NP-MRD: Showing NP-Card for 3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene (NP0259006)

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Record Information

Version

2.0

Created at

2022-09-08 00:43:35 UTC

Updated at

2022-09-08 00:43:35 UTC

NP-MRD ID

NP0259006

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene

Description

3,15-Diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadec-7-ene belongs to the class of organic compounds known as aloperine and related alkaloids. These are lupin Alkaloids with a structure based on the aloperine skeleton. Aloperine is a tetracyclic compound made up of a quinolizidine and a decahydroquinoline joined to form 3,15-diazatetracycloheptadecane. 3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene is found in Sophora flavescens. 3,15-Diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadec-7-ene is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
    0.4273   -1.4740    0.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5156   -0.8106   -0.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7022   -1.5984   -0.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9667   -0.8229   -0.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7285    0.6142   -0.9873 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8386    1.1939   -0.0305 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4977    0.6565   -0.1170 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7106    1.1290    1.0613 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4386    0.0222    2.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4451   -0.9718    1.2753 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6831   -0.2906    0.7828 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6430   -1.3247    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3198   -0.9250   -1.0128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6458    0.5303   -1.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5869    1.4352   -0.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3806    0.7383   -0.1598 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5700    1.7420    0.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1492   -2.4181   -0.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5684   -1.8678   -1.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8287   -2.5592   -0.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7980   -1.2137   -1.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2419   -0.7411    0.5680 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7122    1.1207   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3527    0.6355   -2.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8575    2.2103    0.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0683    1.0384   -1.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2526    1.9230    1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3671   -0.5120    2.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1322    0.3768    2.8995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6755   -1.8266    1.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1684    0.1871    1.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4439   -1.5578    1.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1121   -2.2980    0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2951   -1.4857   -1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6974   -1.2400   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5993    0.6857   -0.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9265    0.7560   -2.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858    2.0379    0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3045    2.1780   -1.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1249    2.2471    1.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2825    2.4800   -0.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17  8  1  0
  8  9  1  0
  9 10  1  0
 10  1  1  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 16  1  0
  7  8  1  0
  7  2  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
 17 40  1  0
 17 41  1  0
  8 27  1  1
  9 28  1  0
  9 29  1  0
 10 30  1  1
  1 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  7 26  1  6
 11 31  1  1
 12 32  1  0
 12 33  1  0
M  END


  Mrv1533004241522152D          

 17 20  0  0  0  0            999 V2000
    6.8413   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8413    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655    0.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.4125    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
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
  6 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
 12 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259006

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C1CCN2CC3CC(C=C4CCCNC34)C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24N2/c1-2-7-17-10-13-9-12(14(17)5-1)8-11-4-3-6-16-15(11)13/h8,12-16H,1-7,9-10H2

> <INCHI_KEY>
SKOLRLSBMUGVOY-UHFFFAOYSA-N

> <FORMULA>
C15H24N2

> <MOLECULAR_WEIGHT>
232.371

> <EXACT_MASS>
232.193948781

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
27.913017995896894

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene

> <ALOGPS_LOGP>
1.74

> <JCHEM_LOGP>
1.650376867999999

> <ALOGPS_LOGS>
-2.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
9.979754334663786

> <JCHEM_POLAR_SURFACE_AREA>
15.27

> <JCHEM_REFRACTIVITY>
71.8011

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      12.770  -0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.770   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.437   2.310   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      10.103   1.540   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       9.014   2.629   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.474   2.629   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.709   0.962   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.014  -1.089   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.103  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.437  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.474  -1.089   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.385  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.385   1.540   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       5.052   2.310   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.718   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.718  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.052  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2   10                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9    1                                                       
CONECT   11    8   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12    6   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   40    0
END

View in JSmol

Synonyms

Value	Source
6-Epi-aloperine	MeSH
Alop1 compound	MeSH
Aloperine	MeSH

Chemical Formula

C₁₅H₂₄N₂

Average Mass

232.3710 Da

Monoisotopic Mass

232.19395 Da

IUPAC Name

3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene

Traditional Name

3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene

CAS Registry Number

Not Available

SMILES

C1CCN2CC3CC(C=C4CCCNC34)C2C1

InChI Identifier

InChI=1S/C15H24N2/c1-2-7-17-10-13-9-12(14(17)5-1)8-11-4-3-6-16-15(11)13/h8,12-16H,1-7,9-10H2

InChI Key

SKOLRLSBMUGVOY-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
Sophora flavescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aloperine and related alkaloids. These are lupin Alkaloids with a structure based on the aloperine skeleton. Aloperine is a tetracyclic compound made up of a quinolizidine and a decahydroquinoline joined to form 3,15-diazatetracycloheptadecane.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Aloperine and related alkaloids

Direct Parent

Aloperine and related alkaloids

Alternative Parents

Substituents

Aloperine skeleton
Quinolizidine
Piperidine
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organoheterocyclic compound
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Hydrocarbon derivative
Organonitrogen compound
Amine
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	1.74	ALOGPS
logP	1.65	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	9.98	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	15.27 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	71.8 m³·mol⁻¹	ChemAxon
Polarizability	27.91 Å³	ChemAxon
Number of Rings	4	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

3772951

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene (NP0259006)

MOL for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

3D MOL for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

3D SDF for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

3D-SDF for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

PDB for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

3D PDB for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

SMILES for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

INCHI for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

Structure for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)

3D Structure for NP0259006 (3,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadec-7-ene)