NP-MRD: Showing NP-Card for (1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one (NP0210751)

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Record Information

Version

2.0

Created at

2022-09-05 08:42:21 UTC

Updated at

2022-09-05 08:42:21 UTC

NP-MRD ID

NP0210751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one

Description

Albine belongs to the class of organic compounds known as tetrahydropyridines. These are derivatives of pyridine in which two double bonds in the pyridine moiety are reduced by adding four hydrogen atoms. (1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one is found in Lupinus albescens and Lupinus albus. (1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one was first documented in 2007 (PMID: 18235911). Based on a literature review a small amount of articles have been published on Albine (PMID: 30159652) (PMID: 27474004) (PMID: 20395002) (PMID: 18433102).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    4.5168   -0.5681    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977   -0.9016   -0.4042 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1682   -1.1259    0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3349   -0.1363   -0.7165 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8251    1.2234   -0.3492 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9323    1.9638    0.5219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5015    2.1752    0.0051 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4523    1.2439   -1.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0474   -0.0305   -0.4216 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2623   -0.7448   -0.3663 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2978   -1.9959    0.4782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7327   -2.3493    0.7823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0107   -3.5399    1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8047   -1.3632    0.7739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4601   -0.0808    0.5650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1156    0.2586    0.3666 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5570    1.5051    0.8594 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5375   -0.4063    0.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2608   -0.4504    1.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8825   -1.0129   -1.4445 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0970   -0.8756    1.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8893   -2.1553   -0.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5489   -0.2540   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1405    1.7425   -1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3757    3.0098    0.4776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9867    1.7031    1.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7308    3.2021   -0.2529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2655    1.5650   -1.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263    1.2155   -1.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0937    0.1162    0.7127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7927   -0.9954   -1.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945   -2.8265   -0.0435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7475   -1.8206    1.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8334   -1.6550    0.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2034    0.7043    0.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2535    1.4342    1.9212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4289    2.2257    0.8615 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  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
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
  9  4  1  0
 16 10  1  0
 17  7  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  6
  5 24  1  0
  6 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
  9 30  1  1
 10 31  1  6
 11 32  1  0
 11 33  1  0
 14 34  1  0
 15 35  1  0
 17 36  1  0
 17 37  1  0
M  END


  Mrv1652309052210422D          

 17 19  0  0  1  0            999 V2000
    4.7780   -0.1928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3988    0.5399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5747    0.5779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1955    1.3105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7273    1.9413    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6573    2.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    3.2951    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9569    2.1862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3735    1.2406    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7427    1.7724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0658    1.3008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3189    1.6512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580    1.1797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2490    2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259    2.9449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    2.5944    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2046    3.2251    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
  4  3  1  1  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  6  0  0  0
  9  8  1  1  0  0  0
  4  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  1  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C=CC[C@@H]1NC[C@H]2C[C@H]1[C@H]1CC(=O)C=CN1C2

> <INCHI_IDENTIFIER>
InChI=1S/C14H20N2O/c1-2-3-13-12-6-10(8-15-13)9-16-5-4-11(17)7-14(12)16/h2,4-5,10,12-15H,1,3,6-9H2/t10-,12-,13+,14-/m1/s1

> <INCHI_KEY>
QJVOZXGJOGJKPT-RUZUBIRVSA-N

> <FORMULA>
C14H20N2O

> <MOLECULAR_WEIGHT>
232.327

> <EXACT_MASS>
232.157563272

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
18.24980439323133

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,9R,12S)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-5-en-4-one

> <JCHEM_LOGP>
1.1627383623333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.469274799382212

> <JCHEM_PKA_STRONGEST_BASIC>
10.238411858412958

> <JCHEM_POLAR_SURFACE_AREA>
32.34

> <JCHEM_REFRACTIVITY>
68.86119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,9R,12S)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-5-en-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

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       8.919  -0.360   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.211   1.008   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.673   1.079   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.965   2.446   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       6.958   3.624   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.827   5.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.650   6.151   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.519   4.081   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.430   2.316   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.253   3.308   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.990   2.428   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.595   3.082   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.668   2.202   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.465   4.617   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.728   5.497   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.123   4.843   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       4.115   6.020   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16    7                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₀N₂O

