NP-MRD: Showing NP-Card for methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate (NP0186312)

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Record Information

Version

2.0

Created at

2022-09-04 02:06:55 UTC

Updated at

2022-09-04 02:06:56 UTC

NP-MRD ID

NP0186312

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate

Description

Methyl (R)-8-Hydroxy-9-decene-4,6-diynoate glucoside 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. Methyl (R)-8-Hydroxy-9-decene-4,6-diynoate glucoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Methyl (R)-8-Hydroxy-9-decene-4,6-diynoate glucoside has been detected, but not quantified in, root vegetables. methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate is found in Helianthus tuberosus. This could make methyl (R)-8-hydroxy-9-decene-4,6-diynoate glucoside a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 47  0  0  0  0  0  0  0  0999 V2000
   -1.6503   -3.9469    1.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9778   -3.2137    0.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -1.7352    0.8159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5220   -1.3439    1.1796 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6556   -1.0378    1.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9928   -0.6944    1.7688 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1385   -0.4121    2.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5362   -0.0890    2.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9052    1.2443    1.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7133    1.1971    0.2009 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5398    1.3698   -0.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7417    0.9774   -0.6948 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4848    0.9461   -2.0774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0949   -1.1809   -0.4416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700   -0.2594   -0.4096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7276    0.9474   -0.8491 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6555    1.9049   -1.0148 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9237    2.6973    0.2704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3684    1.8119    1.2297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526    1.4772   -1.6142 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8543    1.5714   -3.0316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3938    0.0936   -1.2705 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9070    0.0943    0.0366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2314   -0.8649   -1.3316 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5488   -2.1053   -0.7977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6921   -5.0192    1.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -3.4390    2.4151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4806   -3.7042   -0.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5989   -1.2955    1.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1652   -0.8871    1.9048 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7030    0.0350    3.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9810    1.4427    1.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3492    2.0532    2.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4049    1.0784   -2.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0824    1.7092   -2.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8480   -0.0373   -2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5435   -0.2305    0.6327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2201    2.7211   -1.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0166    3.2593    0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7755    3.3885    0.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0763    2.1888    1.8108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7806    2.2074   -1.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7147    1.8540   -3.4014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1889   -0.2117   -1.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1928   -0.8080    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.9335   -2.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1745   -2.8548   -1.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  3  0
  6  5  1  0
  5  4  3  0
  4  3  1  0
  3 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
  3  2  1  0
  2  1  2  3
 24 15  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
  3 29  1  1
 15 37  1  1
 17 38  1  6
 18 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  1
 21 43  1  0
 22 44  1  6
 23 45  1  0
 24 46  1  6
 25 47  1  0
  2 28  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv0541 05061312142D          

 25 25  0  0  0  0            999 V2000
   -1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    7.4250    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
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  5  4  3  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  3  0  0  0  0
  9  7  1  0  0  0  0
 11  3  1  0  0  0  0
 11  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13  9  1  0  0  0  0
 14 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 10  1  0  0  0  0
 19 13  2  0  0  0  0
 20 14  1  0  0  0  0
 21 15  1  0  0  0  0
 22 16  1  0  0  0  0
 23  2  1  0  0  0  0
 23 13  1  0  0  0  0
 24 11  1  0  0  0  0
 24 17  1  0  0  0  0
 25 12  1  0  0  0  0
 25 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186312

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCC#CC#CC(OC1OC(CO)C(O)C(O)C1O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O8/c1-3-11(8-6-4-5-7-9-13(19)23-2)24-17-16(22)15(21)14(20)12(10-18)25-17/h3,11-12,14-18,20-22H,1,7,9-10H2,2H3

> <INCHI_KEY>
AVPBONMPAMZUKG-UHFFFAOYSA-N

> <FORMULA>
C17H22O8

> <MOLECULAR_WEIGHT>
354.3518

> <EXACT_MASS>
354.13146768

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
37.061224423160674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate

> <ALOGPS_LOGP>
0.02

> <JCHEM_LOGP>
-0.24524906600000093

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.199270663309804

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.208448668363165

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810842538717566

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
86.7884

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate

> <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      -2.667   7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002  13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  13.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  13.860   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  13.090   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.669  10.780   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.336  10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.336   8.470   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.002   7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.668  10.010   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -12.003  10.010   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       5.335  15.400   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -10.669   7.700   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -8.002   6.160   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -5.335   7.700   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.668  13.090   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -5.335  10.780   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -8.002  10.780   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2   23                                                            
CONECT    3    1   11                                                       
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   11                                                       
CONECT    9    7   13                                                       
CONECT   10   12   18                                                       
CONECT   11    3    8   24                                                  
CONECT   12   10   14   25                                                  
CONECT   13    9   19   23                                                  
CONECT   14   12   15   20                                                  
CONECT   15   14   16   21                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   24   25                                                  
CONECT   18   10                                                            
CONECT   19   13                                                            
CONECT   20   14                                                            
CONECT   21   15                                                            
CONECT   22   16                                                            
CONECT   23    2   13                                                       
CONECT   24   11   17                                                       
CONECT   25   12   17                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
Methyl (R)-8-hydroxy-9-decene-4,6-diynoic acid glucoside	Generator
Methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoic acid	Generator

Chemical Formula

C₁₇H₂₂O₈

Average Mass

354.3518 Da

Monoisotopic Mass

354.13147 Da

IUPAC Name

methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate

Traditional Name

methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCC#CC#CC(OC1OC(CO)C(O)C(O)C1O)C=C

InChI Identifier

InChI=1S/C17H22O8/c1-3-11(8-6-4-5-7-9-13(19)23-2)24-17-16(22)15(21)14(20)12(10-18)25-17/h3,11-12,14-18,20-22H,1,7,9-10H2,2H3

InChI Key

AVPBONMPAMZUKG-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, 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
Helianthus tuberosus	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
Fatty acid ester
Sugar acid
Fatty acid methyl ester
Oxane
Monosaccharide
Methyl ester
Secondary alcohol
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Acetal
Primary alcohol
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Organic oxygen compound
Alcohol
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	0.02	ALOGPS
logP	-0.25	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.68 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	86.79 m³·mol⁻¹	ChemAxon
Polarizability	37.06 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0040898

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB020734

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

131752979

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate (NP0186312)

MOL for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

3D MOL for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

3D SDF for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

3D-SDF for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

PDB for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

3D PDB for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

SMILES for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

INCHI for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

Structure for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)

3D Structure for NP0186312 (methyl 8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}dec-9-en-4,6-diynoate)