NP-MRD: Showing NP-Card for alotaketal A (NP0038708)

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Record Information

Version

2.0

Created at

2021-06-20 21:19:25 UTC

Updated at

2021-06-30 00:11:38 UTC

NP-MRD ID

NP0038708

Secondary Accession Numbers

None

Natural Product Identification

Common Name

alotaketal A

Provided By

JEOL Database JEOL Logo

Description

Alotaketal A belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. alotaketal A is found in Hamigera sp. alotaketal A was first documented in 2012 (PMID: 23094646). Based on a literature review a small amount of articles have been published on Alotaketal A (PMID: 32391700) (PMID: 23584129) (PMID: 22563931).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202123193D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306202123193D          

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    4.7624    1.6594   -1.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5016    3.4626   -0.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6854   -0.5393   -1.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5554   -4.9836   -2.0803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2884   -4.9493   -2.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7942   -2.9167   -1.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609   -0.7314   -0.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 28  1  6  0  0  0
 15 14  1  0  0  0  0
 20 56  1  1  0  0  0
 15 29  1  0  0  0  0
 27 63  1  1  0  0  0
 14 12  1  0  0  0  0
 10  9  1  0  0  0  0
 24 26  2  0  0  0  0
 24 25  1  0  0  0  0
 22 21  1  0  0  0  0
 21 20  1  0  0  0  0
 22 23  2  0  0  0  0
 27 26  1  0  0  0  0
 17 18  1  0  0  0  0
 27 20  1  0  0  0  0
 18 19  1  0  0  0  0
 12 11  1  0  0  0  0
 12 13  2  3  0  0  0
 11 10  1  0  0  0  0
  9  7  2  0  0  0  0
 10 29  1  0  0  0  0
  7  6  1  0  0  0  0
 24 22  1  0  0  0  0
  6  5  1  0  0  0  0
  5  4  1  0  0  0  0
 27 28  1  0  0  0  0
  4  2  1  0  0  0  0
 20 17  1  0  0  0  0
  2  1  2  3  0  0  0
 17 16  2  0  0  0  0
  2  3  1  0  0  0  0
 16 15  1  0  0  0  0
  7  8  1  0  0  0  0
 14 50  1  0  0  0  0
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 11 46  1  0  0  0  0
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 21 57  1  0  0  0  0
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  3 34  1  0  0  0  0
  8 41  1  0  0  0  0
  8 42  1  0  0  0  0
  8 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0038708

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C1=C([H])[C@]2(O[C@@]([H])(C(\[H])=C(/C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C(=C([H])[H])C([H])([H])[H])C([H])([H])C(=C([H])[H])C2([H])[H])O[C@@]2([H])C([H])=C(C(=O)C([H])([H])[C@@]12[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O4/c1-16(2)7-6-8-17(3)9-21-10-18(4)13-25(28-21)14-20(15-26)22-12-23(27)19(5)11-24(22)29-25/h9,11,14,21-22,24,26H,1,4,6-8,10,12-13,15H2,2-3,5H3/b17-9+/t21-,22-,24-,25+/m0/s1

> <INCHI_KEY>
UIVQQXWRQITZJI-ATUMTDQDSA-N

> <FORMULA>
C25H34O4

> <MOLECULAR_WEIGHT>
398.543

> <EXACT_MASS>
398.245709575

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.15869359437418

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4aS,6'R,8aS)-6'-[(1E)-2,6-dimethylhepta-1,6-dien-1-yl]-4-(hydroxymethyl)-7-methyl-4'-methylidene-4a,5,6,8a-tetrahydrospiro[chromene-2,2'-oxane]-6-one

