NP-MRD: Showing NP-Card for (6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0205172)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 01:01:35 UTC

Updated at

2022-09-05 01:01:35 UTC

NP-MRD ID

NP0205172

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

Description

(6-{[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acids and derivatives. (6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate is found in Ipomoea batatas and Salvia officinalis. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring (6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 04121521062D          

 35 37  0  0  0  0            999 V2000
    2.0792   -9.2563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7436   -8.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2285   -7.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9736   -7.0506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6410   -6.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890   -5.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2820   -6.1241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931   -5.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9381   -5.1679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -4.9964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8762   -4.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0692   -4.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8143   -3.2556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0073   -3.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5447   -3.6972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2476   -2.2995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0546   -2.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3095   -1.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1165   -1.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3714   -0.3872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8194    0.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0743    1.0105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0124    0.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4604    0.6675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7575   -0.7302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4282   -3.5987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733   -2.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2352   -3.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7872   -3.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4901   -4.5548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2971   -4.7264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3085   -7.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0931   -6.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0535   -7.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5384   -8.5026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  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
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 18 25  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  0  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  3 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
   -3.0689    2.0042    1.2062 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    0.8004    1.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5917   -0.1791    0.4814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6863    0.2742   -0.0769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6167   -0.5741   -0.7878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7576   -0.0075   -1.3474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6388   -0.8143   -2.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4101   -2.1555   -2.1480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2884   -3.0131   -2.8302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2911   -2.7199   -1.6009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0371   -4.0658   -1.7136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3821   -1.9155   -0.9109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5630    0.4376    1.7961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6689    1.2769    2.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0640    2.3625    1.6160 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6030    1.8019    0.6183 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9244    1.5379    0.6052 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0180    0.1554    0.5659 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5319   -0.4560   -0.4969 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8967   -0.2824   -1.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8241    0.9959   -2.3134 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4785   -1.8564   -0.2287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4231   -2.4350   -1.0251 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9055   -3.6878   -0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8693   -4.3502   -0.9978 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5637   -1.5056   -1.1921 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8900   -1.2550   -2.5246 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463   -0.2095   -0.5505 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3894    0.9149   -1.2466 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6137    2.0096    1.8441 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0038    2.1090    1.7226 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354    3.4132    2.1418 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8909    3.8875    3.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6577    3.3573    2.4675 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5562    3.0453    3.8183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2951   -1.2228    0.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9115    1.3493   -0.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9112    1.0574   -1.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5360   -0.3811   -2.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1160   -2.5840   -3.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2164   -4.5035   -1.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5254   -2.3969   -0.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564    1.6917    3.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1180    0.5834    2.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9484    2.9128    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3502    2.0202   -0.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9244   -0.8162   -1.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5257   -0.8608   -2.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1541    1.0954   -3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0363   -2.7502   -2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0358   -4.3342   -0.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3474   -3.3944    0.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7406   -4.3950   -0.5093 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4617   -1.8931   -0.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8339   -0.9147   -2.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -0.2212    0.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1960    1.3351   -0.8215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3697    1.3123    2.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2207    2.8141    1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3269    4.0582    1.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4385    4.6101    3.7063 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2645    4.3811    2.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3612    2.5456    4.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 19  1  0
 19 20  1  0
 20 21  1  0
 19 18  1  1
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 15 34  1  0
 34 35  1  0
 34 32  1  0
 32 33  1  0
 32 30  1  0
 30 31  1  0
 19 28  1  0
 28 29  1  0
 28 26  1  0
 26 27  1  0
 26 23  1  0
 30 17  1  0
 12  5  1  0
 25 53  1  0
 24 51  1  0
 24 52  1  0
 23 50  1  6
 20 47  1  0
 20 48  1  0
 21 49  1  0
 17 46  1  6
 15 45  1  6
 14 43  1  0
 14 44  1  0
  3 36  1  0
  4 37  1  0
  6 38  1  0
  7 39  1  0
  9 40  1  0
 11 41  1  0
 12 42  1  0
 34 62  1  1
 35 63  1  0
 32 60  1  6
 33 61  1  0
 30 58  1  1
 31 59  1  0
 28 56  1  1
 29 57  1  0
 26 54  1  1
 27 55  1  0
M  END


