NP-MRD: Showing NP-Card for (1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one (NP0181813)

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Record Information

Version

2.0

Created at

2022-09-03 20:23:50 UTC

Updated at

2022-09-03 20:23:50 UTC

NP-MRD ID

NP0181813

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one

Description

(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadecan-8-one belongs to the class of organic compounds known as sparteine, lupanine, and related alkaloids. These are alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems. (1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one is found in Adenocarpus hispanicus, Anabasis aphylla, Argyrolobium velutinum, Genista monspessulana, Hesperolaburnum platycarpum, Lupinus latifolius, Lupinus mexicanus, Retama monosperma, Sophora davidii and Virgilia oroboides. Based on a literature review very few articles have been published on (1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadecan-8-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -1.0896    2.5663    0.7672 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8892    1.6175   -0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5329    1.4300   -0.5276 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1900    0.3595   -1.5804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3127   -0.7257   -0.6034 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7735   -1.6036   -0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8771   -0.6549   -0.1444 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9884   -1.2260    0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5646   -0.5850    1.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    0.9000    1.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7465    1.4357    0.4105 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4263    0.6198    0.3737 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7372   -0.6603   -0.7723 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4832   -1.5559    0.1788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3846   -0.7075    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2113    0.1719    0.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3182    1.2204   -0.5555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9675    0.7620   -0.4441 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    2.3167   -0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0960    0.0911   -2.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5379    0.7118   -2.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3137   -0.4014    0.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7223   -2.3977    0.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1373   -2.1183   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8295   -1.2944   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7883   -2.3047    0.6869 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6053   -1.0091    1.7674 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183   -0.8981    2.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7019    1.1645    1.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4531    1.3897    2.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4746    2.4721    0.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1858    1.3866   -0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1401    0.6113    1.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1279   -0.7632   -1.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7481   -2.1315    0.7816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0784   -2.2731   -0.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133   -0.1271    1.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0725   -1.4007    1.5620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6910   -0.4784   -0.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9690    0.6743    0.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6211    1.2378   -1.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5019    2.1777   -0.0482 H   0  0  0  0  0  0  0  0  0  0  0  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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  5 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 12  3  1  0
 18 13  1  0
 12  7  1  0
  3 19  1  6
  4 20  1  0
  4 21  1  0
  5 22  1  1
  6 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  1
 13 34  1  6
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
M  END


  Mrv1652309032222232D          

 18 21  0  0  1  0            999 V2000
    0.7686   -0.1362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9093    0.6260    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2478    1.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    2.6178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9093    2.6178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4927    2.0344    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071    2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216    2.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216    1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4927    1.2094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5009    2.0344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2135    2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280    2.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280    1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009    1.2094    0.0000 N   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
  3  4  1  1  0  0  0
  5  4  1  6  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
  3 12  1  0  0  0  0
 12  7  1  1  0  0  0
  5 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
  2 18  1  0  0  0  0
 13 18  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0181813

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1[C@@H]2C[C@H](CN3CCCC[C@@H]23)[C@H]2CCCCN12

> <INCHI_IDENTIFIER>
InChI=1S/C15H24N2O/c18-15-12-9-11(13-5-2-4-8-17(13)15)10-16-7-3-1-6-14(12)16/h11-14H,1-10H2/t11-,12-,13-,14+/m1/s1

> <INCHI_KEY>
YQMWQSMYVPLYDI-SYQHCUMBSA-N

> <FORMULA>
C15H24N2O

> <MOLECULAR_WEIGHT>
248.37

> <EXACT_MASS>
248.188863401

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
29.251354758476744

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-8-one

> <JCHEM_LOGP>
1.3682914969999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.882902755479

> <JCHEM_POLAR_SURFACE_AREA>
23.550000000000004

> <JCHEM_REFRACTIVITY>
71.4962

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-8-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  O   UNK     0       1.435  -0.254   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.024   1.169   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.564   1.169   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.329   2.835   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.024   4.886   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.564   4.886   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       4.653   3.798   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       5.987   4.568   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.320   3.798   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.320   2.258   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.987   1.488   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.653   2.258   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.935   3.798   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.399   4.568   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.732   3.798   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.732   2.258   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.399   1.488   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       0.935   2.258   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    3    7                                                  
CONECT   13    5   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    2   13                                                  
MASTER        0    0    0    0    0    0    0    0   18    0   42    0
END

View in JSmol

Synonyms

Value	Source
(+)-Aphylline	Kegg

Chemical Formula

C₁₅H₂₄N₂O

Average Mass

248.3700 Da

Monoisotopic Mass

248.18886 Da

IUPAC Name

(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-8-one

Traditional Name

(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-8-one

CAS Registry Number

Not Available

SMILES

O=C1[C@@H]2C[C@H](CN3CCCC[C@@H]23)[C@H]2CCCCN12

InChI Identifier

InChI=1S/C15H24N2O/c18-15-12-9-11(13-5-2-4-8-17(13)15)10-16-7-3-1-6-14(12)16/h11-14H,1-10H2/t11-,12-,13-,14+/m1/s1

InChI Key

YQMWQSMYVPLYDI-SYQHCUMBSA-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
Adenocarpus hispanicus	LOTUS Database	35616633
Anabasis aphylla	LOTUS Database	35616633
Argyrolobium velutinum	LOTUS Database	35616633
Cytisus monspessulanus L.	LOTUS Database	35616633
Hesperolaburnum platycarpum	LOTUS Database	35616633
Lupinus latifolius	LOTUS Database	35616633
Lupinus mexicanus	LOTUS Database	35616633
Retama monosperma	LOTUS Database	35616633
Sophora davidii	LOTUS Database	35616633
Virgilia oroboides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sparteine, lupanine, and related alkaloids. These are alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Sparteine, lupanine, and related alkaloids

Direct Parent

Sparteine, lupanine, and related alkaloids

Alternative Parents

Substituents

Sparteine-lupanine skeleton
Quinolizidinone
Quinolizidine
Delta-lactam
Piperidinone
Piperidine
Tertiary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Lactam
Tertiary amine
Tertiary aliphatic amine
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organic nitrogen compound
Amine
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Organopnictogen compound
Carbonyl group
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	1.37	ChemAxon
pKa (Strongest Basic)	8.88	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	23.55 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	71.5 m³·mol⁻¹	ChemAxon
Polarizability	29.25 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

C00002209

Chemspider ID

391243

KEGG Compound ID

C10752

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442940

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one (NP0181813)

MOL for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

3D MOL for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

3D SDF for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

3D-SDF for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

PDB for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

3D PDB for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

SMILES for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

INCHI for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

Structure for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)

3D Structure for NP0181813 ((1r,2r,9r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-8-one)