NP-MRD: Showing NP-Card for (2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one (NP0215466)

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Record Information

Version

2.0

Created at

2022-09-05 15:05:59 UTC

Updated at

2022-09-05 15:05:59 UTC

NP-MRD ID

NP0215466

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one

Description

(2R)-2,3,3,5-tetramethyl-2H,3H,4H,5H-furo[3,2-c]quinolin-4-one belongs to the class of organic compounds known as dihydrofuranoquinolines. These are organic heterocyclic compounds with a structure based on the dihydrofuranoquinoline skeleton. Based on a literature review very few articles have been published on (2R)-2,3,3,5-tetramethyl-2H,3H,4H,5H-furo[3,2-c]quinolin-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
   -3.3545   -1.7239    0.1423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1785   -0.9835    0.6727 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9974   -1.7141    0.3437 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0269   -0.7983    0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4908    0.4688   -0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    1.4950   -0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0851    2.6492   -0.3746 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7274    1.3447   -0.2644 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5499    2.4538   -0.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2051    0.0929   -0.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -0.0936   -0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1298   -1.3396    0.0294 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3037   -2.4236    0.2378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9359   -2.2541    0.2801 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3860   -0.9923    0.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9828    0.3806    0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6289    0.5503   -1.2636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400    1.4271    1.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -2.7831   -0.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1449   -1.8291    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8263   -1.2631   -0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2177   -0.9389    1.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0319    2.7285    0.5105 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3552    2.4084   -1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9375    3.3439   -0.7328 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1856    0.7782   -0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2075   -1.4445   -0.0083 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7425   -3.4122    0.3683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3271   -3.1200    0.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966    0.7893   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4728   -0.2936   -1.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1694    1.4406   -1.7505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4268    0.9868    1.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7669    1.7615    1.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9090    2.3077    0.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 16  2  1  0
 15  4  1  0
 15 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  1
  9 23  1  0
  9 24  1  0
  9 25  1  0
 11 26  1  0
 12 27  1  0
 13 28  1  0
 14 29  1  0
 17 30  1  0
 17 31  1  0
 17 32  1  0
 18 33  1  0
 18 34  1  0
 18 35  1  0
M  END


  Mrv1652309052217062D          

 18 20  0  0  1  0            999 V2000
    4.3613    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8869   -0.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4099   -0.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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  2  0  0  0  0
  4 15  1  0  0  0  0
 10 15  1  0  0  0  0
  5 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215466

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC2=C(C(=O)N(C)C3=CC=CC=C23)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H17NO2/c1-9-15(2,3)12-13(18-9)10-7-5-6-8-11(10)16(4)14(12)17/h5-9H,1-4H3/t9-/m1/s1

> <INCHI_KEY>
JSJSVEVELHLLJW-SECBINFHSA-N

> <FORMULA>
C15H17NO2

> <MOLECULAR_WEIGHT>
243.306

> <EXACT_MASS>
243.125928791

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
26.915675001422336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2,3,3,5-tetramethyl-2H,3H,4H,5H-furo[3,2-c]quinolin-4-one

> <JCHEM_LOGP>
1.9020552080000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.42620685886490384

> <JCHEM_POLAR_SURFACE_AREA>
29.54

> <JCHEM_REFRACTIVITY>
70.95260000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2,3,3,5-tetramethyl-2H-furo[3,2-c]quinolin-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.141   2.271   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.406   2.042   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.307  -3.109   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       2.956  -1.848   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.228  -3.205   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.256  -1.519   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.232  -0.365   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    4   10                                                  
CONECT   16    5    2   17   18                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₇NO₂

Average Mass

243.3060 Da

Monoisotopic Mass

243.12593 Da

IUPAC Name

(2R)-2,3,3,5-tetramethyl-2H,3H,4H,5H-furo[3,2-c]quinolin-4-one

Traditional Name

(2R)-2,3,3,5-tetramethyl-2H-furo[3,2-c]quinolin-4-one

CAS Registry Number

Not Available

SMILES

C[C@H]1OC2=C(C(=O)N(C)C3=CC=CC=C23)C1(C)C

InChI Identifier

InChI=1S/C15H17NO2/c1-9-15(2,3)12-13(18-9)10-7-5-6-8-11(10)16(4)14(12)17/h5-9H,1-4H3/t9-/m1/s1

InChI Key

JSJSVEVELHLLJW-SECBINFHSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydrofuranoquinolines. These are organic heterocyclic compounds with a structure based on the dihydrofuranoquinoline skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Dihydrofuranoquinolines

Direct Parent

Dihydrofuranoquinolines

Alternative Parents

Substituents

Dihydrofuranoquinoline
Dihydroquinolone
Dihydroquinoline
Alkyl aryl ether
Pyridinone
Benzenoid
Pyridine
Heteroaromatic compound
Vinylogous ester
Lactam
Oxacycle
Azacycle
Ether
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
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	1.9	ChemAxon
pKa (Strongest Basic)	-0.43	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.54 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	70.95 m³·mol⁻¹	ChemAxon
Polarizability	26.92 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

163193047

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one (NP0215466)

MOL for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

3D MOL for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

3D SDF for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

3D-SDF for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

PDB for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

3D PDB for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

SMILES for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

INCHI for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

Structure for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)

3D Structure for NP0215466 ((2r)-2,3,3,5-tetramethyl-2h-furo[3,2-c]quinolin-4-one)