NP-MRD: Showing NP-Card for (2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol (NP0215964)

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Record Information

Version

2.0

Created at

2022-09-05 15:45:37 UTC

Updated at

2022-09-05 15:45:37 UTC

NP-MRD ID

NP0215964

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol

Description

Neoraufuracin belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Thus, neoraufuracin is considered to be a flavonoid. (2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol is found in Neorautanenia amboensis. Based on a literature review very few articles have been published on Neoraufuracin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052217452D          

 31 34  0  0  1  0            999 V2000
    1.1809    2.1518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739    2.3234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    1.7103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9851    1.8818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    1.2687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441    1.4402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8961    0.8271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822    0.4841    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8342   -0.1290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    0.3126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4752   -0.5124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    0.9256    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -2.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -2.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -3.5558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -1.3648   -1.2692    2.6016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6607   -1.5094    1.2621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -0.5823    0.7526 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7225   -1.3163    0.4550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6426   -0.3806   -0.0100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0515   -0.9108   -0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1511   -2.0260   -0.8273 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2296   -0.0358   -1.4241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2134    0.8164   -1.9361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9611    0.8196   -1.2833 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4772    0.9533   -2.5804 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9620    0.0261   -0.4893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7966    0.6299   -0.2171 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    0.1747   -0.7251 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0173    1.2268   -1.5387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8207    1.6870   -2.8247 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6000    2.7189   -3.3617 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937    3.3047   -2.6068 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3571    4.3347   -3.1704 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7938    2.8534   -1.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0042    1.8196   -0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0571    1.2375    0.4362 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3934   -0.0355    0.3557 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4520   -1.0351   -0.0721 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185   -1.1763    1.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5063   -0.3592    1.1045 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4019   -0.4902    2.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2090   -1.4438    3.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1208   -1.5662    4.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1024   -2.2820    3.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2365   -2.1195    2.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6431   -2.0333    2.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2580   -1.3597    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9069   -0.2786    2.7880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8021    0.1514    1.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5594    0.5132    0.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6786   -0.1125   -0.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4648   -1.0578    0.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2261   -2.8674   -0.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511   -0.9138   -2.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5844    0.3474   -2.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2923    1.7428   -0.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0434    0.1152   -2.8437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7282   -0.8596   -1.1593 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3250   -0.7164   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0782    1.2907   -3.4784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4538    3.0862   -4.3670 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0883    4.7683   -2.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5768    3.3180   -0.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9991   -0.2518    1.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -1.9999   -0.2329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9237   -0.6970   -1.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6497    0.3852    0.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2769    0.1680    2.1869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9320   -0.9988    5.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9561   -3.0311    3.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3721   -2.7732    1.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 23 22  1  0
 22 21  1  0
 21 20  2  0
 20 18  1  0
 18 19  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 12  3  1  0
 15 14  1  0
 31 25  1  0
 15 21  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  1
  5 36  1  1
  6 37  1  0
  6 38  1  0
  7 39  1  0
  8 40  1  6
  9 41  1  0
 10 42  1  1
 11 43  1  0
 12 44  1  6
 14 45  1  6
 23 50  1  1
 24 51  1  0
 24 52  1  0
 26 53  1  0
 27 54  1  0
 29 55  1  0
 30 56  1  0
 31 57  1  0
 20 49  1  0
 19 48  1  0
 17 47  1  0
 16 46  1  0
M  END


  Mrv1652309052217452D          

 31 34  0  0  1  0            999 V2000
    1.1809    2.1518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739    2.3234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    1.7103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9851    1.8818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    1.2687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441    1.4402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8961    0.8271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822    0.4841    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8342   -0.1290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    0.3126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4752   -0.5124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    0.9256    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -2.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -2.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -3.5558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215964

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1[C@@H](CC2=CC=C(O)C=C2)OC2=CC(O)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O9/c1-28-22-21(19(27)18(26)17(10-23)30-22)31-20-14-7-6-13(25)9-15(14)29-16(20)8-11-2-4-12(24)5-3-11/h2-7,9,16-27H,8,10H2,1H3/t16-,17-,18-,19+,20+,21-,22-/m1/s1

> <INCHI_KEY>
NYWDXRKGBVXINM-OWLUANBVSA-N

> <FORMULA>
C22H26O9

> <MOLECULAR_WEIGHT>
434.441

> <EXACT_MASS>
434.157682417

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.191804893143726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6R)-5-{[(2R,3S)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol

> <JCHEM_LOGP>
1.2745285166666664

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.242246857154383

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.341319590339857

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810834924323153

> <JCHEM_POLAR_SURFACE_AREA>
138.07000000000002

> <JCHEM_REFRACTIVITY>
107.20239999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6R)-5-{[(2R,3S)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       2.204   4.017   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.698   4.337   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.333   3.192   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.839   3.513   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.869   2.368   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.376   2.688   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -5.406   1.544   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.393   0.904   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.424  -0.241   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.887   0.583   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.887  -0.957   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.143   1.728   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.650   1.408   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.591  -2.843   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.126  -2.549   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.320  -3.970   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.090  -5.304   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.630  -5.304   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.400  -6.638   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -3.400  -3.970   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    3   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   15   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   14   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₉

Average Mass

434.4410 Da

Monoisotopic Mass

434.15768 Da

IUPAC Name

(2R,3S,4S,5R,6R)-5-{[(2R,3S)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol

Traditional Name

(2R,3S,4S,5R,6R)-5-{[(2R,3S)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol

CAS Registry Number

Not Available

SMILES

CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1[C@@H](CC2=CC=C(O)C=C2)OC2=CC(O)=CC=C12

InChI Identifier

InChI=1S/C22H26O9/c1-28-22-21(19(27)18(26)17(10-23)30-22)31-20-14-7-6-13(25)9-15(14)29-16(20)8-11-2-4-12(24)5-3-11/h2-7,9,16-27H,8,10H2,1H3/t16-,17-,18-,19+,20+,21-,22-/m1/s1

InChI Key

NYWDXRKGBVXINM-OWLUANBVSA-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
Neorautanenia amboensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Monosaccharide
Oxane
Benzenoid
Secondary alcohol
Oxacycle
Ether
Dialkyl ether
Acetal
Organoheterocyclic compound
Hydrocarbon derivative
Alcohol
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.27	ChemAxon
pKa (Strongest Acidic)	9.34	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	138.07 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	107.2 m³·mol⁻¹	ChemAxon
Polarizability	43.19 Å³	ChemAxon
Number of Rings	4	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

C00008062

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

163087284

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)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol (NP0215964)

MOL for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

3D MOL for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

3D SDF for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

3D-SDF for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

PDB for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

3D PDB for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

SMILES for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

INCHI for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

Structure for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)

3D Structure for NP0215964 ((2r,3s,4s,5r,6r)-5-{[(2r,3s)-6-hydroxy-2-[(4-hydroxyphenyl)methyl]-2,3-dihydro-1-benzofuran-3-yl]oxy}-2-(hydroxymethyl)-6-methoxyoxane-3,4-diol)