NP-MRD: Showing NP-Card for (2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one (NP0244779)

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Record Information

Version

2.0

Created at

2022-09-07 05:39:10 UTC

Updated at

2022-09-07 05:39:10 UTC

NP-MRD ID

NP0244779

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one

Description

(2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one 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. Based on a literature review very few articles have been published on (2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072207392D          

 46 52  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309072207392D          

 46 52  0  0  1  0            999 V2000
    5.9007    4.9054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4882    5.6198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9007    6.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7257    6.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1382    5.6198    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9351    5.4063    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6495    5.8188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6495    6.6438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3640    7.0563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0785    6.6438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0785    5.8188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3640    5.4063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8631    5.5639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3480    6.2313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8631    6.8987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7215    4.6094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1340    3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7215    3.1805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9590    3.8949    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.3715    4.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1965    4.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6090    3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1965    3.1805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3715    3.1805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    4.8229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2102    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  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
    4.6632    5.6198    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2507    4.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4257    4.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0132    5.6198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4257    6.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2507    6.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 16 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 32 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 35 40  1  0  0  0  0
  2 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 41 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244779

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C(\C=C/[C@@H]1[C@@H](CCCC\C=C\C2=CC=C3OCOC3=C2)[C@@H]([C@H]1C1=CC=C2OCOC2=C1)C(=O)N1CCCCC1)N1CCCCC1

> <INCHI_IDENTIFIER>
InChI=1S/C38H46N2O6/c41-35(39-19-7-3-8-20-39)18-15-30-29(12-6-2-1-5-11-27-13-16-31-33(23-27)45-25-43-31)37(38(42)40-21-9-4-10-22-40)36(30)28-14-17-32-34(24-28)46-26-44-32/h5,11,13-18,23-24,29-30,36-37H,1-4,6-10,12,19-22,25-26H2/b11-5+,18-15-/t29-,30-,36+,37+/m1/s1

> <INCHI_KEY>
OMGQCNNMUOGPBW-AEMJZORYSA-N

> <FORMULA>
C38H46N2O6

> <MOLECULAR_WEIGHT>
626.794

> <EXACT_MASS>
626.335587209

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
71.44872230213656

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one

> <JCHEM_LOGP>
6.312612029666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
0.544456530613794

> <JCHEM_POLAR_SURFACE_AREA>
77.54

> <JCHEM_REFRACTIVITY>
178.21199999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one

> <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  O   UNK     0      11.015   9.157   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.245  10.490   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.015  11.824   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.555  11.824   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.325  10.490   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.812  10.092   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.146  10.862   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.146  12.402   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.479  13.172   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.813  12.402   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.813  10.862   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.479  10.092   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      20.278  10.386   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      21.183  11.632   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      20.278  12.878   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      14.414   8.604   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.184   7.271   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.414   5.937   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      16.724   7.271   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      17.494   8.604   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.034   8.604   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.804   7.271   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.034   5.937   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.494   5.937   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.926   9.003   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.592   8.233   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.592   6.693   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.259   5.923   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.259   4.383   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   41  N   UNK     0       8.705  10.490   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0       7.935   9.157   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.395   9.157   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.625  10.490   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.395  11.824   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.935  11.824   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   41                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    7                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    6   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   16    5   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36   32                                                       
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   35                                                       
CONECT   41    2   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₆N₂O₆

Average Mass

626.7940 Da

Monoisotopic Mass

626.33559 Da

IUPAC Name

(2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one

Traditional Name

(2Z)-3-[(1R,2S,3S,4R)-2-(2H-1,3-benzodioxol-5-yl)-4-[(5E)-6-(2H-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

O=C(\C=C/[C@@H]1[C@@H](CCCC\C=C\C2=CC=C3OCOC3=C2)[C@@H]([C@H]1C1=CC=C2OCOC2=C1)C(=O)N1CCCCC1)N1CCCCC1

InChI Identifier

InChI=1S/C38H46N2O6/c41-35(39-19-7-3-8-20-39)18-15-30-29(12-6-2-1-5-11-27-13-16-31-33(23-27)45-25-43-31)37(38(42)40-21-9-4-10-22-40)36(30)28-14-17-32-34(24-28)46-26-44-32/h5,11,13-18,23-24,29-30,36-37H,1-4,6-10,12,19-22,25-26H2/b11-5+,18-15-/t29-,30-,36+,37+/m1/s1

InChI Key

OMGQCNNMUOGPBW-AEMJZORYSA-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

Not Available

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
N-acyl-piperidine
Styrene
Piperidine
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Acetal
Carboxylic acid derivative
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
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	6.31	ChemAxon
pKa (Strongest Basic)	0.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	77.54 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	178.21 m³·mol⁻¹	ChemAxon
Polarizability	71.45 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

162865168

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one (NP0244779)

MOL for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

3D MOL for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

3D SDF for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

3D-SDF for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

PDB for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

3D PDB for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

SMILES for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

INCHI for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

Structure for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)

3D Structure for NP0244779 ((2z)-3-[(1r,2s,3s,4r)-2-(2h-1,3-benzodioxol-5-yl)-4-[(5e)-6-(2h-1,3-benzodioxol-5-yl)hex-5-en-1-yl]-3-(piperidine-1-carbonyl)cyclobutyl]-1-(piperidin-1-yl)prop-2-en-1-one)