NP-MRD: Showing NP-Card for 5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole (NP0143065)

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Record Information

Version

2.0

Created at

2022-09-01 21:44:26 UTC

Updated at

2022-09-01 21:44:26 UTC

NP-MRD ID

NP0143065

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole

Description

(-)-Virgatusin 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. 5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole is found in Phyllanthus urinaria. 5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole was first documented in 2011 (PMID: 21597167). Based on a literature review very few articles have been published on (-)-Virgatusin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309012223442D          

 30 33  0  0  1  0            999 V2000
    5.9481    0.1435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7766    0.9505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9920    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2955    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106    4.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    5.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666    5.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3022    6.3547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8173    7.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    4.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2720    5.0198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7570    4.3523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1160    4.1799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3725    2.6255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1929    2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6779    3.2067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4983    3.1204    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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
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  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
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 12 13  1  0  0  0  0
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 23 26  2  0  0  0  0
 17 26  1  0  0  0  0
 16 27  1  0  0  0  0
  4 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
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   -3.4303   -1.0067    1.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1224   -1.1099    1.4482 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0287    0.2746    1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5821    1.2747    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4953    1.5469    2.4087 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303    1.6617   -0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4516    2.6662   -1.0598 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7906    3.0640   -2.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7445    1.0480   -0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2359   -1.4609    0.6848 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7260   -2.8898    0.4818 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5268   -3.1428   -0.8979 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9470   -4.4376   -1.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9106    0.5377    2.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7294    1.5492    3.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6731    2.2252   -2.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3669    3.8894   -2.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7650    3.4352   -1.9553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2624    1.3928   -1.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3942   -1.1365    1.7401 H   0  0  0  0  0  0  0  0  0  0  0  0
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 25 50  1  0
 25 51  1  0
 26 52  1  0
M  END


  Mrv1652309012223442D          

 30 33  0  0  1  0            999 V2000
    5.9481    0.1435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7766    0.9505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9920    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2955    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106    4.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    5.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666    5.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3022    6.3547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8173    7.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    4.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2720    5.0198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7570    4.3523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1160    4.1799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3725    2.6255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1929    2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6779    3.2067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  4  3  1  1  0  0  0
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  5  6  1  1  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
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  6 11  1  0  0  0  0
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  4 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0143065

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC[C@@H]1[C@@H](COC)[C@@H](O[C@@H]1C1=CC=C2OCOC2=C1)C1=CC=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O7/c1-24-11-16-17(12-25-2)23(15-6-8-19-21(10-15)29-13-28-19)30-22(16)14-5-7-18(26-3)20(9-14)27-4/h5-10,16-17,22-23H,11-13H2,1-4H3/t16-,17-,22+,23-/m1/s1

> <INCHI_KEY>
OGTJJRNJLHLKFF-ROEJJBDBSA-N

> <FORMULA>
C23H28O7

> <MOLECULAR_WEIGHT>
416.47

> <EXACT_MASS>
416.183503242

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
44.542943058954506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(2S,3S,4S,5R)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2H-1,3-benzodioxole

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
2.6326730933333335

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5860319656345534

> <JCHEM_POLAR_SURFACE_AREA>
64.61000000000001

> <JCHEM_REFRACTIVITY>
109.9178

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.03e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(2S,3S,4S,5R)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2H-1,3-benzodioxole

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0      11.103   0.268   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.783   1.774   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.318   2.250   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.998   3.756   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       7.752   5.914   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.259   6.235   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.885   7.641   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.980   8.887   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.606  10.294   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.138  10.455   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.764  11.862   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.859  13.108   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.043   9.209   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      13.574   9.370   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.480   8.124   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.417   7.802   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.029   4.901   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.560   4.740   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      12.465   5.986   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      13.997   5.825   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   27                                                  
CONECT    5    4    6   15                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10    6                                                       
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    5   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   17                                                       
CONECT   27   16    4   28                                                  
CONECT   28   27   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

C₂₃H₂₈O₇

Average Mass

416.4700 Da

Monoisotopic Mass

416.18350 Da

IUPAC Name

5-[(2S,3S,4S,5R)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2H-1,3-benzodioxole

Traditional Name

5-[(2S,3S,4S,5R)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2H-1,3-benzodioxole

CAS Registry Number

Not Available

SMILES

COC[C@@H]1[C@@H](COC)[C@@H](O[C@@H]1C1=CC=C2OCOC2=C1)C1=CC=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C23H28O7/c1-24-11-16-17(12-25-2)23(15-6-8-19-21(10-15)29-13-28-19)30-22(16)14-5-7-18(26-3)20(9-14)27-4/h5-10,16-17,22-23H,11-13H2,1-4H3/t16-,17-,22+,23-/m1/s1

InChI Key

OGTJJRNJLHLKFF-ROEJJBDBSA-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
Phyllanthus urinaria	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
Dimethoxybenzene
O-dimethoxybenzene
Benzodioxole
Methoxybenzene
Anisole
Phenol ether
Phenoxy compound
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Oxolane
Oxacycle
Organoheterocyclic compound
Acetal
Dialkyl ether
Ether
Hydrocarbon derivative
Organooxygen compound
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	2.95	ALOGPS
logP	2.63	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-3.6	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	109.92 m³·mol⁻¹	ChemAxon
Polarizability	44.54 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

8725204

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10549813

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Akiyama K, Tone J, Yamauchi S, Sugahara T, Maruyama M, Kakinuma Y: Disruption of ion homeostasis by verrucosin and a related compound. Biosci Biotechnol Biochem. 2011;75(5):1000-2. doi: 10.1271/bbb.110004. Epub 2011 May 20. [PubMed:21597167 ]
LOTUS database [Link]

Showing NP-Card for 5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole (NP0143065)

MOL for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

3D MOL for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

3D SDF for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

3D-SDF for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

PDB for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

3D PDB for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

SMILES for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

INCHI for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

Structure for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)

3D Structure for NP0143065 (5-[(2s,3s,4s,5r)-5-(3,4-dimethoxyphenyl)-3,4-bis(methoxymethyl)oxolan-2-yl]-2h-1,3-benzodioxole)