NP-MRD: Showing NP-Card for Lunamarine (NP0051240)

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Record Information

Version

2.0

Created at

2022-04-27 22:37:43 UTC

Updated at

2022-04-27 22:37:43 UTC

NP-MRD ID

NP0051240

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lunamarine

Description

2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-methyl-1,4-dihydroquinolin-4-one belongs to the class of organic compounds known as hydroquinolones. Hydroquinolones are compounds containing a hydrogenated quinoline bearing a ketone group. Lunamarine is found in Lunasia amara. 2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-methyl-1,4-dihydroquinolin-4-one is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 41  0  0  0  0  0  0  0  0999 V2000
    6.3271   -0.3447   -0.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9768   -0.1660   -1.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9539   -0.2484   -0.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2048   -0.5174    1.1623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1905   -0.5986    2.0927 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9013   -0.3975    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8448   -0.4704    2.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1332   -0.7182    3.7365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226   -0.2686    2.0666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7069    0.0022    0.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0633    0.2161    0.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038    1.4866    0.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8756    1.7488   -0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6551    0.7143   -0.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1486   -0.5496   -0.6771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8597   -0.8114   -0.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1041   -1.4157   -1.1788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3247   -0.7398   -1.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9525    0.6205   -1.2027 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3244    0.0687   -0.1156 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1141    0.3492   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5956   -0.1261    0.3182 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6525   -0.0551   -0.5778 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5223   -1.1327   -0.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8389   -0.6820   -1.7401 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7737    0.6378   -0.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503   -0.6685    1.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3826   -0.8101    3.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2509   -0.3216    2.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0253    2.3397    0.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2927    2.7651   -0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4708   -1.8166   -0.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7681   -0.9033   -2.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0271   -1.0489   -0.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4826   -0.4677   -2.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9633    0.4726   -1.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369    1.3085   -1.7883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4089    0.1588   -1.6132 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  2  0
  7  9  1  0
  9 10  2  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 19  1  0
 19 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  2  0
 23  3  1  0
 16 11  1  0
 22  6  1  0
 15 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  9 29  1  0
 21 35  1  0
 21 36  1  0
 21 37  1  0
 23 38  1  0
 12 30  1  0
 13 31  1  0
 18 33  1  0
 18 34  1  0
 16 32  1  0
M  END


  Mrv1533004161522592D          

 23 26  0  0  0  0            999 V2000
    6.2102    8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    8.1229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    3.3305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    4.6654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    4.8229    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  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
  3 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  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
 21 22  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051240

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C(=O)C=C(N(C)C2=C1)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H15NO4/c1-19-14(11-3-6-17-18(7-11)23-10-22-17)9-16(20)13-5-4-12(21-2)8-15(13)19/h3-9H,10H2,1-2H3

> <INCHI_KEY>
GOMVNCXQVLUIGA-UHFFFAOYSA-N

> <FORMULA>
C18H15NO4

> <MOLECULAR_WEIGHT>
309.321

> <EXACT_MASS>
309.100107967

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
32.71516001092439

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-methyl-1,4-dihydroquinolin-4-one

> <ALOGPS_LOGP>
2.65

> <JCHEM_LOGP>
2.5493290916666664

> <ALOGPS_LOGS>
-3.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.92924292541455

> <JCHEM_PKA_STRONGEST_BASIC>
1.0836814037981712

> <JCHEM_POLAR_SURFACE_AREA>
48.0

> <JCHEM_REFRACTIVITY>
87.16670000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lunamarine

> <JCHEM_VEBER_RULE>
0

$$$$

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      11.592  15.933   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.259  15.163   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.259  13.623   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.592  12.853   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.592  11.313   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.259  10.543   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.259   9.003   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.592   8.233   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.925   8.233   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.591   9.003   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       7.591  10.543   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.258  11.313   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.925  11.313   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.925  12.853   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.258   8.233   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   5.923   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.590   6.693   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.126   6.217   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.220   7.463   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.126   8.709   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.590   8.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.924   9.003   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14                                                  
CONECT   14   13    3                                                       
CONECT   15   10   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   18   23                                                  
CONECT   23   22   15                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₅NO₄

Average Mass

309.3210 Da

Monoisotopic Mass

309.10011 Da

IUPAC Name

2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-methyl-1,4-dihydroquinolin-4-one

Traditional Name

lunamarine

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C(=O)C=C(N(C)C2=C1)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C18H15NO4/c1-19-14(11-3-6-17-18(7-11)23-10-22-17)9-16(20)13-5-4-12(21-2)8-15(13)19/h3-9H,10H2,1-2H3

InChI Key

GOMVNCXQVLUIGA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Lunasia amara	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroquinolones. Hydroquinolones are compounds containing a hydrogenated quinoline bearing a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Hydroquinolones

Alternative Parents

Substituents

Dihydroquinolone
Dihydroquinoline
Benzodioxole
Anisole
Alkyl aryl ether
Pyridine
Benzenoid
Heteroaromatic compound
Vinylogous amide
Oxacycle
Acetal
Ether
Azacycle
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

quinolines (CHEBI:6565 )
Quinoline alkaloids (C10713 )

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	2.65	ALOGPS
logP	2.55	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	16.93	ChemAxon
pKa (Strongest Basic)	1.08	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	87.17 m³·mol⁻¹	ChemAxon
Polarizability	32.72 Å³	ChemAxon
Number of Rings	4	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

C00002182

Chemspider ID

Not Available

KEGG Compound ID

C10713

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442922

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Lunamarine (NP0051240)

MOL for NP0051240 (Lunamarine)

3D MOL for NP0051240 (Lunamarine)

3D SDF for NP0051240 (Lunamarine)

3D-SDF for NP0051240 (Lunamarine)

PDB for NP0051240 (Lunamarine)

3D PDB for NP0051240 (Lunamarine)

SMILES for NP0051240 (Lunamarine)

INCHI for NP0051240 (Lunamarine)

Structure for NP0051240 (Lunamarine)

3D Structure for NP0051240 (Lunamarine)