NP-MRD: Showing NP-Card for (3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol (NP0204852)

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Record Information

Version

2.0

Created at

2022-09-05 00:37:45 UTC

Updated at

2022-09-05 00:37:45 UTC

NP-MRD ID

NP0204852

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol

Description

(3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. (3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol is found in Sanguisorba minor. Based on a literature review very few articles have been published on (3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202372D          

 32 34  0  0  1  0            999 V2000
   -0.2773   -1.9371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4372   -1.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517   -1.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1517   -2.7621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -3.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3964   -3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3358   -3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6180   -4.5819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5806   -2.7621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3931   -2.6189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8628   -3.5374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6752   -3.6806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5806   -1.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2646   -1.4758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3931   -2.0804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9234   -1.4484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -1.5246    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4596   -0.9515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2526   -1.1789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8461   -0.6059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6465    0.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2399    0.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0330    0.5403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2326   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6391   -0.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -0.7962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9160   -0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287    0.6319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9659    1.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7904    1.3027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777    0.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -0.1254    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  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 17 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    1.1587   -1.5126    2.3245 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9341   -2.4221    1.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3253   -2.1347    0.5349 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4698   -2.1699    1.3156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5367   -2.3958    0.4657 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6043   -3.7995    0.2957 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7619   -2.0599    1.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9415   -2.7818    2.1592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4015   -1.7944   -0.8949 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6974   -1.3330   -1.2439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1044   -2.7637   -1.8567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9851   -2.3201   -3.0602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4555   -0.6482   -0.9897 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0062   -0.5548   -2.3051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284    0.5155   -0.7710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7997    0.4982    0.4027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2762   -0.6964   -0.0573 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9617   -0.7098   -0.7308 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2909    0.3868   -1.3392 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5737    0.8598   -1.5509 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1339    1.6811   -0.5974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4111    2.1561   -0.8013 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0974    1.8061   -1.9408 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281    0.9777   -2.8991 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470    0.4992   -2.6980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    0.1844    0.9638 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2120    1.4765    1.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1497    1.8311    2.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1160    3.1246    3.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1429    4.1492    2.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2032    3.8753    0.7961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2365    2.5502    0.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6833   -0.7568    1.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7625   -2.4703    0.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8299   -3.4120    1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3769   -2.8407   -0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0721   -4.2790    0.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416   -2.8434    2.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3608   -1.9808   -0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7974   -1.9818   -3.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1545   -1.0856   -2.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7034    0.9253    0.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6008    1.9669    0.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8852    2.8141   -0.0575 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0941    2.2025   -2.0561 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1216    0.7390   -3.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8147   -0.1458   -3.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1268    1.0559    3.3502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0681    3.3384    4.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1180    5.2004    2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2255    4.6788    0.0538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2898    2.3997   -0.6658 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  6
  5  7  1  0
  7  8  1  0
  5  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
  9 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 13 17  1  0
 17 18  1  6
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 17 26  1  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 17  3  1  0
 25 20  1  0
 32 27  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  6
  6 37  1  0
  8 38  1  0
 10 39  1  0
 12 40  1  0
 14 41  1  0
 16 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 28 48  1  0
 29 49  1  0
 30 50  1  0
 31 51  1  0
 32 52  1  0
M  END


  Mrv1652309052202372D          

 32 34  0  0  1  0            999 V2000
   -0.2773   -1.9371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4372   -1.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517   -1.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1517   -2.7621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -3.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3964   -3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3358   -3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6180   -4.5819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5806   -2.7621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3931   -2.6189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8628   -3.5374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6752   -3.6806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5806   -1.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2646   -1.4758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3931   -2.0804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9234   -1.4484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -1.5246    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4596   -0.9515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2526   -1.1789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8461   -0.6059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6465    0.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2399    0.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0330    0.5403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2326   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6391   -0.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -0.7962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9160   -0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287    0.6319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9659    1.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7904    1.3027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777    0.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -0.1254    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  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 17 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0204852

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1OC(O)(OO)[C@](O)(OO)[C@@](O)(OO)[C@@]1(OOC1=CC=CC=C1)OC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O14/c19-11-14-15(26-12-7-3-1-4-8-12,32-28-13-9-5-2-6-10-13)16(20,29-23)17(21,30-24)18(22,27-14)31-25/h1-10,14,19-25H,11H2/t14-,15-,16+,17-,18?/m1/s1

> <INCHI_KEY>
GMVKZIGIYSHLJD-IHAUNJBESA-N

> <FORMULA>
C18H20O14

> <MOLECULAR_WEIGHT>
460.344

> <EXACT_MASS>
460.085305324

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.38095503193804

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol

> <JCHEM_LOGP>
2.2840644923333326

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.128942078354799

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.61927238125737

> <JCHEM_PKA_STRONGEST_BASIC>
-3.028304845744234

> <JCHEM_POLAR_SURFACE_AREA>
206.21999999999994

> <JCHEM_REFRACTIVITY>
96.59570000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol

> <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  O   UNK     0      -0.518  -3.616   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.816  -2.846   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.150  -3.616   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.150  -5.156   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.483  -5.926   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.473  -7.106   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       2.494  -7.106   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       3.020  -8.553   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.817  -5.156   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.334  -4.889   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       5.344  -6.603   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       6.860  -6.871   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.817  -3.616   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.094  -2.755   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       6.334  -3.883   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       7.324  -2.704   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.483  -2.846   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.591  -1.776   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.072  -2.201   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.179  -1.131   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.807   0.363   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.915   1.433   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.395   1.009   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.767  -0.486   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.660  -1.555   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.760  -1.486   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.577  -0.180   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.854   1.179   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.670   2.485   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.209   2.432   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.932   1.072   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.116  -0.234   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7    9                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10   11   13                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11                                                            
CONECT   13    9   14   15   17                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17   13    3   18   26                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   17   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀O₁₄

Average Mass

460.3440 Da

Monoisotopic Mass

460.08531 Da

IUPAC Name

(3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol

Traditional Name

(3R,4R,5R,6R)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol

CAS Registry Number

Not Available

SMILES

OC[C@H]1OC(O)(OO)[C@](O)(OO)[C@@](O)(OO)[C@@]1(OOC1=CC=CC=C1)OC1=CC=CC=C1

InChI Identifier

InChI=1S/C18H20O14/c19-11-14-15(26-12-7-3-1-4-8-12,32-28-13-9-5-2-6-10-13)16(20,29-23)17(21,30-24)18(22,27-14)31-25/h1-10,14,19-25H,11H2/t14-,15-,16+,17-,18?/m1/s1

InChI Key

GMVKZIGIYSHLJD-IHAUNJBESA-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
Sanguisorba minor	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol ethers

Sub Class

Not Available

Direct Parent

Phenol ethers

Alternative Parents

Substituents

Phenoxy compound
Phenol ether
Oxane
Monosaccharide
Monocyclic benzene moiety
Orthocarboxylic acid derivative
Hydroperoxide
Alkyl hydroperoxide
Oxacycle
Organoheterocyclic compound
Polyol
Peroxol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
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	2.28	ChemAxon
pKa (Strongest Acidic)	6.62	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	206.22 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	96.6 m³·mol⁻¹	ChemAxon
Polarizability	39.38 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

162817110

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol (NP0204852)

MOL for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

3D MOL for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

3D SDF for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

3D-SDF for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

PDB for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

3D PDB for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

SMILES for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

INCHI for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

Structure for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)

3D Structure for NP0204852 ((3r,4r,5r,6r)-2,3,4-trihydroperoxy-6-(hydroxymethyl)-5-phenoxy-5-(phenylperoxy)oxane-2,3,4-triol)