NP-MRD: Showing NP-Card for 4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol (NP0330575)

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Record Information

Version

2.0

Created at

2022-09-12 16:03:22 UTC

Updated at

2022-09-12 16:03:22 UTC

NP-MRD ID

NP0330575

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol

Description

Rayalinol belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units. Based on a literature review very few articles have been published on Rayalinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122218032D          

 30 33  0  0  1  0            999 V2000
   -1.1092   -3.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543   -2.8347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0473   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0146    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5666    1.8102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0937    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417    1.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7966    2.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036    2.7664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585    3.5510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1556    2.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626    2.3248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007    1.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5666   -2.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3117   -3.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8637   -3.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088   -4.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5047   -3.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2498   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018   -4.6740    0.0000 C   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11  8  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 13 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 11 23  1  0  0  0  0
  6 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
   -3.2940   -2.2954   -2.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2337   -1.5784   -2.0160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8043   -0.8790   -0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4505   -0.8705   -0.5717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0296   -0.1777    0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6559   -0.0983    0.9632 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2354    1.1802    1.3392 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719    0.9115    1.7387 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8126    2.1922    1.8652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522    1.9923    2.2581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6514   -0.0922    0.7811 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5717    0.4311   -0.2226 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9136   -0.1367   -0.3012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4163   -0.9808    0.6318 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7124   -1.5106    0.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4901   -1.1770   -0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7915   -1.7031   -0.6734 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0007   -0.3210   -1.5093 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8286   -0.0088   -2.5780 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7128    0.1940   -1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9124    0.4444   -1.4382 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5475    0.3364   -1.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -0.5140    0.0145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9885    0.5127    1.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3254    0.5044    0.9318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2814    1.1882    1.6739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9102    1.9196    2.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7527   -0.1987   -0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0975   -0.1988   -0.5031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7059    0.7347   -1.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7891   -2.8537   -3.6216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5959   -1.5787   -3.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7690   -3.0428   -2.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7147   -1.4020   -1.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5314   -0.7282    1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788    0.4833    2.7726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6934    2.9035    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3622    2.7200    2.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6390    2.8168    2.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699   -0.9760    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7371    1.5366    0.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8999   -1.3141    1.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1212   -2.1835    1.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3490   -1.4436   -1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4403    0.6291   -3.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3747    0.8655   -2.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1484    1.3574   -1.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1314   -0.2086   -2.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4199   -1.5859   -0.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6933    1.0790    2.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7570    1.1807    3.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0282    2.5418    2.6387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8027    2.5186    3.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4504    0.1726   -1.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3223    1.4834   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0280    1.2562   -2.0253 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 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  2  0
 28 29  1  0
 29 30  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 23  1  0
 23 22  1  0
 22 21  1  0
 21 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 28  3  1  0
 23  6  1  0
 20 13  1  0
 12 11  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 24 50  1  0
 27 51  1  0
 27 52  1  0
 27 53  1  0
 30 54  1  0
 30 55  1  0
 30 56  1  0
  6 35  1  1
  8 36  1  1
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  1
 23 49  1  6
 22 47  1  0
 22 48  1  0
 12 41  1  1
 14 42  1  0
 15 43  1  0
 17 44  1  0
 19 45  1  0
 20 46  1  0
M  END


  Mrv1652309122218032D          

 30 33  0  0  1  0            999 V2000
   -1.1092   -3.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543   -2.8347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0473   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0146    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5666    1.8102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0937    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417    1.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7966    2.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036    2.7664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585    3.5510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1556    2.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626    2.3248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007    1.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5666   -2.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3117   -3.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8637   -3.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088   -4.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5047   -3.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2498   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018   -4.6740    0.0000 C   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11  8  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 13 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 11 23  1  0  0  0  0
  6 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330575

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)[C@@H]1O[C@H](CO)[C@H]2[C@@H]1CO[C@@H]2C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O8/c1-26-16-7-12(8-17(27-2)22(16)28-3)20-13-10-29-21(19(13)18(9-23)30-20)11-4-5-14(24)15(25)6-11/h4-8,13,18-21,23-25H,9-10H2,1-3H3/t13-,18+,19+,20-,21+/m0/s1

> <INCHI_KEY>
OWPQEEIAMIZUDX-LKDANELNSA-N

> <FORMULA>
C22H26O8

> <MOLECULAR_WEIGHT>
418.442

> <EXACT_MASS>
418.162767797

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.754194145378364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(1S,3aR,4R,6S,6aS)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol

> <JCHEM_LOGP>
1.4897533396666662

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.660881604281759

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.213707629643334

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9471226065677785

> <JCHEM_POLAR_SURFACE_AREA>
106.84000000000002

> <JCHEM_REFRACTIVITY>
107.52590000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-[(1S,3aR,4R,6S,6aS)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.071  -6.756   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.595  -5.291   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.088  -4.971   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.388  -3.507   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.894  -3.186   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.465  -0.476   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.894   2.235   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.924   3.379   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.834   0.294   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.775   2.235   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.744   3.379   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.220   4.844   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.727   5.164   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.203   6.629   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.757   4.019   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.264   4.340   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.281   2.555   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.204  -0.476   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.924  -4.331   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.449  -5.795   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.479  -6.940   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.003  -8.405   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.942  -6.116   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.466  -7.580   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.497  -8.725   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   23                                                  
CONECT   12   11   13   21                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   13                                                       
CONECT   21   12   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   11    6                                                  
CONECT   24    5   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25    3   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₈

Average Mass

418.4420 Da

Monoisotopic Mass

418.16277 Da

IUPAC Name

4-[(1S,3aR,4R,6S,6aS)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol

Traditional Name

4-[(1S,3aR,4R,6S,6aS)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)[C@@H]1O[C@H](CO)[C@H]2[C@@H]1CO[C@@H]2C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C22H26O8/c1-26-16-7-12(8-17(27-2)22(16)28-3)20-13-10-29-21(19(13)18(9-23)30-20)11-4-5-14(24)15(25)6-11/h4-8,13,18-21,23-25H,9-10H2,1-3H3/t13-,18+,19+,20-,21+/m0/s1

InChI Key

OWPQEEIAMIZUDX-LKDANELNSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Not Available

Direct Parent

Furanoid lignans

Alternative Parents

Substituents

Furanoid lignan
Furofuran lignan skeleton
Anisole
Catechol
Phenoxy compound
Furofuran
Phenol ether
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Oxolane
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Alcohol
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
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	1.49	ChemAxon
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	106.84 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	107.53 m³·mol⁻¹	ChemAxon
Polarizability	42.75 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

Not Available

Chemspider ID

28287340

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102173972

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol (NP0330575)

MOL for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

3D MOL for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

3D SDF for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

3D-SDF for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

PDB for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

3D PDB for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

SMILES for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

INCHI for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

Structure for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)

3D Structure for NP0330575 (4-[(1s,3ar,4r,6s,6as)-6-(hydroxymethyl)-4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]benzene-1,2-diol)