NP-MRD: Showing NP-Card for 8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one (NP0246384)

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Record Information

Version

2.0

Created at

2022-09-07 07:50:19 UTC

Updated at

2022-09-07 07:50:20 UTC

NP-MRD ID

NP0246384

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one

Description

Plakinidine A belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring. Based on a literature review very few articles have been published on Plakinidine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 41  0  0  0  0  0  0  0  0999 V2000
   -2.3519    3.6750    0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7103    2.3008    0.4511 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8383    1.3971    0.2790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1775    0.0712    0.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2149   -0.9289   -0.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1188   -0.5740   -0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -1.4652   -0.2672 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4123   -1.0492   -0.1919 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269   -1.9678   -0.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429   -1.5641   -0.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0265   -0.2398   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    0.7030    0.1347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6999    0.2837    0.0588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6989    1.2132    0.2364 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5655    2.5594    0.4903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2288    2.8651    0.5509 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4941    1.7537    0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4138    0.7464    0.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5637   -2.2763   -0.4088 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9227   -2.5583   -0.8082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9176   -1.7570    0.0088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5790   -0.3174   -0.0421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4281    0.5972   -0.1443 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7217    3.7825    1.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7103    4.0639   -0.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2467    4.3230    0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9326   -2.4438   -0.4534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1638   -2.9993   -0.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5740   -2.2744   -0.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0657    0.1051    0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2001    1.7297    0.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4176    3.2081    0.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9063   -3.0669   -0.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0411   -2.2043   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1795   -3.6227   -0.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9046   -1.9214   -0.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9002   -2.1470    1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 18  1  0
 18  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  6  5  1  0
  5  4  2  0
  4 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
  4  3  1  0
 18 17  1  0
 13  8  1  0
 19  5  1  0
 13 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 15 32  1  0
  7 27  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 21 36  1  0
 21 37  1  0
 20 34  1  0
 20 35  1  0
 19 33  1  0
M  END


  Mrv1652309072209502D          

 23 27  0  0  0  0            999 V2000
    3.3394   -0.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9893   -0.1647    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4612    0.5120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1112    1.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5831    1.9357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4051    1.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    2.4856    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9598    2.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5621    2.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3515    2.5699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5386    1.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9363    1.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1469    1.4423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5446    0.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    0.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7810   -0.2163    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2832    0.4416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7552    1.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2331    2.6828    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4111    2.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9391    2.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2892    1.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8173    0.6527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  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  2  0  0  0  0
  9 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
  8 13  1  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
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  2  0  0  0  0
 14 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0246384

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN=C1C2=NC=C3C2=C(NC2=CC=CC=C32)C2=C1C(=O)CCN2

> <INCHI_IDENTIFIER>
InChI=1S/C18H14N4O/c1-19-15-14-12(23)6-7-20-17(14)18-13-10(8-21-16(13)15)9-4-2-3-5-11(9)22-18/h2-5,8,20,22H,6-7H2,1H3

> <INCHI_KEY>
AMDBWMKCBSPPND-UHFFFAOYSA-N

> <FORMULA>
C18H14N4O

> <MOLECULAR_WEIGHT>
302.337

> <EXACT_MASS>
302.116761087

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
32.71601738065771

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0^{2,7}.0^{9,20}.0^{13,18}]icosa-1(20),2(7),9,11,13,15,17-heptaen-6-one

> <JCHEM_LOGP>
1.0205810441088852

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.06212329564028

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.865293113849562

> <JCHEM_PKA_STRONGEST_BASIC>
8.697761528385069

> <JCHEM_POLAR_SURFACE_AREA>
70.14

> <JCHEM_REFRACTIVITY>
88.7482

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0^{2,7}.0^{9,20}.0^{13,18}]icosa-1(20),2(7),9,11,13,15,17-heptaen-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       6.233  -1.702   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       5.580  -0.307   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       6.461   0.956   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.808   2.350   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.689   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.223   3.482   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       9.651   4.640   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      11.125   4.192   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.249   5.245   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.723   4.797   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.072   3.297   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.948   2.245   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.474   2.692   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.350   1.640   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.380   0.100   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       8.924  -0.404   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       7.995   0.824   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.876   2.087   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       6.035   5.008   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       4.501   5.139   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.620   3.876   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.273   2.482   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.392   1.218   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6   19                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    3   18                                                  
CONECT   18   17    6   14                                                  
CONECT   19    5   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    4   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄N₄O

Average Mass

302.3370 Da

Monoisotopic Mass

302.11676 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN=C1C2=NC=C3C2=C(NC2=CC=CC=C32)C2=C1C(=O)CCN2

InChI Identifier

InChI=1S/C18H14N4O/c1-19-15-14-12(23)6-7-20-17(14)18-13-10(8-21-16(13)15)9-4-2-3-5-11(9)22-18/h2-5,8,20,22H,6-7H2,1H3

InChI Key

AMDBWMKCBSPPND-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 phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Phenanthrolines

Sub Class

Not Available

Direct Parent

Phenanthrolines

Alternative Parents

Substituents

1,10-phenanthroline
Benzoquinoline
Acridine
Pyrroloquinoline
Pyrrolo[4,3,2-de]quinoline
Quinolone
Tetrahydroquinolone
Aminoquinoline
Quinoline
Tetrahydroquinoline
Indole or derivatives
Indole
Aryl alkyl ketone
Aryl ketone
Secondary aliphatic/aromatic amine
Benzenoid
Pyridine
Heteroaromatic compound
Vinylogous amide
Secondary ketimine
Pyrrole
Ketone
Azacycle
Secondary amine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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

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

135409164

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one (NP0246384)

MOL for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

3D MOL for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

3D SDF for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

3D-SDF for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

PDB for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

3D PDB for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

SMILES for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

INCHI for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

Structure for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)

3D Structure for NP0246384 (8-(methylimino)-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(20),2(7),9,11,13(18),14,16-heptaen-6-one)