NP-MRD: Showing NP-Card for Verproside (NP0057431)

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Record Information

Version

2.0

Created at

2022-04-28 02:52:11 UTC

Updated at

2022-04-28 02:52:11 UTC

NP-MRD ID

NP0057431

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Verproside

Description

(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl 3,4-dihydroxybenzoate 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. Verproside is found in Paederota lutea, Vernoica cymbalaria, Veronica anagallis, Veronica anagallis-aquatica , Veronica austriaca, Veronica austriaca L. , Veronica besseya, Veronica cuneifolia, Veronica cymbalaria, Veronica filiformis, Veronica fuhsii, Veronica kellereri, Veronica lavaudiana, Veronica liwanensis, Veronica longifolia, Veronica officinalis , Veronica pectinata, Veronica perfoliata, Veronica persica , Veronica pulvinaris, Veronica salicifolia G. Forst. and Veronica turrilliana. Based on a literature review very few articles have been published on (1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl 3,4-dihydroxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204522D          

 35 39  0  0  1  0            999 V2000
    0.7327   -1.5964    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5364   -0.7950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1323   -0.2244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9243   -0.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1206   -1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5248   -1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9360    0.5769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.1475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3356    1.9488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9314    2.5194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7235    2.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9198    1.4874    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3239    0.9168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5202    0.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119    1.2567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3194    2.8594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7352    3.3208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    3.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2863   -0.7341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5986   -1.4977    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0312   -2.0306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0298   -2.8534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6523   -3.3175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3953   -2.9590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5913   -4.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2733   -4.6045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2123   -5.4272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693   -5.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2127   -5.3216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1517   -4.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -6.6085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8944   -5.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038   -0.8455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3117    0.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0385    0.4809    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  2  0  0  0  0
  1  6  1  6  0  0  0
  3  7  1  6  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 12 15  1  1  0  0  0
 11 16  1  1  0  0  0
 10 17  1  1  0  0  0
 17 18  1  0  0  0  0
  2 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
 28 31  1  0  0  0  0
 27 32  1  0  0  0  0
 20 33  1  6  0  0  0
 19 33  1  0  0  0  0
 19 34  1  1  0  0  0
 34 35  1  0  0  0  0
M  END

     RDKit          3D

 61 65  0  0  0  0  0  0  0  0999 V2000
    4.3184   -1.1331    2.5750 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3442   -0.6400    1.4222 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1592   -0.5716    0.7350 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9143   -1.0125    1.2243 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9044    0.0843    1.3391 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4637    1.4336    1.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6299    2.4205    1.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6650    2.1585    0.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0939    0.8486    0.2395 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9197    0.9702   -0.8680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2525    0.6224   -0.6196 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5841   -0.3175   -1.5719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9141   -0.6667   -1.4525 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2870   -1.2749   -0.1218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5556   -2.4401    0.0659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8374    0.4708   -1.7975 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1567    0.0372   -1.5701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5271    1.6736   -0.9439 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0648    1.5602    0.3381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0388    1.9009   -0.9014 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6537    2.4567   -2.1199 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1260    0.0507    0.0319 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0154   -1.4147   -0.1719 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3128   -2.1414   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0306   -3.4107    0.4865 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0392   -1.9583   -0.9519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2418   -2.0443    0.3959 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6234   -0.1806    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7514   -0.2929    1.6899 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0031    0.1152    1.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0974    0.6623    0.0309 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3253    1.1123   -0.4793 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9949    0.8032   -0.8088 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1148    1.3603   -2.0806 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7694    0.3737   -0.3465 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0583   -1.4248    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2070   -0.0720    2.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4374    1.7003    1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9733    3.4622    1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6919    0.4602    1.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3325    0.3137    0.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1726   -1.4846   -2.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1454   -0.5355    0.6596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3829   -1.5047   -0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7047   -2.7246    1.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7593    0.7571   -2.8768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7542    0.7634   -1.9167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9608    2.6072   -1.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3547    2.4518    0.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8227    2.6723   -0.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7224    2.1793   -2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7243    0.5251   -0.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7361   -2.2914   -1.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0131   -1.6673    0.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5397   -3.9377   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1595   -3.0986    0.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6661   -0.7324    2.6964 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8924    0.0196    1.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.0402    1.6553   -2.3604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8781    0.4518   -0.9404 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 28  1  0
 28 35  2  0
 35 33  1  0
 33 34  1  0
 33 31  2  0
 31 32  1  0
 31 30  1  0
 30 29  2  0
  4 27  1  0
 27 26  1  0
 26 23  1  0
 23 24  1  1
 24 25  1  0
 23 22  1  0
 11 20  1  0
 20 21  1  0
 20 18  1  0
 18 19  1  0
 18 16  1  0
 16 17  1  0
 16 13  1  0
 22  9  1  0
 22  5  1  0
 29 28  1  0
 23 27  1  0
 15 45  1  0
 14 43  1  0
 14 44  1  0
 13 42  1  6
 11 41  1  1
  9 40  1  1
  7 39  1  0
  6 38  1  0
  5 37  1  1
  4 36  1  1
 35 61  1  0
 34 60  1  0
 32 59  1  0
 30 58  1  0
 29 57  1  0
 27 56  1  1
 24 53  1  0
 24 54  1  0
 25 55  1  0
 22 52  1  6
 20 50  1  1
 21 51  1  0
 18 48  1  6
 19 49  1  0
 16 46  1  6
 17 47  1  0
M  END


  Mrv1652304282204522D          

 35 39  0  0  1  0            999 V2000
    0.7327   -1.5964    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5364   -0.7950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1323   -0.2244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9243   -0.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1206   -1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5248   -1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9360    0.5769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.1475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3356    1.9488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9314    2.5194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7235    2.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9198    1.4874    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3239    0.9168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5202    0.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119    1.2567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3194    2.8594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7352    3.3208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    3.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2863   -0.7341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5986   -1.4977    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0312   -2.0306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0298   -2.8534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6523   -3.3175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3953   -2.9590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5913   -4.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2733   -4.6045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2123   -5.4272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693   -5.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2127   -5.3216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1517   -4.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -6.6085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8944   -5.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038   -0.8455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3117    0.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0385    0.4809    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  2  0  0  0  0
  1  6  1  6  0  0  0
  3  7  1  6  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 12 15  1  1  0  0  0
 11 16  1  1  0  0  0
 10 17  1  1  0  0  0
 17 18  1  0  0  0  0
  2 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
 28 31  1  0  0  0  0
 27 32  1  0  0  0  0
 20 33  1  6  0  0  0
 19 33  1  0  0  0  0
 19 34  1  1  0  0  0
 34 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057431

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@@H]1O[C@@H](O[C@@H]2OC=C[C@@H]3[C@H](OC(=O)C4=CC(O)=C(O)C=C4)[C@@H]4O[C@]4(CO)[C@@H]23)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O13/c23-6-12-14(27)15(28)16(29)21(32-12)34-20-13-9(3-4-31-20)17(18-22(13,7-24)35-18)33-19(30)8-1-2-10(25)11(26)5-8/h1-5,9,12-18,20-21,23-29H,6-7H2/t9-,12-,13+,14+,15+,16-,17-,18-,20-,21-,22+/m0/s1

> <INCHI_KEY>
DBUOUVZMYWYRRI-RIWUNSSHSA-N

> <FORMULA>
C22H26O13

> <MOLECULAR_WEIGHT>
498.437

> <EXACT_MASS>
498.137340897

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
47.496410143733655

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl 3,4-dihydroxybenzoate

> <ALOGPS_LOGP>
-0.46

> <JCHEM_LOGP>
-1.5436344043333325

> <ALOGPS_LOGS>
-1.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.88229004148916

