NP-MRD: Showing NP-Card for 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol (NP0303447)

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Record Information

Version

2.0

Created at

2022-09-10 17:48:14 UTC

Updated at

2022-09-10 17:48:15 UTC

NP-MRD ID

NP0303447

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol

Description

2-({[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol 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. 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol is found in Atractylodes lancea. 2-({[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004191513252D          

 32 33  0  0  0  0            999 V2000
   -3.1526   -2.9314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3322   -2.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9966   -2.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1761   -2.0052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8406   -1.2515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3255   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9899    0.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4492    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6777    3.9692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5846    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1661    1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3155   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1360   -0.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0201   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4648   -1.8327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4815   -1.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9664   -0.7566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -0.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9363    0.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4212    1.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0856    1.9994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5706    2.6669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3911    2.5806    0.0000 O   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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  3  0  0  0  0
 26 27  1  0  0  0  0
 27 28  3  0  0  0  0
 29 28  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END


  Mrv1533004191513252D          

 32 33  0  0  0  0            999 V2000
   -3.1526   -2.9314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3322   -2.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9966   -2.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1761   -2.0052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8406   -1.2515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3255   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9899    0.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4492    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6777    3.9692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5846    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1661    1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3155   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1360   -0.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0201   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4648   -1.8327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4815   -1.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9664   -0.7566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -0.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9363    0.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4212    1.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0856    1.9994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5706    2.6669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3911    2.5806    0.0000 O   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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  3  0  0  0  0
 26 27  1  0  0  0  0
 27 28  3  0  0  0  0
 29 28  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303447

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C#CC#CC=CCO

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O11/c1-2-13(8-6-4-3-5-7-9-22)31-19-17(26)16(25)15(24)14(32-19)10-29-20-18(27)21(28,11-23)12-30-20/h5,7,13-20,22-28H,2,9-12H2,1H3

> <INCHI_KEY>
GSJDAQQWMTXNPK-UHFFFAOYSA-N

> <FORMULA>
C21H30O11

> <MOLECULAR_WEIGHT>
458.46

> <EXACT_MASS>
458.178811786

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
48.08850121437891

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.28

> <JCHEM_LOGP>
-1.8420127039999996

> <ALOGPS_LOGS>
-2.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.317064261820434

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.70447170333313

> <JCHEM_PKA_STRONGEST_BASIC>
-2.550541112544824

> <JCHEM_POLAR_SURFACE_AREA>
178.53

> <JCHEM_REFRACTIVITY>
110.02529999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.48e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -5.885  -5.472   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.353  -5.311   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.727  -3.904   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.195  -3.743   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.569  -2.336   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.474  -1.090   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.848   0.317   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.753   1.562   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.127   2.969   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.032   4.215   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.572   4.215   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.048   5.680   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.802   6.585   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.832   7.729   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.771   7.729   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.265   7.409   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.556   5.680   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.091   6.156   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.316   0.478   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.310   1.884   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.589  -0.768   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.120  -0.607   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.037  -2.175   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.868  -3.421   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -4.632  -2.658   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.537  -1.412   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.443  -0.166   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -7.348   1.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -8.253   2.325   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.627   3.732   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.532   4.978   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0     -10.063   4.817   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   17                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17   13   10   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    5   24                                                  
CONECT   24   23                                                            
CONECT   25    3   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₁₁

Average Mass

458.4600 Da

Monoisotopic Mass

458.17881 Da

IUPAC Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol

Traditional Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CCC(OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C#CC#CC=CCO

InChI Identifier

InChI=1S/C21H30O11/c1-2-13(8-6-4-3-5-7-9-22)31-19-17(26)16(25)15(24)14(32-19)10-29-20-18(27)21(28,11-23)12-30-20/h5,7,13-20,22-28H,2,9-12H2,1H3

InChI Key

GSJDAQQWMTXNPK-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Atractylodes lancea	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
Disaccharide
Glycosyl compound
O-glycosyl compound
Fatty alcohol
Oxane
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
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	-0.28	ALOGPS
logP	-1.8	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	11.7	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	178.53 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	110.03 m³·mol⁻¹	ChemAxon
Polarizability	48.09 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

85414667

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol (NP0303447)

MOL for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

3D MOL for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

3D SDF for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

3D-SDF for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

PDB for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

3D PDB for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

SMILES for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

INCHI for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

Structure for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)

3D Structure for NP0303447 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(10-hydroxydec-8-en-4,6-diyn-3-yl)oxy]oxane-3,4,5-triol)