NP-MRD: Showing NP-Card for 4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole (NP0205074)

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Record Information

Version

2.0

Created at

2022-09-05 00:54:15 UTC

Updated at

2022-09-05 00:54:15 UTC

NP-MRD ID

NP0205074

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole

Description

Sesartemin 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. Sesartemin is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Sesartemin has been detected, but not quantified in, alcoholic beverages and herbs and spices. 4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole is found in Achillea cretica, Achillea holosericea, Artemisia absinthium, Artemisia arborescens, Hernandia ovigera, Peperomia obtusifolia and Sesamum alatum. This could make sesartemin a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241214382D          

 31 35  0  0  0  0            999 V2000
    1.6505    1.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3112    1.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3934    2.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1370    2.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5495    2.2705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0541    1.6098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1370    0.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4763    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7335    0.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9907    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2470    0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9907    0.8670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9907    0.0411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2470   -0.8662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9907   -0.6188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8799    0.4536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5405    0.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5405   -0.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8799   -0.2885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1370   -0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4763   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6505   -0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5683   -1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2290   -1.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0541   -1.4439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7147   -1.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6317   -2.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1460   -2.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031   -2.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  9  1  0  0  0  0
  2  3  1  0  0  0  0
  2  6  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7 18  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 17  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 24  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 19  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 30  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 57 61  0  0  0  0  0  0  0  0999 V2000
   -4.5061    2.3310    1.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1541    1.4054    1.0506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439    0.4466    0.3492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675    0.3190    0.4442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3852   -0.6481   -0.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9149   -0.8123   -0.1815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3815   -0.9844   -1.4828 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9662   -0.8878   -1.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1586    0.2592   -0.3033 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9914   -0.1966    0.8479 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4294    0.1071    0.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0222    0.5772   -0.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3955    0.8434   -0.4493 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9679    1.3211   -1.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1419    1.5313   -2.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.6350    0.6665 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5954    0.1621    1.8328 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2279   -0.0946    1.8556 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6228    0.0558    2.7671 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8628   -0.0208    2.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5516    0.8040    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4146    0.2814    2.0080 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433    0.3147    1.8061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2010    0.4167    0.3386 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1462   -1.4713   -1.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5100   -1.3742   -1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2409   -2.2220   -2.0117 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5459   -3.2120   -2.7422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1750   -0.4036   -0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5364   -0.2987   -0.5850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1065    0.5361   -1.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2480    3.0632    2.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7517    2.9246    1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0738    1.8095    2.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5513    0.9977    1.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6421   -1.6854    0.4450 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5422   -0.7594   -2.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2780   -1.8350   -0.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5060    1.1870   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237   -1.3236    0.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4265    0.7477   -1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6620    2.0845   -3.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7371    0.5498   -3.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3003    2.1933   -2.4309 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7949   -0.4576    2.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0358   -1.0433    1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6965    0.3744    2.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3821   -0.6241    2.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4347    1.1471    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6889    1.3577    0.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6175   -2.2319   -1.6339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6943   -2.7619   -3.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2255   -3.7816   -3.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0575   -3.9001   -1.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2118    0.5391   -1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7684    1.5909   -1.4791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8087    0.1164   -2.5729 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 16  2  0
 16 21  1  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 18 11  1  0
 11 12  2  0
 11 10  1  0
 10 22  1  0
 22 23  1  0
 23 24  1  0
 24  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 29  2  0
 29 30  1  0
 30 31  1  0
 29 26  1  0
 26 27  1  0
 27 28  1  0
 26 25  2  0
 12 13  1  0
  9 10  1  0
 25  5  1  0
 17 16  1  0
  6 24  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 20 46  1  0
 20 47  1  0
 18 45  1  0
 12 41  1  0
 10 40  1  1
 23 48  1  0
 23 49  1  0
 24 50  1  1
  9 39  1  6
  8 37  1  0
  8 38  1  0
  6 36  1  1
  4 35  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 31 55  1  0
 31 56  1  0
 31 57  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
 25 51  1  0
M  END


  Mrv0541 02241214382D          

 31 35  0  0  0  0            999 V2000
    1.6505    1.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3112    1.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3934    2.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1370    2.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5495    2.2705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0541    1.6098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1370    0.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4763    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7335    0.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9907    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2470    0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9907    0.8670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9907    0.0411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2470   -0.8662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9907   -0.6188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8799    0.4536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5405    0.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5405   -0.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8799   -0.2885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1370   -0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4763   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6505   -0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5683   -1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2290   -1.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0541   -1.4439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7147   -1.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6317   -2.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1460   -2.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031   -2.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  9  1  0  0  0  0
  2  3  1  0  0  0  0
  2  6  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7 18  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 17  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 24  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 19  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 30  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205074

