NP-MRD: Showing NP-Card for Undulatoside A (NP0139243)

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Record Information

Version

2.0

Created at

2022-06-29 19:45:40 UTC

Updated at

2022-06-29 19:45:41 UTC

NP-MRD ID

NP0139243

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Undulatoside A

Description

Undulatoside A 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. Undulatoside A is found in Camellia sinensis, Helichrysum arenarium and Sinoadina racemosa. Undulatoside A was first documented in 2006 (PMID: 17135054). Based on a literature review a significant number of articles have been published on Undulatoside A (PMID: 20708173) (PMID: 22932311) (PMID: 34738433) (PMID: 35807260) (PMID: 32364737) (PMID: 28882671).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
   -6.0466    1.6541    2.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1244    0.9528    1.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6420    0.2339    0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8074   -0.4113   -0.7535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2082   -1.0829   -1.7372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4469   -0.3136   -0.5487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5473   -0.9386   -1.4037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0355   -1.6654   -2.4709 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1835   -0.8506   -1.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7050   -0.1272   -0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6319   -0.0154    0.0730 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7047   -0.5322   -0.6185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4646   -1.3999    0.1627 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4177   -0.7946    0.9360 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8205    0.0595    2.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8297    0.6518    2.7914 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4869   -0.0712    0.1554 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7242   -0.6781    0.2282 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9900   -0.0198   -1.2947 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8376    0.7475   -2.0825 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5940    0.5627   -1.2267 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1431    0.8987   -2.5040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6122    0.4957    0.7008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9752    0.4165    0.5225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8240    1.0148    1.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4202    2.0010    3.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7889    0.9444    2.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5888    2.4752    1.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7100    0.1705   -0.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4852   -2.1488   -3.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5518   -1.3617   -1.9169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3808   -1.1296   -1.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9541   -1.6315    1.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2603   -0.6195    2.7198 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1353    0.8200    1.6512 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7927    0.3879    3.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5279    0.9887    0.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8904   -1.1374   -0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8916   -1.0634   -1.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0237    0.2213   -2.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5847    1.4793   -0.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8742    0.0522   -2.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2573    1.0738    1.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  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  1  0
 23 24  2  0
 24 25  1  0
 25  2  1  0
 24  6  1  0
 21 12  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  8 30  1  0
  9 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  1
 18 38  1  0
 19 39  1  6
 20 40  1  0
 21 41  1  1
 22 42  1  0
 23 43  1  0
M  END


  Mrv1652306292221452D          

 25 27  0  0  1  0            999 V2000
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
  9 13  1  0  0  0  0
 14 13  1  1  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
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 18 20  1  1  0  0  0
 20 21  1  0  0  0  0
 17 22  1  6  0  0  0
 16 23  1  1  0  0  0
 15 24  1  6  0  0  0
  7 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139243

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C2=C(O)C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O9/c1-6-2-8(18)12-9(19)3-7(4-10(12)23-6)24-16-15(22)14(21)13(20)11(5-17)25-16/h2-4,11,13-17,19-22H,5H2,1H3/t11-,13-,14+,15-,16-/m1/s1

> <INCHI_KEY>
BYYDEEAJCDGLER-YMILTQATSA-N

> <FORMULA>
C16H18O9

> <MOLECULAR_WEIGHT>
354.311

> <EXACT_MASS>
354.09508216

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
33.85617526527812

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-2-methyl-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

> <ALOGPS_LOGP>
-0.62

> <JCHEM_LOGP>
-0.35364546733333296

> <ALOGPS_LOGS>
-1.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.200087398926849

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.331252325957404

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343758667

> <JCHEM_POLAR_SURFACE_AREA>
145.91000000000003

> <JCHEM_REFRACTIVITY>
83.21340000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.75e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-2-methyl-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.670  -2.310   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      13.337  -0.000   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11    2                                                       
CONECT   13    9   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16   24                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   14                                                       
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   17                                                            
CONECT   23   16                                                            
CONECT   24   15                                                            
CONECT   25    7                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₈O₉

Average Mass

354.3110 Da

Monoisotopic Mass

354.09508 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2=C(O)C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2O1

InChI Identifier

InChI=1S/C16H18O9/c1-6-2-8(18)12-9(19)3-7(4-10(12)23-6)24-16-15(22)14(21)13(20)11(5-17)25-16/h2-4,11,13-17,19-22H,5H2,1H3/t11-,13-,14+,15-,16-/m1/s1

InChI Key

BYYDEEAJCDGLER-YMILTQATSA-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
Camellia sinensis	LOTUS Database	35616633
Helichrysum arenarium	LOTUS Database	35616633
Sinoadina racemosa	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
Hexose monosaccharide
Chromone
O-glycosyl compound
Benzopyran
1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Monosaccharide
Oxane
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Organoheterocyclic compound
Polyol
Oxacycle
Acetal
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
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

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

4479215

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5321494

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hakki Z, Cao B, Heskes AM, Goodger JQ, Woodrow IE, Williams SJ: Synthesis of the monoterpenoid esters cypellocarpin C and cuniloside B and evidence for their widespread occurrence in Eucalyptus. Carbohydr Res. 2010 Sep 23;345(14):2079-84. doi: 10.1016/j.carres.2010.07.029. Epub 2010 Jul 21. [PubMed:20708173 ]
Kim SB, Ahn JH, Han SB, Hwang BY, Kim SY, Lee MK: Anti-adipogenic chromone glycosides from Cnidium monnieri fruits in 3T3-L1 cells. Bioorg Med Chem Lett. 2012 Oct 1;22(19):6267-71. doi: 10.1016/j.bmcl.2012.07.103. Epub 2012 Aug 8. [PubMed:22932311 ]
Duan ZW, Zhang J, Chen XJ, Pang X, Ma BP: [Non-alkaloid constituents of Hymenocallis littoralis]. Zhongguo Zhong Yao Za Zhi. 2021 Oct;46(20):5304-5309. doi: 10.19540/j.cnki.cjcmm.20210610.320. [PubMed:34738433 ]
Rahayu I, Timotius KH: Phytochemical Analysis, Antimutagenic and Antiviral Activity of Moringa oleifera L. Leaf Infusion: In Vitro and In Silico Studies. Molecules. 2022 Jun 22;27(13):4017. doi: 10.3390/molecules27134017. [PubMed:35807260 ]
Pereira LCO, Abreu LS, Silva JPRE, Machado FSVL, Queiroga CS, do Espi Rito-Santo RF, Agnelo-Silva DF, Villarreal CF, Agra MF, Scotti MT, Costa VCO, Tavares JF, Silva MSD: Bioactive Compounds from the Aerial Parts of Evolvulus linarioides. J Nat Prod. 2020 May 22;83(5):1515-1523. doi: 10.1021/acs.jnatprod.9b01189. Epub 2020 May 4. [PubMed:32364737 ]
Yu J, Song X, Wang D, Wang X, Wang X: Five new chromone glycosides from Scindapsus officinalis (Roxb.) Schott. Fitoterapia. 2017 Oct;122:101-106. doi: 10.1016/j.fitote.2017.09.002. Epub 2017 Sep 4. [PubMed:28882671 ]
Peng B, Bai RF, Li P, Han XY, Wang H, Zhu CC, Zeng ZP, Chai XY: Two new glycosides from Dryopteris fragrans with anti-inflammatory activities. J Asian Nat Prod Res. 2016;18(1):59-64. doi: 10.1080/10286020.2015.1121853. Epub 2015 Dec 24. [PubMed:26700189 ]
Wang YB, Huang R, Zhang HB, Li L: Chromone glycosides from Knoxia corymbosa. J Asian Nat Prod Res. 2006 Oct-Nov;8(7):663-70. doi: 10.1080/10286020500246303. [PubMed:17135054 ]

Showing NP-Card for Undulatoside A (NP0139243)

MOL for NP0139243 (Undulatoside A)

3D MOL for NP0139243 (Undulatoside A)

3D SDF for NP0139243 (Undulatoside A)

3D-SDF for NP0139243 (Undulatoside A)

PDB for NP0139243 (Undulatoside A)

3D PDB for NP0139243 (Undulatoside A)

SMILES for NP0139243 (Undulatoside A)

INCHI for NP0139243 (Undulatoside A)

Structure for NP0139243 (Undulatoside A)

3D Structure for NP0139243 (Undulatoside A)