NP-MRD: Showing NP-Card for 3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione (NP0225280)

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Record Information

Version

2.0

Created at

2022-09-06 03:57:30 UTC

Updated at

2022-09-06 03:57:30 UTC

NP-MRD ID

NP0225280

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione

Description

260397-58-8 Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. 3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione is found in Salvia glutinosa and Salvia miltiorrhiza. 260397-58-8 Is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 38  0  0  0  0  0  0  0  0999 V2000
   -4.8234   -0.0697   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6020   -0.1220    0.2026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6827   -0.3493    1.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5568   -0.3966    2.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024   -0.2100    1.7356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2206    0.0164    0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0097    0.2019   -0.2076 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504    0.4279   -1.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1114    0.4697   -2.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3378    0.2911   -1.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3772    0.0642   -0.4022 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3332    0.6353   -2.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426    0.8420   -3.5327 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5397    0.5919   -1.4881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700    0.7641   -2.0471 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073    0.3459   -0.0450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619    0.1619    0.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5503   -0.0374    1.9201 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9042   -0.3042    2.1340 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.2710    0.9141 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6365   -0.6508    0.3918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7347   -0.1428   -0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7692   -0.8528   -1.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8241    0.9258   -1.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6794   -0.4874    1.9644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6398   -0.5767    3.3921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -0.2463    2.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0200    0.6510   -3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2710    0.3180   -2.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3223    0.2226    3.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0543   -1.3953    2.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0185    1.2590    1.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1152   -0.1813   -0.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2364   -1.6604    0.1455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3655   -0.7767    1.2377 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  2  0
 14 12  1  0
 12 13  2  0
 12  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
 16 20  1  0
  7  8  1  0
  7 17  1  0
  6 11  1  0
 21 33  1  0
 21 34  1  0
 21 35  1  0
 20 32  1  1
 19 30  1  0
 19 31  1  0
  9 28  1  0
 10 29  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  5 27  1  0
M  END


  Mrv1533004171509282D          

 21 24  0  0  0  0            999 V2000
    1.9927    0.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    0.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9919   -0.2141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1264    0.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3939    0.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3563    1.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6238    2.1830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0512    2.2481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0136    3.0722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7838    1.8686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4787    2.3132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2112    1.9337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2488    1.1096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9813    0.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6763    1.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0190   -0.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3240   -0.5387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5915   -0.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539    0.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8214    1.0445    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
  5 21  1  0  0  0  0
 11 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0225280

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1COC2=C1C(=O)C(=O)C1=CC=C3C(C)=CC=CC3=C21

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O3/c1-9-4-3-5-12-11(9)6-7-13-15(12)18-14(10(2)8-21-18)17(20)16(13)19/h3-7,10H,8H2,1-2H3

> <INCHI_KEY>
KWKITVVBQQLHBB-UHFFFAOYSA-N

> <FORMULA>
C18H14O3

> <MOLECULAR_WEIGHT>
278.307

> <EXACT_MASS>
278.094294311

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
29.959217545049995

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,14-dimethyl-16-oxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1,3,5,7,9,13(17)-hexaene-11,12-dione

> <ALOGPS_LOGP>
3.69

> <JCHEM_LOGP>
3.3554682296666667

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.864170996964634

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
81.397

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,14-dimethyl-16-oxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1,3,5,7,9,13(17)-hexaene-11,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       3.720   0.998   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.239   0.746   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.929  -0.630   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.451  -0.400   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.703   1.120   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.335   1.828   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.265   3.366   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.898   4.075   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.562   4.196   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.492   5.735   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.930   3.488   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.227   4.318   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.594   3.610   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.664   2.071   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.032   1.363   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.329   2.193   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.102  -0.176   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.805  -1.006   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.437  -0.297   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.367   1.241   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.000   1.950   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    2    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   21                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20    5   11                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄O₃

Average Mass

278.3070 Da

Monoisotopic Mass

278.09429 Da

IUPAC Name

6,14-dimethyl-16-oxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1,3,5,7,9,13(17)-hexaene-11,12-dione

Traditional Name

6,14-dimethyl-16-oxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1,3,5,7,9,13(17)-hexaene-11,12-dione

CAS Registry Number

Not Available

SMILES

CC1COC2=C1C(=O)C(=O)C1=CC=C3C(C)=CC=CC3=C21

InChI Identifier

InChI=1S/C18H14O3/c1-9-4-3-5-12-11(9)6-7-13-15(12)18-14(10(2)8-21-18)17(20)16(13)19/h3-7,10H,8H2,1-2H3

InChI Key

KWKITVVBQQLHBB-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
Salvia glutinosa	LOTUS Database	35616633
Salvia miltiorrhiza	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Naphthofuran
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
Vinylogous ester
Dihydrofuran
Ketone
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.69	ALOGPS
logP	3.36	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	81.4 m³·mol⁻¹	ChemAxon
Polarizability	29.96 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

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

75024890

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione (NP0225280)

MOL for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

3D MOL for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

3D SDF for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

3D-SDF for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

PDB for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

3D PDB for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

SMILES for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

INCHI for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

Structure for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)

3D Structure for NP0225280 (3,8-dimethyl-2h,3h-phenanthro[4,3-b]furan-4,5-dione)