> <ALOGPS_LOGP>
3.52

> <JCHEM_LOGP>
4.599376794999999

> <ALOGPS_LOGS>
-4.37

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.201035485175762

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.119062259420023

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7464136635428504

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
118.31049999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.72e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aS,6'R,8aS)-6'-[(1E)-2,6-dimethylhepta-1,6-dien-1-yl]-4-(hydroxymethyl)-7-methyl-4'-methylidene-5,8a-dihydro-4aH-spiro[chromene-2,2'-oxane]-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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 27 63  1  1
 14 12  1  0
 10  9  1  0
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 17 18  1  0
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 27 28  1  0
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 20 17  1  0
  2  1  2  3
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 16 15  1  0
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 14 50  1  0
 14 51  1  0
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  8 41  1  0
  8 42  1  0
  8 43  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.506  -1.585   6.292  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.802  -0.745   5.286  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.222  -0.296   5.058  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.200  -0.173   4.300  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.672  -0.565   4.499  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.615   0.129   3.506  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.360  -0.224   2.053  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.665  -1.647   1.671  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.910   0.716   1.195  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.551   0.548  -0.258  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.608   1.199  -1.165  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.152   1.135  -2.601  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.910   0.651  -3.597  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.739   1.644  -2.798  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.242   1.045  -1.752  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.539   1.827  -1.772  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.768   1.278  -1.845  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.057   2.056  -1.868  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.843   3.427  -1.570  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.894  -0.236  -1.871  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.261  -0.734  -3.270  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.335  -2.245  -3.305  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.143  -2.828  -4.026  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.357  -3.023  -2.487  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.325  -4.504  -2.694  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.544  -2.365  -1.644  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.582  -0.888  -1.389  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.471  -0.332  -2.086  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.275   1.190  -0.422  0.00  0.00           O+0
HETATM   30  H   UNK     0       1.276  -1.957   6.962  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.503  -1.933   6.486  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.916  -0.731   5.785  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.293   0.794   5.141  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.558  -0.592   4.059  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.126   0.922   4.340  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.118  -0.478   3.295  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.785  -1.653   4.421  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.989  -0.285   5.512  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.650  -0.140   3.753  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.548   1.214   3.658  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.889  -2.319   2.050  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.744  -1.794   0.591  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.627  -1.955   2.096  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.743   1.725   1.573  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.436  -0.513  -0.503  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.736   2.256  -0.899  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.578   0.705  -1.031  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.543   0.608  -4.618  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.916   0.284  -3.419  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.779   2.736  -2.692  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.387   1.419  -3.813  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.430   2.908  -1.721  0.00  0.00           H+0
HETATM   53  H   UNK     0       4.521   1.993  -2.857  0.00  0.00           H+0
HETATM   54  H   UNK     0       4.762   1.659  -1.130  0.00  0.00           H+0
HETATM   55  H   UNK     0       3.502   3.463  -0.661  0.00  0.00           H+0
HETATM   56  H   UNK     0       3.685  -0.539  -1.171  0.00  0.00           H+0
HETATM   57  H   UNK     0       2.535  -0.410  -4.026  0.00  0.00           H+0
HETATM   58  H   UNK     0       4.245  -0.345  -3.559  0.00  0.00           H+0
HETATM   59  H   UNK     0       2.109  -4.741  -3.741  0.00  0.00           H+0
HETATM   60  H   UNK     0       1.555  -4.984  -2.080  0.00  0.00           H+0
HETATM   61  H   UNK     0       3.288  -4.949  -2.427  0.00  0.00           H+0
HETATM   62  H   UNK     0       0.794  -2.917  -1.082  0.00  0.00           H+0
HETATM   63  H   UNK     0       1.461  -0.731  -0.308  0.00  0.00           H+0
CONECT    1    2   30   31                                                  
CONECT    2    4    1    3                                                  
CONECT    3    2   32   33   34                                             
CONECT    4    5    2   35   36                                             
CONECT    5    6    4   37   38                                             
CONECT    6    7    5   39   40                                             
CONECT    7    9    6    8                                                  
CONECT    8    7   41   42   43                                             
CONECT    9   10    7   44                                                  
CONECT   10    9   11   29   45                                             
CONECT   11   12   10   46   47                                             
CONECT   12   14   11   13                                                  
CONECT   13   12   48   49                                                  
CONECT   14   15   12   50   51                                             
CONECT   15   28   14   29   16                                             
CONECT   16   17   15   52                                                  
CONECT   17   18   20   16                                                  
CONECT   18   17   19   53   54                                             
CONECT   19   18   55                                                       
CONECT   20   56   21   27   17                                             
CONECT   21   22   20   57   58                                             
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   26   25   22                                                  
CONECT   25   24   59   60   61                                             
CONECT   26   24   27   62                                                  
CONECT   27   63   26   20   28                                             
CONECT   28   15   27                                                       
CONECT   29   15   10                                                       
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    3                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    4                                                            
CONECT   36    4                                                            
CONECT   37    5                                                            
CONECT   38    5                                                            
CONECT   39    6                                                            
CONECT   40    6                                                            
CONECT   41    8                                                            
CONECT   42    8                                                            
CONECT   43    8                                                            
CONECT   44    9                                                            
CONECT   45   10                                                            
CONECT   46   11                                                            
CONECT   47   11                                                            
CONECT   48   13                                                            
CONECT   49   13                                                            
CONECT   50   14                                                            
CONECT   51   14                                                            
CONECT   52   16                                                            
CONECT   53   18                                                            
CONECT   54   18                                                            
CONECT   55   19                                                            
CONECT   56   20                                                            
CONECT   57   21                                                            
CONECT   58   21                                                            
CONECT   59   25                                                            
CONECT   60   25                                                            
CONECT   61   25                                                            
CONECT   62   26                                                            
CONECT   63   27                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

