NP-MRD: Showing NP-Card for 12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol (NP0287348)

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Record Information

Version

2.0

Created at

2022-09-09 16:22:46 UTC

Updated at

2022-09-09 16:22:46 UTC

NP-MRD ID

NP0287348

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol

Description

12-Ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]Nonadeca-2,4,6,8,13-pentaen-9-ol belongs to the class of organic compounds known as melodinus alkaloids. These are alkaloids with a structure that is based on the melodinus skeleton. This backbone is a pentacyclic structure that contains a tetrahydroquinoline and an indolizine joined to each other through a cyclopentane. 12-Ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]Nonadeca-2,4,6,8,13-pentaen-9-ol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -3.8338    0.3439   -0.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5893    0.7743    0.1206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5596    0.3551   -0.8095 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1116   -0.5665   -1.8603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2689   -1.8092   -1.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9279   -2.2272   -0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8298   -1.5442    0.5575 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0429   -0.9108    1.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0613    0.2423    1.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4320    0.4906    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8194    0.0629    0.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2090   -1.2173    0.6696 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4890   -1.6920    0.5205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4295   -0.8409   -0.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0939    0.4408   -0.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7617    0.8865   -0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4554    2.2121   -0.6157 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1461    2.6964   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9096    3.9032   -0.6660 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0567    1.8020   -0.0580 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7663    1.5149   -1.3396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309   -0.4742   -0.2666 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6443    0.6365    0.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1426   -0.3347   -0.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3867    1.4415    0.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3220   -0.1746   -2.8223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6666   -2.5323   -2.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6084   -3.3105   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8336   -2.2939    0.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -1.6660    2.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0695   -0.6465    2.0658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7981   -0.0135    2.5898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5332    1.1239    2.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4707   -1.8778    1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7649   -2.7154    0.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4406   -1.2061   -0.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8145    1.1322   -0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2328    2.8179   -1.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6145    2.3701    0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0921    1.2449   -2.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4070    2.3972   -1.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1510   -0.8357   -1.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  3  2  1  1
  3 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  1  1
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  7 22  1  0
  4  3  1  0
 22  3  1  0
 10 20  1  0
 22 10  1  0
 11 16  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
 21 40  1  0
 21 41  1  0
 20 39  1  1
 17 38  1  0
 15 37  1  0
 14 36  1  0
 13 35  1  0
 12 34  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
  6 28  1  0
  6 29  1  0
  5 27  1  0
  4 26  1  0
 22 42  1  6
M  END


  Mrv1533004171510512D          

 22 26  0  0  0  0            999 V2000
    0.4832    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2979    1.0965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8178    0.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1916    1.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0065    1.0632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6471    1.5831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5172    2.3978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176    1.2882    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5476    0.4735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3181    0.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4480   -0.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8074   -1.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0369   -0.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9070   -0.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1365    0.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7204   -0.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1891   -0.9239    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3924   -1.1383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8084   -0.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0211    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018   -0.1268    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
  3  4  1  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
  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  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
  3 21  1  0  0  0  0
 18 22  1  0  0  0  0
  3 22  1  0  0  0  0
 15 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287348

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C=CC12CC3C(=O)NC4=CC=CC=C4C33CCN(CC=C1)C23

> <INCHI_IDENTIFIER>
InChI=1S/C19H20N2O/c1-2-18-8-5-10-21-11-9-19(17(18)21)13-6-3-4-7-15(13)20-16(22)14(19)12-18/h2-8,14,17H,1,9-12H2,(H,20,22)

> <INCHI_KEY>
BEMFQIDPZLYEBJ-UHFFFAOYSA-N

> <FORMULA>
C19H20N2O

> <MOLECULAR_WEIGHT>
292.382

> <EXACT_MASS>
292.157563272

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
31.82812767667224

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,13-tetraen-9-one

> <ALOGPS_LOGP>
2.64

> <JCHEM_LOGP>
2.280492633666666

> <ALOGPS_LOGS>
-2.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.602833790437522

> <JCHEM_PKA_STRONGEST_BASIC>
9.142528314137381

> <JCHEM_POLAR_SURFACE_AREA>
32.34

> <JCHEM_REFRACTIVITY>
89.44040000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,13-tetraen-9-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       0.902   1.804   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.423   2.047   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.393   0.851   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.091   2.224   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.612   1.985   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.808   2.955   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.565   4.476   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       8.246   2.405   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       8.489   0.884   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.927   0.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.170  -1.187   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.974  -2.158   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.536  -1.607   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.293  -0.086   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.855   0.464   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.945  -0.624   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.247  -1.997   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       4.086  -1.725   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       2.599  -2.125   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.509  -1.037   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.906   0.451   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.483  -0.237   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21   22                                             
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14    5   16   22                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    3                                                       
CONECT   22   18    3   15                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀N₂O

Average Mass

292.3820 Da

Monoisotopic Mass

292.15756 Da

IUPAC Name

12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,13-tetraen-9-one

Traditional Name

12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,13-tetraen-9-one

CAS Registry Number

Not Available

SMILES

C=CC12CC3C(=O)NC4=CC=CC=C4C33CCN(CC=C1)C23

InChI Identifier

InChI=1S/C19H20N2O/c1-2-18-8-5-10-21-11-9-19(17(18)21)13-6-3-4-7-15(13)20-16(22)14(19)12-18/h2-8,14,17H,1,9-12H2,(H,20,22)

InChI Key

BEMFQIDPZLYEBJ-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as melodinus alkaloids. These are alkaloids with a structure that is based on the melodinus skeleton. This backbone is a pentacyclic structure that contains a tetrahydroquinoline and an indolizine joined to each other through a cyclopentane.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Melodinus alkaloids

Sub Class

Not Available

Direct Parent

Melodinus alkaloids

Alternative Parents

Substituents

Melodinus skeleton
Tetrahydroquinolone
Quinolone
Tetrahydroquinoline
Aralkylamine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Amino acid or derivatives
Carboxamide group
Lactam
Secondary carboxylic acid amide
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
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	2.64	ALOGPS
logP	2.28	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	13.6	ChemAxon
pKa (Strongest Basic)	9.14	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.34 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	89.44 m³·mol⁻¹	ChemAxon
Polarizability	31.83 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

14263660

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol (NP0287348)

MOL for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

3D MOL for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

3D SDF for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

3D-SDF for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

PDB for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

3D PDB for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

SMILES for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

INCHI for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

Structure for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)

3D Structure for NP0287348 (12-ethenyl-8,16-diazapentacyclo[10.6.1.0¹,¹⁰.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,8,13-pentaen-9-ol)