NP-MRD: Showing NP-Card for (5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one (NP0222015)

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Record Information

Version

2.0

Created at

2022-09-05 23:44:22 UTC

Updated at

2022-09-05 23:44:22 UTC

NP-MRD ID

NP0222015

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one

Description

(5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one belongs to the class of organic compounds known as curcuminoids. These are aromatic compounds containing a curcumin moiety, which is composed of two aryl buten-2-one (feruloyl) chromophores joined by a methylene group. (5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one is found in Betula papyrifera and Betula pendula. Based on a literature review very few articles have been published on (5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062201442D          

 43 46  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309062201442D          

 43 46  0  0  1  0            999 V2000
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    0.2211   -5.5539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -5.5539    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4586   -4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -3.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -2.6961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -1.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836   -1.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -1.2671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.6961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836   -3.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836   -6.2684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6961   -5.5539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -5.5539    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9336   -4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -4.8395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9336   -6.2684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7586   -6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -6.9829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9336   -7.6974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -6.9829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2836   -7.6974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -8.4118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5165   -8.4981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6881   -9.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9736   -9.7175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4585  -10.3850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3605  -10.2696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5320  -11.0765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3605   -9.1655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5535   -9.3370    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  1  0  0  0  0
  4  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
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 13 23  1  6  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 35 34  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  6  0  0  0
 40 41  1  0  0  0  0
 38 42  1  0  0  0  0
 35 42  1  0  0  0  0
 42 43  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0222015

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](O[C@@H](CCC2=CC=C(O)C=C2)CC(=O)CCC2=CC=C(O)C=C2)[C@H](O[C@@H]2OC[C@](O)(CO)[C@H]2O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O13/c31-14-23-24(36)25(37)26(43-29-27(38)30(39,15-32)16-40-29)28(42-23)41-22(12-6-18-3-9-20(34)10-4-18)13-21(35)11-5-17-1-7-19(33)8-2-17/h1-4,7-10,22-29,31-34,36-39H,5-6,11-16H2/t22-,23+,24+,25-,26+,27-,28+,29-,30+/m0/s1

> <INCHI_KEY>
NUACGMYJCUJZFV-BYWUESOHSA-N

> <FORMULA>
C30H40O13

> <MOLECULAR_WEIGHT>
608.637

> <EXACT_MASS>
608.246891348

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
62.25465241984015

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one

> <JCHEM_LOGP>
0.6679576916666663

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.347708617868221

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.438257127477497

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810837682577036

> <JCHEM_POLAR_SURFACE_AREA>
215.82999999999996

> <JCHEM_REFRACTIVITY>
148.60340000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0       0.413  -7.700   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -0.357  -9.034   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.897  -9.034   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.207  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.977  -9.034   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.517  -9.034   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.287  -7.700   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.827  -7.700   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -6.517  -6.366   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.977  -6.366   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.413 -10.367   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.953 -10.367   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.723  -9.034   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.953  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.723  -6.366   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.953  -5.033   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.723  -3.699   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.263  -3.699   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.033  -2.365   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.033  -5.033   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.263  -6.366   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.723 -11.701   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.263 -11.701   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.033 -10.367   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.573 -10.367   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.343  -9.034   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.883  -9.034   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.343 -11.701   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.883 -11.701   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.573 -13.035   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.343 -14.368   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.033 -13.035   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.263 -14.368   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.033 -15.702   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.564 -15.863   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       6.884 -17.369   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.551 -18.139   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.456 -19.385   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       4.406 -19.170   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.726 -20.676   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.406 -17.109   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       2.900 -17.429   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5                                                       
CONECT   12    2   13                                                       
CONECT   13   12   14   23                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16                                                       
CONECT   23   13   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   42                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40   42                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40                                                            
CONECT   42   38   35   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₀O₁₃

Average Mass

608.6370 Da

Monoisotopic Mass

608.24689 Da

IUPAC Name

(5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one

Traditional Name

(5S)-5-{[(2R,3R,4S,5S,6R)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](O[C@@H](CCC2=CC=C(O)C=C2)CC(=O)CCC2=CC=C(O)C=C2)[C@H](O[C@@H]2OC[C@](O)(CO)[C@H]2O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C30H40O13/c31-14-23-24(36)25(37)26(43-29-27(38)30(39,15-32)16-40-29)28(42-23)41-22(12-6-18-3-9-20(34)10-4-18)13-21(35)11-5-17-1-7-19(33)8-2-17/h1-4,7-10,22-29,31-34,36-39H,5-6,11-16H2/t22-,23+,24+,25-,26+,27-,28+,29-,30+/m0/s1

InChI Key

NUACGMYJCUJZFV-BYWUESOHSA-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
Betula papyrifera	LOTUS Database	35616633
Betula pendula	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as curcuminoids. These are aromatic compounds containing a curcumin moiety, which is composed of two aryl buten-2-one (feruloyl) chromophores joined by a methylene group.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Linear diarylheptanoids

Direct Parent

Curcuminoids

Alternative Parents

Substituents

Bis-desmethoxycurcumin
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Oxane
Tetrahydrofuran
Tertiary alcohol
Ketone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	0.67	ChemAxon
pKa (Strongest Acidic)	9.44	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	215.83 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	148.6 m³·mol⁻¹	ChemAxon
Polarizability	62.25 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

162985559

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one (NP0222015)

MOL for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

3D MOL for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

3D SDF for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

3D-SDF for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

PDB for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

3D PDB for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

SMILES for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

INCHI for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

Structure for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)

3D Structure for NP0222015 ((5s)-5-{[(2r,3r,4s,5s,6r)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,7-bis(4-hydroxyphenyl)heptan-3-one)