NP-MRD: Showing NP-Card for 1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium (NP0215220)

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Record Information

Version

2.0

Created at

2022-09-05 14:45:40 UTC

Updated at

2022-09-05 14:45:40 UTC

NP-MRD ID

NP0215220

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium

Description

ZINC104205424 belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group. 1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium is found in Arctotis fastuosa, Arctotis hirsuta and Arctotis venusta. Based on a literature review very few articles have been published on ZINC104205424.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052216452D          

 26 27  0  0  0  0            999 V2000
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    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
   -0.0000    0.0000    0.0000 N   0  3  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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    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
    1.0214    0.4309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5451    0.1559    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  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  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  1  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
 17 18  1  0  0  0  0
 18 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
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 10 26  1  0  0  0  0
M  CHG  2  10   1  13   1
M  END

     RDKit          3D

 76 77  0  0  0  0  0  0  0  0999 V2000
   -9.5208   -1.7186    2.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5460   -0.3725    1.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2652   -0.2104    0.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1291   -0.2829    1.7235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7667   -0.1333    1.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5588   -1.2207    0.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2080   -1.1533   -0.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0124    0.1113   -1.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.2985   -2.1020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5194    0.3178   -1.4190 N   0  0  2  0  0  4  0  0  0  0  0  0
   -0.9625   -1.0143   -1.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5738   -0.8941   -1.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8729    0.3463   -0.5697 N   0  0  2  0  0  4  0  0  0  0  0  0
    2.1487    0.3764    0.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2546    0.9094   -0.7718 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5611    0.9061   -0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0106   -0.4550    0.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3080   -0.4359    1.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4487    0.1077    0.3574 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7013    0.0664    1.2203 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8539    0.6112    0.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1178    0.5846    1.2424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.5958    0.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4634    0.9679   -0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7005    1.4037   -1.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5984    1.1222   -2.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8021   -2.4089    1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1882   -1.6246    3.2771 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5177   -2.1827    2.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5936    0.4041    2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4505   -0.3202    0.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2361   -1.0597    0.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2547    0.7273    0.1775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2300    0.4867    2.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1262   -1.3041    2.1966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0282   -0.2470    1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7252    0.8833    0.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3431   -1.1800   -0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6885   -2.1929    0.5990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4688   -1.3198    0.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1136   -1.9916   -1.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8413    0.1480   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2384    1.0248   -0.7257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6898   -0.5428   -2.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549    1.2608   -2.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2179   -1.4179   -0.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3313   -1.6350   -2.0920 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0462   -1.7290   -0.7505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8595   -0.7749   -2.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -0.6173    0.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0711    1.0574    0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4198    0.3649   -1.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.9797   -1.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3691    1.3890   -0.6182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4954    1.5335    0.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2762   -1.0107    1.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1881   -1.0555   -0.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5155   -1.4620    1.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1486    0.1684    2.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6339   -0.5609   -0.5002 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2763    1.1170   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9028   -1.0002    1.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5488    0.6360    2.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9563   -0.0666   -0.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6428    1.6291    0.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9017    1.1891    0.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9119    1.0843    2.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4305   -0.4665    1.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1884   -0.2727    1.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2362    1.4632    1.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2543    0.6507    0.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5670    2.0808   -0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6179    2.3840   -1.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5329    1.3866   -2.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1475    2.0276   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4348    0.5331   -3.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
 10  9  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 13 23  1  0
 23 24  1  0
 13 25  1  0
 25 26  1  0
 24 10  1  0
 26 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 15 52  1  0
 15 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 22 67  1  0
 22 68  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 25 73  1  0
 25 74  1  0
 26 75  1  0
 26 76  1  0
M  CHG  2  10   1  13   1
M  END


  Mrv1652309052216452D          

 26 27  0  0  0  0            999 V2000
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    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
   -0.0000    0.0000    0.0000 N   0  3  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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    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
    1.0214    0.4309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5451    0.1559    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  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  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  1  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
 17 18  1  0  0  0  0
 18 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
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 10 26  1  0  0  0  0
M  CHG  2  10   1  13   1
M  END
> <DATABASE_ID>
NP0215220

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC[N+]12CC[N+](CCCCCCCCC)(CC1)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C24H50N2/c1-3-5-7-9-11-13-15-17-25-19-22-26(23-20-25,24-21-25)18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3/q+2

> <INCHI_KEY>
QVOQAFZRUJLJRH-UHFFFAOYSA-N

> <FORMULA>
C24H50N2

> <MOLECULAR_WEIGHT>
366.677

> <EXACT_MASS>
366.396302458

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
51.40421042928263

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium

> <JCHEM_LOGP>
-1.365424452276826

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
139.65359999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.669   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.000   0.000   0.000  0.00  0.00           N+1
HETATM   11  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.667   1.540   0.000  0.00  0.00           N+1
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.907   0.804   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.017   0.291   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   24   26                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   23   25                                             
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                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   13   24                                                       
CONECT   24   23   10                                                       
CONECT   25   13   26                                                       
CONECT   26   25   10                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₅₀N₂

Average Mass

366.6770 Da

Monoisotopic Mass

366.39630 Da

IUPAC Name

1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium

Traditional Name

1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium

CAS Registry Number

Not Available

SMILES

CCCCCCCCC[N+]12CC[N+](CCCCCCCCC)(CC1)CC2

InChI Identifier

InChI=1S/C24H50N2/c1-3-5-7-9-11-13-15-17-25-19-22-26(23-20-25,24-21-25)18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3/q+2

InChI Key

QVOQAFZRUJLJRH-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
Arctotis fastuosa	LOTUS Database	35616633
Arctotis hirsuta	LOTUS Database	35616633
Arctotis venusta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazinanes

Sub Class

Piperazines

Direct Parent

N-alkylpiperazines

Alternative Parents

Substituents

N-alkylpiperazine
Tetraalkylammonium salt
Quaternary ammonium salt
Azacycle
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organic salt
Organonitrogen compound
Amine
Organic cation
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-1.4	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	139.65 m³·mol⁻¹	ChemAxon
Polarizability	51.4 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

382334

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

432316

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium (NP0215220)

MOL for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

3D MOL for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

3D SDF for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

3D-SDF for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

PDB for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

3D PDB for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

SMILES for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

INCHI for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

Structure for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)

3D Structure for NP0215220 (1,4-dinonyl-1,4-diazabicyclo[2.2.2]octane-1,4-diium)