NP-MRD: Showing NP-Card for (1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose (NP0351233)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2025-06-28 17:50:25 UTC

Updated at

2025-12-20 03:39:45 UTC

NP-MRD ID

NP0351233

Natural Product DOI

https://doi.org/10.57994/4223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose

Description

Based on a literature review very few articles have been published on (1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01022311002D          

 33 35  0  0  1  0            999 V2000
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    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  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  0  0  0  0
 13 14  1  0  0  0  0
  9 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
 16 18  2  0  0  0  0
 13 19  1  6  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
 21 31  2  0  0  0  0
 11 32  1  6  0  0  0
 32 33  1  0  0  0  0
M  END


  Mrv2104 01022311002D          

 33 35  0  0  1  0            999 V2000
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    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  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  0  0  0  0
 13 14  1  0  0  0  0
  9 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
 16 18  2  0  0  0  0
 13 19  1  6  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
 21 31  2  0  0  0  0
 11 32  1  6  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0351233

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1[C@@H](O)C(OC(=O)\C=C\C2=CC=C(O)C=C2)[C@@H](CO)O[C@H]1OC1CCCCC1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O10/c1-13(25)30-22-20(29)21(33-19(28)11-8-14-6-9-15(26)10-7-14)18(12-24)32-23(22)31-17-5-3-2-4-16(17)27/h6-11,16-18,20-24,26-27,29H,2-5,12H2,1H3/b11-8+/t16?,17?,18-,20+,21?,22?,23-/m1/s1

> <INCHI_KEY>
LDZUHBXDDJEQBQ-WSSVQWSESA-N

> <FORMULA>
C23H30O10

> <MOLECULAR_WEIGHT>
466.483

> <EXACT_MASS>
466.183897166

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.59705273162554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4S,6R)-5-(acetyloxy)-4-hydroxy-6-[(2-hydroxycyclohexyl)oxy]-2-(hydroxymethyl)oxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
1.6064050169999997

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.888950788142846

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398443151983576

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981808352060531

> <JCHEM_POLAR_SURFACE_AREA>
151.98000000000002

> <JCHEM_REFRACTIVITY>
113.7504

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,6R)-5-(acetyloxy)-4-hydroxy-6-[(2-hydroxycyclohexyl)oxy]-2-(hydroxymethyl)oxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-JAN-23         0                                  
HETATM    1  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.336 -11.550   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.336 -14.630   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.002 -16.940   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      12.003 -16.170   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      14.670 -14.630   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      21.339 -16.940   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.005 -16.170   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      24.006 -16.940   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      16.004 -12.320   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      14.670 -10.010   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   32                                                  
CONECT   12   11   13   20                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13                                                            
CONECT   20   12   21                                                       
CONECT   21   20   22   31                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
CONECT   30   27                                                            
CONECT   31   21                                                            
CONECT   32   11   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₁₀

Average Mass

466.4830 Da

Monoisotopic Mass

466.18390 Da

IUPAC Name

(2R,4S,6R)-5-(acetyloxy)-4-hydroxy-6-[(2-hydroxycyclohexyl)oxy]-2-(hydroxymethyl)oxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

(2R,4S,6R)-5-(acetyloxy)-4-hydroxy-6-[(2-hydroxycyclohexyl)oxy]-2-(hydroxymethyl)oxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1[C@@H](O)C(OC(=O)\C=C\C2=CC=C(O)C=C2)[C@@H](CO)O[C@H]1OC1CCCCC1O

InChI Identifier

InChI=1S/C23H30O10/c1-13(25)30-22-20(29)21(33-19(28)11-8-14-6-9-15(26)10-7-14)18(12-24)32-23(22)31-17-5-3-2-4-16(17)27/h6-11,16-18,20-24,26-27,29H,2-5,12H2,1H3/b11-8+/t16?,17?,18-,20+,21?,22?,23-/m1/s1

InChI Key

LDZUHBXDDJEQBQ-WSSVQWSESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 850 MHz, C2D6OS, experimental)	Not Available	Dongguk University	Hyunwoo Kim	2025-06-25	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 850 MHz, C2D6OS, experimental)	Not Available	Dongguk University	Hyunwoo Kim	2025-06-25	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 850 MHz, C2D6OS, experimental)	Not Available	Dongguk University	Hyunwoo Kim	2025-06-25	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 214 MHz, C2D6OS, experimental)	Not Available	Dongguk University	Hyunwoo Kim	2025-06-25	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 850 MHz, C2D6OS, experimental)	Not Available	Dongguk University	Hyunwoo Kim	2025-06-25	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Idesia polycarpa		Not Available

Chemical Taxonomy

Classification

Not classified

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	1.61	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	113.75 m³·mol⁻¹	ChemAxon
Polarizability	47.6 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose (NP0351233)

MOL for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

3D MOL for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

3D SDF for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

3D-SDF for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

PDB for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

3D PDB for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

SMILES for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

INCHI for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

Structure for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)

3D Structure for NP0351233 ((1S,2R)-1-O-(1,2-dihydroxycyclohexyl)-2-O-acetyl-4-O-(E)-p-coumaroyl-β-D-glucopyranose)