NP-MRD: Showing NP-Card for [3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate (NP0327669)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 10:27:47 UTC

Updated at

2022-09-12 10:27:48 UTC

NP-MRD ID

NP0327669

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate

Description

[3,4,5-Trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]Pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate 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. [3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate is found in Urospermum picroides. Based on a literature review very few articles have been published on [3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]Pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122212272D          

 41 45  0  0  0  0            999 V2000
    3.6818   -1.0926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5434   -0.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8041    0.0867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0733   -0.2963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9237    0.9030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7370    1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1784    1.7385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0027    1.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6197    2.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7954    2.4692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124    3.1999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881    3.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2051    3.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3808    3.9980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9978    4.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1735    4.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2678    4.0654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2095    5.4931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0338    5.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4751    4.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2994    4.8635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6824    5.5942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067    5.6279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2411    6.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4168    6.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6465    4.6613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2635    5.3921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4708    4.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9121    5.3247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537    3.8969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6781    3.8632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4440    2.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2683    2.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6513    1.6374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100    0.9403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3857    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9443    0.2770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177   -0.2559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3484    0.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0877   -0.2390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200    0.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 13 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
 11 30  1  0  0  0  0
 30 31  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  1  0  0  0  0
 34 33  1  4  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 35 39  1  0  0  0  0
 39 40  2  0  0  0  0
 37 41  1  0  0  0  0
  2 41  1  0  0  0  0
  6 41  1  0  0  0  0
M  END

     RDKit          3D

 73 77  0  0  0  0  0  0  0  0999 V2000
   -4.9619   -3.5268   -2.3363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3007   -2.3982   -2.3966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9217   -2.1891   -2.9000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1367   -3.1133   -3.2674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6847   -0.8208   -2.8833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3863   -0.3742   -1.7068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6860   -0.9265   -0.5490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2826   -0.3955    0.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8413   -0.5695    1.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1522    0.6123    1.1540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0448    1.3321   -0.0405 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2470    1.3371   -0.4476 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1452    2.1909    0.1062 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5586    1.7672    1.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1973    0.5074    1.5270 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3592    0.1642    0.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9193    1.0831    0.2292 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0346   -1.1361    0.9495 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2998   -1.1678    0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5194   -0.8459    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6418   -0.8984    0.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6467   -1.2611   -1.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8055   -1.3080   -2.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4291   -1.5783   -1.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2612   -1.5349   -1.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5925    3.6074    0.1797 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3002    3.8814    1.5042 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3038    3.6653   -0.6398 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5581    3.1241   -1.8807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6227    2.6897    0.0963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7022    3.0616    1.4471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107    0.3625    1.5731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8583   -0.5199    2.5397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3555   -0.4554    2.3780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9718   -0.8016    1.2918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3835   -1.8168    0.3343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5380   -0.8654   -0.8322 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9624   -0.8216   -0.8248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1847   -0.4859    0.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2279   -0.0010    1.0871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7511   -1.0602   -1.9997 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4752   -4.4289   -2.6853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9663   -3.5296   -1.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5295    0.7079   -1.7048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4326   -2.0142   -0.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9260   -0.9837    2.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3195   -1.3650    0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6173    0.7593   -0.8487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0360    2.1942   -0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7049    1.6632    2.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1975    2.5570    1.9843 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1626   -1.4472    2.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3488   -1.8897    0.4980 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4811   -0.5656    1.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5870   -0.6373    0.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7189   -1.0783   -1.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3804   -1.8647   -2.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3116   -1.7974   -1.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620    4.3502   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5460    4.8026    1.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0494    4.6924   -0.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5172    3.2424   -2.1078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6333    2.7945   -0.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5028    2.3259    2.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720    1.0974    2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8336    0.9800    1.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6544   -0.1285    3.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4995   -1.5680    2.5420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0077   -0.1016    3.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1715   -2.6140    0.2229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4383   -2.1950    0.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3298    0.2258   -0.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1466   -0.4711   -2.8645 H   0  0  0  0  0  0  0  0  0  0  0  0
 29 28  1  0
 28 26  1  0
 26 27  1  0
 26 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 41  1  0
 41 37  1  0
 37 36  1  0
 36 35  1  0
 35 34  2  0
 34 33  1  0
 33 32  1  0
 35 39  1  0
 39 40  2  0
 39 38  1  0
 11 30  1  0
 30 31  1  0
 30 28  1  0
 25 19  1  0
 32  8  1  0
 41  6  1  0
 38 37  1  0
 29 62  1  0
 28 61  1  6
 26 59  1  6
 27 60  1  0
 13 49  1  6
 14 50  1  0
 14 51  1  0
 18 52  1  0
 18 53  1  0
 20 54  1  0
 21 55  1  0
 23 56  1  0
 24 57  1  0
 25 58  1  0
 11 48  1  6
  9 46  1  0
  9 47  1  0
  7 45  1  0
  6 44  1  1
  1 42  1  0
  1 43  1  0
 41 73  1  6
 37 72  1  1
 36 70  1  0
 36 71  1  0
 34 69  1  0
 33 67  1  0
 33 68  1  0
 32 65  1  0
 32 66  1  0
 30 63  1  6
 31 64  1  0
M  END


