NP-MRD: Showing NP-Card for 10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene (NP0190581)

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Record Information

Version

2.0

Created at

2022-09-04 07:16:54 UTC

Updated at

2022-09-04 07:16:54 UTC

NP-MRD ID

NP0190581

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene

Description

10,14-Dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]Octadeca-7(18),8,10,14,16-pentaene belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic. 10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene is found in Papaver orientale. 10,14-Dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]Octadeca-7(18),8,10,14,16-pentaene is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 45  0  0  0  0  0  0  0  0999 V2000
   -3.4837   -3.3171   -0.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5399   -2.6868    0.2525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0527   -1.4067    0.0178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4980   -0.7816   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0199    0.5629   -1.3823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1635    1.1709   -0.6003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6091    2.5221   -0.8048 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9111    2.5477   -0.7966 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5009    1.2444   -0.4520 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7926    0.9117   -0.7972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2677   -0.3688   -0.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4641   -1.3144    0.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9347   -2.5756    0.4704 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2197   -3.0321    0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1611   -0.9823    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7943    0.2718    0.1766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6152    0.5067    0.6332 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7283    1.4835    1.7529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395    2.7087    1.4003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0449    3.4266    0.2671 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1122   -0.8292    0.9565 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0820   -1.6239    1.1386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0456   -3.3967   -1.6058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4765   -2.8641   -0.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5933   -4.3663   -0.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2048   -1.2651   -1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3981    1.0376   -2.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9935    2.9881   -1.7430 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243    3.3337   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3039    2.8849   -1.7893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    1.5715   -1.2961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2809   -0.6677   -0.7405 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2902   -4.0972    0.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4639   -2.8921   -0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9597   -2.4688    0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2496    1.7196    2.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2982    0.9654    2.5799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5935    2.4242    1.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4804    3.4020    2.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2914    4.0790    0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5925   -0.8265    1.9716 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  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  1
 18 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 21  3  1  0
 17  6  1  0
 20  7  1  0
 16  9  1  0
 22 15  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  7 28  1  6
  8 29  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 18 36  1  0
 18 37  1  0
 19 38  1  0
 19 39  1  0
 20 40  1  0
 21 41  1  1
M  END


  Mrv1533004161519202D          

 22 26  0  0  0  0            999 V2000
    0.0567   -2.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8638   -2.4218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1191   -1.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5601   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8730   -0.2960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8469   -0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4371    0.6365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2556    0.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5543   -0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3790   -0.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6907   -0.9743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1707   -1.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4882   -2.3919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3064   -2.4976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3221   -1.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6104   -1.9798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9449   -1.4771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1595   -0.6451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3144   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1721    0.8410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8935    1.2248    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0315   -0.7687    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  2  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  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  7 21  1  0  0  0  0
 18 22  1  0  0  0  0
  9 22  1  0  0  0  0
 15 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0190581

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C3CC4=CC=C(OC)C5=C4C2(CCN3)C1O5

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO3/c1-20-13-5-3-10-9-12-11-4-6-14(21-2)17-18(11,7-8-19-12)15(10)16(13)22-17/h3-6,12,17,19H,7-9H2,1-2H3

> <INCHI_KEY>
QKQQEIVDLRUZRP-UHFFFAOYSA-N

> <FORMULA>
C18H19NO3

> <MOLECULAR_WEIGHT>
297.354

> <EXACT_MASS>
297.136493476

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
31.34077283945233

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene

> <ALOGPS_LOGP>
1.90

> <JCHEM_LOGP>
1.1491616916666674

> <ALOGPS_LOGS>
-2.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.325603899573128

> <JCHEM_POLAR_SURFACE_AREA>
39.72

> <JCHEM_REFRACTIVITY>
85.36500000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.02e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       0.106  -4.840   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.612  -4.521   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.089  -3.056   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.046  -1.936   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.630  -0.553   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.447  -0.278   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.549   1.188   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.077   1.168   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.635  -0.229   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.174  -0.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.756  -1.819   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.785  -3.043   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.378  -4.465   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.905  -4.662   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.201  -2.868   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.873  -3.696   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.630  -2.757   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.031  -1.204   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.454  -0.087   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.188   1.570   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       3.534   2.286   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       5.659  -1.435   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8   21                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16    3   18                                                  
CONECT   18   17    6   19   22                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    7                                                       
CONECT   22   18    9   15                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₉NO₃

Average Mass

297.3540 Da

Monoisotopic Mass

297.13649 Da

IUPAC Name

10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene

Traditional Name

10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C3CC4=CC=C(OC)C5=C4C2(CCN3)C1O5

InChI Identifier

InChI=1S/C18H19NO3/c1-20-13-5-3-10-9-12-11-4-6-14(21-2)17-18(11,7-8-19-12)15(10)16(13)22-17/h3-6,12,17,19H,7-9H2,1-2H3

InChI Key

QKQQEIVDLRUZRP-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
Papaver orientale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Morphinans

Sub Class

Not Available

Direct Parent

Morphinans

Alternative Parents

Substituents

Morphinan
Phenanthrene
Tetralin
Coumaran
Anisole
Alkyl aryl ether
Aralkylamine
Piperidine
Benzenoid
Secondary aliphatic amine
Ether
Oxacycle
Secondary amine
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Organopnictogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Amine
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	1.9	ALOGPS
logP	1.15	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Basic)	9.33	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	39.72 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	85.36 m³·mol⁻¹	ChemAxon
Polarizability	31.34 Å³	ChemAxon
Number of Rings	5	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

12313596

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene (NP0190581)

MOL for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

3D MOL for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

3D SDF for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

3D-SDF for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

PDB for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

3D PDB for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

SMILES for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

INCHI for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

Structure for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)

3D Structure for NP0190581 (10,14-dimethoxy-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7,9,11(18),14,16-pentaene)