NP-MRD: Showing NP-Card for (2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane (NP0304492)

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Record Information

Version

2.0

Created at

2022-09-10 19:37:22 UTC

Updated at

2022-09-10 19:37:22 UTC

NP-MRD ID

NP0304492

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane

Description

Epigrandisin belongs to the class of organic compounds known as 7,7'-epoxylignans. These are lignans with a structure based on a 2,5-diaryl-3, 4-dimethyltetrahydrofuran skeleton. (2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane is found in Aglaia leptantha, Bonamia spectabilis, Rhaphidophora decursiva and Saururus chinensis. (2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane was first documented in 2000 (PMID: 10843571). Based on a literature review very few articles have been published on epigrandisin (PMID: 11421741).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102221372D          

 31 33  0  0  1  0            999 V2000
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  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
    0.7145   -0.4125    0.0000 C   0  0  0  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
    1.3819   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7378   -3.6695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2227   -4.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7311   -5.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4257   -5.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6052   -5.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    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 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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
  9 20  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
  5 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
    3.2026    4.1177    0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1896    3.1520   -0.1006 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9735    1.7851    0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7311    1.3010    0.3446 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4584   -0.0525    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1432   -0.4814    0.8199 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0993    0.1747    0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9703   -0.3792    0.8579 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2777    0.0797    0.3875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2039    0.4615    1.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4653    0.9103    1.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3972    1.2951    1.9866 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1270    1.2561    3.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8271    0.9847   -0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0819    1.4279   -0.7055 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0919    0.4257   -0.8307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9262    0.6111   -1.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3162    0.6959   -2.6135 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3842    0.3101   -3.6059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6530    0.1598   -0.9235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7312   -1.8518    0.6832 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2318   -2.5470    1.9315 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7806   -1.9069    0.5804 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1597   -2.4668   -0.7311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5022   -0.9379    0.2465 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7451   -0.4624   -0.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7713   -1.3571   -0.3054 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -2.7403   -0.1853 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9958    0.9103   -0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2764    1.3226   -0.5465 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5773    1.4659   -1.9235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5749    3.9406    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5770    4.3263   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    5.0871    0.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9094    2.0129    0.5205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9316   -0.2742    1.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7896   -0.1022    1.9111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9758    0.4249    2.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0907    1.3549    3.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6733    0.2939    3.6892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4644    2.0977    3.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8587   -0.1898   -1.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0976    0.8793   -0.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0190   -0.2333    0.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0404   -0.7178   -3.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8220    0.3246   -4.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869    0.9470   -3.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9499   -0.1319   -1.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2356   -2.2008   -0.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9994   -1.8515    2.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7574   -3.5311    2.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -2.7148    1.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1236   -2.5939    1.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -3.4278   -0.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7112   -1.7244   -1.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2409   -2.6989   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3719   -2.0053    0.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4215   -3.3502   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6820   -3.0012   -0.8804 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -3.0352    0.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6640    1.6319   -2.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2654    0.5194   -2.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0098    2.2797   -2.3991 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
 30 31  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  2  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 29  3  1  0
 23  6  1  0
 20  9  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
 25 57  1  0
 28 58  1  0
 28 59  1  0
 28 60  1  0
 31 61  1  0
 31 62  1  0
 31 63  1  0
  6 36  1  1
  8 37  1  1
 21 49  1  6
 22 50  1  0
 22 51  1  0
 22 52  1  0
 23 53  1  1
 24 54  1  0
 24 55  1  0
 24 56  1  0
 10 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
M  END


  Mrv1652309102221372D          

 31 33  0  0  1  0            999 V2000
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  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
    0.7145   -0.4125    0.0000 C   0  0  0  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
    1.3819   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7378   -3.6695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2227   -4.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7311   -5.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4257   -5.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6052   -5.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    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 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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
  9 20  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
  5 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0304492

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-13-14(2)22(16-11-19(27-5)24(30-8)20(12-16)28-6)31-21(13)15-9-17(25-3)23(29-7)18(10-15)26-4/h9-14,21-22H,1-8H3/t13-,14-,21-,22+/m1/s1

> <INCHI_KEY>
ZPINJJOPURFFNV-SRLQQUAWSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.24747082812278

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,4R,5S)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane

> <JCHEM_LOGP>
3.8827453349999987

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8865422782624868

> <JCHEM_POLAR_SURFACE_AREA>
64.61000000000001

> <JCHEM_REFRACTIVITY>
116.84150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5S)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.580  -3.215   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.009  -5.926   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.540  -5.765   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.446  -7.011   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.977  -6.850   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.882  -8.096   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.819  -8.417   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.724  -9.663   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.098 -11.070   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.288  -8.578   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.661  -9.985   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.130 -10.146   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.382  -7.333   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564  -4.680   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.342  -5.926   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.088  -3.215   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.377  -2.739   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17    9                                                       
CONECT   21    8   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    6   24                                                  
CONECT   24   23                                                            
CONECT   25    5   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26    3   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

(2R,3R,4R,5S)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane

Traditional Name

(2R,3R,4R,5S)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C24H32O7/c1-13-14(2)22(16-11-19(27-5)24(30-8)20(12-16)28-6)31-21(13)15-9-17(25-3)23(29-7)18(10-15)26-4/h9-14,21-22H,1-8H3/t13-,14-,21-,22+/m1/s1

InChI Key

ZPINJJOPURFFNV-SRLQQUAWSA-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
Aglaia leptantha	LOTUS Database	35616633
Bonamia spectabilis	LOTUS Database	35616633
Rhaphidophora decursiva	LOTUS Database	35616633
Saururus chinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7,7'-epoxylignans. These are lignans with a structure based on a 2,5-diaryl-3, 4-dimethyltetrahydrofuran skeleton.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Tetrahydrofuran lignans

Direct Parent

7,7'-epoxylignans

Alternative Parents

Substituents

7,7p-epoxylignan
Dibenzylbutane lignan skeleton
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Oxolane
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	3.88	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	64.61 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	116.84 m³·mol⁻¹	ChemAxon
Polarizability	47.25 Å³	ChemAxon
Number of Rings	3	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

C00045892

Chemspider ID

10235652

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21603492

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang HJ, Tamez PA, Vu DH, Ghee TT, Nguyen VH, Le TX, Le MH, Nguyen MC, Do TT, Soejarto DD, Fong HH, Pezzuto JM: Antimalarial compounds from Rhaphidophora decursiva. J Nat Prod. 2001 Jun;64(6):772-7. doi: 10.1021/np010037c. [PubMed:11421741 ]
Greger H, Pacher T, Vajrodaya S, Bacher M, Hofer O: Infraspecific variation of sulfur-containing bisamides from Aglaia leptantha. J Nat Prod. 2000 May;63(5):616-20. doi: 10.1021/np990542y. [PubMed:10843571 ]
LOTUS database [Link]

Showing NP-Card for (2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane (NP0304492)

MOL for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

3D MOL for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

3D SDF for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

3D-SDF for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

PDB for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

3D PDB for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

SMILES for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

INCHI for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

Structure for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)

3D Structure for NP0304492 ((2r,3r,4r,5s)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane)