NP-MRD: Showing NP-Card for (2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol (NP0307042)

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Record Information

Version

2.0

Created at

2022-09-10 23:54:15 UTC

Updated at

2022-09-10 23:54:15 UTC

NP-MRD ID

NP0307042

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol

Description

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. (2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol is found in Breynia rostrata. Based on a literature review very few articles have been published on (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112201542D          

 31 33  0  0  1  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -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
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  2  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   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    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
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  2  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
   -1.4289   -1.6500    0.0000 C   0  0  1  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
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 12 17  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
 18 31  2  0  0  0  0
  4 31  1  0  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
   -1.2129    7.5521    1.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5877    6.1995    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2591    5.1412    1.5270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7051    3.7879    1.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3532    3.2751    1.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8258    2.0309    1.6986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2664    1.2453    0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7326   -0.0225    0.4456 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480   -0.7351    1.0771 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0830   -0.5452    0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3208   -2.1564    1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3386   -2.9686    1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2656   -2.9423    3.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838   -3.6886    3.9880 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1351   -4.4309    3.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -4.4414    1.9557 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643   -3.6917    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8012    1.7078   -0.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4494    1.0213   -0.9905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3252   -0.2314   -1.5110 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2103   -0.1530   -2.9044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1688   -1.4296   -3.4475 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6154   -1.4882   -4.8518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6487   -2.8460   -5.2491 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5817   -1.9694   -3.3898 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7453   -3.1678   -4.0751 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8343   -2.2049   -1.9040 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1203   -2.6817   -1.7147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6019   -0.9778   -1.1144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4685   -1.3145    0.2319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2778    3.0174    0.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7560    8.3652    0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0503    7.7561    2.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2950    7.5702    0.8771 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5020    6.2261    0.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8015    6.0676   -0.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3307    5.1218    1.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1228    5.3762    2.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7964    3.9074    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6864    1.6111    2.2568 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -0.3155    2.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9010   -0.2505    1.0565 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4166   -1.4389   -0.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9222    0.2292   -0.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3370   -2.1690    1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1368   -2.5437    0.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5123   -2.3541    3.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1607   -3.6950    5.0720 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8721   -5.0359    3.8920 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9219   -5.0127    1.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2933   -3.7125    0.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4610   -0.8164   -1.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5412   -2.0431   -2.7427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1955   -0.8956   -5.5789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4491   -1.1896   -4.8675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0085   -3.3772   -4.7287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2952   -1.1799   -3.7033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -3.6142   -3.6166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0546   -2.9629   -1.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5858   -2.0869   -1.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4634   -0.2910   -1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3045   -1.5270    0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1240    3.3891   -0.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  3  4  1  0
  4  5  2  0
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 23 24  1  0
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 25 27  1  0
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 27 29  1  0
 29 30  1  0
 18 31  2  0
 31  4  1  0
 17 12  1  0
 29 20  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  5 39  1  0
  6 40  1  0
  9 41  1  1
 10 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 13 47  1  0
 14 48  1  0
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 16 50  1  0
 17 51  1  0
 20 52  1  1
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 23 54  1  0
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 24 56  1  0
 25 57  1  6
 26 58  1  0
 27 59  1  1
 28 60  1  0
 29 61  1  1
 30 62  1  0
 31 63  1  0
M  END


  Mrv1652309112201542D          

 31 33  0  0  1  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -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
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  2  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   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  2  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
   -1.4289   -1.6500    0.0000 C   0  0  1  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
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0307042

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=CC=C(O[C@H](C)CC2=CC=CC=C2)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-3-7-16-10-11-18(29-15(2)12-17-8-5-4-6-9-17)19(13-16)30-24-23(28)22(27)21(26)20(14-25)31-24/h4-6,8-11,13,15,20-28H,3,7,12,14H2,1-2H3/t15-,20-,21-,22+,23-,24-/m1/s1

> <INCHI_KEY>
ZKVRSNBRTIQMBB-CTYPUASWSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.53018892927801

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol

> <JCHEM_LOGP>
3.076209201666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.19604365899411

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.200014712444528

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092354911012

> <JCHEM_POLAR_SURFACE_AREA>
108.61000000000001

> <JCHEM_REFRACTIVITY>
114.67610000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   31                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    7   19   31                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   20   30                                                  
CONECT   30   29                                                            
CONECT   31   18    4                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol

Traditional Name

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-{[(2R)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CCCC1=CC=C(O[C@H](C)CC2=CC=CC=C2)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

InChI Identifier

InChI=1S/C24H32O7/c1-3-7-16-10-11-18(29-15(2)12-17-8-5-4-6-9-17)19(13-16)30-24-23(28)22(27)21(26)20(14-25)31-24/h4-6,8-11,13,15,20-28H,3,7,12,14H2,1-2H3/t15-,20-,21-,22+,23-,24-/m1/s1

InChI Key

ZKVRSNBRTIQMBB-CTYPUASWSA-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
Breynia rostrata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Phenolic glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Phenylpropane
Phenoxy compound
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Monosaccharide
Benzenoid
Oxane
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Ether
Acetal
Polyol
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Primary alcohol
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	3.08	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	108.61 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	114.68 m³·mol⁻¹	ChemAxon
Polarizability	46.53 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

163193821

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol (NP0307042)

MOL for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

3D MOL for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

3D SDF for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

3D-SDF for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

PDB for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

3D PDB for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

SMILES for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

INCHI for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

Structure for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)

3D Structure for NP0307042 ((2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-{[(2r)-1-phenylpropan-2-yl]oxy}-5-propylphenoxy)oxane-3,4,5-triol)