11-[5-(1-hydroxytridecyl)oxolan-2-yl]undecyl}-3-(2-oxopropyl)oxolan-2-one

Traditional Name

5-{6,11-dihydroxy-11-[5-(1-hydroxytridecyl)oxolan-2-yl]undecyl}-3-(2-oxopropyl)oxolan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC(O)C1CCC(O1)C(O)CCCCC(O)CCCCCC1CC(CC(C)=O)C(=O)O1

InChI Identifier

InChI=1S/C35H64O7/c1-3-4-5-6-7-8-9-10-11-15-21-31(38)33-23-24-34(42-33)32(39)22-17-16-19-29(37)18-13-12-14-20-30-26-28(25-27(2)36)35(40)41-30/h28-34,37-39H,3-26H2,1-2H3

InChI Key

DGQPZGGOYKKJLX-UHFFFAOYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Annona muricata	Plant	KNApSAcK
Annona reticulata	LOTUS Database	35616633
Asimina longifolia	LOTUS Database	35616633
Asimina triloba	LOTUS Database	35616633
Goniothalamus gardneri	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Long chain fatty alcohol
Gamma butyrolactone
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Alcohol
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	6.61	ALOGPS
logP	7.5	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	13.9	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	167.49 m³·mol⁻¹	ChemAxon
Polarizability	74.72 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

HMDB0041035

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB021543

KNApSAcK ID

Not Available

Chemspider ID

113519

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

128014

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (2,4-trans)-10R-annonacin-A-one (NP0083660)

MOL for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

3D MOL for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

3D SDF for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

3D-SDF for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

PDB for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

3D PDB for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

SMILES for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

INCHI for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

Structure for NP0083660 ((2,4-trans)-10R-annonacin-A-one)

3D Structure for NP0083660 ((2,4-trans)-10R-annonacin-A-one)