NP-MRD: Showing NP-Card for Forsythoside B (NP0071241)

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Record Information

Version

2.0

Created at

2022-04-28 16:38:01 UTC

Updated at

2022-04-28 16:38:01 UTC

NP-MRD ID

NP0071241

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Forsythoside B

Description

Forsythoside B belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. Forsythoside B is found in Amphilophium crucigerum, Ballota nigra, Barleria lupulina , Buddleja yunnanensis, Callicarpa japonica, Callicarpa japonica Thunb.var.luxurians Rehd., Forsythia koreana, Forsythia suspensa , Jasminum nudiflorum, Phlomoides rotata, Lippia alba , Marrubium alysson, Marrubium velutinum, Marrubium vulgare , Pedicularis nordmanniana, Penstemon griffinii, Phlomis armeniaca, Phlomis aurea, Phlomis brunneogaleata, Phlomis caucasica, Phlomis herba-venti, Phlomis lycia, Phlomis spinidens, Phlomoides tuberosa, Phlomoides umbrosa, Phtheirospermum japonicum, Pithecotenium crucigerum (L.) A.H Gentry, Verbascum phlomoides, Verbascum thapsus and Verbascum wiedemannianum. Forsythoside B was first documented in 2021 (PMID: 35153761). Based on a literature review a small amount of articles have been published on Forsythoside B (PMID: 34678528) (PMID: 34184069) (PMID: 33920316) (PMID: 33916300).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218382D          

 53 57  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652304282218382D          

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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
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 48 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0071241

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OCCC3=CC=C(O)C(O)=C3)O[C@H](CO[C@@H]3OC[C@](O)(CO)[C@H]3O)[C@H]2OC(=O)\C=C\C2=CC(O)=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H44O19/c1-15-24(41)25(42)26(43)32(50-15)53-29-27(44)31(47-9-8-17-3-6-19(37)21(39)11-17)51-22(12-48-33-30(45)34(46,13-35)14-49-33)28(29)52-23(40)7-4-16-2-5-18(36)20(38)10-16/h2-7,10-11,15,22,24-33,35-39,41-46H,8-9,12-14H2,1H3/b7-4+/t15-,22+,24-,25+,26+,27+,28+,29+,30-,31+,32-,33+,34+/m0/s1

> <INCHI_KEY>
JMBINOWGIHWPJI-UNSOMVRXSA-N

> <FORMULA>
C34H44O19

> <MOLECULAR_WEIGHT>
756.707

> <EXACT_MASS>
756.247679197

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
73.61695011232143

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R,5R,6R)-2-({[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.41

> <JCHEM_LOGP>
-0.4570736996666669

> <ALOGPS_LOGS>
-2.62

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.641420318014273

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.009667028487426

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9475494467417507

> <JCHEM_POLAR_SURFACE_AREA>
304.21

> <JCHEM_REFRACTIVITY>
175.0733

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.82e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5R,6R)-2-({[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <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      -3.796 -12.640   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.701 -13.886   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.233 -13.725   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.859 -12.318   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.954 -11.072   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.422 -11.233   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.517  -9.988   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.143  -8.581   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.238  -7.335   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.714  -5.870   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.468  -4.965   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.222  -5.870   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.698  -7.335   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -3.224  -3.623   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.712  -3.623   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.172  -3.607   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -5.179  -5.394   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -8.390 -12.157   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -9.017 -10.751   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -10.548 -10.590   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -11.175  -9.183   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.706  -9.022   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -13.333  -7.615   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -12.428  -6.369   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -10.896  -6.530   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -10.270  -7.937   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -9.991  -5.284   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -13.054  -4.962   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -7.138 -14.971   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -4.075 -15.293   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.980 -16.539   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -6.511 -16.378   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -7.417 -17.624   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.790 -19.031   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.259 -19.192   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.353 -17.946   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.822 -18.107   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -4.632 -20.599   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -7.695 -20.277   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -8.948 -17.463   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -2.264 -12.801   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -1.359 -11.555   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -1.985 -10.149   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       0.173 -11.716   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.078 -10.470   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.609 -10.631   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.514  -9.386   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       5.046  -9.547   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.672 -10.953   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       4.767 -12.199   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       3.236 -12.038   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       7.204 -11.114   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       5.951  -8.301   0.000  0.00  0.00           O+0
CONECT    1    2    6   41                                                  
CONECT    2    1    3   30                                                  
CONECT    3    2    4   29                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12   14   15                                             
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14   11                                                            
CONECT   15   11   16                                                       
CONECT   16   15                                                            
CONECT   17   10                                                            
CONECT   18    4   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   21                                                       
CONECT   27   25                                                            
CONECT   28   24                                                            
CONECT   29    3                                                            
CONECT   30    2   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   40                                                  
CONECT   34   33   35   39                                                  
CONECT   35   34   36   38                                                  
CONECT   36   35   31   37                                                  
CONECT   37   36                                                            
CONECT   38   35                                                            
CONECT   39   34                                                            
CONECT   40   33                                                            
CONECT   41    1   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   53                                                  
CONECT   49   48   50   52                                                  
CONECT   50   49   51                                                       
CONECT   51   50   46                                                       
CONECT   52   49                                                            
CONECT   53   48                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₄O₁₉

Average Mass

756.7070 Da

Monoisotopic Mass

756.24768 Da

IUPAC Name

(2R,3R,4R,5R,6R)-2-({[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OCCC3=CC=C(O)C(O)=C3)O[C@H](CO[C@@H]3OC[C@](O)(CO)[C@H]3O)[C@H]2OC(=O)\C=C\C2=CC(O)=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C34H44O19/c1-15-24(41)25(42)26(43)32(50-15)53-29-27(44)31(47-9-8-17-3-6-19(37)21(39)11-17)51-22(12-48-33-30(45)34(46,13-35)14-49-33)28(29)52-23(40)7-4-16-2-5-18(36)20(38)10-16/h2-7,10-11,15,22,24-33,35-39,41-46H,8-9,12-14H2,1H3/b7-4+/t15-,22+,24-,25+,26+,27+,28+,29+,30-,31+,32-,33+,34+/m0/s1