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OCOC2=CC(=C1)C1OCC2C1COC2C1=CC(OC)=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O8/c1-24-16-5-12(6-17(25-2)22(16)27-4)20-14-9-29-21(15(14)10-28-20)13-7-18(26-3)23-19(8-13)30-11-31-23/h5-8,14-15,20-21H,9-11H2,1-4H3

> <INCHI_KEY>
DHWUVPPRBIJJKS-UHFFFAOYSA-N

> <FORMULA>
C23H26O8

> <MOLECULAR_WEIGHT>
430.4477

> <EXACT_MASS>
430.162767808

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
45.620834587600655

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2H-1,3-benzodioxole

> <ALOGPS_LOGP>
2.57

> <JCHEM_LOGP>
2.192781127

> <ALOGPS_LOGS>
-4.50

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7072502015420414

> <JCHEM_POLAR_SURFACE_AREA>
73.84000000000002

> <JCHEM_REFRACTIVITY>
109.83170000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2H-1,3-benzodioxole

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       3.081   2.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.314   3.622   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.468   5.162   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.856   5.470   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.626   4.238   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.701   3.005   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.856   1.463   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.622   0.693   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.236   1.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.849   0.385   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.461   0.847   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.461   2.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.849   1.618   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.849   0.077   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.461  -0.384   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.461  -1.617   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.849  -1.155   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       7.242   0.847   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.476   1.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.476  -1.309   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -7.242  -0.539   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -5.856  -1.155   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.622  -0.230   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.081  -0.847   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.927  -2.387   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.161  -3.312   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.701  -2.695   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.934  -3.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -6.779  -5.162   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.006  -4.853   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.619  -5.470   0.000  0.00  0.00           C+0
CONECT    1    2    9                                                       
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    2    5    7                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    1    8   10                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   11   14   16                                                  
CONECT   16   15   17                                                       
CONECT   17   10   16                                                       
CONECT   18    7   19                                                       
CONECT   19   18                                                            
CONECT   20   21                                                            
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   14   23   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   30                                                  
CONECT   27   22   26   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   26   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
(+)-Sesartemin	HMDB
2-(3-Methoxy-4,5-methylenedioxyphenyl)-6-(3,4,5-trimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane	HMDB
3,3',4',5'-Tetramethoxy-4,5-methylenedioxy-7,9',7',9-diepoxylignan	HMDB
4-Methoxy-6-[tetrahydro-4-(3,4,5-trimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]-1,3-benzodioxole, 9ci	HMDB
Sesartemin-(+)	HMDB

Chemical Formula

C₂₃H₂₆O₈

Average Mass

430.4477 Da

Monoisotopic Mass

430.16277 Da

IUPAC Name

4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2H-1,3-benzodioxole

Traditional Name

4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2H-1,3-benzodioxole

CAS Registry Number

Not Available

SMILES

COC1=C2OCOC2=CC(=C1)C1OCC2C1COC2C1=CC(OC)=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C23H26O8/c1-24-16-5-12(6-17(25-2)22(16)27-4)20-14-9-29-21(15(14)10-28-20)13-7-18(26-3)23-19(8-13)30-11-31-23/h5-8,14-15,20-21H,9-11H2,1-4H3

InChI Key

DHWUVPPRBIJJKS-UHFFFAOYSA-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
Achillea cretica	LOTUS Database	35616633
Achillea holosericea	LOTUS Database	35616633
Artemisia absinthium	LOTUS Database	35616633
Artemisia arborescens	LOTUS Database	35616633
Hernandia ovigera	LOTUS Database	35616633
Peperomia obtusifolia	LOTUS Database	35616633
Sesamum alatum	LOTUS Database	35616633

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
Benzodioxole
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Furofuran
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Acetal
Oxacycle
Organoheterocyclic compound
Dialkyl ether
Ether
Hydrocarbon derivative
Organic oxygen compound
Organooxygen 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	2.57	ALOGPS
logP	2.19	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	73.84 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	109.83 m³·mol⁻¹	ChemAxon
Polarizability	45.62 Å³	ChemAxon
Number of Rings	5	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

HMDB0038931

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018403

KNApSAcK ID

Not Available

Chemspider ID

2962390

KEGG Compound ID

C10884

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3732009

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole (NP0205074)

MOL for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

3D MOL for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

3D SDF for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

3D-SDF for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

PDB for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

3D PDB for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

SMILES for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

INCHI for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

Structure for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)

3D Structure for NP0205074 (4-methoxy-6-[4-(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2h-1,3-benzodioxole)