NP-MRD: Showing NP-Card for 2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol (NP0253710)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 17:39:35 UTC

Updated at

2022-09-07 17:39:35 UTC

NP-MRD ID

NP0253710

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol

Description

2-[3-(3-{[4-(2,3-Dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. 2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol is found in Pieris formosa. Based on a literature review very few articles have been published on 2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072219392D          

 39 41  0  0  0  0            999 V2000
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2295   -3.5549    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  2  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
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 11  2  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
 12 15  2  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  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  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  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  1  0  0  0  0
 28 36  1  0  0  0  0
 36 37  1  0  0  0  0
 23 38  2  0  0  0  0
 17 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END

     RDKit          3D

 78 80  0  0  0  0  0  0  0  0999 V2000
    2.1616    0.4123   -3.1141 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626    0.6907   -1.7374 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1587    0.4548   -0.9245 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3028   -0.0474   -1.5194 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4345   -0.3081   -0.7764 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6828   -0.8526   -1.4056 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5128    0.3192   -1.8281 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8886    1.1399   -2.7365 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8763   -0.0931   -2.3250 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6796    1.0101   -2.5275 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3638   -0.0449    0.5703 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2398    0.4558    1.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2451    0.7008    2.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4259    0.4200    3.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1192    0.7103    0.4398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9406    1.2247    1.0390 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9202    0.3638    1.5548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0467   -0.9853    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828   -1.5622    0.8621 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2322   -2.9728    0.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0394   -1.7729    1.9827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0722   -1.2167    2.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2174    0.1741    2.6720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4408    0.7151    3.3046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4797    1.2016    2.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9712    0.0905    1.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9452    0.5980    0.5664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4230   -0.3684   -0.3090 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.7482   -0.6278    0.0741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5113    0.4871   -0.2319 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.7633    0.5768    0.5947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8114    0.4308   -1.7123 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.2412    1.6823   -2.1696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6375   -0.0755   -2.4843 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5158    0.6375   -3.6807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3255    0.0496   -1.7444 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3851   -0.6970   -2.4537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1964    0.9300    2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3037    2.3153    2.2300 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2500   -0.6758   -3.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319    0.7365   -3.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9946    0.9185   -3.6176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3559   -0.2553   -2.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4080   -1.5304   -2.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2496   -1.3656   -0.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6917    0.9349   -0.9001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2443    2.0576   -2.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3701   -0.8116   -1.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7447   -0.6386   -3.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4981    1.0052   -1.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2380   -0.2406    1.1758 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2633    1.1022    3.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1520    0.4975    4.3938 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7069   -0.6344    3.1098 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8422    2.2612    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2144   -3.3458    0.4638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3906   -3.4276    0.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1407   -3.3276    1.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1565   -2.8636    1.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8488   -1.8653    2.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1372    1.5896    3.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708   -0.0160    4.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1592    2.0787    1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3946    1.4701    2.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3321   -0.7272    2.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1358   -0.2629    0.8210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8758   -1.3138   -0.0828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8944    1.4087   -0.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5024    0.2758    1.6512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5651   -0.0861    0.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1017    1.6339    0.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6758   -0.2649   -1.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0350    1.9128   -1.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7580   -1.1429   -2.7710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8256    0.1008   -4.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0651    1.1367   -1.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4125   -1.6414   -2.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0807    2.7623    2.6590 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  5 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  2  0
 22 23  1  0
 23 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  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 23 38  2  0
 38 39  1  0
 15  3  1  0
 38 17  1  0
 36 28  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  4 43  1  0
  6 44  1  0
  6 45  1  0
  7 46  1  1
  8 47  1  0
  9 48  1  0
  9 49  1  0
 10 50  1  0
 11 51  1  0
 14 52  1  0
 14 53  1  0
 14 54  1  0
 16 55  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 21 59  1  0
 22 60  1  0
 24 61  1  0
 24 62  1  0
 25 63  1  0
 25 64  1  0
 26 65  1  0
 26 66  1  0
 28 67  1  6
 30 68  1  6
 31 69  1  0
 31 70  1  0
 31 71  1  0
 32 72  1  1
 33 73  1  0
 34 74  1  6
 35 75  1  0
 36 76  1  1
 37 77  1  0
 39 78  1  0
M  END


  Mrv1652309072219392D          

 39 41  0  0  0  0            999 V2000
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2295   -3.5549    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  2  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
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 11  2  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
 12 15  2  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  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  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  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  1  0  0  0  0
 28 36  1  0  0  0  0
 36 37  1  0  0  0  0
 23 38  2  0  0  0  0
 17 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253710

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CC(O)CO)=CC(OC)=C1NC1=C(OC)C=CC(CCCOC2OC(C)C(O)C(O)C2O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H39NO11/c1-14-23(31)25(33)26(34)27(39-14)38-9-5-6-16-7-8-18(35-2)22(24(16)32)28-21-19(36-3)11-15(10-17(30)13-29)12-20(21)37-4/h7-8,11-12,14,17,23,25-34H,5-6,9-10,13H2,1-4H3

> <INCHI_KEY>
XGBWRXIJOYLKPR-UHFFFAOYSA-N

> <FORMULA>
C27H39NO11

> <MOLECULAR_WEIGHT>
553.605

> <EXACT_MASS>
553.25231108

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
58.80375467227617

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol

> <JCHEM_LOGP>
0.7695233920000009

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.222663415933631

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.011097062832658

> <JCHEM_PKA_STRONGEST_BASIC>
3.358369708657227

> <JCHEM_POLAR_SURFACE_AREA>
179.56

> <JCHEM_REFRACTIVITY>
140.48960000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -6.668 -11.550   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -6.668 -14.630   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -4.001  -5.390   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.428  -6.636   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    5   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12    3   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   38                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   38                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   28   37                                                  
CONECT   37   36                                                            
CONECT   38   23   17   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₉NO₁₁

Average Mass

553.6050 Da

Monoisotopic Mass

553.25231 Da

IUPAC Name

2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol

Traditional Name

2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

COC1=CC(CC(O)CO)=CC(OC)=C1NC1=C(OC)C=CC(CCCOC2OC(C)C(O)C(O)C2O)=C1O

InChI Identifier

InChI=1S/C27H39NO11/c1-14-23(31)25(33)26(34)27(39-14)38-9-5-6-16-7-8-18(35-2)22(24(16)32)28-21-19(36-3)11-15(10-17(30)13-29)12-20(21)37-4/h7-8,11-12,14,17,23,25-34H,5-6,9-10,13H2,1-4H3

InChI Key

XGBWRXIJOYLKPR-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
Pieris formosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Dimethoxybenzene
M-dimethoxybenzene
Aminophenyl ether
Methoxyaniline
Aminophenol
Anisole
Phenoxy compound
O-aminophenol
Phenol ether
Aniline or substituted anilines
Methoxybenzene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Monosaccharide
Oxane
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Ether
Secondary amine
Primary alcohol
Organopnictogen compound
Alcohol
Amine
Organic nitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organonitrogen compound
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	0.77	ChemAxon
pKa (Strongest Acidic)	10.01	ChemAxon
pKa (Strongest Basic)	3.36	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	179.56 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	140.49 m³·mol⁻¹	ChemAxon
Polarizability	58.8 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

163014372

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol (NP0253710)

MOL for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

3D MOL for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

3D SDF for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

3D-SDF for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

PDB for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

3D PDB for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

SMILES for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

INCHI for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

Structure for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)

3D Structure for NP0253710 (2-[3-(3-{[4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl]amino}-2-hydroxy-4-methoxyphenyl)propoxy]-6-methyloxane-3,4,5-triol)