NP-MRD: Showing NP-Card for 12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid (NP0324697)

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Record Information

Version

2.0

Created at

2022-09-12 04:56:02 UTC

Updated at

2022-09-12 04:56:02 UTC

NP-MRD ID

NP0324697

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid

Description

12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienimidic acid belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. 12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid is found in Piper nigrum. 12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514012D          

 28 29  0  0  0  0            999 V2000
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9012   -6.7395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5657   -7.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7452   -7.4070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  7  1  4  0  0  0
  9 10  2  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  4  0  0  0
 18 19  2  0  0  0  0
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 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
M  END

     RDKit          3D

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    9.6848   -0.6544   -0.1801 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9701    2.0187    0.0827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9054    2.1022   -0.9593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6747    1.0253   -1.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5035   -0.1346   -0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5891   -0.2165    0.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4025   -1.0722   -1.1689 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4265   -0.3277   -1.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6629    0.7882   -2.2700 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.7548   -0.7112   -1.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6994   -0.5148    0.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5279   -0.1605   -1.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6635    1.5953   -0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2982    1.9101    2.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1328    3.0948    1.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4455    2.9412    0.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1489    3.4046    2.4063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2015    0.9129    3.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -0.2834    2.4602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4445    2.9050    0.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0317    3.0319   -1.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4776   -1.1669    0.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1515   -0.0161   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8731   -0.8876   -2.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
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  7  8  2  0
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 18 55  1  0
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 21 57  1  0
 22 58  1  0
 27 60  1  0
 27 61  1  0
 25 59  1  0
M  END


  Mrv1533004191514012D          

 28 29  0  0  0  0            999 V2000
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8592   -6.1875    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  7  1  4  0  0  0
  9 10  2  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
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 23 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324697

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCNC(=O)C=CC=CCCCCCC=CC1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H33NO3/c1-20(2)16-17-25-24(26)13-11-9-7-5-3-4-6-8-10-12-21-14-15-22-23(18-21)28-19-27-22/h7,9-15,18,20H,3-6,8,16-17,19H2,1-2H3,(H,25,26)

> <INCHI_KEY>
DWPMNGYHFAAZBH-UHFFFAOYSA-N

> <FORMULA>
C24H33NO3

> <MOLECULAR_WEIGHT>
383.532

> <EXACT_MASS>
383.246043927

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
46.5510767103252

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienamide

> <ALOGPS_LOGP>
6.34

> <JCHEM_LOGP>
6.0642459623333345

> <ALOGPS_LOGS>
-6.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.38846148996581

> <JCHEM_PKA_STRONGEST_BASIC>
-0.19931886428374168

> <JCHEM_POLAR_SURFACE_AREA>
47.56

> <JCHEM_REFRACTIVITY>
117.6101

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.36e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -2.667  -9.240   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334 -11.550   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.670 -10.010   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      18.482 -12.580   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      17.856 -13.987   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      16.324 -13.826   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23   28                                                  
CONECT   28   27   20                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
12-(2H-1,3-Benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienimidate	Generator

Chemical Formula

C₂₄H₃₃NO₃

Average Mass

383.5320 Da

Monoisotopic Mass

383.24604 Da

IUPAC Name

12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienamide

Traditional Name

12-(2H-1,3-benzodioxol-5-yl)-N-(3-methylbutyl)dodeca-2,4,11-trienamide

CAS Registry Number

Not Available

SMILES

CC(C)CCNC(=O)C=CC=CCCCCCC=CC1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C24H33NO3/c1-20(2)16-17-25-24(26)13-11-9-7-5-3-4-6-8-10-12-21-14-15-22-23(18-21)28-19-27-22/h7,9-15,18,20H,3-6,8,16-17,19H2,1-2H3,(H,25,26)

InChI Key

DWPMNGYHFAAZBH-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
Piper nigrum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Styrene
Benzenoid
Acetal
Carboximidic acid
Carboximidic acid derivative
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Oxacycle
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Organic nitrogen compound
Organonitrogen compound
Hydrocarbon derivative
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	6.34	ALOGPS
logP	6.06	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	16.39	ChemAxon
pKa (Strongest Basic)	-0.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.56 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	117.61 m³·mol⁻¹	ChemAxon
Polarizability	46.55 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72757529

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid (NP0324697)

MOL for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

3D MOL for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

3D SDF for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

3D-SDF for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

PDB for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

3D PDB for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

SMILES for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

INCHI for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

Structure for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)

3D Structure for NP0324697 (12-(2h-1,3-benzodioxol-5-yl)-n-(3-methylbutyl)dodeca-2,4,11-trienimidic acid)