NP-MRD: Showing NP-Card for 14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one (NP0209832)

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Record Information

Version

2.0

Created at

2022-09-05 07:23:54 UTC

Updated at

2022-09-05 07:23:54 UTC

NP-MRD ID

NP0209832

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one

Description

CHEMBL467697 belongs to the class of organic compounds known as aristolactams. These are phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system. 14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one is found in Houttuynia cordata and Piper caldense. CHEMBL467697 is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
    3.7096   -2.8474   -0.9773 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843   -1.5729   -0.6997 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8374   -1.3139   -0.5372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8652   -2.2776   -0.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4617   -1.9624   -0.4592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7699   -0.6500   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973   -0.4617   -0.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5292    0.8162    0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6088    1.8410    0.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0823    3.1308    0.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1861    4.1701    0.5906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1581    3.9502    0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6539    2.6628    0.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2443    1.6337    0.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2022    0.3487   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5047    0.0275   -0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5362    0.9304   -0.1728 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2373    0.9620    1.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7380   -1.7220   -0.2220 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1480   -1.9522   -0.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7249   -2.6844   -0.4811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8427   -3.9184   -0.6925 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8156   -2.7718   -1.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3429   -3.5342   -0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3866   -3.2385   -1.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1148   -3.2894   -0.8363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042    0.9726    0.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1528    3.2660    0.6502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5608    5.1684    0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8774    4.7656    0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6898    2.5899    0.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7192    1.9405    1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5032    0.7633    1.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9907    0.1773    1.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4044   -2.9744    0.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5836   -1.1945    0.5398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5903   -1.7513   -1.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
  7 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 16  3  1  0
 21  5  1  0
 15  6  1  0
 14  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  8 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 18 32  1  0
 18 33  1  0
 18 34  1  0
 20 35  1  0
 20 36  1  0
 20 37  1  0
M  END


  Mrv1533004231518412D          

 22 25  0  0  0  0            999 V2000
   -0.1637   -2.6759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -2.4209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925   -1.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794   -1.0619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0960    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -0.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771   -1.3590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1902   -1.9110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0186   -2.7180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.0000    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
  5 22  2  0  0  0  0
 10 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209832

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C(=CC4=CC=CC=C4C3=C1OC)N(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H15NO3/c1-19-13-8-10-6-4-5-7-11(10)16-15(13)12(18(19)20)9-14(21-2)17(16)22-3/h4-9H,1-3H3

> <INCHI_KEY>
DPJMELSPGMOETA-UHFFFAOYSA-N

> <FORMULA>
C18H15NO3

> <MOLECULAR_WEIGHT>
293.322

> <EXACT_MASS>
293.105193347

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
31.607600381789982

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2,4,6,8,12(16),13-heptaen-11-one

> <ALOGPS_LOGP>
3.27

> <JCHEM_LOGP>
2.619561856333333

> <ALOGPS_LOGS>
-4.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.685057172977696

> <JCHEM_POLAR_SURFACE_AREA>
38.769999999999996

> <JCHEM_REFRACTIVITY>
84.47619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.64e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2,4,6,8,12(16),13-heptaen-11-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -0.306  -4.995   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.159  -4.519   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.479  -3.013   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.335  -1.982   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.655  -0.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.250   0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.790   0.770   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       0.655   2.016   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       0.179   3.481   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.453   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.454  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.264  -1.030   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.944  -2.537   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.088  -3.567   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.768  -5.074   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.120   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17   19   22                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   18    5   10                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₅NO₃

Average Mass

293.3220 Da

Monoisotopic Mass

293.10519 Da

IUPAC Name

14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2,4,6,8,12(16),13-heptaen-11-one

Traditional Name

14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2,4,6,8,12(16),13-heptaen-11-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C(=CC4=CC=CC=C4C3=C1OC)N(C)C2=O

InChI Identifier

InChI=1S/C18H15NO3/c1-19-13-8-10-6-4-5-7-11(10)16-15(13)12(18(19)20)9-14(21-2)17(16)22-3/h4-9H,1-3H3

InChI Key

DPJMELSPGMOETA-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
Houttuynia cordata	LOTUS Database	35616633
Piper caldense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aristolactams. These are phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aristolactams

Sub Class

Not Available

Direct Parent

Aristolactams

Alternative Parents

Substituents

Aristolactam
Phenanthrene
Isoindolone
Naphthalene
Indole or derivatives
Isoindole or derivatives
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Carboxylic acid derivative
Ether
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.27	ALOGPS
logP	2.62	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.77 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	84.48 m³·mol⁻¹	ChemAxon
Polarizability	31.61 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

21680139

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one (NP0209832)

MOL for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

3D MOL for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

3D SDF for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

3D-SDF for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

PDB for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

3D PDB for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

SMILES for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

INCHI for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

Structure for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)

3D Structure for NP0209832 (14,15-dimethoxy-10-methyl-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one)