  Mrv1652309122212272D          

 41 45  0  0  0  0            999 V2000
    3.6818   -1.0926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5434   -0.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8041    0.0867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0733   -0.2963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9237    0.9030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7370    1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1784    1.7385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0027    1.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6197    2.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7954    2.4692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124    3.1999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881    3.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2051    3.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3808    3.9980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9978    4.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1735    4.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2678    4.0654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2095    5.4931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0338    5.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4751    4.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2994    4.8635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6824    5.5942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067    5.6279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2411    6.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4168    6.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6465    4.6613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2635    5.3921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4708    4.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9121    5.3247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537    3.8969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6781    3.8632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4440    2.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2683    2.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6513    1.6374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100    0.9403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3857    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9443    0.2770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177   -0.2559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3484    0.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0877   -0.2390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200    0.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 13 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
 11 30  1  0  0  0  0
 30 31  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  1  0  0  0  0
 34 33  1  4  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 35 39  1  0  0  0  0
 39 40  2  0  0  0  0
 37 41  1  0  0  0  0
  2 41  1  0  0  0  0
  6 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0327669

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1C(O)C(COC(=O)CC2=CC=C(O)C=C2)OC(OCC2=CC3OC(=O)C(=C)C3C3CC(=CCC2)C(=O)O3)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C29H32O12/c1-14-23-19(39-27(14)35)9-16(3-2-4-17-11-20(23)40-28(17)36)12-38-29-26(34)25(33)24(32)21(41-29)13-37-22(31)10-15-5-7-18(30)8-6-15/h4-9,19-21,23-26,29-30,32-34H,1-3,10-13H2

> <INCHI_KEY>
OKCHBIUSLHZRMY-UHFFFAOYSA-N

> <FORMULA>
C29H32O12

> <MOLECULAR_WEIGHT>
572.563

> <EXACT_MASS>
572.18937647

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
56.61460790582635

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0^{2,6}]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate

> <JCHEM_LOGP>
1.4807950096666662

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.212867921584651

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.495588894453883

> <JCHEM_PKA_STRONGEST_BASIC>
-3.649085218095647

> <JCHEM_POLAR_SURFACE_AREA>
178.27999999999997

> <JCHEM_REFRACTIVITY>
139.78440000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0^{2,6}]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl (4-hydroxyphenyl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.873  -2.040   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.614  -0.521   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.234   0.162   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.870  -0.553   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       5.458   1.686   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.976   1.944   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.800   3.245   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.338   3.182   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.623   4.546   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.085   4.609   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.370   5.973   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.831   6.036   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.116   7.400   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.578   7.463   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.863   8.827   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.324   8.890   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.500   7.589   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.391  10.254   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.930  10.317   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.754   9.016   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.292   9.079   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.007  10.443   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -6.546  10.505   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.183  11.744   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.645  11.681   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.940   8.701   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.225  10.065   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.479   8.638   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.303   9.939   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.194   7.274   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.732   7.211   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      10.162   4.483   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.701   4.420   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.416   3.056   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.592   1.755   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.053   1.818   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.229   0.517   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      10.486  -0.478   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.850   0.237   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      13.230  -0.446   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.691   0.580   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   41                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   41                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   19                                                       
CONECT   26   13   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   11   31                                                  
CONECT   31   30                                                            
CONECT   32    8   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   39                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   41                                                  
CONECT   38   37   39                                                       
CONECT   39   38   35   40                                                  
CONECT   40   39                                                            
CONECT   41   37    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
[3,4,5-Trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0,]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetic acid	Generator

Chemical Formula

C₂₉H₃₂O₁₂

Average Mass

572.5630 Da

Monoisotopic Mass

572.18938 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1C(O)C(COC(=O)CC2=CC=C(O)C=C2)OC(OCC2=CC3OC(=O)C(=C)C3C3CC(=CCC2)C(=O)O3)C1O

InChI Identifier

InChI=1S/C29H32O12/c1-14-23-19(39-27(14)35)9-16(3-2-4-17-11-20(23)40-28(17)36)12-38-29-26(34)25(33)24(32)21(41-29)13-37-22(31)10-15-5-7-18(30)8-6-15/h4-9,19-21,23-26,29-30,32-34H,1-3,10-13H2

InChI Key

OKCHBIUSLHZRMY-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
Urospermum picroides	LOTUS Database	35616633

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

O-glycosyl compound
Tricarboxylic acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Gamma butyrolactone
Monosaccharide
Benzenoid
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
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

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

162912189

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate (NP0327669)

MOL for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

3D MOL for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

3D SDF for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

3D-SDF for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

PDB for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

3D PDB for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

SMILES for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

INCHI for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

Structure for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)

3D Structure for NP0327669 ([3,4,5-trihydroxy-6-({3-methylidene-4,13-dioxo-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-dien-8-yl}methoxy)oxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate)