NP-MRD: Showing NP-Card for Fuliginol (NP0084004)

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Record Information

Version

2.0

Created at

2022-04-29 04:52:26 UTC

Updated at

2022-04-29 04:52:27 UTC

NP-MRD ID

NP0084004

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Fuliginol

Description

Fuliginol belongs to the class of organic compounds known as phenylnaphthalenes. Phenylnaphthalenes are compounds containing a phenylnaphthalene skeleton, which consists of a naphthalene bound to a phenyl group. Fuliginol is found in Macropidia fuliginosa. Based on a literature review very few articles have been published on Fuliginol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 41  0  0  0  0  0  0  0  0999 V2000
   -1.8585    2.2838    0.7304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1690    1.7406   -0.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1336    1.2797   -0.2896 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1881    2.1873   -0.4398 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8598    3.5032   -0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5014    1.8287   -0.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7737    0.4964   -0.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7390   -0.4136    0.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0111   -1.7415    0.3183 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881   -2.6489    0.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277   -2.2821    0.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6399   -0.9331    0.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0557   -0.6572   -0.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5420   -0.2682   -1.3143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -0.0200   -1.5125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8022   -0.1561   -0.4973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3385   -0.5462    0.7411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9964   -0.7906    0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860   -0.0396   -0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4159   -2.1352    0.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6449   -3.3560    0.6662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4895   -1.1648    0.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8007   -1.5684    0.3749 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1826    0.0899    0.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507    2.0967    0.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5084    1.8585    1.6865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7490    3.3988    0.7559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5559    4.2057   -0.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3056    2.5436   -0.4663 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2065   -3.6816    0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1402   -2.9752    0.4781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8667   -0.1559   -2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2438    0.2856   -2.4969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8634    0.0354   -0.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0683   -0.6481    1.5330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6093   -1.0951    1.8910 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5026   -1.4208   -0.3387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9515    0.8643   -0.1106 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
  4  6  1  0
  6  7  2  0
  7 24  1  0
 24 22  2  0
 22 23  1  0
 22 20  1  0
 20 21  2  0
 20  9  1  0
  9  8  1  0
  8 19  2  0
 19 12  1  0
 12 11  2  0
 11 10  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 19  3  1  0
 18 13  1  0
  8  7  1  0
 10  9  2  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  0
  6 29  1  0
 24 38  1  0
 23 37  1  0
 11 31  1  0
 10 30  1  0
 14 32  1  0
 15 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  0
M  END


  Mrv1652304292206522D          

 24 27  0  0  0  0            999 V2000
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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
    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 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
    1.4289    0.8250    0.0000 O   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
    2.1434   -0.4125    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
    2.8579    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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   -0.4125    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
    2.8579   -1.6500    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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 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  2  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13 24  1  0  0  0  0
  6 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084004

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2C=C(O)C(=O)C3=C2C1=C(C=C3)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H14O4/c1-24-20-16(22)10-12-9-15(21)19(23)14-8-7-13(18(20)17(12)14)11-5-3-2-4-6-11/h2-10,21-22H,1H3

> <INCHI_KEY>
XOLLRELLRMGBMG-UHFFFAOYSA-N

> <FORMULA>
C20H14O4

> <MOLECULAR_WEIGHT>
318.328

> <EXACT_MASS>
318.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
33.17405640619644

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,5-dihydroxy-6-methoxy-7-phenyl-1H-phenalen-1-one

> <ALOGPS_LOGP>
3.53

> <JCHEM_LOGP>
3.573887342999999

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.308336994060225

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.194994762391504

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5831452844331872

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
92.81690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.96e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,5-dihydroxy-6-methoxy-7-phenylphenalen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   24                                                  
CONECT   14   13   15   21                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   14   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    2   24                                                  
CONECT   24   23   13    6                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₄O₄

Average Mass

318.3280 Da

Monoisotopic Mass

318.08921 Da

IUPAC Name

2,5-dihydroxy-6-methoxy-7-phenyl-1H-phenalen-1-one

Traditional Name

2,5-dihydroxy-6-methoxy-7-phenylphenalen-1-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2C=C(O)C(=O)C3=C2C1=C(C=C3)C1=CC=CC=C1

InChI Identifier

InChI=1S/C20H14O4/c1-24-20-16(22)10-12-9-15(21)19(23)14-8-7-13(18(20)17(12)14)11-5-3-2-4-6-11/h2-10,21-22H,1H3

InChI Key

XOLLRELLRMGBMG-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
Macropidia fuliginosa	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylnaphthalenes. Phenylnaphthalenes are compounds containing a phenylnaphthalene skeleton, which consists of a naphthalene bound to a phenyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenylnaphthalene
Phenalen-1-one
Phenalen
2-naphthol
Aryl ketone
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Ketone
Ether
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.53	ALOGPS
logP	3.57	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	9.19	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.82 m³·mol⁻¹	ChemAxon
Polarizability	33.17 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

C00053181

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

132553603

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Fuliginol (NP0084004)

MOL for NP0084004 (Fuliginol)

3D MOL for NP0084004 (Fuliginol)

3D SDF for NP0084004 (Fuliginol)

3D-SDF for NP0084004 (Fuliginol)

PDB for NP0084004 (Fuliginol)

3D PDB for NP0084004 (Fuliginol)

SMILES for NP0084004 (Fuliginol)

INCHI for NP0084004 (Fuliginol)

Structure for NP0084004 (Fuliginol)

3D Structure for NP0084004 (Fuliginol)