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.555943535708302

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
208.13

> <JCHEM_REFRACTIVITY>
110.97529999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.01e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl 3,4-dihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.368  -2.980   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.001  -1.484   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.114  -0.419   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.592  -0.850   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.958  -2.345   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.846  -3.411   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.747   1.077   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.859   2.142   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.493   3.638   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.605   4.703   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.084   4.272   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.450   2.777   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.338   1.711   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.704   0.216   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       6.929   2.346   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.196   5.337   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.239   6.199   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.351   7.264   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.534  -1.370   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.117  -2.796   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.058  -3.790   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.056  -5.326   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.218  -6.193   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.604  -5.523   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.104  -7.729   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.377  -8.595   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.263 -10.131   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.876 -10.800   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.397  -9.934   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.283  -8.398   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.762 -12.336   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.536 -10.997   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -2.060  -1.578   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.582   0.169   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.939   0.898   0.000  0.00  0.00           O+0
CONECT    1    2    6   21                                                  
CONECT    2    1    3   19                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    3    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13                                                            
CONECT   15   12                                                            
CONECT   16   11                                                            
CONECT   17   10   18                                                       
CONECT   18   17                                                            
CONECT   19    2   20   33   34                                             
CONECT   20   19   21   33                                                  
CONECT   21   20    1   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31   28                                                            
CONECT   32   27                                                            
CONECT   33   20   19                                                       
CONECT   34   19   35                                                       
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,4S,5S,6S,10S)-2-(Hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0,]dec-7-en-5-yl 3,4-dihydroxybenzoic acid	Generator

Chemical Formula

C₂₂H₂₆O₁₃

Average Mass

498.4370 Da

Monoisotopic Mass

498.13734 Da

IUPAC Name

(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl 3,4-dihydroxybenzoate

Traditional Name

(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl 3,4-dihydroxybenzoate

CAS Registry Number

Not Available

SMILES

OC[C@@H]1O[C@@H](O[C@@H]2OC=C[C@@H]3[C@H](OC(=O)C4=CC(O)=C(O)C=C4)[C@@H]4O[C@]4(CO)[C@@H]23)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C22H26O13/c23-6-12-14(27)15(28)16(29)21(32-12)34-20-13-9(3-4-31-20)17(18-22(13,7-24)35-18)33-19(30)8-1-2-10(25)11(26)5-8/h1-5,9,12-18,20-21,23-29H,6-7H2/t9-,12-,13+,14+,15+,16-,17-,18-,20-,21-,22+/m0/s1

InChI Key

DBUOUVZMYWYRRI-RIWUNSSHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Paederota lutea	LOTUS Database	35616633
Vernoica cymbalaria	-	KNApSAcK
Veronica anagallis	LOTUS Database	35616633
Veronica anagallis-aquatica	Plant	KNApSAcK
Veronica austriaca	LOTUS Database	35616633
Veronica austriaca L.	Plant	KNApSAcK
Veronica besseya	LOTUS Database	35616633
Veronica cuneifolia	Plant	KNApSAcK
Veronica cymbalaria	Plant	KNApSAcK
Veronica filiformis	LOTUS Database	35616633
Veronica fuhsii	LOTUS Database	35616633
Veronica kellereri	LOTUS Database	35616633
Veronica lavaudiana	LOTUS Database	35616633
Veronica liwanensis	LOTUS Database	35616633
Veronica longifolia	Plant	KNApSAcK
Veronica officinalis	Plant	KNApSAcK
Veronica pectinata	Plant	KNApSAcK
Veronica perfoliata	Plant	KNApSAcK
Veronica persica	Plant	KNApSAcK
Veronica pulvinaris	LOTUS Database	35616633
Veronica salicifolia G. Forst.	Plant	KNApSAcK
Veronica turrilliana	Plant	KNApSAcK

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

Hexose monosaccharide
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
O-glycosyl compound
Dihydroxybenzoic acid
Benzoate ester
Benzoic acid or derivatives
Catechol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	-1.5	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	208.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	110.98 m³·mol⁻¹	ChemAxon
Polarizability	47.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

162994915

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Verproside (NP0057431)

MOL for NP0057431 (Verproside)

3D MOL for NP0057431 (Verproside)

3D SDF for NP0057431 (Verproside)

3D-SDF for NP0057431 (Verproside)

PDB for NP0057431 (Verproside)

3D PDB for NP0057431 (Verproside)

SMILES for NP0057431 (Verproside)

INCHI for NP0057431 (Verproside)

Structure for NP0057431 (Verproside)

3D Structure for NP0057431 (Verproside)