NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0201989)

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Record Information

Version

2.0

Created at

2022-09-04 21:07:39 UTC

Updated at

2022-09-04 21:07:39 UTC

NP-MRD ID

NP0201989

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

(3S,5S)-1-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]decane-3,5-diol belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. (2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Zingiber officinale. Based on a literature review very few articles have been published on (3S,5S)-1-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]decane-3,5-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223072D          

 32 33  0  0  1  0            999 V2000
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.4328   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.8618   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.4328   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -6.6000    0.0000 C   0  0  0  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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
 16 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  2  0  0  0  0
 13 32  1  0  0  0  0
M  END

     RDKit          3D

 70 71  0  0  0  0  0  0  0  0999 V2000
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   -3.3567   -0.5207   -0.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6769   -0.1931    0.1872 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0527   -0.6116    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3430   -0.4258    1.7897 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6673   -1.3177    2.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0036   -1.1474    3.3860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3774   -0.5762    0.7509 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.4972    0.2282    1.0326 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9496   -0.2780   -0.6496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.7826   -0.8880   -1.5993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5556   -0.7333   -0.9141 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1240   -0.1100   -2.1033 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0819   -0.3311   -0.7126 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6281   -1.1871   -0.8885 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4744   -1.6090    0.6592 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9385   -1.5650    0.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    0.7849   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4647    1.8319   -0.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7756    1.2364    1.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9992    3.4319    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8824    3.5304   -1.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2718    2.1494   -0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309042223072D          

 32 33  0  0  1  0            999 V2000
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2881   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   13.5749   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.2894   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.4328   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   17.8618   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.4328   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   15.0039   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0201989

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC[C@H](O)C[C@@H](O)CCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H38O9/c1-3-4-5-6-15(25)12-16(26)9-7-14-8-10-17(18(11-14)30-2)31-23-22(29)21(28)20(27)19(13-24)32-23/h8,10-11,15-16,19-29H,3-7,9,12-13H2,1-2H3/t15-,16-,19+,20+,21-,22+,23+/m0/s1

> <INCHI_KEY>
NIZBVVCYJIIIMW-MTLKXPBVSA-N

> <FORMULA>
C23H38O9

> <MOLECULAR_WEIGHT>
458.548

> <EXACT_MASS>
458.251582804

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
50.020074840248995

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-2-{4-[(3S,5S)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
0.9122494496666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.187889483064883

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.199090419450592

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7208398973095154

> <JCHEM_POLAR_SURFACE_AREA>
149.07

> <JCHEM_REFRACTIVITY>
116.39210000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-2-{4-[(3S,5S)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <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      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670 -14.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      17.338 -16.170   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      20.005 -16.170   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006 -13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.340 -14.630   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.674 -13.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.674 -12.320   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      28.007 -11.550   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      29.341 -12.320   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      30.675 -11.550   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      32.008 -12.320   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      33.342 -11.550   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      33.342 -10.010   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      32.008 -13.860   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      33.342 -14.630   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      30.675 -14.630   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      30.675 -16.170   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      29.341 -13.860   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      28.007 -14.630   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      25.340 -11.550   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      25.340 -10.010   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      24.006  -9.240   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      24.006 -12.320   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   32                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27                                                            
CONECT   29   16   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   13                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
(3S,5S)-1-[3-Methoxy-4-(b-D-glucopyranosyloxy)phenyl]decane-3,5-diol	Generator
(3S,5S)-1-[3-Methoxy-4-(β-D-glucopyranosyloxy)phenyl]decane-3,5-diol	Generator

Chemical Formula

C₂₃H₃₈O₉

Average Mass

458.5480 Da

Monoisotopic Mass

458.25158 Da

IUPAC Name

(2S,3R,4S,5S,6R)-2-{4-[(3S,5S)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3R,4S,5S,6R)-2-{4-[(3S,5S)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](O)C[C@@H](O)CCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(OC)=C1

InChI Identifier

InChI=1S/C23H38O9/c1-3-4-5-6-15(25)12-16(26)9-7-14-8-10-17(18(11-14)30-2)31-23-22(29)21(28)20(27)19(13-24)32-23/h8,10-11,15-16,19-29H,3-7,9,12-13H2,1-2H3/t15-,16-,19+,20+,21-,22+,23+/m0/s1

InChI Key

NIZBVVCYJIIIMW-MTLKXPBVSA-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
Zingiber officinale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
O-glycosyl compound
Fatty alcohol
Phenoxy compound
Methoxybenzene
Anisole
Phenol ether
Alkyl aryl ether
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Monosaccharide
Oxane
Secondary alcohol
Organoheterocyclic compound
Ether
Oxacycle
Polyol
Acetal
Hydrocarbon derivative
Alcohol
Primary alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	0.91	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	149.07 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	116.39 m³·mol⁻¹	ChemAxon
Polarizability	50.02 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

8727236

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10551845

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0201989)

MOL for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0201989 ((2s,3r,4s,5s,6r)-2-{4-[(3s,5s)-3,5-dihydroxydecyl]-2-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol)