NP-MRD: Showing NP-Card for Eleganoside A (NP0075314)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 20:36:24 UTC

Updated at

2022-04-28 20:36:24 UTC

NP-MRD ID

NP0075314

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Eleganoside A

Description

Methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. Eleganoside A is found in Fridericia elegans and Pseudocalymma elegans. Based on a literature review very few articles have been published on methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222362D          

 33 35  0  0  1  0            999 V2000
    3.3523    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7812    3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8212    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3018    2.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5314    2.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.2900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  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  1  0  0  0
 12 15  1  6  0  0  0
 11 16  1  1  0  0  0
 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
 20 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 27  1  6  0  0  0
 19 28  1  1  0  0  0
  4 29  1  6  0  0  0
  3 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
   -1.6176    6.2468    3.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0394    4.9872    2.9239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6922    3.9016    2.3697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8629    4.0292    1.9988 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9976    2.6445    2.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2525    2.5647    2.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9642    1.3802    2.5405 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4865    0.4869    1.5118 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3053   -0.6290    1.4268 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0187   -0.6229    0.2334 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9279   -1.8196   -0.3659 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8328   -2.2465   -1.2555 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1415   -3.7179   -0.9305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9912   -4.4932   -1.0195 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1096   -1.5266   -1.4013 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4197   -1.2464   -2.7352 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2071   -0.2223   -0.6539 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5151    0.1819   -0.4885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4831   -0.4160    0.6607 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6258    0.6443    1.5214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9349    0.1849    1.8934 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7071    1.4953    1.6456 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9793    1.3043    2.1665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7550    1.5312    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6326    0.1249   -0.3525 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5718   -0.3434   -1.1915 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3056   -0.8442   -2.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6467   -1.2670   -3.0224 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4312   -1.9922   -4.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5040   -0.1732   -3.1421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6595   -0.7057    0.9115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0974   -2.0733    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9872   -0.7605    1.3646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1750    6.3010    4.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3226    6.4665    2.2901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7905    7.0021    3.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7682    3.4261    3.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017    1.0734    0.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7417    0.2642   -0.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343   -2.2919   -2.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5422   -3.8254    0.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8851   -4.1283   -1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5948   -4.4839   -1.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9762   -2.1502   -1.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0434   -0.4848   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6487    0.5385   -1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7149    0.1562    0.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8667   -1.3875    1.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7449    0.2794    2.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9904   -0.1427    2.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9764    1.4844    3.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9166    2.1769   -0.2148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6788    2.0424   -0.1496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6315    0.0121   -0.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7066   -1.7712   -2.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8492   -0.1677   -3.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1713   -1.9843   -2.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -2.6275   -4.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2818   -2.6949   -4.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3617   -1.2885   -5.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9059    0.0839   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3305   -2.2735    1.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -2.8100    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7567   -2.3099   -0.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0348   -1.0930    2.2931 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  8 21  1  0
 21 31  1  0
 31 32  1  0
 31 33  1  1
 31 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  1  1
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 22  5  1  0
 19 10  1  0
 22 21  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  6 37  1  0
  8 38  1  6
 10 39  1  6
 12 40  1  6
 13 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  1
 16 45  1  0
 17 46  1  6
 18 47  1  0
 19 48  1  1
 20 49  1  0
 21 50  1  1
 32 62  1  0
 32 63  1  0
 32 64  1  0
 33 65  1  0
 25 54  1  6
 24 52  1  0
 24 53  1  0
 23 51  1  0
 27 55  1  0
 27 56  1  0
 28 57  1  1
 29 58  1  0
 29 59  1  0
 29 60  1  0
 30 61  1  0
M  END


  Mrv1652304282222362D          

 33 35  0  0  1  0            999 V2000
    3.3523    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7812    3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8212    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3018    2.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5314    2.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.2900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  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  1  0  0  0
 12 15  1  6  0  0  0
 11 16  1  1  0  0  0
 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
 20 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 27  1  6  0  0  0
 19 28  1  1  0  0  0
  4 29  1  6  0  0  0
  3 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0075314

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]2[C@@](C)(O)[C@H](C[C@]12O)OC[C@H](C)O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O13/c1-8(22)6-30-11-4-20(28)9(16(26)29-3)7-31-18(15(20)19(11,2)27)33-17-14(25)13(24)12(23)10(5-21)32-17/h7-8,10-15,17-18,21-25,27-28H,4-6H2,1-3H3/t8-,10+,11-,12+,13-,14+,15+,17-,18-,19-,20-/m0/s1

> <INCHI_KEY>
KNWPUFRWLDYCQJ-VKTYGPIQSA-N

> <FORMULA>
C20H32O13

> <MOLECULAR_WEIGHT>
480.463

> <EXACT_MASS>
480.18429109

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.19016391242354

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
-1.86

> <JCHEM_LOGP>
-3.940478245333336

> <ALOGPS_LOGS>
-1.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.88719000752316

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.15353172223536

> <JCHEM_PKA_STRONGEST_BASIC>
-2.86318458225751

> <JCHEM_POLAR_SURFACE_AREA>
204.82999999999998

> <JCHEM_REFRACTIVITY>
105.43449999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.16e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,5H,6H,7aH-cyclopenta[c]pyran-4-carboxylate

> <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  O   UNK     0       6.258   3.613   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.258   8.233   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.591   9.003   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.925   8.233   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.925   6.693   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.591   5.923   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.591   4.383   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      10.259   5.923   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      10.259   9.003   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.591  10.543   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.925  11.313   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.320   2.843   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.090   1.509   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.630   1.509   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.400   0.175   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.400   2.843   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.430   5.598   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.992   5.131   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.429   0.541   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.924  -0.237   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.590  -1.007   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.258  -1.007   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.258  -2.547   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5   21   29                                             
CONECT    5    4    6   19                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    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    5   20   27   28                                             
CONECT   20   19   21   22                                                  
CONECT   21   20    4                                                       
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   19                                                            
CONECT   28   19                                                            
CONECT   29    4                                                            
CONECT   30    3   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,4ar,6S,7R,7as)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₂₀H₃₂O₁₃

Average Mass

480.4630 Da

Monoisotopic Mass

480.18429 Da

IUPAC Name

methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

Traditional Name

methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(2S)-2-hydroxypropoxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,5H,6H,7aH-cyclopenta[c]pyran-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]2[C@@](C)(O)[C@H](C[C@]12O)OC[C@H](C)O

InChI Identifier

InChI=1S/C20H32O13/c1-8(22)6-30-11-4-20(28)9(16(26)29-3)7-31-18(15(20)19(11,2)27)33-17-14(25)13(24)12(23)10(5-21)32-17/h7-8,10-15,17-18,21-25,27-28H,4-6H2,1-3H3/t8-,10+,11-,12+,13-,14+,15+,17-,18-,19-,20-/m0/s1

InChI Key

KNWPUFRWLDYCQJ-VKTYGPIQSA-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
Fridericia elegans	LOTUS Database	35616633
Pseudocalymma elegans	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
Hexose monosaccharide
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Bicyclic monoterpenoid
Monoterpenoid
Monosaccharide
Oxane
Cyclic alcohol
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Methyl ester
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Polyol
Acetal
Dialkyl ether
Ether
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Primary alcohol
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-1.9	ALOGPS
logP	-3.9	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	204.83 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	105.43 m³·mol⁻¹	ChemAxon
Polarizability	47.19 Å³	ChemAxon
Number of Rings	3	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

162875518

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Eleganoside A (NP0075314)

MOL for NP0075314 (Eleganoside A)

3D MOL for NP0075314 (Eleganoside A)

3D SDF for NP0075314 (Eleganoside A)

3D-SDF for NP0075314 (Eleganoside A)

PDB for NP0075314 (Eleganoside A)

3D PDB for NP0075314 (Eleganoside A)

SMILES for NP0075314 (Eleganoside A)

INCHI for NP0075314 (Eleganoside A)

Structure for NP0075314 (Eleganoside A)

3D Structure for NP0075314 (Eleganoside A)