NP-MRD: Showing NP-Card for [(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate (NP0144671)

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Record Information

Version

2.0

Created at

2022-09-01 23:42:23 UTC

Updated at

2022-09-01 23:42:23 UTC

NP-MRD ID

NP0144671

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate

Description

[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate 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. Based on a literature review very few articles have been published on [(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201422D          

 43 46  0  0  1  0            999 V2000
   -5.1577    5.1360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3507    4.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0339    3.2237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5240    1.6545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8830    1.2129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6281    0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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 40 41  1  6  0  0  0
  6 42  1  0  0  0  0
 42 43  2  0  0  0  0
  3 43  1  0  0  0  0
M  END

     RDKit          3D

 79 82  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309022201422D          

 43 46  0  0  1  0            999 V2000
   -5.1577    5.1360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8914   -4.2966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3763   -4.9640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0407   -5.7177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2202   -5.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7353   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9148   -5.2227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5793   -5.9764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7588   -6.0627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2739   -5.3952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4232   -6.8163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9082   -7.4838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0642   -6.6439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8847   -6.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3696   -7.2251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1901   -7.1388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1968   -4.8778    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6817   -5.5452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5323   -4.1241    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.3528   -4.0379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0474   -3.4567    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3829   -2.7030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8476   -0.6697    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6322   -0.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3929    2.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6478    3.5668    0.0000 C   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  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  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  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 20 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 18 38  1  0  0  0  0
 38 39  1  6  0  0  0
 15 40  1  0  0  0  0
 11 40  1  0  0  0  0
 40 41  1  6  0  0  0
  6 42  1  0  0  0  0
 42 43  2  0  0  0  0
  3 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144671

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C(=O)OC[C@@]1(O)CO[C@@H](OC[C@H]2O[C@@H](OC3=CC=C(C=C3OC)[C@@H](O)CO)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O15/c1-37-16-6-3-14(4-7-16)25(35)40-12-28(36)13-41-27(24(28)34)39-11-20-21(31)22(32)23(33)26(43-20)42-18-8-5-15(17(30)10-29)9-19(18)38-2/h3-9,17,20-24,26-27,29-34,36H,10-13H2,1-2H3/t17-,20+,21+,22-,23+,24-,26+,27+,28+/m0/s1

> <INCHI_KEY>
IYWMXLVTJMHOKZ-XCKGQVDLSA-N

> <FORMULA>
C28H36O15

> <MOLECULAR_WEIGHT>
612.581

> <EXACT_MASS>
612.205420459

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
60.36170858380999

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate

> <ALOGPS_LOGP>
-0.46

> <JCHEM_LOGP>
-1.0926140510000004

> <ALOGPS_LOGS>
-2.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.289334910620575

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.684985830048433

> <JCHEM_PKA_STRONGEST_BASIC>
-2.980726531385308

> <JCHEM_POLAR_SURFACE_AREA>
223.28999999999996

> <JCHEM_REFRACTIVITY>
142.3803

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.93e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate

> <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      -9.628   9.587   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -8.121   9.267   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -7.646   7.802   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.139   7.482   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.663   6.018   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.694   4.873   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.218   3.409   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.712   3.088   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -7.248   2.264   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -6.772   0.799   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.803  -0.345   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -8.833   0.799   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -6.557  -1.250   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -7.033  -2.715   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -8.573  -2.715   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -9.478  -3.961   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -8.852  -5.368   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.757  -6.613   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -9.131  -8.020   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0     -10.036  -9.266   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -9.409 -10.673   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -7.878 -10.834   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.973  -9.588   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.441  -9.749   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.815 -11.156   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.283 -11.317   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.378 -10.071   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.657 -12.724   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.562 -13.970   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.720 -12.402   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.251 -12.241   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -8.157 -13.487   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -9.688 -13.326   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -11.567  -9.105   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -12.472 -10.351   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -12.194  -7.698   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -13.725  -7.537   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0     -11.288  -6.452   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0     -11.915  -5.046   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -9.049  -1.250   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -10.513  -0.774   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -8.200   5.193   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -8.676   6.658   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   43                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   40                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   40                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   38                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28                                                            
CONECT   30   25   31                                                       
CONECT   31   30   22   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   20   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   18   39                                                  
CONECT   39   38                                                            
CONECT   40   15   11   41                                                  
CONECT   41   40                                                            
CONECT   42    6   43                                                       
CONECT   43   42    3                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Value	Source
[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoic acid	Generator

Chemical Formula

C₂₈H₃₆O₁₅

Average Mass

612.5810 Da

Monoisotopic Mass

612.20542 Da

IUPAC Name

[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate

Traditional Name

[(3S,4R,5R)-5-{[(2R,3S,4S,5R,6S)-6-{4-[(1R)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C(=O)OC[C@@]1(O)CO[C@@H](OC[C@H]2O[C@@H](OC3=CC=C(C=C3OC)[C@@H](O)CO)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

InChI Identifier

InChI=1S/C28H36O15/c1-37-16-6-3-14(4-7-16)25(35)40-12-28(36)13-41-27(24(28)34)39-11-20-21(31)22(32)23(33)26(43-20)42-18-8-5-15(17(30)10-29)9-19(18)38-2/h3-9,17,20-24,26-27,29-34,36H,10-13H2,1-2H3/t17-,20+,21+,22-,23+,24-,26+,27+,28+/m0/s1

InChI Key

IYWMXLVTJMHOKZ-XCKGQVDLSA-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 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
Disaccharide
O-glycosyl compound
P-methoxybenzoic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Anisole
Phenoxy compound
Benzoyl
Methoxybenzene
Phenol ether
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Oxane
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Ether
Polyol
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Monocarboxylic acid or derivatives
Oxacycle
Hydrocarbon derivative
Primary alcohol
Organic oxide
Alcohol
Aromatic alcohol
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	-0.46	ALOGPS
logP	-1.1	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	11.68	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	223.29 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	142.38 m³·mol⁻¹	ChemAxon
Polarizability	60.36 Å³	ChemAxon
Number of Rings	4	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

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

162949577

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate (NP0144671)

MOL for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

3D MOL for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

3D SDF for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

3D-SDF for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

PDB for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

3D PDB for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

SMILES for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

INCHI for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

Structure for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)

3D Structure for NP0144671 ([(3s,4r,5r)-5-{[(2r,3s,4s,5r,6s)-6-{4-[(1r)-1,2-dihydroxyethyl]-2-methoxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate)