NP-MRD: Showing NP-Card for 5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione (NP0270523)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 16:28:51 UTC

Updated at

2022-09-08 16:28:51 UTC

NP-MRD ID

NP0270523

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione

Description

5-Hydroxy-7-methoxy-3-methyl-2H,6H,9H,10H-cyclohexa[g]isoquinoline-6,9,10-trione belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). 5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione is found in Coniocarpon cinnabarinum and Fusarium martii. Based on a literature review very few articles have been published on 5-hydroxy-7-methoxy-3-methyl-2H,6H,9H,10H-cyclohexa[g]isoquinoline-6,9,10-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
    5.3344    1.3606    0.6284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6750    0.8831   -0.5305 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4744    0.2037   -0.3781 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4936   -1.0968   -0.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2367   -1.8088   -0.0797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -3.0597    0.0532 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9375   -1.1593   -0.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9057    0.2318   -0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3037    0.8907   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4268    2.2409   -0.3397 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4839    0.1823   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7143    0.8166   -0.0353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8801    0.0947    0.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2012    0.8013    0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8046   -1.2207    0.2560 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484   -1.9225    0.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4471   -1.2522    0.1037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2311   -1.8901    0.0920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1804   -3.1319    0.2223 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1853    0.9030   -0.3682 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2189    2.1591   -0.5056 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2766    1.8778    0.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900    2.0810    1.1766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6026    0.4794    1.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4352   -1.6707   -0.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2576    2.9085   -0.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7398    1.8904   -0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7935    0.3868    0.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0810    1.8831    0.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7401    0.6874   -0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6994   -1.7529    0.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6101   -2.9968    0.3683 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
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
  8 20  1  0
 20 21  2  0
 20  3  1  0
 18  7  1  0
 17 11  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
 10 26  1  0
 12 27  1  0
 14 28  1  0
 14 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
M  END


  Mrv1652309082218282D          

 21 23  0  0  0  0            999 V2000
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   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
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
  8 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0270523

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=O)C2=C(C(O)=C3C=C(C)NC=C3C2=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H11NO5/c1-6-3-7-8(5-16-6)14(19)11-9(17)4-10(21-2)15(20)12(11)13(7)18/h3-5,16,18H,1-2H3

> <INCHI_KEY>
GRDUAFOUVFRDBR-UHFFFAOYSA-N

> <FORMULA>
C15H11NO5

> <MOLECULAR_WEIGHT>
285.255

> <EXACT_MASS>
285.063722458

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
27.941613555766253

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-7-methoxy-3-methyl-2H,6H,9H,10H-cyclohexa[g]isoquinoline-6,9,10-trione

> <JCHEM_LOGP>
0.09878547966666676

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.088070695044685

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.34283862879972

> <JCHEM_PKA_STRONGEST_BASIC>
-4.778869955395912

> <JCHEM_POLAR_SURFACE_AREA>
92.69999999999999

> <JCHEM_REFRACTIVITY>
78.81379999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-7-methoxy-3-methyl-2H-cyclohexa[g]isoquinoline-6,9,10-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       0.000   1.540   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   18                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17    7   19                                                  
CONECT   19   18                                                            
CONECT   20    8    3   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₁NO₅

Average Mass

285.2550 Da

Monoisotopic Mass

285.06372 Da

IUPAC Name

5-hydroxy-7-methoxy-3-methyl-2H,6H,9H,10H-cyclohexa[g]isoquinoline-6,9,10-trione

Traditional Name

5-hydroxy-7-methoxy-3-methyl-2H-cyclohexa[g]isoquinoline-6,9,10-trione

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C2=C(C(O)=C3C=C(C)NC=C3C2=O)C1=O

InChI Identifier

InChI=1S/C15H11NO5/c1-6-3-7-8(5-16-6)14(19)11-9(17)4-10(21-2)15(20)12(11)13(7)18/h3-5,16,18H,1-2H3

InChI Key

GRDUAFOUVFRDBR-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
Coniocarpon cinnabarinum	LOTUS Database	35616633
Fusarium martii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Naphthoquinone
Isoquinoline
Aryl ketone
Quinone
Methylpyridine
Pyridine
Heteroaromatic compound
Vinylogous ester
Vinylogous amide
Vinylogous acid
Ketone
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
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	0.099	ChemAxon
pKa (Strongest Acidic)	7.34	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	92.7 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	78.81 m³·mol⁻¹	ChemAxon
Polarizability	27.94 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

4572202

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5458195

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione (NP0270523)

MOL for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

3D MOL for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

3D SDF for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

3D-SDF for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

PDB for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

3D PDB for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

SMILES for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

INCHI for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

Structure for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)

3D Structure for NP0270523 (5-hydroxy-7-methoxy-3-methyl-2h-cyclohexa[g]isoquinoline-6,9,10-trione)