NP-MRD: Showing NP-Card for (2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol (NP0241633)

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Record Information

Version

2.0

Created at

2022-09-07 01:45:55 UTC

Updated at

2022-09-07 01:45:56 UTC

NP-MRD ID

NP0241633

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol

Description

CHEMBL612191 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. (2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol is found in Betula platyphylla. Based on a literature review very few articles have been published on CHEMBL612191.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072203452D          

 32 34  0  0  1  0            999 V2000
    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 C   0  0  1  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 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
   -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
   -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
    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  2  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  2  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
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5165   -0.4170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3234   -0.2455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6590    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4795    0.5944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7359   -0.9600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5564   -1.0462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1839   -1.5731    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3554   -2.3800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  1  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  2  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  1  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
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
  2 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  1  0  0  0
 15 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
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    2.2461   -1.6089    0.3989 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7452   -1.4679    0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.8218    0.1092   -0.4354 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9146    0.0021    0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5325   -0.0321    1.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7057    0.1177    0.1792 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6716   -0.1891    0.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2997    0.6253    0.9996 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6586    0.1071    1.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4436    0.0658    0.2408 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7286   -0.4023    0.4883 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0640   -1.5021   -0.2476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0424   -1.1806   -1.1481 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.3916   -1.7466   -0.7227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3715   -1.4081   -1.6526 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0854    0.3155   -1.2642 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0870    0.7349   -2.1284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6736    0.7265    0.1345 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.7619    0.7818    0.9987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3634    2.0532    0.5096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4885    2.9481    1.5702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2140    2.3923   -0.4073 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5984    2.2888   -1.7503 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0054    1.5377   -0.1626 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7439    2.1683    0.8501 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0357   -3.5243   -0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9133   -3.2234    0.7998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0364   -1.2879    1.4642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1037   -1.9952   -0.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7171    0.5926   -0.5088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9973    0.3361    1.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5805    0.1175   -2.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9903    0.1766   -2.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2204    0.1638   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5883   -0.0302    1.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1295   -0.0909    2.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787    0.0150    1.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6578    0.6085    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5317   -0.9492    1.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0919    0.6823    2.2094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8746   -0.6556    1.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8184   -1.6283   -2.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7141   -1.3289    0.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3354   -2.8416   -0.6078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7045   -2.2070   -2.1188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0832    0.7019   -1.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5710    0.0100   -2.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1668    1.7118    0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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 29 30  1  0
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 31 32  1  0
 11  5  1  0
 31 13  1  0
 25 18  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  1
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  6 41  1  0
  7 42  1  0
  9 43  1  0
 10 44  1  0
 11 45  1  0
 13 46  1  1
 15 47  1  1
 16 48  1  0
 16 49  1  0
 18 50  1  1
 20 51  1  6
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 22 54  1  0
 23 55  1  6
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 25 57  1  6
 26 58  1  0
 27 59  1  6
 28 60  1  0
 29 61  1  1
 30 62  1  0
 31 63  1  6
 32 64  1  0
M  END


  Mrv1652309072203452D          

 32 34  0  0  1  0            999 V2000
    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 C   0  0  1  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 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
   -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
   -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
    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  2  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  2  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
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5165   -0.4170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3234   -0.2455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6590    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4795    0.5944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7359   -0.9600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5564   -1.0462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1839   -1.5731    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3554   -2.3800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  1  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  2  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  1  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
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
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 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0241633

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CCC1=CC=C(O)C=C1)O[C@@H]1O[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O11/c1-10(2-3-11-4-6-12(23)7-5-11)30-21-19(28)17(26)16(25)14(32-21)9-29-20-18(27)15(24)13(8-22)31-20/h4-7,10,13-28H,2-3,8-9H2,1H3/t10-,13-,14+,15-,16+,17-,18+,19+,20+,21+/m0/s1

> <INCHI_KEY>
DJDISCKFJXDADJ-IMNWWGSQSA-N

> <FORMULA>
C21H32O11

> <MOLECULAR_WEIGHT>
460.476

> <EXACT_MASS>
460.19446185

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.12238707794726

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6R)-2-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2S)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.859200727666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.949476569048112

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.286351262592424

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981143337099244

> <JCHEM_POLAR_SURFACE_AREA>
178.53

> <JCHEM_REFRACTIVITY>
107.49370000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6R)-2-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2S)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-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       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.164  -0.778   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.670  -0.458   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.297   0.949   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      15.828   1.110   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.440  -1.792   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      15.972  -1.953   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      13.410  -2.936   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.730  -4.443   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5                                                       
CONECT   12    2   13                                                       
CONECT   13   12   14   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   18   26                                                  
CONECT   26   25                                                            
CONECT   27   15   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   13   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₂O₁₁

Average Mass

460.4760 Da

Monoisotopic Mass

460.19446 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H](CCC1=CC=C(O)C=C1)O[C@@H]1O[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C21H32O11/c1-10(2-3-11-4-6-12(23)7-5-11)30-21-19(28)17(26)16(25)14(32-21)9-29-20-18(27)15(24)13(8-22)31-20/h4-7,10,13-28H,2-3,8-9H2,1H3/t10-,13-,14+,15-,16+,17-,18+,19+,20+,21+/m0/s1

InChI Key

DJDISCKFJXDADJ-IMNWWGSQSA-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
Betula platyphylla	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
Disaccharide
Glycosyl compound
O-glycosyl compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Oxane
Oxolane
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Organic oxygen compound
Organooxygen 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

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

24658988

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

38347392

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,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol (NP0241633)

MOL for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

3D MOL for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

3D SDF for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

3D-SDF for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

PDB for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

3D PDB for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

SMILES for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

INCHI for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

Structure for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)

3D Structure for NP0241633 ((2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2s)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol)