NP-MRD: Showing NP-Card for 4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde (NP0255844)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 20:29:00 UTC

Updated at

2022-09-07 20:29:00 UTC

NP-MRD ID

NP0255844

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde

Description

4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. 4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde is found in Cyclopia intermedia. Based on a literature review very few articles have been published on 4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072222292D          

 29 31  0  0  1  0            999 V2000
    8.0931   -4.8027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2726   -4.8889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7877   -4.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -4.3077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -3.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -2.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.2192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -2.3054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1769   -3.0591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564   -3.1453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0208   -3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -3.9852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715   -2.4779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0510   -2.5641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070   -1.7242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7221   -1.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0275   -1.6380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3631   -0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781   -0.2169    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0531   -0.2169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    1.0527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9136    1.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7627    2.4504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331    0.5678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9177    0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6383   -2.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1232   -3.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  1  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 22 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  6  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
  3 29  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    5.9309   -4.0359   -1.6643 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1874   -4.1515   -0.6568 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -3.1166   -0.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4286   -3.2444    0.8101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265   -2.2880    1.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3739   -1.0945    0.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4506   -0.1649    0.8610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2110    1.0281    0.2305 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4892    2.1026    1.0866 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4807    3.2831    0.3546 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1040    4.4288    1.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4032    4.6476    2.2791 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0543    3.5690   -0.0443 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1213    4.8075   -0.6167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3314    2.4392   -1.0083 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5328    2.6565   -1.6204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2474    1.1820   -0.2086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7342    0.0645   -0.8222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7536   -0.5139   -0.1145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4475   -1.8305    0.3030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6578   -2.1738    0.9095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6403   -1.9075   -0.2120 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6686   -3.0316   -1.0142 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0199   -1.5913    0.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4883   -2.6464    1.0628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0214   -0.7080   -0.8932 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7760   -0.9663   -2.2400 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1866   -0.9664   -0.6597 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1033   -1.9586   -1.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2767   -5.0477   -0.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5395   -4.1621    1.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9065   -2.4327    2.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8422    1.1613   -0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0607    3.1080   -0.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9631    5.3393    0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1775    4.2856    1.2312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9700    4.8931    3.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5765    3.4045    0.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8391    5.2946   -0.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4781    2.4314   -1.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5410    2.3306   -2.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8213    1.3430    0.7403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033    0.0286    0.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8140   -1.4411    1.7257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6844   -3.2247    1.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4181   -2.9516   -1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6743   -1.4484   -0.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9683   -0.6460    0.9065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4272   -2.4793    2.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6552    0.1906   -0.8252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4040   -1.8701   -2.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1539   -0.0934   -1.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7272   -1.8326   -1.8889 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  3 29  1  0
 29 28  2  0
  8 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 22 26  1  0
 26 27  1  0
 17 15  1  0
 15 16  1  0
 15 13  1  0
 13 14  1  0
 13 10  1  0
 28  6  1  0
 26 19  1  0
 12 37  1  0
 11 35  1  0
 11 36  1  0
 10 34  1  6
  8 33  1  6
  5 32  1  0
  4 31  1  0
  2 30  1  0
 29 53  1  0
 28 52  1  0
 17 42  1  1
 19 43  1  1
 21 44  1  0
 21 45  1  0
 23 46  1  0
 24 47  1  0
 24 48  1  0
 25 49  1  0
 26 50  1  6
 27 51  1  0
 15 40  1  6
 16 41  1  0
 13 38  1  1
 14 39  1  0
M  END


  Mrv1652309072222292D          

 29 31  0  0  1  0            999 V2000
    8.0931   -4.8027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2726   -4.8889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7877   -4.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -4.3077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -3.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -2.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.2192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -2.3054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1769   -3.0591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564   -3.1453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0208   -3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -3.9852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715   -2.4779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0510   -2.5641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070   -1.7242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7221   -1.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0275   -1.6380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3631   -0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781   -0.2169    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0531   -0.2169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    1.0527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9136    1.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7627    2.4504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331    0.5678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9177    0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6383   -2.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1232   -3.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  1  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 22 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  6  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
  3 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255844

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](OC2=CC=C(C=O)C=C2)[C@H](O[C@@H]2OC[C@@](O)(CO)[C@@H]2O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O11/c19-5-9-1-3-10(4-2-9)27-16-14(13(23)12(22)11(6-20)28-16)29-17-15(24)18(25,7-21)8-26-17/h1-5,11-17,20-25H,6-8H2/t11-,12-,13+,14-,15-,16-,17+,18+/m1/s1

> <INCHI_KEY>
WNBIKNLJJFCZAQ-OKOXNFRXSA-N

> <FORMULA>
C18H24O11

> <MOLECULAR_WEIGHT>
416.379

> <EXACT_MASS>
416.131861593

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
40.18828397802352

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde

> <JCHEM_LOGP>
-2.162384314333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.652098425518506

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.807562255405655

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810925692672834

> <JCHEM_POLAR_SURFACE_AREA>
175.37

> <JCHEM_REFRACTIVITY>
93.43750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde

> <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  O   UNK     0      15.107  -8.965   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      13.576  -9.126   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.670  -7.880   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.139  -8.041   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.234  -6.795   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.860  -5.388   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.955  -4.142   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.423  -4.303   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.797  -5.710   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.265  -5.871   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.639  -7.278   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.107  -7.439   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.360  -4.625   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.829  -4.786   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.986  -3.219   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.081  -1.973   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.518  -3.058   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.144  -1.651   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.239  -0.405   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.699  -0.405   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.223   1.060   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.469   1.965   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.439   3.109   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.500   3.109   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.024   4.574   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.715   1.060   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.180   1.536   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.392  -5.227   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.297  -6.473   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   26                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   22   19   27                                                  
CONECT   27   26                                                            
CONECT   28    6   29                                                       
CONECT   29   28    3                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₄O₁₁

Average Mass

416.3790 Da

Monoisotopic Mass

416.13186 Da

IUPAC Name

4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde

Traditional Name

4-{[(2S,3R,4S,5S,6R)-3-{[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](OC2=CC=C(C=O)C=C2)[C@H](O[C@@H]2OC[C@@](O)(CO)[C@@H]2O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C18H24O11/c19-5-9-1-3-10(4-2-9)27-16-14(13(23)12(22)11(6-20)28-16)29-17-15(24)18(25,7-21)8-26-17/h1-5,11-17,20-25H,6-8H2/t11-,12-,13+,14-,15-,16-,17+,18+/m1/s1

InChI Key

WNBIKNLJJFCZAQ-OKOXNFRXSA-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
Cyclopia intermedia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Disaccharide
O-glycosyl compound
Phenoxy compound
Benzaldehyde
Benzoyl
Phenol ether
Aryl-aldehyde
Monocyclic benzene moiety
Oxane
Benzenoid
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Primary alcohol
Aldehyde
Alcohol
Hydrocarbon derivative
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	-2.2	ChemAxon
pKa (Strongest Acidic)	11.81	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	175.37 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	93.44 m³·mol⁻¹	ChemAxon
Polarizability	40.19 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

162909307

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde (NP0255844)

MOL for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

3D MOL for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

3D SDF for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

3D-SDF for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

PDB for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

3D PDB for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

SMILES for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

INCHI for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

Structure for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)

3D Structure for NP0255844 (4-{[(2s,3r,4s,5s,6r)-3-{[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde)