NP-MRD: Showing NP-Card for trans-Neochlorogenic acid (NP0337442)

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Record Information

Version

2.0

Created at

2024-09-11 10:53:04 UTC

Updated at

2024-09-11 10:53:04 UTC

NP-MRD ID

NP0337442

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trans-Neochlorogenic acid

Description

Isochlorogenic acid, also known as isochlorogenate, belongs to the class of organic compounds known as quinic acids and derivatives. Quinic acids and derivatives are compounds containing a quinic acid moiety (or a derivative thereof), which is a cyclitol made up of a cyclohexane ring that bears four hydroxyl groups at positions 1,3.4, And 5, as well as a carboxylic acid at position 1. trans-Neochlorogenic acid was first documented in 2022 (PMID: 36055055). Based on a literature review a small amount of articles have been published on Isochlorogenic acid (PMID: 36068780) (PMID: 35959429) (PMID: 35930833) (PMID: 35921697).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
   -0.3388    1.9664   -1.3283 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2645    1.0800   -0.6833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7261    1.1089   -0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4434    0.2056   -0.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943    0.1797    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7199    1.0759   -0.6056 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1003    1.0053   -0.5320 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6839   -0.0041    0.2008 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0680   -0.0744    0.2743 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8783   -0.9212    0.8442 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4786   -1.9481    1.5897 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5044   -0.8211    0.7495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4866    0.1470   -0.0276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8875    0.2105   -0.0966 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5329    0.3678    1.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0490    0.3322    1.0163 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3121    1.2164   -0.0202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7887    0.7315    2.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6859    0.0603    3.2644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5959    1.8409    2.1985 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3552   -1.0953    0.5961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8160   -1.2330   -0.8145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5077   -0.3400   -1.6209 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3424   -1.0355   -0.8159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6897   -2.1278   -0.3012 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    1.8769   -1.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8436   -0.5373    0.5016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2762    1.8702   -1.1820 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7387    1.7336   -1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6445    0.5893   -0.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8836   -2.6106    2.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9358   -1.5755    1.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.0706   -0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3049   -0.4696    1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3186    1.3632    1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8176    2.0633    0.1051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4528    2.6509    1.6154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7983   -1.7815    1.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4391   -1.2947    0.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0282   -2.2744   -1.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2783   -0.8327   -2.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0172   -0.9170   -1.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3196   -2.8526   -0.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 16  1  0
 16 17  1  6
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 14 24  1  0
 24 25  1  0
 16 18  1  0
 18 20  1  0
 18 19  2  0
 24 22  1  0
 12  5  1  0
 23 41  1  0
 22 40  1  6
 21 38  1  0
 21 39  1  0
 17 36  1  0
 15 34  1  0
 15 35  1  0
 14 33  1  6
  3 26  1  0
  4 27  1  0
  6 28  1  0
  7 29  1  0
  9 30  1  0
 11 31  1  0
 12 32  1  0
 24 42  1  6
 25 43  1  0
 20 37  1  0
M  END


  Mrv1652309092215552D          

 25 26  0  0  1  0            999 V2000
    2.1434   -1.2375    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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   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
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8125    0.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    1.7435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2481    2.2322    0.0000 O   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
    1.4289    0.8250    0.0000 C   0  0  1  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
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
  2 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0337442

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1C[C@](O)(C[C@@H](OC(=O)\C=C\C2=CC=C(O)C(O)=C2)[C@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24,15(22)23)6-11(19)14(12)21/h1-5,11-12,14,17-19,21,24H,6-7H2,(H,22,23)/b4-2+/t11-,12-,14+,16+/m1/s1

> <INCHI_KEY>
CWVRJTMFETXNAD-BMNNCGMMSA-N

> <FORMULA>
C16H18O9

> <MOLECULAR_WEIGHT>
354.311

> <EXACT_MASS>
354.09508216

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
33.428987202837874

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,4S,5R)-3-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid

> <JCHEM_LOGP>
-0.26852975799999984

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.20854914523281

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3338531471838464

> <JCHEM_PKA_STRONGEST_BASIC>
-3.231823980915407

> <JCHEM_POLAR_SURFACE_AREA>
164.75

> <JCHEM_REFRACTIVITY>
83.23469999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4S,5R)-3-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+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       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.517   1.273   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.527   2.987   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.043   3.255   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.463   4.167   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5                                                       
CONECT   13    2   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   21                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   14   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
Isochlorogenate	Generator
(1S,3R,4S,5R)-3-(((2E)-3-(3,4-Dihydroxyphenyl)-2-propenoyl)oxy)-1,4,5-trihydroxycyclohexanecarboxylic acid	MeSH

