NP-MRD: Showing NP-Card for (1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene (NP0281992)

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Record Information

Version

2.0

Created at

2022-09-09 08:39:08 UTC

Updated at

2022-09-09 08:39:08 UTC

NP-MRD ID

NP0281992

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene

Description

(1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2,4,6,8-tetraene belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. (1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene is found in Kopsia arborea. Based on a literature review very few articles have been published on (1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2,4,6,8-tetraene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 45  0  0  0  0  0  0  0  0999 V2000
    1.7868    1.9560    1.8483 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1545    0.8895    1.4979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2981    0.9191    1.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486    1.5203    1.8222 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5102    1.1239    1.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7987    1.5459    1.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8877    1.0233    0.9583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6635    0.0893   -0.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3954   -0.3117   -0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2709    0.1952    0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8315    0.0103    0.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3287    0.4973   -1.1852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1639   -0.8392   -1.9263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812   -1.7246   -0.9210 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8014   -1.5800   -0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3499   -0.5560   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3079    0.2412   -0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8543    0.1384   -1.8481 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8347   -0.4512    1.3472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7165   -1.4968    1.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2551   -1.3388    0.2869 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2423    2.9016    1.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8387    2.0191    2.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9757    2.2772    2.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9053    1.3363    1.2108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5185   -0.3233   -0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1966   -1.0500   -1.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1117    1.0810   -1.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6060    1.0209   -1.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5519   -0.6812   -2.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1186   -1.1791   -2.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2299   -2.5672   -0.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2111   -1.4555   -1.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7327    0.9983    0.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1657   -0.8974   -2.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0841    0.5372   -2.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7293    0.8021   -1.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5664   -0.6337    2.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2077   -2.4806    1.3154 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2112   -1.4911    2.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0855   -2.0661    0.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 21  1  0
 21 20  1  0
 20 19  1  0
 19  2  1  0
  2  1  2  3
  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
 19 16  1  0
 10  5  1  0
 21 14  1  0
  3 11  1  0
 10 11  1  0
 18 35  1  0
 18 36  1  0
 18 37  1  0
 17 34  1  0
 15 32  1  0
 15 33  1  0
 13 30  1  0
 13 31  1  0
 12 28  1  0
 12 29  1  0
 21 41  1  1
 20 39  1  0
 20 40  1  0
 19 38  1  1
  1 22  1  0
  1 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
M  END


  Mrv1652309092210392D          

 21 25  0  0  1  0            999 V2000
    2.1949    2.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965    1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0003    1.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.7571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3466    1.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1713    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6027    0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533    0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766    0.5160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2714   -0.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881   -0.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -0.3673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0039    0.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7871    0.9265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2946    0.3105    0.0000 C   0  0  1  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  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 11 10  1  6  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 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  2  0  0  0  0
 17 18  1  4  0  0  0
 16 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 20  1  1  0  0  0
 14 21  1  0  0  0  0
 11 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281992

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C1CN2CC[C@@]34[C@@H]2C[C@@H]1C(=C)C3=NC1=CC=CC=C41

> <INCHI_IDENTIFIER>
InChI=1S/C19H20N2/c1-3-13-11-21-9-8-19-15-6-4-5-7-16(15)20-18(19)12(2)14(13)10-17(19)21/h3-7,14,17H,2,8-11H2,1H3/t14-,17+,19-/m1/s1

> <INCHI_KEY>
KFXIUXCXSKTCNK-DKSSEZFCSA-N

> <FORMULA>
C19H20N2

> <MOLECULAR_WEIGHT>
276.383

> <EXACT_MASS>
276.162648652

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
31.57112720663048

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,8-tetraene

> <JCHEM_LOGP>
3.660623756666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.784406033986231

> <JCHEM_POLAR_SURFACE_AREA>
15.6

> <JCHEM_REFRACTIVITY>
88.6567

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,8-tetraene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       4.097   4.932   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.100   3.392   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.601   2.616   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       7.019   3.280   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       8.114   2.191   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.653   2.232   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.458   0.919   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.724  -0.435   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.185  -0.476   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.379   0.837   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.743   0.963   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.107  -0.666   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.831  -1.608   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       3.508  -0.686   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       1.932  -0.284   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.495   1.319   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.007   1.657   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.051   0.524   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.599   2.609   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.336   1.729   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.283   0.580   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    3   12   21                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16    2   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   14   11                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀N₂

Average Mass

276.3830 Da

Monoisotopic Mass

276.16265 Da

IUPAC Name

(1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,8-tetraene

Traditional Name

(1R,11S,17S)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,8-tetraene

CAS Registry Number

Not Available

SMILES

CC=C1CN2CC[C@@]34[C@@H]2C[C@@H]1C(=C)C3=NC1=CC=CC=C41

InChI Identifier

InChI=1S/C19H20N2/c1-3-13-11-21-9-8-19-15-6-4-5-7-16(15)20-18(19)12(2)14(13)10-17(19)21/h3-7,14,17H,2,8-11H2,1H3/t14-,17+,19-/m1/s1

InChI Key

KFXIUXCXSKTCNK-DKSSEZFCSA-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
Kopsia arborea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Strychnan skeleton
Stemmadenine-skeleton
3-alkylindole
Indolizidine
Indole or derivatives
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Piperidine
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Ketimine
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Imine
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	3.66	ChemAxon
pKa (Strongest Basic)	9.78	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	15.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	88.66 m³·mol⁻¹	ChemAxon
Polarizability	31.57 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

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

162891330

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene (NP0281992)

MOL for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

3D MOL for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

3D SDF for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

3D-SDF for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

PDB for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

3D PDB for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

SMILES for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

INCHI for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

Structure for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)

3D Structure for NP0281992 ((1r,11s,17s)-12-ethylidene-10-methylidene-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,8-tetraene)