  Mrv0541 04121521062D          

 35 37  0  0  0  0            999 V2000
    2.0792   -9.2563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7436   -8.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2285   -7.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9736   -7.0506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6410   -6.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890   -5.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2820   -6.1241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931   -5.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9381   -5.1679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -4.9964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8762   -4.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0692   -4.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8143   -3.2556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0073   -3.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5447   -3.6972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2476   -2.2995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0546   -2.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3095   -1.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1165   -1.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3714   -0.3872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8194    0.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0743    1.0105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0124    0.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4604    0.6675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7575   -0.7302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4282   -3.5987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733   -2.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2352   -3.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7872   -3.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4901   -4.5548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2971   -4.7264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3085   -7.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0931   -6.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0535   -7.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5384   -8.5026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  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
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 18 25  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  0  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  3 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205172

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(CO)(OC2OC(COC(=O)C=CC3=CC=C(O)C(O)=C3)C(O)C(O)C2O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O14/c22-6-12-16(28)19(31)21(8-23,34-12)35-20-18(30)17(29)15(27)13(33-20)7-32-14(26)4-2-9-1-3-10(24)11(25)5-9/h1-5,12-13,15-20,22-25,27-31H,6-8H2

> <INCHI_KEY>
UZUDNVXQOKQTDO-UHFFFAOYSA-N

> <FORMULA>
C21H28O14

> <MOLECULAR_WEIGHT>
504.441

> <EXACT_MASS>
504.147905582

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.62471864332321

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
-1.24

> <JCHEM_LOGP>
-2.102074889

> <ALOGPS_LOGS>
-1.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.775361205534262

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.207628137551078

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4558260660598448

> <JCHEM_POLAR_SURFACE_AREA>
236.05999999999997

> <JCHEM_REFRACTIVITY>
112.30360000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.42e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  O   UNK     0       3.881 -17.278   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.255 -15.872   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.160 -14.626   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.684 -13.161   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.930 -12.256   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.899 -11.111   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.393 -11.432   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       5.960 -11.111   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.484  -9.647   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.978  -9.327   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.502  -7.862   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.996  -7.542   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.520  -6.077   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.014  -5.757   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.017  -6.901   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.462  -4.292   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.969  -3.972   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.444  -2.508   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.951  -2.187   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.427  -0.723   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.396   0.422   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.872   1.886   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.890   0.102   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.859   1.246   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.414  -1.363   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.533  -6.718   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.057  -5.253   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.039  -7.038   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.070  -5.893   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.515  -8.502   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.021  -8.823   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.176 -13.161   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.640 -12.685   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.700 -14.626   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.605 -15.872   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   34                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8   32                                             
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   26                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   18                                                       
CONECT   26   11   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    9   31                                                  
CONECT   31   30                                                            
CONECT   32    5   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32    3   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

View in JSmol

Synonyms

Value	Source
(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₁H₂₈O₁₄

Average Mass

504.4410 Da

Monoisotopic Mass

504.14791 Da

IUPAC Name

(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

Traditional Name

(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

OCC1OC(CO)(OC2OC(COC(=O)C=CC3=CC=C(O)C(O)=C3)C(O)C(O)C2O)C(O)C1O

InChI Identifier

InChI=1S/C21H28O14/c22-6-12-16(28)19(31)21(8-23,34-12)35-20-18(30)17(29)15(27)13(33-20)7-32-14(26)4-2-9-1-3-10(24)11(25)5-9/h1-5,12-13,15-20,22-25,27-31H,6-8H2

InChI Key

UZUDNVXQOKQTDO-UHFFFAOYSA-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

Species Name	Source	Reference
Ipomoea batatas	LOTUS Database	35616633
Salvia officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Cinnamic acid ester
C-glycosyl compound
Disaccharide
Glycosyl compound
O-glycosyl compound
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Ketal
Fatty acid ester
Phenol
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Oxane
Oxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Acetal
Polyol
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Primary alcohol
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	-1.2	ALOGPS
logP	-2.1	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	236.06 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	112.3 m³·mol⁻¹	ChemAxon
Polarizability	47.62 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

85116664

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0205172)

MOL for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D MOL for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D SDF for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D-SDF for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

PDB for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D PDB for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

SMILES for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

INCHI for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

Structure for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D Structure for NP0205172 ((6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate)