NP-MRD: Showing NP-Card for Paeonoside (NP0051552)

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Record Information

Version

2.0

Created at

2022-04-27 22:52:29 UTC

Updated at

2022-04-27 22:52:29 UTC

NP-MRD ID

NP0051552

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Paeonoside

Description

Paeonoside belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Paeonoside is found in Exacum affine, Paeonia daurica, Paeonia arborea, Rhodiola wallichiana, Spiranthes australis (R.BROWN) LINDL. and Spiranthes vernalis. Paeonoside was first documented in 2006 (PMID: 16343840). Based on a literature review a small amount of articles have been published on Paeonoside (PMID: 34199016) (PMID: 22070681).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
    4.3940    3.1346    1.2226 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0896    2.6925    0.9064 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8838    1.3240    0.6413 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9237    0.4457    0.6903 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7264   -0.8760    0.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4560   -1.3486    0.1182 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3279   -2.7543   -0.1358 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0974   -3.4918   -0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3842   -3.4797   -0.0571 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3522   -0.5017    0.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1319   -0.7933   -0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1010   -1.0879   -0.5021 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6846   -0.2134   -1.4343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8971    0.2902   -1.0694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4537    1.1025   -2.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219    2.1639   -2.5706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7119    1.1841    0.1457 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9631    1.7689    0.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2876    0.2537    1.2628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2233    0.8738    1.9290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9152   -1.1129    0.8086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9590   -2.0146    0.7501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6451    0.8581    0.3323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6663    2.6393    2.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1010    2.8512    0.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3332    4.2504    1.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9087    0.7738    0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5929   -1.5567    0.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3557   -3.3904    0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7171   -3.1323   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3075   -4.5782   -0.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3137   -2.1106   -0.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6738   -0.4521   -0.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4272    1.5575   -1.9187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6382    0.4922   -3.1104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5212    2.8187   -1.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9761    1.9947   -0.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4460    1.2790    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1264    0.2415    1.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2383    0.5306    2.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1990   -1.5346    1.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8481   -2.6683    0.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8318    1.5765    0.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  6 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10 23  2  0
 23  3  1  0
 21 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
 12 32  1  6
 14 33  1  1
 15 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  6
 18 38  1  0
 19 39  1  1
 20 40  1  0
 21 41  1  1
 22 42  1  0
 23 43  1  0
M  END


  Mrv1652304282200522D          

 23 24  0  0  1  0            999 V2000
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  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
   -1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    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
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 12  1  0  0  0  0
 13 12  1  1  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  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  1  0  0  0
 19 20  1  0  0  0  0
 16 21  1  6  0  0  0
 15 22  1  1  0  0  0
 14 23  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0051552

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C(C)=O)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O8/c1-7(17)9-4-3-8(21-2)5-10(9)22-15-14(20)13(19)12(18)11(6-16)23-15/h3-5,11-16,18-20H,6H2,1-2H3/t11-,12-,13+,14-,15-/m1/s1

> <INCHI_KEY>
AVIUTYMRHHBXPB-UXXRCYHCSA-N

> <FORMULA>
C15H20O8

> <MOLECULAR_WEIGHT>
328.317

> <EXACT_MASS>
328.115817604

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
31.954136000497087

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)ethan-1-one

> <ALOGPS_LOGP>
-0.80

> <JCHEM_LOGP>
-1.1984113459999997

> <ALOGPS_LOGS>
-1.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.195021739505783

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.199989279625125

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092346267867

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
77.0493

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
paeonoside

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2    6   12                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    3   11                                                       
CONECT   11   10                                                            
CONECT   12    1   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   23                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   16                                                            
CONECT   22   15                                                            
CONECT   23   14                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₈

Average Mass

328.3170 Da

Monoisotopic Mass

328.11582 Da

IUPAC Name

1-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)ethan-1-one

Traditional Name

paeonoside

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C(C)=O)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

InChI Identifier

InChI=1S/C15H20O8/c1-7(17)9-4-3-8(21-2)5-10(9)22-15-14(20)13(19)12(18)11(6-16)23-15/h3-5,11-16,18-20H,6H2,1-2H3/t11-,12-,13+,14-,15-/m1/s1

InChI Key

AVIUTYMRHHBXPB-UXXRCYHCSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Exacum affine	LOTUS Database	35616633
Paeonia daurica	LOTUS Database	35616633
Paeonia suffruticosa	Plant	KNApSAcK
Rhodiola wallichiana	LOTUS Database	35616633
Spiranthes australis (R.BROWN) LINDL.	Plant	KNApSAcK
Spiranthes vernalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Alkyl-phenylketone
Hexose monosaccharide
O-glycosyl compound
Acetophenone
Phenylketone
Phenoxy compound
Anisole
Benzoyl
Phenol ether
Aryl ketone
Aryl alkyl ketone
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Oxane
Monosaccharide
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Acetal
Polyol
Ether
Hydrocarbon derivative
Alcohol
Primary alcohol
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

glycoside (CHEBI:7892 )

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	-0.8	ALOGPS
logP	-1.2	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	77.05 m³·mol⁻¹	ChemAxon
Polarizability	31.95 Å³	ChemAxon
Number of Rings	2	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

C00002706

Chemspider ID

391227

KEGG Compound ID

C10717

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442924

PDB ID

Not Available

ChEBI ID

7892

Good Scents ID

Not Available

References

General References

Park KR, Lee JY, Cho M, Hong JT, Yun HM: Biological Mechanisms of Paeonoside in the Differentiation of Pre-Osteoblasts and the Formation of Mineralized Nodules. Int J Mol Sci. 2021 Jun 27;22(13). pii: ijms22136899. doi: 10.3390/ijms22136899. [PubMed:34199016 ]
Lin B: Polyphenols and neuroprotection against ischemia and neurodegeneration. Mini Rev Med Chem. 2011 Dec;11(14):1222-38. doi: 10.2174/13895575111091222. [PubMed:22070681 ]
Chen G, Zhang L, Zhu Y: Determination of glycosides and sugars in Moutan Cortex by capillary electrophoresis with electrochemical detection. J Pharm Biomed Anal. 2006 Apr 11;41(1):129-34. doi: 10.1016/j.jpba.2005.11.001. Epub 2005 Dec 15. [PubMed:16343840 ]

Showing NP-Card for Paeonoside (NP0051552)

MOL for NP0051552 (Paeonoside)

3D MOL for NP0051552 (Paeonoside)

3D SDF for NP0051552 (Paeonoside)

3D-SDF for NP0051552 (Paeonoside)

PDB for NP0051552 (Paeonoside)

3D PDB for NP0051552 (Paeonoside)

SMILES for NP0051552 (Paeonoside)

INCHI for NP0051552 (Paeonoside)

Structure for NP0051552 (Paeonoside)

3D Structure for NP0051552 (Paeonoside)