Chemical Formula

C₁₆H₁₈O₉

Average Mass

354.3110 Da

Monoisotopic Mass

354.09508 Da

IUPAC Name

(1S,3R,4S,5R)-3-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid

Traditional Name

(1S,3R,4S,5R)-3-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

O[C@@H]1C[C@](O)(C[C@@H](OC(=O)\C=C\C2=CC=C(O)C(O)=C2)[C@H]1O)C(O)=O

InChI Identifier

InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24,15(22)23)6-11(19)14(12)21/h1-5,11-12,14,17-19,21,24H,6-7H2,(H,22,23)/b4-2+/t11-,12-,14+,16+/m1/s1

InChI Key

CWVRJTMFETXNAD-BMNNCGMMSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinic acids and derivatives. Quinic acids and derivatives are compounds containing a quinic acid moiety (or a derivative thereof), which is a cyclitol made up of a cyclohexane ring that bears four hydroxyl groups at positions 1,3.4, And 5, as well as a carboxylic acid at position 1.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Quinic acids and derivatives

Alternative Parents

Substituents

Quinic acid
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Cyclohexanol
Fatty acid ester
Phenol
Fatty acyl
Hydroxy acid
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha-hydroxy acid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Polyol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	-0.27	ChemAxon
pKa (Strongest Acidic)	3.33	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	164.75 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	83.23 m³·mol⁻¹	ChemAxon
Polarizability	33.43 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

C00002751

Chemspider ID

4940887

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Chlorogenic acid

METLIN ID

Not Available

PubChem Compound

6436237

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhu Y, Gu W, Tian R, Li C, Ji Y, Li T, Wei C, Chen Z: Morphological, physiological, and secondary metabolic responses of Taraxacum officinale to salt stress. Plant Physiol Biochem. 2022 Oct 15;189:71-82. doi: 10.1016/j.plaphy.2022.08.002. Epub 2022 Aug 19. [PubMed:36055055 ]
Xavier-Santos JB, Passos JGR, Gomes JAS, Cruz JVC, Alves JSF, Garcia VB, da Silva RM, Lopes NP, Araujo-Junior RF, Zucolotto SM, Silva-Junior AA, Felix-Silva J, Fernandes-Pedrosa MF: Topical gel containing phenolic-rich extract from Ipomoea pes-capre leaf (Convolvulaceae) has anti-inflammatory, wound healing, and antiophidic properties. Biomed Pharmacother. 2022 May;149:112921. doi: 10.1016/j.biopha.2022.112921. Epub 2022 Apr 7. [PubMed:36068780 ]
Zheng L, Lin G, Li R, Gan H, Huang X, Yao N, Cai D, Zhao Z, Hu Z, Li M, Xu H, Li L, Peng S, Zhao X, Lai Y, Chen Y, Huang D: Isochlorogenic Acid C Alleviates High-Fat Diet-Induced Hyperlipemia by Promoting Cholesterol Reverse Transport. Front Pharmacol. 2022 Jul 25;13:881078. doi: 10.3389/fphar.2022.881078. eCollection 2022. [PubMed:35959429 ]
Bian GL, Wang DM, Cheng XJ, Li DQ: Rapid screening of natural-origin tyrosinase regulators from Vernonia anthelmintica (L.) Willd. by offline two-dimensional liquid chromatography coupled with mass spectrometry. J Pharm Biomed Anal. 2022 Sep 20;219:114978. doi: 10.1016/j.jpba.2022.114978. Epub 2022 Aug 1. [PubMed:35930833 ]
Tian Z, Sun L, Chi B, Du Z, Zhang X, Liu Y, Zhou H: Affinity ultrafiltration and UPLC-HR-Orbitrap-MS based screening of neuraminidase inhibitors from Angelica pubescens. J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Oct 1;1208:123398. doi: 10.1016/j.jchromb.2022.123398. Epub 2022 Jul 28. [PubMed:35921697 ]

Showing NP-Card for trans-Neochlorogenic acid (NP0337442)

MOL for NP0337442 (trans-Neochlorogenic acid)

3D MOL for NP0337442 (trans-Neochlorogenic acid)

3D SDF for NP0337442 (trans-Neochlorogenic acid)

3D-SDF for NP0337442 (trans-Neochlorogenic acid)

PDB for NP0337442 (trans-Neochlorogenic acid)

3D PDB for NP0337442 (trans-Neochlorogenic acid)

SMILES for NP0337442 (trans-Neochlorogenic acid)

INCHI for NP0337442 (trans-Neochlorogenic acid)

Structure for NP0337442 (trans-Neochlorogenic acid)

3D Structure for NP0337442 (trans-Neochlorogenic acid)