RDKit          3D

63 65  0  0  0  0  0  0  0  0999 V2000
    0.5058   -1.5850    6.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8015   -0.7450    5.2857 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5779    0.7054   -1.0311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5433    0.6079   -4.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9163    0.2843   -3.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3869    1.4192   -3.8127 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7624    1.6594   -1.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2447   -0.3453   -3.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2884   -4.9493   -2.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7942   -2.9167   -1.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609   -0.7314   -0.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 28  1  6
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 15 29  1  0
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 10  9  1  0
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 17 18  1  0
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  4  2  1  0
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  2  1  2  3
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  4 35  1  0
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  1 30  1  0
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  3 34  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₄

Average Mass

398.5430 Da

Monoisotopic Mass

398.24571 Da

IUPAC Name

(2R,4aS,6'R,8aS)-6'-[(1E)-2,6-dimethylhepta-1,6-dien-1-yl]-4-(hydroxymethyl)-7-methyl-4'-methylidene-4a,5,6,8a-tetrahydrospiro[chromene-2,2'-oxane]-6-one

Traditional Name

(2R,4aS,6'R,8aS)-6'-[(1E)-2,6-dimethylhepta-1,6-dien-1-yl]-4-(hydroxymethyl)-7-methyl-4'-methylidene-5,8a-dihydro-4aH-spiro[chromene-2,2'-oxane]-6-one

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])C1=C([H])[C@]2(O[C@@]([H])(C(\[H])=C(/C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C(=C([H])[H])C([H])([H])[H])C([H])([H])C(=C([H])[H])C2([H])[H])O[C@@]2([H])C([H])=C(C(=O)C([H])([H])[C@@]12[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C25H34O4/c1-16(2)7-6-8-17(3)9-21-10-18(4)13-25(28-21)14-20(15-26)22-12-23(27)19(5)11-24(22)29-25/h9,11,14,21-22,24,26H,1,4,6-8,10,12-13,15H2,2-3,5H3/b17-9+/t21-,22-,24-,25+/m0/s1

InChI Key

UIVQQXWRQITZJI-ATUMTDQDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Hamigera sp. (in: Fungi)	JEOL database	Forestieri, R., et al, Org. Lett. 11, 5166 (2009)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Bicyclic monoterpenoid
Monoterpenoid
Ketal
Cyclohexenone
Pyran
Oxane
Ketone
Cyclic ketone
Acetal
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aldehyde
Alcohol
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	3.52	ALOGPS
logP	4.6	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	15.12	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	118.31 m³·mol⁻¹	ChemAxon
Polarizability	46.16 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

Not Available

Chemspider ID

28287015

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44542224

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lee J, Kim J, Lee HY: Au(I)-Catalyzed Cyclization of Epoxyalkynes to Allylic Alcohol Containing Spiroketals and Application to the Total Synthesis of (-)-Alotaketal A. Org Lett. 2020 Jun 5;22(11):4073-4077. doi: 10.1021/acs.orglett.0c01130. Epub 2020 May 11. [PubMed:32391700 ]
Huang J, Yang JR, Zhang J, Yang J: Total synthesis and structure-activity relationship study of the potent cAMP signaling agonist (-)-alotaketal A. Org Biomol Chem. 2013 May 21;11(19):3212-22. doi: 10.1039/c3ob40120k. Epub 2013 Apr 12. [PubMed:23584129 ]
Xuan M, Paterson I, Dalby SM: Total synthesis of alotaketal A. Org Lett. 2012 Nov 2;14(21):5492-5. doi: 10.1021/ol302570k. Epub 2012 Oct 24. [PubMed:23094646 ]
Huang J, Yang JR, Zhang J, Yang J: Total synthesis of the potent cAMP signaling agonist (-)-alotaketal A. J Am Chem Soc. 2012 May 30;134(21):8806-9. doi: 10.1021/ja303529z. Epub 2012 May 16. [PubMed:22563931 ]
Forestieri, R., et al. (2009). Forestieri, R., et al, Org. Lett. 11, 5166 (2009). Org. Lett..

Showing NP-Card for alotaketal A (NP0038708)

MOL for NP0038708 (alotaketal A)

3D MOL for NP0038708 (alotaketal A)

3D SDF for NP0038708 (alotaketal A)

3D-SDF for NP0038708 (alotaketal A)

PDB for NP0038708 (alotaketal A)

3D PDB for NP0038708 (alotaketal A)

SMILES for NP0038708 (alotaketal A)

INCHI for NP0038708 (alotaketal A)

Structure for NP0038708 (alotaketal A)

3D Structure for NP0038708 (alotaketal A)