NP-MRD: Showing NP-Card for Arteannumonoside D (NP0331502)

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Record Information

Version

2.0

Created at

2023-02-08 08:00:54 UTC

Updated at

2024-09-03 04:15:56 UTC

NP-MRD ID

NP0331502

Natural Product DOI

https://doi.org/10.57994/0462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Arteannumonoside D

Description

Arteannumonoside D 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. Arteannumonoside D was first documented in 2023 (PMID: 36740572). Based on a literature review very few articles have been published on Arteannumonoside D.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652302082309002D          

 32 33  0  0  1  0            999 V2000
    3.2762   -3.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4557   -3.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1201   -2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6051   -2.0052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695   -1.2515    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4490   -1.1653    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9641   -1.8327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7544   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4189    0.1696    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9038    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5682    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0531    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0136    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9136    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7627    4.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984    0.2558    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2628    1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1135   -0.4116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2930   -0.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9708   -4.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3063   -4.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8214   -5.5149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1540   -5.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4888   -5.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3365   -6.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6720   -6.9360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1268   -4.9337    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 20  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
  2 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 32  2  0  0  0  0
M  END


  Mrv1652302082309002D          

 32 33  0  0  1  0            999 V2000
    3.2762   -3.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4557   -3.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1201   -2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6051   -2.0052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695   -1.2515    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4490   -1.1653    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9641   -1.8327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7544   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4189    0.1696    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9038    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5682    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0531    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0136    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9136    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7627    4.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984    0.2558    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2628    1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1135   -0.4116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2930   -0.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9708   -4.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3063   -4.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8214   -5.5149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1540   -5.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4888   -5.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3365   -6.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6720   -6.9360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1268   -4.9337    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 20  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
  2 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 32  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0331502

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CO[C@@H]1O[C@H](COC2OCC(O)(CO)C2O)[C@@H](O)[C@H](O)[C@H]1O)=C/C(=O)C(C)(C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O11/c1-5-20(3,4)13(23)6-11(2)7-29-18-16(26)15(25)14(24)12(32-18)8-30-19-17(27)21(28,9-22)10-31-19/h5-6,12,14-19,22,24-28H,1,7-10H2,2-4H3/b11-6+/t12-,14-,15+,16-,17?,18-,19?,21?/m1/s1

> <INCHI_KEY>
YKUZSVDRTPSLKE-ROWLOWAOSA-N

> <FORMULA>
C21H34O11

> <MOLECULAR_WEIGHT>
462.492

> <EXACT_MASS>
462.210111915

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.62377818445092

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5E)-7-{[(2R,3R,4S,5S,6R)-6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3,3,6-trimethylhepta-1,5-dien-4-one

> <JCHEM_LOGP>
-0.8954196746666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.318197098706097

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.705005079922756

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1423790163389214

> <JCHEM_POLAR_SURFACE_AREA>
175.37

> <JCHEM_REFRACTIVITY>
110.00369999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5E)-7-{[(2R,3R,4S,5S,6R)-6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3,3,6-trimethylhepta-1,5-dien-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-FEB-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-FEB-23         0                                  
HETATM    1  C   UNK     0       6.116  -6.557   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.584  -6.396   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.958  -4.989   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.863  -3.743   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.236  -2.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.705  -2.175   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.800  -3.421   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       5.142  -1.090   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.515   0.317   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.420   1.562   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.794   2.969   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.699   4.215   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.223   5.680   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.759   6.156   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.469   6.585   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.439   7.729   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.500   7.729   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.024   9.194   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.715   5.680   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.239   4.215   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.984   0.478   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.357   1.884   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.078  -0.768   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.547  -0.607   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.679  -7.642   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.305  -9.049   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.400 -10.294   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.154  -9.389   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.646 -11.200   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.495 -11.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.121 -12.947   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.837  -9.210   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   21                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   19                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19   12                                                       
CONECT   21    9   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    6   24                                                  
CONECT   24   23                                                            
CONECT   25    2   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31                                                       
CONECT   31   30                                                            
CONECT   32   26                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₄O₁₁

Average Mass

462.4920 Da

Monoisotopic Mass

462.21011 Da

IUPAC Name

(5E)-7-{[(2R,3R,4S,5S,6R)-6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3,3,6-trimethylhepta-1,5-dien-4-one

Traditional Name

(5E)-7-{[(2R,3R,4S,5S,6R)-6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3,3,6-trimethylhepta-1,5-dien-4-one

CAS Registry Number

Not Available

SMILES

C\C(CO[C@@H]1O[C@H](COC2OCC(O)(CO)C2O)[C@@H](O)[C@H](O)[C@H]1O)=C/C(=O)C(C)(C)C=C

InChI Identifier

InChI=1S/C21H34O11/c1-5-20(3,4)13(23)6-11(2)7-29-18-16(26)15(25)14(24)12(32-18)8-30-19-17(27)21(28,9-22)10-31-19/h5-6,12,14-19,22,24-28H,1,7-10H2,2-4H3/b11-6+/t12-,14-,15+,16-,17?,18-,19?,21?/m1/s1

InChI Key

YKUZSVDRTPSLKE-ROWLOWAOSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
1D_DEPT NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD3OD, experimental)	qiguo_wu@163.com	Not Available	Not Available	2024-05-11	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 500.11, CD₃OD, simulated)	Not Available	Not Available	Not Available	2024-05-11	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
annua		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These 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
Glycerolipid
Oxane
Monosaccharide
Alpha,beta-unsaturated ketone
Tetrahydrofuran
Tertiary alcohol
Enone
Acryloyl-group
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	-0.9	ChemAxon
pKa (Strongest Acidic)	11.71	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	175.37 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	110 m³·mol⁻¹	ChemAxon
Polarizability	47.62 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu QG, Huang LY, Fan MH, Chou GX, Wang YL: Anti-Inflammatory Activities of Monoterpene and Sesquiterpene Glycosides from the Aqueous Extract of Artemisia annua L. Chem Biodivers. 2023 Mar;20(3):e202201237. doi: 10.1002/cbdv.202201237. Epub 2023 Feb 21. [PubMed:36740572 ]

Showing NP-Card for Arteannumonoside D (NP0331502)

MOL for NP0331502 (Arteannumonoside D)

3D MOL for NP0331502 (Arteannumonoside D)

3D SDF for NP0331502 (Arteannumonoside D)

3D-SDF for NP0331502 (Arteannumonoside D)

PDB for NP0331502 (Arteannumonoside D)

3D PDB for NP0331502 (Arteannumonoside D)

SMILES for NP0331502 (Arteannumonoside D)

INCHI for NP0331502 (Arteannumonoside D)

Structure for NP0331502 (Arteannumonoside D)

3D Structure for NP0331502 (Arteannumonoside D)