NP-MRD: Showing NP-Card for (-)-Lyoniresinol (NP0138554)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-06-29 17:34:54 UTC

Updated at

2022-06-29 17:34:54 UTC

NP-MRD ID

NP0138554

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Lyoniresinol

Description

(-)-Lyoniresinol belongs to the class of organic compounds known as 9,9p-dihydroxyaryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton carrying a hydroxyl group at the 9- and the 9'- position. (-)-Lyoniresinol is found in Ailanthus altissima, Berberis koreana, Betula maximowicziana, Laguncularia racemosa, Litsea glutinosa, Phellodendron amurense, Ulmus thomasii and Zanthoxylum ailanthoides. (-)-Lyoniresinol was first documented in 2019 (PMID: 31703459). Based on a literature review a small amount of articles have been published on (-)-Lyoniresinol (PMID: 32237421) (PMID: 35238199).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292219342D          

 30 32  0  0  1  0            999 V2000
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    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
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  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
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   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
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  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
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12  5  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 21  1  0  0  0  0
 16 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 24  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  1  0  0  0
 27 28  1  0  0  0  0
 13 29  1  6  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
   -3.4510   -0.3321    3.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0796   -0.4231    2.4230 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4209   -0.1824    1.2055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0894    0.1650    1.1480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4143    0.4083   -0.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0194    0.7909   -0.1558 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9501   -0.2284   -0.5558 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2231    0.2871   -0.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2543   -0.4907   -1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0254   -1.8498   -1.4392 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0521   -2.6766   -1.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3155   -2.1349   -2.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7846   -2.3801   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5821   -3.7489   -1.3412 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7519   -1.5569   -0.7234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4647   -2.1690   -0.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7227   -2.7657    0.8150 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4078    1.7718   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8785    2.1333    0.7572 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8818    1.6677    1.8066 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4771    2.0788    3.0636 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5131    1.5749    1.0106 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3781    2.7655    1.3349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4494    3.6313    0.2181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1722    0.2793   -1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5035   -0.0644   -1.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2482   -0.1902   -2.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7391    0.0159   -3.6511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1039   -0.2901    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4362   -0.6376    0.0695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8602   -1.2700    3.8221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2233   -0.1949    4.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    0.5127    3.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5441    0.2394    2.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0223    1.5560   -1.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272   -0.0509   -1.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0343   -2.9774   -2.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3243   -1.5192   -3.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6258   -1.5254   -1.2933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3326   -4.3385   -1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3071   -3.8050    0.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8133   -2.8675    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3584   -2.1289    1.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595    2.3703   -1.4179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5000    1.9495   -0.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8742    3.2372    0.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0411    0.5665    1.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8324    2.1920    1.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5606    1.3648    3.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5661    0.9069    1.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1071    3.3528    2.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4060    2.5175    1.5692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7592    4.5183    0.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6975    0.4579   -2.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1968   -0.8873   -4.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5458    0.2525   -4.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9898    0.8522   -3.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9818   -0.7303   -0.7673 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  2  0
 29 30  1  0
  5  6  1  0
  6 22  1  0
 22 23  1  0
 23 24  1  0
 22 19  1  0
 19 20  1  0
 20 21  1  0
 19 18  1  0
 18  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15  7  2  0
 29  3  1  0
  7  6  1  0
  7  8  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 25 54  1  0
 28 55  1  0
 28 56  1  0
 28 57  1  0
 30 58  1  0
  6 35  1  6
 22 50  1  1
 23 51  1  0
 23 52  1  0
 24 53  1  0
 19 46  1  6
 20 47  1  0
 20 48  1  0
 21 49  1  0
 18 44  1  0
 18 45  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 14 40  1  0
 17 41  1  0
 17 42  1  0
 17 43  1  0
M  END


  Mrv1652306292219342D          

 30 32  0  0  1  0            999 V2000
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    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
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  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
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   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
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  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
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12  5  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 21  1  0  0  0  0
 16 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 24  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  1  0  0  0
 27 28  1  0  0  0  0
 13 29  1  6  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138554

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1O)[C@H]1[C@H](CO)[C@@H](CO)CC2=CC(OC)=C(O)C(OC)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O8/c1-27-15-7-12(8-16(28-2)20(15)25)18-14(10-24)13(9-23)5-11-6-17(29-3)21(26)22(30-4)19(11)18/h6-8,13-14,18,23-26H,5,9-10H2,1-4H3/t13-,14-,18+/m1/s1

> <INCHI_KEY>
ZDVZKBOFCHOPLM-LBTNJELSSA-N

> <FORMULA>
C22H28O8

> <MOLECULAR_WEIGHT>
420.458

> <EXACT_MASS>
420.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
43.61555532527343

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6S,7S,8R)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-ol

> <ALOGPS_LOGP>
1.60

> <JCHEM_LOGP>
1.4650958043333349

> <ALOGPS_LOGS>
-3.80

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.883692268442651

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.243662764577333

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6036881189792025

> <JCHEM_POLAR_SURFACE_AREA>
117.84000000000002

> <JCHEM_REFRACTIVITY>
110.79899999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.62e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6S,7S,8R)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -6.930   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       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10                                                            
CONECT   12    5   13   21                                                  
CONECT   13   12   14   29                                                  
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   12   16                                                  
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24   19                                                            
CONECT   25   18   26                                                       
CONECT   26   25                                                            
CONECT   27   14   28                                                       
CONECT   28   27                                                            
CONECT   29   13   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₈

Average Mass

420.4580 Da

Monoisotopic Mass

420.17842 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

31768-94-2

SMILES

COC1=CC(=CC(OC)=C1O)[C@H]1[C@H](CO)[C@@H](CO)CC2=CC(OC)=C(O)C(OC)=C12

InChI Identifier

InChI=1S/C22H28O8/c1-27-15-7-12(8-16(28-2)20(15)25)18-14(10-24)13(9-23)5-11-6-17(29-3)21(26)22(30-4)19(11)18/h6-8,13-14,18,23-26H,5,9-10H2,1-4H3/t13-,14-,18+/m1/s1

InChI Key

ZDVZKBOFCHOPLM-LBTNJELSSA-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
Ailanthus altissima	LOTUS Database	35616633
Berberis koreana	LOTUS Database	35616633
Betula maximowicziana	LOTUS Database	35616633
Laguncularia racemosa	LOTUS Database	35616633
Litsea glutinosa	LOTUS Database	35616633
Phellodendron amurense	LOTUS Database	35616633
Ulmus thomasii	LOTUS Database	35616633
Zanthoxylum ailanthoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 9,9p-dihydroxyaryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton carrying a hydroxyl group at the 9- and the 9'- position.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Aryltetralin lignans

Sub Class

9,9p-dihydroxyaryltetralin lignans

Direct Parent

9,9p-dihydroxyaryltetralin lignans

Alternative Parents

Substituents

9,9p-dihydroxyaryltetralin lignan
M-dimethoxybenzene
Dimethoxybenzene
Tetralin
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Ether
Alcohol
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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

C00036284

Chemspider ID

8064050

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9888378

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wang D, Wu XM, Zhang DD, Zhu BR, Wang SC, Wang CX, Jia Q, Li YM: [Study on chemical constituents of Cinnamomi Ramulus]. Zhongguo Zhong Yao Za Zhi. 2020 Jan;45(1):124-132. doi: 10.19540/j.cnki.cjcmm.20190829.201. [PubMed:32237421 ]
Shi X, Li Z, Cai W, Liu Y, Li S, Ai M, Sun J, Hou B, Ni L, Qiu L: Chemical Constituents from Albiziae Cortex and Their Ability to Ameliorate Steatosis and Promote Proliferation and Anti-Oxidation In Vitro. Molecules. 2019 Nov 7;24(22). pii: molecules24224041. doi: 10.3390/molecules24224041. [PubMed:31703459 ]
Luong TM, Pilkington LI, Barker D: Total Asymmetric Synthesis and Stereochemical Confirmation of (+)- and (-)-Lyoniresinol and Its Deuterated Analogues. J Org Chem. 2022 Mar 18;87(6):4254-4262. doi: 10.1021/acs.joc.1c03085. Epub 2022 Mar 3. [PubMed:35238199 ]

Showing NP-Card for (-)-Lyoniresinol (NP0138554)

MOL for NP0138554 ((-)-Lyoniresinol)

3D MOL for NP0138554 ((-)-Lyoniresinol)

3D SDF for NP0138554 ((-)-Lyoniresinol)

3D-SDF for NP0138554 ((-)-Lyoniresinol)

PDB for NP0138554 ((-)-Lyoniresinol)

3D PDB for NP0138554 ((-)-Lyoniresinol)

SMILES for NP0138554 ((-)-Lyoniresinol)

INCHI for NP0138554 ((-)-Lyoniresinol)

Structure for NP0138554 ((-)-Lyoniresinol)

3D Structure for NP0138554 ((-)-Lyoniresinol)