NP-MRD: Showing NP-Card for [(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate (NP0195586)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 13:28:28 UTC

Updated at

2022-09-04 13:28:29 UTC

NP-MRD ID

NP0195586

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate

Description

4-Hydroxyphenethyl 6-O-[5-O-(4-methoxybenzoyl)-D-apio-beta-D-furanosyl]-beta-D-glucopyranoside belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review very few articles have been published on 4-Hydroxyphenethyl 6-O-[5-O-(4-methoxybenzoyl)-D-apio-beta-D-furanosyl]-beta-D-glucopyranoside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042215282D          

 40 43  0  0  1  0            999 V2000
    2.5948   -0.8667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4017   -1.0382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6567   -1.8228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4636   -1.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7186   -2.7790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1665   -3.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4215   -4.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2285   -4.3482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694   -4.7898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -5.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0203   -5.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2398   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849   -7.4570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -7.4570    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6749   -8.1245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0105   -8.8782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256   -9.5456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8611  -10.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762  -10.9667    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7118  -11.7204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2268  -12.3878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624  -13.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775  -13.8089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130  -14.5626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9281  -15.2301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1076  -15.1438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6227  -15.8113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7721  -14.3901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2570  -13.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5557  -10.8805    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0708  -11.5479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2202  -10.1268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3997  -10.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7051   -9.4594    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3695   -8.7057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049   -6.6724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1203   -6.4175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3596   -3.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1046   -2.4359    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  1  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
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  1  6  0  0  0
 15 37  1  0  0  0  0
 11 37  1  0  0  0  0
 37 38  1  6  0  0  0
  6 39  1  0  0  0  0
 39 40  2  0  0  0  0
  3 40  1  0  0  0  0
M  END

     RDKit          3D

 74 77  0  0  0  0  0  0  0  0999 V2000
   10.5187    2.0362    2.3397 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5079    1.6033    0.9956 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2828    1.4654    0.3600 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0972    1.7387    1.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8699    1.6044    0.3817 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7933    1.1829   -0.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846    1.0403   -1.6038 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5259    0.6557   -2.7903 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3059    1.3034   -0.9898 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448    1.1873   -1.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6972   -0.2469   -1.8331 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5571   -0.8349   -2.7704 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7744   -1.1105   -0.5981 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7184   -2.0134   -0.6774 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6802   -1.2966   -1.2506 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1588   -0.7034   -0.3531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4584   -1.1717   -0.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387   -0.4695    0.6416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5885   -1.0203    0.5058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5715   -0.4987    1.3068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2597   -1.5135    1.8897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5724   -1.6742    1.7094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1533   -2.0059    0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9191   -1.0654   -0.6943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9106   -1.2679   -1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7599   -0.3308   -2.6280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5743    0.7769   -2.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4129    1.7030   -3.6976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5781    0.9694   -1.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7597    0.0541   -0.7496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9977    0.4719    2.3381 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9075    1.7307    1.7597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7666   -0.0090    3.0088 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0329   -0.8379    4.1057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8249   -0.6549    2.0354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5221   -0.1334    2.1765 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2668   -0.3988   -2.2779 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1891   -0.9410   -3.5706 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9830    0.9120   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2104    1.0466   -0.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5441    2.0839    2.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0219    3.0451    2.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8697    1.3398    2.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1660    2.0704    2.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9481    1.8307    0.9262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0517    1.7188   -2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2672    1.6340   -0.8615 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -1.7854   -2.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494   -1.5601   -0.4159 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5342   -0.4247    0.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0575   -2.0584   -1.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4326   -2.2420   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9560   -1.1081   -1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4030    0.6119    0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2456    0.1286    0.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0944   -0.7907    2.1947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8901   -2.5267    2.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8120   -3.0551    0.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2843   -2.1321    0.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768   -2.1606   -1.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9787   -0.4574   -3.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8102    2.4902   -3.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2297    1.8510   -1.8131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5383    0.2026   -0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7896    0.5495    3.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4160    1.8336    0.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2335    0.9143    3.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425   -1.1951    4.4188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6886   -1.7531    2.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1808   -0.4491    3.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8305    0.6294   -2.2658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1153   -1.9207   -3.4526 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9261    0.5776   -2.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1257    0.8240   -1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 39  1  0
 39 40  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 20 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 15 37  1  0
 37 38  1  0
 40  3  1  0
 37 11  1  0
 35 18  1  0
 30 24  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  4 44  1  0
  5 45  1  0
 39 73  1  0
 40 74  1  0
 10 46  1  0
 10 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 15 51  1  6
 17 52  1  0
 17 53  1  0
 18 54  1  6
 20 55  1  6
 22 56  1  0
 22 57  1  0
 23 58  1  0
 23 59  1  0
 25 60  1  0
 26 61  1  0
 28 62  1  0
 29 63  1  0
 30 64  1  0
 31 65  1  1
 32 66  1  0
 33 67  1  1
 34 68  1  0
 35 69  1  1
 36 70  1  0
 37 71  1  6
 38 72  1  0
M  END


  Mrv1652309042215282D          

 40 43  0  0  1  0            999 V2000
    2.5948   -0.8667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4017   -1.0382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6567   -1.8228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4636   -1.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7186   -2.7790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1665   -3.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4215   -4.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2285   -4.3482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694   -4.7898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -5.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0203   -5.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2398   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849   -7.4570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -7.4570    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6749   -8.1245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0105   -8.8782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256   -9.5456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8611  -10.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762  -10.9667    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7118  -11.7204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2268  -12.3878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624  -13.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775  -13.8089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130  -14.5626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9281  -15.2301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1076  -15.1438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6227  -15.8113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7721  -14.3901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2570  -13.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5557  -10.8805    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0708  -11.5479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2202  -10.1268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3997  -10.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7051   -9.4594    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3695   -8.7057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049   -6.6724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1203   -6.4175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3596   -3.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1046   -2.4359    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  1  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
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  1  6  0  0  0
 15 37  1  0  0  0  0
 11 37  1  0  0  0  0
 37 38  1  6  0  0  0
  6 39  1  0  0  0  0
 39 40  2  0  0  0  0
  3 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195586

> <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](OCCC3=CC=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O13/c1-35-18-8-4-16(5-9-18)24(33)38-13-27(34)14-39-26(23(27)32)37-12-19-20(29)21(30)22(31)25(40-19)36-11-10-15-2-6-17(28)7-3-15/h2-9,19-23,25-26,28-32,34H,10-14H2,1H3/t19-,20-,21+,22-,23+,25-,26-,27-/m1/s1

> <INCHI_KEY>
USMNLFDFNCAKRV-AFBUJPPUSA-N

> <FORMULA>
C27H34O13

> <MOLECULAR_WEIGHT>
566.556

> <EXACT_MASS>
566.199941155

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
56.221368254818

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3S,4R,5R)-3,4-dihydroxy-5-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate

> <JCHEM_LOGP>
0.4812858093333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.70405578904446

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.188466749168711

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648667947423088

> <JCHEM_POLAR_SURFACE_AREA>
193.82999999999998

> <JCHEM_REFRACTIVITY>
134.97850000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(3S,4R,5R)-3,4-dihydroxy-5-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.844  -1.618   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.350  -1.938   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.826  -3.403   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.332  -3.723   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.808  -5.187   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.778  -6.332   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.253  -7.796   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.760  -8.117   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       7.223  -8.941   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.699 -10.406   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.638 -10.406   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.914 -12.455   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.438 -13.920   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.898 -13.920   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.993 -15.166   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.620 -16.573   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.714 -17.818   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.341 -19.225   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.436 -20.471   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.062 -21.878   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.157 -23.124   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.783 -24.531   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.878 -25.777   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.504 -27.184   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.599 -28.429   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.068 -28.268   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.162 -29.514   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.441 -26.862   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.346 -25.616   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.904 -20.310   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.999 -21.556   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.278 -18.903   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.746 -18.742   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.183 -17.657   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.556 -16.251   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.423 -12.455   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.958 -11.979   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       6.271  -6.012   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.795  -4.547   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   39                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   37                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   37                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   35                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24                                                       
CONECT   31   20   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   18   36                                                  
CONECT   36   35                                                            
CONECT   37   15   11   38                                                  
CONECT   38   37                                                            
CONECT   39    6   40                                                       
CONECT   40   39    3                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Value	Source
4-Hydroxyphenethyl 6-O-[5-O-(4-methoxybenzoyl)-D-apio-b-D-furanosyl]-b-D-glucopyranoside	Generator
4-Hydroxyphenethyl 6-O-[5-O-(4-methoxybenzoyl)-D-apio-β-D-furanosyl]-β-D-glucopyranoside	Generator

Chemical Formula

C₂₇H₃₄O₁₃

Average Mass

566.5560 Da

Monoisotopic Mass

566.19994 Da

IUPAC Name

[(3S,4R,5R)-3,4-dihydroxy-5-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate

Traditional Name

[(3S,4R,5R)-3,4-dihydroxy-5-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-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](OCCC3=CC=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

InChI Identifier

InChI=1S/C27H34O13/c1-35-18-8-4-16(5-9-18)24(33)38-13-27(34)14-39-26(23(27)32)37-12-19-20(29)21(30)22(31)25(40-19)36-11-10-15-2-6-17(28)7-3-15/h2-9,19-23,25-26,28-32,34H,10-14H2,1H3/t19-,20-,21+,22-,23+,25-,26-,27-/m1/s1

InChI Key

USMNLFDFNCAKRV-AFBUJPPUSA-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 o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
O-glycosyl compound
P-methoxybenzoic acid or derivatives
Benzoate ester
Tyrosol derivative
Benzoic acid or derivatives
Phenoxy compound
Anisole
Methoxybenzene
Benzoyl
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Oxane
Tertiary alcohol
Oxolane
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
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	0.48	ChemAxon
pKa (Strongest Acidic)	10.19	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	193.83 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	134.98 m³·mol⁻¹	ChemAxon
Polarizability	56.22 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

10191002

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21579201

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)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate (NP0195586)

MOL for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

3D MOL for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

3D SDF for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

3D-SDF for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

PDB for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

3D PDB for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

SMILES for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

INCHI for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

Structure for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)

3D Structure for NP0195586 ([(3s,4r,5r)-3,4-dihydroxy-5-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy}oxolan-3-yl]methyl 4-methoxybenzoate)