NP-MRD: Showing NP-Card for 1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane (NP0141907)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-01 20:19:43 UTC

Updated at

2022-09-01 20:19:43 UTC

NP-MRD ID

NP0141907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane

Description

18-Epiormosanine belongs to the class of organic compounds known as ormosia-type alkaloids. These are aloperine alkaloids with a structure based on the ormosanine skeleton. 1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane is found in Ammopiptanthus mongolicus, Bowdichia virgilioides, Hovea linearis, Ormosia jamaicensis, Ormosia macrocalyx, Ormosia monosperma, Ormosia ormondii, Ormosia sumatrana and Templetonia retusa. 18-Epiormosanine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    4.5648   -0.8559    0.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8637   -1.3407   -0.9741 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6034   -0.4741   -1.1183 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557   -0.7514    0.0788 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4192   -0.0720    0.0643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2698   -0.4869    1.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6972   -0.0034    1.4190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7265    1.4694    1.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    2.0823    1.0717 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5477    3.5480    0.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5554    3.9954   -0.1354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3629    3.3121   -1.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1519    1.8824   -1.3314 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776    1.4125    0.0190 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4273   -0.6684    0.2703 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3869   -1.6904    0.8898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2496   -2.1794   -0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3919   -2.8719   -1.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9460   -2.5347   -1.1924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5923   -1.3151   -0.6306 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4231   -0.6658   -1.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4060   -0.4827    1.3297 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6642   -1.1912    1.4622 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7044    0.2322    0.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5390   -1.3590    0.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5028   -1.2612   -1.8717 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5658   -2.4086   -0.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9748    0.5686   -1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1035   -0.8196   -2.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5419   -1.8588    0.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2833   -1.5834    1.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3350   -0.1231    2.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1116   -0.2817    2.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2185    1.9627    2.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3196    1.7668    0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1809    1.9800    2.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6571    4.1627    1.6853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5056    3.6542    0.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5528    3.8435    0.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4210    5.0949   -0.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5703    3.7321   -1.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1801    3.5753   -2.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8809    1.4338   -1.9510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350    1.7390    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0734    0.0754   -0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9553   -1.2131    1.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7453   -2.5270    1.2339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0891   -2.8014    0.1205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7264   -1.2677   -0.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5183   -3.9827   -1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8252   -2.6907   -2.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3922   -3.3652   -0.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5461   -2.5875   -2.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1814   -1.3950   -1.6699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053    0.1701   -1.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5612    0.5235    1.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5067   -2.2690    1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1634   -0.8376    2.3737 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 22  1  0
 22 23  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
  7 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
 23  1  1  0
 14  5  1  0
 20 15  1  0
  5 21  1  6
 14  9  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  1
 22 56  1  0
 23 57  1  0
 23 58  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  1
  8 34  1  0
  8 35  1  0
  9 36  1  1
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  1
 15 45  1  6
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 21 54  1  0
 21 55  1  0
M  END


  Mrv1533004161515452D          

 23 27  0  0  0  0            999 V2000
    4.0658   -1.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2479   -1.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9322   -0.2897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4344    0.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524    0.2571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5681   -0.5051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1187    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4572    2.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2937    3.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1187    3.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021    2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4165    2.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1310    2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1310    1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4165    1.2978    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021    1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7103    2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9959    2.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2814    2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2814    1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9959    1.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7103    1.7103    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2937    1.1270    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
  1  6  1  0  0  0  0
  4  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
  7 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 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
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0141907

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C1CCC(NC1)C12CC(CC3CCCNC13)C1CCCCN1C2

> <INCHI_IDENTIFIER>
InChI=1S/C20H35N3/c1-3-9-21-18(8-1)20-13-16(12-15-6-5-10-22-19(15)20)17-7-2-4-11-23(17)14-20/h15-19,21-22H,1-14H2

> <INCHI_KEY>
YUKCLPPRYNXRAF-UHFFFAOYSA-N

> <FORMULA>
C20H35N3

> <MOLECULAR_WEIGHT>
317.521

> <EXACT_MASS>
317.283098139

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
38.93072751578814

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane

> <ALOGPS_LOGP>
2.38

> <JCHEM_LOGP>
2.4254148443333343

> <ALOGPS_LOGS>
-4.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
3

> <JCHEM_PKA_STRONGEST_BASIC>
11.062457246786598

> <JCHEM_POLAR_SURFACE_AREA>
27.299999999999997

> <JCHEM_REFRACTIVITY>
95.38999999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.87e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       7.590  -2.165   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.063  -1.964   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.473  -0.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.411   0.681   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.938   0.480   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       8.527  -0.943   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.822   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.587   3.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.282   5.822   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.822   5.822   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.911   4.733   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.244   5.503   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.578   4.733   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.578   3.193   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       8.244   2.423   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.911   3.193   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.193   4.733   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.859   5.503   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.525   4.733   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.525   3.193   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.859   2.423   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       3.193   3.193   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       4.282   2.104   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8   16   23                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    7   11                                                  
CONECT   17    9   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22    7                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₅N₃

Average Mass

317.5210 Da

Monoisotopic Mass

317.28310 Da

IUPAC Name

1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane

Traditional Name

1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane

CAS Registry Number

Not Available

SMILES

C1CCC(NC1)C12CC(CC3CCCNC13)C1CCCCN1C2

InChI Identifier

InChI=1S/C20H35N3/c1-3-9-21-18(8-1)20-13-16(12-15-6-5-10-22-19(15)20)17-7-2-4-11-23(17)14-20/h15-19,21-22H,1-14H2

InChI Key

YUKCLPPRYNXRAF-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
Ammopiptanthus mongolicus	LOTUS Database	35616633
Bowdichia virgilioides	LOTUS Database	35616633
Hovea linearis	LOTUS Database	35616633
Ormosia jamaicensis	LOTUS Database	35616633
Ormosia macrocalyx	LOTUS Database	35616633
Ormosia monosperma	LOTUS Database	35616633
Ormosia ormondii	LOTUS Database	35616633
Ormosia sumatrana	LOTUS Database	35616633
Templetonia retusa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ormosia-type alkaloids. These are aloperine alkaloids with a structure based on the ormosanine skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Aloperine and related alkaloids

Direct Parent

Ormosia-type alkaloids

Alternative Parents

Substituents

Ormosia-type alkaloid
Quinolizidine
Quinolidine
Piperidine
Tertiary amine
Tertiary aliphatic amine
Secondary amine
Secondary aliphatic amine
Azacycle
Organoheterocyclic compound
Amine
Hydrocarbon derivative
Organopnictogen compound
Organic nitrogen compound
Organonitrogen compound
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	2.38	ALOGPS
logP	2.43	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	11.06	ChemAxon
Physiological Charge	3	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	27.3 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	95.39 m³·mol⁻¹	ChemAxon
Polarizability	38.93 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

558826

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane (NP0141907)

MOL for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

3D MOL for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

3D SDF for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

3D-SDF for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

PDB for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

3D PDB for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

SMILES for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

INCHI for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

Structure for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)

3D Structure for NP0141907 (1-(piperidin-2-yl)-3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecane)