NP-MRD: Showing NP-Card for 2-acetyl-9-methylfuro[3,2-c]chromen-4-one (NP0167508)

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Record Information

Version

2.0

Created at

2022-09-03 03:05:56 UTC

Updated at

2022-09-03 03:05:56 UTC

NP-MRD ID

NP0167508

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-acetyl-9-methylfuro[3,2-c]chromen-4-one

Description

Pterophyllin 4 belongs to the class of organic compounds known as angular furanocoumarins. These are furanocoumarins, with a structure characterized by a furan ring angularly fused to a coumarin. 2-acetyl-9-methylfuro[3,2-c]chromen-4-one is found in Ekebergia pterophylla. 2-acetyl-9-methylfuro[3,2-c]chromen-4-one was first documented in 2017 (PMID: 28805845). Based on a literature review very few articles have been published on Pterophyllin 4 (PMID: 29288027).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 28 30  0  0  0  0  0  0  0  0999 V2000
    3.7463    1.8232   -0.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6124    0.3365   -0.4281 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6284   -0.3944   -0.5330 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2827   -0.2510   -0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0379   -1.6063   -0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957   -1.7500    0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776   -2.8821    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4492   -4.0390    0.1502 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3683   -2.7123    0.3371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9335   -1.5284    0.3660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3025   -1.4123    0.5402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9345   -0.1878    0.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1718    0.9363    0.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7883    0.8936    0.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9768    2.1310    0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015   -0.3554    0.2261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1597   -0.4798    0.0532 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1426    0.4018   -0.1084 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7733    2.1127   -0.1489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5736    2.1690   -1.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9500    2.3053    0.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7411   -2.4230   -0.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9032   -2.3037    0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9976   -0.1636    0.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6689    1.8982    0.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7045    2.9767   -0.0482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3215    2.1185   -0.7713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4423    2.3861    1.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6 17  2  0
 17 18  1  0
 17 16  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
 18  4  1  0
 10 16  1  0
  7  6  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
 15 26  1  0
 15 27  1  0
 15 28  1  0
 13 25  1  0
 12 24  1  0
 11 23  1  0
M  END


  Mrv1652309032205052D          

 18 20  0  0  0  0            999 V2000
    0.6864   -1.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4134   -1.6293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4392   -2.4539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1752   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8849   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2803   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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  2  0  0  0  0
  7  9  1  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 17  2  0  0  0  0
 17 18  1  0  0  0  0
  4 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0167508

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C1=CC2=C(O1)C1=C(C)C=CC=C1OC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H10O4/c1-7-4-3-5-10-12(7)13-9(14(16)18-10)6-11(17-13)8(2)15/h3-6H,1-2H3

> <INCHI_KEY>
QZSWQZATUQOFHE-UHFFFAOYSA-N

> <FORMULA>
C14H10O4

> <MOLECULAR_WEIGHT>
242.23

> <EXACT_MASS>
242.057908802

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
24.438444711536953

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-acetyl-9-methyl-4H-furo[3,2-c]chromen-4-one

> <ALOGPS_LOGP>
2.46

> <JCHEM_LOGP>
1.976644117

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.237999595170347

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2394335269160224

> <JCHEM_POLAR_SURFACE_AREA>
56.510000000000005

> <JCHEM_REFRACTIVITY>
64.65150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-acetyl-9-methylfuro[3,2-c]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       1.281  -2.313   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.638  -3.041   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.686  -4.581   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.947  -2.230   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.060  -0.694   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.556  -0.327   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.284   1.030   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.473   2.339   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       7.823   1.078   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.635  -0.231   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.174  -0.183   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.985  -1.492   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.257  -2.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.718  -2.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.990  -4.254   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.907  -1.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.367  -1.636   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.373  -2.812   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16    6   18                                                  
CONECT   18   17    4                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₀O₄

Average Mass

242.2300 Da

Monoisotopic Mass

242.05791 Da

IUPAC Name

2-acetyl-9-methyl-4H-furo[3,2-c]chromen-4-one

Traditional Name

2-acetyl-9-methylfuro[3,2-c]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC(=O)C1=CC2=C(O1)C1=C(C)C=CC=C1OC2=O

InChI Identifier

InChI=1S/C14H10O4/c1-7-4-3-5-10-12(7)13-9(14(16)18-10)6-11(17-13)8(2)15/h3-6H,1-2H3

InChI Key

QZSWQZATUQOFHE-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
Ekebergia pterophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as angular furanocoumarins. These are furanocoumarins, with a structure characterized by a furan ring angularly fused to a coumarin.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Furanocoumarins

Direct Parent

Angular furanocoumarins

Alternative Parents

Substituents

Angular furanocoumarin
Benzopyran
1-benzopyran
Furopyran
Aryl alkyl ketone
Aryl ketone
Pyranone
Benzenoid
Pyran
Furan
Heteroaromatic compound
Ketone
Lactone
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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	2.46	ALOGPS
logP	1.98	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	14.24	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	56.51 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	64.65 m³·mol⁻¹	ChemAxon
Polarizability	24.44 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

62909504

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15838083

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pergomet JL, Di Liberto MG, Derita MG, Bracca ABJ, Kaufman TS: Activity of the pterophyllins 2 and 4 against postharvest fruit pathogenic fungi. Comparison with a synthetic analog and related intermediates. Fitoterapia. 2018 Mar;125:98-105. doi: 10.1016/j.fitote.2017.12.021. Epub 2017 Dec 27. [PubMed:29288027 ]
Pergomet JL, Bracca ABJ, Kaufman TS: Total syntheses of gerberinol I and the pterophyllins 2 and 4 using the Casnati-Skattebol reaction under different conditions. Org Biomol Chem. 2017 Aug 23;15(33):7040-7049. doi: 10.1039/c7ob01471f. [PubMed:28805845 ]
LOTUS database [Link]

Showing NP-Card for 2-acetyl-9-methylfuro[3,2-c]chromen-4-one (NP0167508)

MOL for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

3D MOL for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

3D SDF for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

3D-SDF for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

PDB for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

3D PDB for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

SMILES for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

INCHI for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

Structure for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)

3D Structure for NP0167508 (2-acetyl-9-methylfuro[3,2-c]chromen-4-one)