NP-MRD: Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0182509)

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Record Information

Version

2.0

Created at

2022-09-03 21:13:15 UTC

Updated at

2022-09-03 21:13:15 UTC

NP-MRD ID

NP0182509

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

Betulalbuside A belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. (2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Erigeron breviscapus and Pimpinella anisum. (2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol was first documented in 2004 (PMID: 15340194). Based on a literature review a small amount of articles have been published on Betulalbuside A (PMID: 30145331) (PMID: 21842649) (PMID: 20209954).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 51  0  0  0  0  0  0  0  0999 V2000
    6.5133   -0.5609   -0.7789 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8168    0.4627   -0.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3754    0.3466    0.0785 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6224    1.4310   -0.6432 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398    0.5647    1.4618 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8379   -0.9997   -0.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4185   -1.2694    0.0627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3990   -0.4433   -0.5652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5693    0.2865    0.1478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6490    0.2893    1.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4485    1.1442   -0.5027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7103    0.7438   -0.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0596   -0.5382   -0.4414 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0920   -0.4739   -1.3634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3016   -0.0920   -0.8723 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4443    1.4098   -1.1718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3756    1.5872   -2.5598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6231   -0.3465    0.5272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4345   -1.4963    0.6615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4804   -0.5359    1.4871 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9196    0.6847    1.8165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4229   -1.3415    0.7613 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8993   -2.6095    0.4227 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5554   -0.4586   -1.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0528   -1.5363   -0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3191    1.4157   -0.2006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1041    1.0761   -1.5453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9088    1.9254    0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3572    2.2252   -0.9775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3683    1.5450    1.5899 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458   -1.7545    0.3261 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0797   -1.2806   -1.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2151   -2.3362   -0.2727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151   -1.2150    1.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3017   -0.4258   -1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204    0.8058    1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5840   -0.7013    2.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1354    0.9153    2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3361    1.1686   -1.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3038    2.1718   -0.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2027   -1.0183   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0846   -0.5678   -1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6862    1.9892   -0.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4335    1.7233   -0.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5463    1.1838   -2.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2433    0.4903    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -1.4708    1.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8227   -1.0606    2.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5926    1.3533    2.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5642   -1.4930    1.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6228   -2.9135   -0.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  1
  3  2  1  0
  2  1  2  3
 22 13  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 13 41  1  6
 15 42  1  6
 16 43  1  0
 16 44  1  0
 17 45  1  0
 18 46  1  1
 19 47  1  0
 20 48  1  1
 21 49  1  0
 22 50  1  1
 23 51  1  0
  8 35  1  0
  7 33  1  0
  7 34  1  0
  6 31  1  0
  6 32  1  0
  4 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  2 26  1  0
  1 24  1  0
  1 25  1  0
M  END


  Mrv1652309032223132D          

 23 23  0  0  1  0            999 V2000
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    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
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0182509

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C/CCC(C)(O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C16H28O7/c1-4-16(3,21)7-5-6-10(2)9-22-15-14(20)13(19)12(18)11(8-17)23-15/h4,6,11-15,17-21H,1,5,7-9H2,2-3H3/b10-6+/t11-,12-,13+,14-,15-,16?/m1/s1

> <INCHI_KEY>
WEHZDNHJZBEGME-GTQRNPCRSA-N

> <FORMULA>
C16H28O7

> <MOLECULAR_WEIGHT>
332.393

> <EXACT_MASS>
332.183503242

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
34.49418589699117

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(2E)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.40411434966666676

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200070462264431

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210511039444665

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2849634550554079

> <JCHEM_POLAR_SURFACE_AREA>
119.61000000000001

> <JCHEM_REFRACTIVITY>
84.39459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(2E)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  13.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  12.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.127  10.780   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.207  10.780   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₈O₇

Average Mass

332.3930 Da

Monoisotopic Mass

332.18350 Da

IUPAC Name

(2R,3R,4S,5S,6R)-2-{[(2E)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2R,3R,4S,5S,6R)-2-{[(2E)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

C\C(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C/CCC(C)(O)C=C

InChI Identifier

InChI=1S/C16H28O7/c1-4-16(3,21)7-5-6-10(2)9-22-15-14(20)13(19)12(18)11(8-17)23-15/h4,6,11-15,17-21H,1,5,7-9H2,2-3H3/b10-6+/t11-,12-,13+,14-,15-,16?/m1/s1

InChI Key

WEHZDNHJZBEGME-GTQRNPCRSA-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
Erigeron breviscapus	LOTUS Database	35616633
Pimpinella anisum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Monoterpenoid
Monocyclic monoterpenoid
Oxane
Monosaccharide
Tertiary alcohol
Secondary alcohol
Polyol
Oxacycle
Acetal
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
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	-0.4	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	119.61 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	84.39 m³·mol⁻¹	ChemAxon
Polarizability	34.49 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

C00031629

Chemspider ID

28425445

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14484636

PDB ID

Not Available

ChEBI ID

174515

Good Scents ID

Not Available

References

General References

Morikawa H, Kasai R, Otsuka H, Hirata E, Shinzato T, Aramoto M, Takeda Y: Terpenic and phenolic glycosides from leaves of Breynia officinalis HEMSL. Chem Pharm Bull (Tokyo). 2004 Sep;52(9):1086-90. doi: 10.1248/cpb.52.1086. [PubMed:15340194 ]
Gou P, Xiao Y, Lv L, Xie H: Hydroquinone and terpene glucosides from Leontopodium leontopodioides and their lipase inhibitory activity. Fitoterapia. 2018 Oct;130:89-93. doi: 10.1016/j.fitote.2018.08.010. Epub 2018 Aug 23. [PubMed:30145331 ]
Zhang J, Li X, Ren L, Fang C, Wang F: [Chemical constituents from Exochorda racemosa]. Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1198-201. [PubMed:21842649 ]
Yan C, Wang Y, Hao X: [Water-soluble chemical constituents from fruits of Phellodendron chinense var. glabriusculum]. Zhongguo Zhong Yao Za Zhi. 2009 Nov;34(22):2895-7. [PubMed:20209954 ]
LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0182509)

MOL for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0182509 ((2r,3r,4s,5s,6r)-2-{[(2e)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)