InChI Key

JMBINOWGIHWPJI-UNSOMVRXSA-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
Amphilophium crucigerum	LOTUS Database	35616633
Ballota nigra	LOTUS Database	35616633
Barleria lupulina	Plant	KNApSAcK
Buddleja yunnanensis	LOTUS Database	35616633
Callicarpa japonica	LOTUS Database	35616633
Callicarpa japonica Thunb.var.luxurians Rehd.	Plant	KNApSAcK
Forsythia koreana	LOTUS Database	35616633
Forsythia suspensa	Plant	KNApSAcK
Jasminum nudiflorum	LOTUS Database	35616633
Lamiophlomis rotata	LOTUS Database	35616633
Lippia alba	Plant	KNApSAcK
Marrubium alysson	LOTUS Database	35616633
Marrubium velutinum	Plant	KNApSAcK
Marrubium vulgare	Plant	KNApSAcK
Pedicularis nordmanniana	Plant	KNApSAcK
Penstemon griffinii	LOTUS Database	35616633
Phlomis armeniaca	LOTUS Database	35616633
Phlomis aurea	LOTUS Database	35616633
Phlomis brunneogaleata	Plant	KNApSAcK
Phlomis caucasica	Plant	KNApSAcK
Phlomis herba-venti	LOTUS Database	35616633
Phlomis lycia	LOTUS Database	35616633
Phlomis spinidens	Plant	KNApSAcK
Phlomoides tuberosa	LOTUS Database	35616633
Phlomoides umbrosa	LOTUS Database	35616633
Phtheirospermum japonicum	LOTUS Database	35616633
Pithecotenium crucigerum (L.) A.H Gentry	-	KNApSAcK
Verbascum phlomoides	LOTUS Database	35616633
Verbascum thapsus	LOTUS Database	35616633
Verbascum wiedemannianum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Glycosyl compound
O-glycosyl compound
Tyrosol derivative
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Monocyclic benzene moiety
Oxane
Fatty acyl
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Oxolane
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Acetal
Carbonyl group
Primary alcohol
Alcohol
Organic oxide
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	0.41	ALOGPS
logP	-0.46	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9.01	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	304.21 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	175.07 m³·mol⁻¹	ChemAxon
Polarizability	73.62 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

C00030317

Chemspider ID

22912890

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Forsythoside B

METLIN ID

Not Available

PubChem Compound

23928102

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li Y, Yang Y, Kang X, Li X, Wu Y, Xiao J, Ye Y, Yang J, Yang Y, Liu H: Study on The Anti-Inflammatory Effects of Callicarpa nudiflora Based on The Spectrum-Effect Relationship. Front Pharmacol. 2022 Jan 27;12:806808. doi: 10.3389/fphar.2021.806808. eCollection 2021. [PubMed:35153761 ]
Yang D, Li J, Liang C, Tian L, Shi C, Hui N, Liu Y, Ling M, Xin L, Wan M, Li H, Zhao Q, Ren X, Liu H, Cao W: Syringa microphylla Diels: A comprehensive review of its phytochemical, pharmacological, pharmacokinetic, and toxicological characteristics and an investigation into its potential health benefits. Phytomedicine. 2021 Dec;93:153770. doi: 10.1016/j.phymed.2021.153770. Epub 2021 Oct 12. [PubMed:34678528 ]
Kim JC, Kim HB, Shim WS, Kwak IS, Chung BY, Kang SY, Park CW, Kim HO: Activation of Transient Receptor Potential Vanilloid-3 Channels in Keratinocytes Induces Pruritus in Humans. Acta Derm Venereol. 2021 Aug 18;101(8):adv00517. doi: 10.2340/00015555-3855. [PubMed:34184069 ]
Torres-Vega J, Gomez-Alonso S, Perez-Navarro J, Alarcon-Enos J, Pastene-Navarrete E: Polyphenolic Compounds Extracted and Purified from Buddleja Globosa Hope (Buddlejaceae) Leaves Using Natural Deep Eutectic Solvents and Centrifugal Partition Chromatography. Molecules. 2021 Apr 10;26(8). pii: molecules26082192. doi: 10.3390/molecules26082192. [PubMed:33920316 ]
Senol Deniz FS, Eren G, Orhan IE, Sener B, Ozgen U, Aldaba R, Calis I: Outlining In Vitro and In Silico Cholinesterase Inhibitory Activity of Twenty-Four Natural Products of Various Chemical Classes: Smilagenin, Kokusaginine, and Methyl Rosmarinate as Emboldening Inhibitors. Molecules. 2021 Apr 1;26(7). pii: molecules26072024. doi: 10.3390/molecules26072024. [PubMed:33916300 ]

Showing NP-Card for Forsythoside B (NP0071241)

MOL for NP0071241 (Forsythoside B)

3D MOL for NP0071241 (Forsythoside B)

3D SDF for NP0071241 (Forsythoside B)

3D-SDF for NP0071241 (Forsythoside B)

PDB for NP0071241 (Forsythoside B)

3D PDB for NP0071241 (Forsythoside B)

SMILES for NP0071241 (Forsythoside B)

INCHI for NP0071241 (Forsythoside B)

Structure for NP0071241 (Forsythoside B)

3D Structure for NP0071241 (Forsythoside B)