NP-MRD: Showing NP-Card for [(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate (NP0149090)

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Record Information

Version

2.0

Created at

2022-09-02 04:55:51 UTC

Updated at

2022-09-02 04:55:51 UTC

NP-MRD ID

NP0149090

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

Description

Benzoylalbiflorin belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. [(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate is found in Paeonia lactiflora. [(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate was first documented in 2007 (PMID: 18038896). Based on a literature review a significant number of articles have been published on Benzoylalbiflorin (PMID: 28468284) (PMID: 30111055) (PMID: 33558884) (PMID: 28567056) (PMID: 17199256).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206552D          

 42 47  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309022206552D          

 42 47  0  0  1  0            999 V2000
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    3.4361   -2.1164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2089   -2.9095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8630   -1.5231    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0625   -1.7228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3246   -0.8410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1829   -1.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3896   -2.0065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2518   -2.8199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8874   -3.3459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5215   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6592   -3.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4325   -4.2082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0681   -3.6822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9304   -2.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1570   -2.5814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -0.4139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2057   -0.7288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7036    0.4249    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  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  1  0  0  0
  8 29  1  0  0  0  0
  6 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 29 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
  2 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149090

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12C[C@@H](O)C3C[C@@]1(O[C@@H]1O[C@H](COC(=O)C4=CC=CC=C4)[C@@H](O)[C@H](O)[C@H]1O)C3(COC(=O)C1=CC=CC=C1)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C30H32O12/c1-28-13-19(31)18-12-30(28,29(18,27(37)42-28)15-39-25(36)17-10-6-3-7-11-17)41-26-23(34)22(33)21(32)20(40-26)14-38-24(35)16-8-4-2-5-9-16/h2-11,18-23,26,31-34H,12-15H2,1H3/t18?,19-,20-,21-,22+,23-,26+,28?,29?,30+/m1/s1

> <INCHI_KEY>
ZHQGREQIJCCKHT-TUSVETBFSA-N

> <FORMULA>
C30H32O12

> <MOLECULAR_WEIGHT>
584.574

> <EXACT_MASS>
584.18937647

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
58.38363773124823

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(1R,4R)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0^{3,9}]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

> <ALOGPS_LOGP>
0.82

> <JCHEM_LOGP>
1.3801929433333335

> <ALOGPS_LOGS>
-3.14

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.204492532284476

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.21044514378269

> <JCHEM_PKA_STRONGEST_BASIC>
-2.887210474601969

> <JCHEM_POLAR_SURFACE_AREA>
178.28

> <JCHEM_REFRACTIVITY>
140.45740000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(1R,4R)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0^{3,9}]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       2.502   2.662   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.878   1.090   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.421   1.488   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.238   0.136   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.907   0.061   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.247  -1.115   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.464  -2.242   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.259  -0.459   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.551  -0.102   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.768  -1.363   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.263  -0.990   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.333  -2.097   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.827  -1.725   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.897  -2.832   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.391  -2.459   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.815  -0.979   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      13.461  -3.567   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.955  -3.194   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.025  -4.302   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.601  -5.782   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.107  -6.155   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.037  -5.048   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.908  -3.578   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.978  -4.686   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.414  -3.951   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.990  -5.431   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.344  -2.843   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.850  -3.216   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.473  -1.570   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.208  -3.195   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.727  -3.745   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.470  -5.264   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.657  -6.246   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.973  -5.800   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.230  -7.319   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.674  -7.855   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.860  -6.873   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.603  -5.355   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.160  -4.819   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.089  -0.773   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -0.384  -1.360   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       1.313   0.793   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8   42                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   29                                                  
CONECT    7    6    8                                                       
CONECT    8    7    2    9   29                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   12   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   10   28                                                  
CONECT   28   27                                                            
CONECT   29    8    6   30   40                                             
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
CONECT   40   29   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40    2                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₂O₁₂

Average Mass

584.5740 Da

Monoisotopic Mass

584.18938 Da

IUPAC Name

[(2R,3S,4S,5R,6S)-6-{[(1R,4R)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0^{3,9}]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

Traditional Name

[(2R,3S,4S,5R,6S)-6-{[(1R,4R)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0^{3,9}]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