Average Mass

232.3270 Da

Monoisotopic Mass

232.15756 Da

IUPAC Name

(1R,2R,9R,12S)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-5-en-4-one

Traditional Name

(1R,2R,9R,12S)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-5-en-4-one

CAS Registry Number

Not Available

SMILES

C=CC[C@@H]1NC[C@H]2C[C@H]1[C@H]1CC(=O)C=CN1C2

InChI Identifier

InChI=1S/C14H20N2O/c1-2-3-13-12-6-10(8-15-13)9-16-5-4-11(17)7-14(12)16/h2,4-5,10,12-15H,1,3,6-9H2/t10-,12-,13+,14-/m1/s1

InChI Key

QJVOZXGJOGJKPT-RUZUBIRVSA-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
Lupinus albescens	LOTUS Database	35616633
Lupinus albus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydropyridines. These are derivatives of pyridine in which two double bonds in the pyridine moiety are reduced by adding four hydrogen atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Hydropyridines

Direct Parent

Tetrahydropyridines

Alternative Parents

Substituents

Tetrahydropyridine
Piperidine
Vinylogous amide
Ketone
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Secondary aliphatic amine
Secondary amine
Enamine
Azacycle
Allylamine
Carbonyl group
Organic oxygen compound
Amine
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Hydrocarbon derivative
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	1.16	ChemAxon
pKa (Strongest Acidic)	18.47	ChemAxon
pKa (Strongest Basic)	10.24	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.34 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	68.86 m³·mol⁻¹	ChemAxon
Polarizability	18.25 Å³	ChemAxon
Number of Rings	3	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

C00002204

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Albine

METLIN ID

Not Available

PubChem Compound

91747723

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Flamm H: [The Austrian Plague Commission in Bombay 1897 and the last fatal Plague Cases in Vienna 1898]. Wien Med Wochenschr. 2018 Nov;168(15-16):375-383. doi: 10.1007/s10354-018-0653-z. Epub 2018 Aug 29. [PubMed:30159652 ]
Chiebao DP, Pena HFJ, Cabral AD, Rocca MP, Lopes EG, Valadas SYOB, Keid LB, Grisi Filho JHH, Soares RM: Infection of mice with oocysts of Toxoplasma gondii by oral route showed differences of virulence from Brazilian RFLP genotypes BrI and BrIII. Res Vet Sci. 2016 Aug;107:257-260. doi: 10.1016/j.rvsc.2016.06.010. Epub 2016 Jun 20. [PubMed:27474004 ]
Salva S, Villena J, Alvarez S: Immunomodulatory activity of Lactobacillus rhamnosus strains isolated from goat milk: impact on intestinal and respiratory infections. Int J Food Microbiol. 2010 Jun 30;141(1-2):82-9. doi: 10.1016/j.ijfoodmicro.2010.03.013. Epub 2010 Mar 18. [PubMed:20395002 ]
Boschin G, Annicchiarico P, Resta D, D'Agostina A, Arnoldi A: Quinolizidine alkaloids in seeds of lupin genotypes of different origins. J Agric Food Chem. 2008 May 28;56(10):3657-63. doi: 10.1021/jf7037218. [PubMed:18433102 ]
Araf D, Moura Eda M, Rodrigues CJ, Figueiredo LA: [Homologous scleral and dura mater grafts in rabbit eyes: a comparative histopathological analysis]. Arq Bras Oftalmol. 2007 Nov-Dec;70(6):981-7. doi: 10.1590/s0004-27492007000600018. [PubMed:18235911 ]
LOTUS database [Link]

Showing NP-Card for (1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one (NP0210751)

MOL for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

3D MOL for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

3D SDF for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

3D-SDF for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

PDB for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

3D PDB for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

SMILES for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

INCHI for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

Structure for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)

3D Structure for NP0210751 ((1r,2r,9r,12s)-12-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-5-en-4-one)