NP-MRD: Showing NP-Card for 3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate (NP0256614)

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Record Information

Version

2.0

Created at

2022-09-07 21:30:14 UTC

Updated at

2022-09-07 21:30:14 UTC

NP-MRD ID

NP0256614

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate

Description

7-Demethoxylegonol-2-methylbutanoate belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 7-Demethoxylegonol-2-methylbutanoate is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate is found in Styrax agrestis. Based on a literature review very few articles have been published on 7-demethoxylegonol-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223302D          

 28 31  0  0  1  0            999 V2000
    0.8250   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -8.5248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2539   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -9.7623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -8.5248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8263   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5408   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5408   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2552   -7.2873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9697   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7543   -7.4448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2393   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0643   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4768   -7.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3018   -7.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7143   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3018   -8.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4768   -8.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8538   -9.4398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6075   -9.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5212   -8.2838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7543   -8.7797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9697   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2552   -8.9373    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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
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 15 16  1  0  0  0  0
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 19 20  2  0  0  0  0
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 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 16 26  2  0  0  0  0
 26 27  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  2  0  0  0  0
 11 28  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    5.6889   -2.1452   -2.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9724   -0.8353   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2359   -0.3606   -0.4322 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7684   -1.3113    0.6268 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5855    0.9552   -0.1654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299    1.4639   -1.1110 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6999    1.5779    1.0567 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0905    2.8082    1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.0524   -1.4317   -1.4703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8185   -1.8916   -1.8368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6667   -1.3537   -1.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0208   -2.8713   -2.7954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3670   -3.3036   -2.7544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993   -2.1469   -2.2196 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2269   -0.1718    0.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3997    0.5951    0.8404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0231    0.6722    1.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1816    2.0319    3.1173 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1688    3.0618    3.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3444    2.9589    3.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.1165   -0.0909   -0.2428 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.7670   -3.6091   -3.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4122   -4.1537   -2.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8647   -0.9116   -0.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6051    0.0286    0.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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 17 18  2  0
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 22 17  1  0
 27 14  1  0
 21 20  1  0
  1 29  1  0
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  1 31  1  0
  2 32  1  0
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  3 34  1  6
  4 35  1  0
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  8 38  1  0
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 26 51  1  0
 28 52  1  0
 18 46  1  0
 19 47  1  0
 24 49  1  0
 24 50  1  0
 22 48  1  0
M  END


  Mrv1652309072223302D          

 28 31  0  0  1  0            999 V2000
    0.8250   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -8.5248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2539   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -9.7623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -8.5248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8263   -8.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5408   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5408   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2552   -7.2873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9697   -7.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7543   -7.4448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2393   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0643   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4768   -7.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3018   -7.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7143   -8.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3018   -8.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4768   -8.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8538   -9.4398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6075   -9.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5212   -8.2838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7543   -8.7797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9697   -8.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2552   -8.9373    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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
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 14 27  1  0  0  0  0
 27 28  2  0  0  0  0
 11 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256614

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)C(=O)OCCCC1=CC=C2OC(=CC2=C1)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O5/c1-3-15(2)23(24)25-10-4-5-16-6-8-19-18(11-16)13-21(28-19)17-7-9-20-22(12-17)27-14-26-20/h6-9,11-13,15H,3-5,10,14H2,1-2H3/t15-/m0/s1

> <INCHI_KEY>
MBOVWBBJDJPNSN-HNNXBMFYSA-N

> <FORMULA>
C23H24O5

> <MOLECULAR_WEIGHT>
380.44

> <EXACT_MASS>
380.162373873

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
43.40429802785639

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[2-(2H-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2S)-2-methylbutanoate

> <JCHEM_LOGP>
5.417925473333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.911881937337796

> <JCHEM_POLAR_SURFACE_AREA>
57.900000000000006

> <JCHEM_REFRACTIVITY>
104.80550000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-[2-(2H-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2S)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.540 -15.913   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.874 -16.683   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.207 -15.913   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.207 -14.373   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.541 -16.683   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.541 -18.223   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.875 -15.913   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.208 -16.683   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.542 -15.913   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.876 -16.683   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.209 -15.913   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.209 -14.373   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.543 -13.603   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.877 -14.373   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.341 -13.897   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      17.247 -15.143   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.787 -15.143   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.557 -13.809   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.097 -13.809   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.867 -15.143   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.097 -16.477   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.557 -16.477   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      22.127 -17.621   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      23.534 -16.995   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      23.373 -15.463   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      16.341 -16.389   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.877 -15.913   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.543 -16.683   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21   17                                                       
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   16   27                                                       
CONECT   27   26   14   28                                                  
CONECT   28   27   11                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
7-Demethoxylegonol-2-methylbutanoic acid	Generator

Chemical Formula

C₂₃H₂₄O₅

Average Mass

380.4400 Da

Monoisotopic Mass

380.16237 Da

IUPAC Name

3-[2-(2H-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2S)-2-methylbutanoate

Traditional Name

3-[2-(2H-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2S)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@H](C)C(=O)OCCCC1=CC=C2OC(=CC2=C1)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C23H24O5/c1-3-15(2)23(24)25-10-4-5-16-6-8-19-18(11-16)13-21(28-19)17-7-9-20-22(12-17)27-14-26-20/h6-9,11-13,15H,3-5,10,14H2,1-2H3/t15-/m0/s1

InChI Key

MBOVWBBJDJPNSN-HNNXBMFYSA-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
Styrax agrestis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
Benzodioxole
Benzofuran
Fatty acid ester
Fatty acyl
Benzenoid
Heteroaromatic compound
Furan
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

1-benzofurans (CHEBI:69551 )
benzodioxoles (CHEBI:69551 )
fatty acid ester (CHEBI:69551 )

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	5.42	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.9 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	104.81 m³·mol⁻¹	ChemAxon
Polarizability	43.4 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

26635849

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

56673143

PDB ID

Not Available

ChEBI ID

69551

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate (NP0256614)

MOL for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

3D MOL for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

3D SDF for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

3D-SDF for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

PDB for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

3D PDB for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

SMILES for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

INCHI for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

Structure for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)

3D Structure for NP0256614 (3-[2-(2h-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propyl (2s)-2-methylbutanoate)