NP-MRD: Showing NP-Card for (1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine (NP0210889)

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Record Information

Version

2.0

Created at

2022-09-05 08:54:36 UTC

Updated at

2022-09-05 08:54:36 UTC

NP-MRD ID

NP0210889

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine

Description

Mirabilin F belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. (1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine is found in Mycale mirabilis. (1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine was first documented in 2010 (PMID: 20066277). Based on a literature review very few articles have been published on Mirabilin F.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
   -2.0672   -4.8154    0.3010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2283   -4.2176    0.1077 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3856   -2.9386   -0.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2465   -2.1261   -0.3014 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4814   -0.7052   -0.4558 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4557    0.1482   -0.1095 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7227   -0.3375    0.4285 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7061    0.4384    0.7908 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9473   -0.1597    1.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0862    0.2621    0.4092 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3443    1.6281   -0.2206 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3079    2.1530   -1.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0405    2.1209   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0962    1.1048   -0.4396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6369    0.7086    0.9357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7415   -0.2329    0.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9369   -1.0615   -0.5770 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6340   -2.2974    0.0480 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7606   -0.2238   -0.9998 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6860   -2.5423   -0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8692   -1.3948    0.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6300    1.5032    0.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1449    0.1330    2.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8990   -1.2734    1.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624    0.2624    0.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8316    1.2737    0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0988   -0.4464   -0.4495 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6976    2.0693    0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6732    2.3877   -2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7791    3.0875   -0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0245    1.3843   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3314    2.9247    0.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0577    2.6598   -1.4186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0078    1.4885   -0.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0452    1.5575    1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9224    0.0863    1.4745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1779   -0.8297    1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4454    0.4032   -0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6051   -1.2551   -1.4509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3901   -2.7588    0.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7278   -0.1690   -2.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  3 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 14 19  1  0
 11  6  1  0
 19  5  1  0
 19 17  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
  9 23  1  0
  9 24  1  0
  8 22  1  0
  7 21  1  0
  4 20  1  0
  2  1  1  0
 18 40  1  0
 17 39  1  6
 16 37  1  0
 16 38  1  0
 15 35  1  0
 15 36  1  0
 14 34  1  6
 13 32  1  0
 13 33  1  0
 11 28  1  1
 12 29  1  0
 12 30  1  0
 12 31  1  0
 19 41  1  6
M  END


  Mrv1652309052210542D          

 18 20  0  0  1  0            999 V2000
   -0.1610    4.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927    3.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6790    3.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326    2.8071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    1.9867    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6198    1.8373    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.6813    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.3457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7713   -0.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463   -0.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.3457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9377    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514    1.5017    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0978    1.8373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588    0.8306    0.0000 C   0  0  1  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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  6  0  0  0
 14 18  1  0  0  0  0
 18  6  1  1  0  0  0
 11 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210889

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C\C1=C2NC(=N)N[C@H]3CC[C@@H](C[C@@H]1C)[C@@H]23

> <INCHI_IDENTIFIER>
InChI=1S/C15H23N3/c1-3-4-5-11-9(2)8-10-6-7-12-13(10)14(11)18-15(16)17-12/h4-5,9-10,12-13H,3,6-8H2,1-2H3,(H3,16,17,18)/b5-4+/t9-,10-,12-,13+/m0/s1

> <INCHI_KEY>
YSZQKSLEUOCOPD-GWZQUTHXSA-N

> <FORMULA>
C15H23N3

> <MOLECULAR_WEIGHT>
245.37

> <EXACT_MASS>
245.189197753

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.883415805891197

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,10S,12R)-9-[(1E)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0^{4,12}]dodec-8-en-6-imine

> <JCHEM_LOGP>
2.0938083716666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
11.865276730275003

> <JCHEM_POLAR_SURFACE_AREA>
47.910000000000004

> <JCHEM_REFRACTIVITY>
86.79419999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,10S,12R)-9-[(1E)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0^{4,12}]dodec-8-en-6-imine

> <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      -0.300   8.024   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.106   7.398   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.267   5.866   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.674   5.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.835   3.708   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.242   3.082   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       5.971   3.708   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       7.217   2.803   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.624   3.430   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0       7.056   1.272   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       5.649   0.645   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.173  -0.819   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.633  -0.819   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.157   0.645   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.750   1.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.589   2.803   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.182   3.430   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.403   1.550   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   16                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15    5   17                                                  
CONECT   17   16                                                            
CONECT   18   14    6   11                                                  
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₃N₃

Average Mass

245.3700 Da

Monoisotopic Mass

245.18920 Da

IUPAC Name

(1S,4S,10S,12R)-9-[(1E)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0^{4,12}]dodec-8-en-6-imine

Traditional Name

(1S,4S,10S,12R)-9-[(1E)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0^{4,12}]dodec-8-en-6-imine

CAS Registry Number

Not Available

SMILES

CC\C=C\C1=C2NC(=N)N[C@H]3CC[C@@H](C[C@@H]1C)[C@@H]23

InChI Identifier

InChI=1S/C15H23N3/c1-3-4-5-11-9(2)8-10-6-7-12-13(10)14(11)18-15(16)17-12/h4-5,9-10,12-13H,3,6-8H2,1-2H3,(H3,16,17,18)/b5-4+/t9-,10-,12-,13+/m0/s1

InChI Key

YSZQKSLEUOCOPD-GWZQUTHXSA-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
Arenochalina mirabilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Quinazoline
1,4,5,6-tetrahydropyrimidine
Hydropyrimidine
Guanidine
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
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	2.09	ChemAxon
pKa (Strongest Basic)	11.87	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	47.91 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	86.79 m³·mol⁻¹	ChemAxon
Polarizability	28.88 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

34258935

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45100977

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

El-Naggar M, Conte M, Capon RJ: Mirabilins revisited: polyketide alkaloids from a southern Australian marine sponge, Clathria sp. Org Biomol Chem. 2010 Jan 21;8(2):407-12. doi: 10.1039/b915624k. Epub 2009 Oct 30. [PubMed:20066277 ]
LOTUS database [Link]

Showing NP-Card for (1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine (NP0210889)

MOL for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

3D MOL for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

3D SDF for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

3D-SDF for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

PDB for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

3D PDB for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

SMILES for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

INCHI for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

Structure for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)

3D Structure for NP0210889 ((1s,4s,10s,12r)-9-[(1e)-but-1-en-1-yl]-10-methyl-5,7-diazatricyclo[6.3.1.0⁴,¹²]dodec-8-en-6-imine)