CAS Registry Number

Not Available

SMILES

CC12C[C@@H](O)C3C[C@@]1(O[C@@H]1O[C@H](COC(=O)C4=CC=CC=C4)[C@@H](O)[C@H](O)[C@H]1O)C3(COC(=O)C1=CC=CC=C1)C(=O)O2

InChI Identifier

InChI=1S/C30H32O12/c1-28-13-19(31)18-12-30(28,29(18,27(37)42-28)15-39-25(36)17-10-6-3-7-11-17)41-26-23(34)22(33)21(32)20(40-26)14-38-24(35)16-8-4-2-5-9-16/h2-11,18-23,26,31-34H,12-15H2,1H3/t18?,19-,20-,21-,22+,23-,26+,28?,29?,30+/m1/s1

InChI Key

ZHQGREQIJCCKHT-TUSVETBFSA-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
Paeonia lactiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Terpene lactone
O-glycosyl compound
Glycosyl compound
Monoterpenoid
Nopinane monoterpenoid
Pinane monoterpenoid
Benzoate ester
Aromatic monoterpenoid
Tricarboxylic acid or derivatives
Benzoic acid or derivatives
Caprolactone
Benzoyl
Oxepane
Benzenoid
Oxane
Monosaccharide
Gamma butyrolactone
Monocyclic benzene moiety
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	0.82	ALOGPS
logP	1.38	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	178.28 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	140.46 m³·mol⁻¹	ChemAxon
Polarizability	58.38 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

102000323

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Bi X, Han L, Qu T, Mu Y, Guan P, Qu X, Wang Z, Huang X: Anti-Inflammatory Effects, SAR, and Action Mechanism of Monoterpenoids from Radix Paeoniae Alba on LPS-Stimulated RAW 264.7 Cells. Molecules. 2017 Apr 29;22(5):715. doi: 10.3390/molecules22050715. [PubMed:28468284 ]
Li R, Li YC, Wu YZ, Wang LY, Qiu BL, Zhang JF, Lin S: [Chemical constituents from water-soluble extract of dry roots of Paeonia lactiflora]. Zhongguo Zhong Yao Za Zhi. 2018 Jul;43(14):2956-2963. doi: 10.19540/j.cnki.cjcmm.20170512.010. [PubMed:30111055 ]
Wu Y, Jiang Y, Zhang L, Zhou J, Yu Y, Zhou Y, Kang T: Chemical Profiling and Antioxidant Evaluation of Paeonia lactiflora Pall. "Zhongjiang" by HPLC-ESI-MS Combined with DPPH Assay. J Chromatogr Sci. 2021 Sep 29;59(9):795-805. doi: 10.1093/chromsci/bmab005. [PubMed:33558884 ]
Zhou C, Wang X: Rapid Determination of Isomeric Benzoylpaeoniflorin and Benzoylalbiflorin in Rat Plasma by LC-MS/MS Method. Int J Anal Chem. 2017;2017:1693464. doi: 10.1155/2017/1693464. Epub 2017 May 8. [PubMed:28567056 ]
Yen PH, Kiem PV, Nhiem NX, Tung NH, Quang TH, Minh CV, Kim JW, Choi EM, Kim YH: A new monoterpene glycoside from the roots of Paeonia lactiflora increases the differentiation of osteoblastic MC3T3-E1 cells. Arch Pharm Res. 2007 Oct;30(10):1179-85. doi: 10.1007/BF02980258. [PubMed:18038896 ]
Li R, Wang X, Zhou Y, Cai M, Ding L: Analysis of sodium adduct paeoniflorin, albiflorin and their derivatives by (+)ESI-MSn, DFT calculations and computer-aided mass spectrometry analysis program. J Mass Spectrom. 2007 Mar;42(3):335-45. doi: 10.1002/jms.1164. [PubMed:17199256 ]
LOTUS database [Link]

Showing NP-Card for [(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate (NP0149090)

MOL for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D MOL for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D SDF for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D-SDF for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

PDB for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D PDB for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

SMILES for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

INCHI for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

Structure for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D Structure for NP0149090 ([(2r,3s,4s,5r,6s)-6-{[(1r,4r)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)