NP-MRD: Showing NP-Card for [(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0184261)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 23:21:05 UTC

Updated at

2022-09-03 23:21:05 UTC

NP-MRD ID

NP0184261

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Description

Isobetonyoside F belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. [(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate is found in Prostanthera melissifolia. Based on a literature review very few articles have been published on Isobetonyoside F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042201212D          

 53 57  0  0  1  0            999 V2000
    3.9487   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2843   -4.3828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7994   -3.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1349   -2.9617    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6500   -2.2943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8295   -2.3805    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4940   -3.1342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9789   -3.8016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6735   -3.2204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3379   -3.9741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -4.0603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1819   -4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6668   -5.4814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6386   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9742   -5.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -5.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1302   -6.4938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -6.5801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4356   -5.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2561   -5.9989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1000   -5.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850   -4.4915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796   -5.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1886   -2.5530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -1.7993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0392   -1.1319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3747   -0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8898    0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7405    1.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0760    2.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8965    2.5503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2321    3.3039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814    1.8828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2019    1.9691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0459    1.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3446   -1.7131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6801   -0.9594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9554   -2.8755    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2910   -2.1218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8060   -1.4544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9810   -1.4544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7261   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3935   -0.1848    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8415    0.4283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456    0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7525    0.2567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0610   -0.6697    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8456   -0.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4403   -3.5429    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2608   -3.4567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1048   -4.2966    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5897   -4.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  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
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 25 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  6  0  0  0
  4 39  1  0  0  0  0
 39 40  1  6  0  0  0
 41 40  1  6  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  6  0  0  0
 46 47  1  0  0  0  0
 44 48  1  0  0  0  0
 41 48  1  0  0  0  0
 48 49  1  1  0  0  0
 39 50  1  0  0  0  0
 50 51  1  6  0  0  0
 50 52  1  0  0  0  0
  2 52  1  0  0  0  0
 52 53  1  1  0  0  0
M  END

     RDKit          3D

 97101  0  0  0  0  0  0  0  0999 V2000
   -3.3390   -3.0214   -2.9668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1556   -1.8789   -2.0337 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3576   -2.2172   -0.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8221   -1.2407    0.1651 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5622   -1.0033   -0.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5249   -1.3219    0.5579 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3844   -2.3575    0.0154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2415   -3.5428    0.7845 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8428   -2.0314   -0.0364 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6224   -3.0210   -0.8386 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980   -2.9055   -0.8098 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7141   -1.8453   -1.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1654   -0.8589   -1.7737 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1899   -1.8578   -1.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7898   -2.8860   -0.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2153   -3.0227   -0.4858 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7835   -4.1531    0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1286   -4.3368    0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9817   -3.3373   -0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3387   -3.5205    0.0046 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4559   -2.2014   -0.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3316   -1.2206   -1.1560 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0852   -2.0449   -0.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0400   -0.7051   -0.4042 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6139    0.0770    0.6476 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9484    1.3977    0.3124 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7804    1.9948    1.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1198    3.4256    0.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9100    4.2567    0.6599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2460    4.3048   -0.5559 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1135    5.0782   -0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3800    5.8130    0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078    6.5766    0.1994 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2810    5.7654    1.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1957    6.4997    2.6519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4205    4.9891    1.7134 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1494   -0.0404    0.8992 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1602    0.3537    2.2312 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7434   -0.0434    0.0009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0218   -0.2646    0.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5460    0.4503    1.4038 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0904   -0.4315    2.3159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4024   -0.6946    1.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9552    0.6144    1.4221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.4870    1.2809    2.5253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0397    0.4364    0.4021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5193    1.6954    0.0249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7171    1.2532    0.8770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6959    2.5785    1.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5624    0.4318   -1.4231 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1656    1.6289   -1.7001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0177   -0.6815   -2.3787 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7709   -0.2094   -3.6660 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9920   -2.7010   -3.8039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3629   -3.2927   -3.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7129   -3.9441   -2.4714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065   -1.5246   -2.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8402   -1.6566    1.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9391   -1.7258    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0875   -2.6150   -1.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3649   -3.3527    1.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2508   -2.1021    1.0184 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437   -2.9714   -1.8986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3667   -4.0380   -0.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7554   -1.0196   -1.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1578   -3.7046   -0.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0856   -4.9327    0.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5471   -5.2137    0.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9548   -2.7782   -0.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9700   -0.3788   -1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7452   -1.1315   -1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1454   -0.1432    1.6048 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2457    2.1267    2.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    1.4872    1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7304    3.3964   -0.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439    3.8796    1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316    3.7302   -1.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3695    5.0852   -1.6580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9843    6.6107   -0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0117    7.0782    2.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    4.9917    2.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3190    0.8099    0.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0112    1.3232    2.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3232    0.7477    0.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8496    1.1782    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3701   -1.4067    1.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0015   -1.1357    2.7420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9516    1.0768    3.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8936   -0.1191    0.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6966   -0.0941   -0.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2452    1.9553    0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7874    1.1977   -0.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2033    2.7275    2.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4759    0.5476   -1.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8206    1.6012   -2.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0986   -0.8690   -2.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4290   -0.7046   -4.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
  9 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  2  0
 25 37  1  0
 37 38  1  0
  4 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  1
 44 46  1  0
 46 47  1  0
 44 48  1  0
 48 49  1  0
 39 50  1  0
 50 51  1  0
 50 52  1  0
 52 53  1  0
 52  2  1  0
 37  6  1  0
 48 41  1  0
 23 16  1  0
 36 29  1  0
  1 54  1  0
  1 55  1  0
  1 56  1  0
  2 57  1  1
  4 58  1  1
  6 59  1  1
  7 60  1  6
  8 61  1  0
  9 62  1  1
 10 63  1  0
 10 64  1  0
 14 65  1  0
 15 66  1  0
 17 67  1  0
 18 68  1  0
 20 69  1  0
 22 70  1  0
 23 71  1  0
 25 72  1  1
 27 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 30 77  1  0
 31 78  1  0
 33 79  1  0
 35 80  1  0
 36 81  1  0
 37 82  1  6
 38 83  1  0
 39 84  1  1
 41 85  1  1
 43 86  1  0
 43 87  1  0
 45 88  1  0
 46 89  1  0
 46 90  1  0
 47 91  1  0
 48 92  1  6
 49 93  1  0
 50 94  1  6
 51 95  1  0
 52 96  1  6
 53 97  1  0
M  END


  Mrv1652309042201212D          

 53 57  0  0  1  0            999 V2000
    3.9487   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2843   -4.3828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7994   -3.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1349   -2.9617    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6500   -2.2943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8295   -2.3805    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4940   -3.1342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9789   -3.8016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6735   -3.2204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3379   -3.9741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -4.0603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1819   -4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6668   -5.4814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6386   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9742   -5.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -5.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1302   -6.4938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -6.5801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4356   -5.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2561   -5.9989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1000   -5.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850   -4.4915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796   -5.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1886   -2.5530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -1.7993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0392   -1.1319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3747   -0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8898    0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7405    1.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0760    2.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8965    2.5503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2321    3.3039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814    1.8828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2019    1.9691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0459    1.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3446   -1.7131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6801   -0.9594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9554   -2.8755    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2910   -2.1218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8060   -1.4544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9810   -1.4544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7261   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3935   -0.1848    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8415    0.4283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456    0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7525    0.2567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0610   -0.6697    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8456   -0.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4403   -3.5429    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2608   -3.4567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1048   -4.2966    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5897   -4.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  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
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 25 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  6  0  0  0
  4 39  1  0  0  0  0
 39 40  1  6  0  0  0
 41 40  1  6  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  6  0  0  0
 46 47  1  0  0  0  0
 44 48  1  0  0  0  0
 41 48  1  0  0  0  0
 48 49  1  1  0  0  0
 39 50  1  0  0  0  0
 50 51  1  6  0  0  0
 50 52  1  0  0  0  0
  2 52  1  0  0  0  0
 52 53  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0184261

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](COC(=O)\C=C\C3=CC=C(O)C(O)=C3)O[C@@H](OCCC3=CC=C(O)C(O)=C3)[C@@H]2O)[C@H](O[C@@H]2OC[C@](O)(CO)[C@H]2O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H44O19/c1-15-24(41)26(43)29(53-33-30(45)34(46,13-35)14-49-33)32(50-15)52-28-25(42)22(12-48-23(40)7-4-16-2-5-18(36)20(38)10-16)51-31(27(28)44)47-9-8-17-3-6-19(37)21(39)11-17/h2-7,10-11,15,22,24-33,35-39,41-46H,8-9,12-14H2,1H3/b7-4+/t15-,22+,24-,25+,26+,27+,28-,29+,30-,31+,32-,33-,34+/m0/s1

> <INCHI_KEY>
XQTBLJOROUNENZ-PWYLGMGVSA-N

> <FORMULA>
C34H44O19

> <MOLECULAR_WEIGHT>
756.707

> <EXACT_MASS>
756.247679197

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
74.68978338540299

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3R,4S,5R,6R)-4-{[(2S,3R,4R,5R,6S)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-0.4570736996666669

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.641895045983745

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.00982772385854

> <JCHEM_PKA_STRONGEST_BASIC>
-3.683395991788644

> <JCHEM_POLAR_SURFACE_AREA>
304.21

> <JCHEM_REFRACTIVITY>
175.07330000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R,4S,5R,6R)-4-{[(2S,3R,4R,5R,6S)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.371  -9.588   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.997  -8.181   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.092  -6.935   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.719  -5.529   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.813  -4.283   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.282  -4.444   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.655  -5.850   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.561  -7.096   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.124  -6.011   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.497  -7.418   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.966  -7.579   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.340  -8.986   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.245 -10.232   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.192  -9.147   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.818 -10.554   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.350 -10.715   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.976 -12.122   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.508 -12.283   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.413 -11.037   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -7.945 -11.198   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -5.787  -9.630   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -6.692  -8.384   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.255  -9.469   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.219  -4.766   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.845  -3.359   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.940  -2.113   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.566  -0.706   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.661   0.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.287   1.947   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.382   3.193   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.009   4.600   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.540   4.761   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.166   6.167   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.445   3.515   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.977   3.676   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.819   2.108   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.377  -3.198   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       5.003  -1.791   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.250  -5.368   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.876  -3.961   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.971  -2.715   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       7.431  -2.715   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       6.955  -1.250   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       8.201  -0.345   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       7.171   0.799   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       9.232   0.799   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      10.738   0.479   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       9.447  -1.250   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      10.912  -0.774   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      10.155  -6.613   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      11.687  -6.452   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       9.529  -8.020   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      10.434  -9.266   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   52                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   39                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   37                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   24                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16                                                       
CONECT   24    9   25                                                       
CONECT   25   24   26   37                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29                                                       
CONECT   37   25    6   38                                                  
CONECT   38   37                                                            
CONECT   39    4   40   50                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   48                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45   46   48                                             
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46                                                            
CONECT   48   44   41   49                                                  
CONECT   49   48                                                            
CONECT   50   39   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50    2   53                                                  
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₄O₁₉

Average Mass

756.7070 Da

Monoisotopic Mass

756.24768 Da

IUPAC Name

[(2R,3R,4S,5R,6R)-4-{[(2S,3R,4R,5R,6S)-3-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](COC(=O)\C=C\C3=CC=C(O)C(O)=C3)O[C@@H](OCCC3=CC=C(O)C(O)=C3)[C@@H]2O)[C@H](O[C@@H]2OC[C@](O)(CO)[C@H]2O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C34H44O19/c1-15-24(41)26(43)29(53-33-30(45)34(46,13-35)14-49-33)32(50-15)52-28-25(42)22(12-48-23(40)7-4-16-2-5-18(36)20(38)10-16)51-31(27(28)44)47-9-8-17-3-6-19(37)21(39)11-17/h2-7,10-11,15,22,24-33,35-39,41-46H,8-9,12-14H2,1H3/b7-4+/t15-,22+,24-,25+,26+,27+,28-,29+,30-,31+,32-,33-,34+/m0/s1

InChI Key

XQTBLJOROUNENZ-PWYLGMGVSA-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
Prostanthera melissifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Hydroxycinnamic acid or derivatives
Cinnamic acid or derivatives
Cinnamic acid ester
Coumaric acid or derivatives
O-glycosyl compound
Glycosyl compound
Tyrosol derivative
Styrene
Catechol
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Fatty acid ester
Fatty acyl
Monocyclic benzene moiety
Oxane
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Oxolane
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Carbonyl group
Primary alcohol
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-0.46	ChemAxon
pKa (Strongest Acidic)	9.01	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	304.21 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	175.07 m³·mol⁻¹	ChemAxon
Polarizability	74.69 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

101035919

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0184261)

MOL for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D MOL for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D SDF for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D-SDF for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

PDB for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D PDB for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

SMILES for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

INCHI for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

Structure for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D Structure for NP0184261 ([(2r,3r,4s,5r,6r)-4-{[(2s,3r,4r,5r,6s)-3-{[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)