NP-MRD: Showing NP-Card for (4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one (NP0314755)

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Record Information

Version

2.0

Created at

2022-09-11 13:01:28 UTC

Updated at

2022-09-11 13:01:29 UTC

NP-MRD ID

NP0314755

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one

Description

(4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-2H,3H,4H,9H-furo[2,3-b]quinolin-2-ylidene]propyl}-2H,3H,4H,5H,6H-pyrano[3,2-c]quinolin-5-one belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine. (4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one is found in Ptelea trifoliata. Based on a literature review very few articles have been published on (4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-2H,3H,4H,9H-furo[2,3-b]quinolin-2-ylidene]propyl}-2H,3H,4H,5H,6H-pyrano[3,2-c]quinolin-5-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112215012D          

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 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 24 34  1  0  0  0  0
 34 35  2  0  0  0  0
 25 36  1  0  0  0  0
 22 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314755

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2=C(C\C(O2)=C(\C)C[C@@H]2CC(C)(C)OC3=C2C(=O)N(C)C2=CC=CC=C32)C(=O)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C30H30N2O4/c1-17(24-15-21-26(33)19-10-6-8-12-22(19)32(5)29(21)35-24)14-18-16-30(2,3)36-27-20-11-7-9-13-23(20)31(4)28(34)25(18)27/h6-13,18H,14-16H2,1-5H3/b24-17+/t18-/m1/s1

> <INCHI_KEY>
YZAPTPVRHPBWGT-ZDSQJECRSA-N

> <FORMULA>
C30H30N2O4

> <MOLECULAR_WEIGHT>
482.58

> <EXACT_MASS>
482.220557454

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
54.31475669175203

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-2H,3H,4H,9H-furo[2,3-b]quinolin-2-ylidene]propyl}-2H,3H,4H,5H,6H-pyrano[3,2-c]quinolin-5-one

> <JCHEM_LOGP>
4.0698423953333345

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3884854139097159

> <JCHEM_POLAR_SURFACE_AREA>
59.08

> <JCHEM_REFRACTIVITY>
152.09439999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-3H-furo[2,3-b]quinolin-2-ylidene]propyl}-3H,4H-pyrano[3,2-c]quinolin-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      15.349 -14.635   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.579 -13.301   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.349 -11.967   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.889 -11.967   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.659 -13.301   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.199 -13.301   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.932 -14.817   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.646 -13.828   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      19.969 -11.967   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      19.199 -10.633   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.659 -10.633   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.889  -9.300   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      15.349  -9.300   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      17.659  -7.966   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      16.889  -6.632   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.199  -7.966   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.969  -6.632   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.509  -6.632   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.279  -7.966   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.509  -9.300   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.969  -9.300   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.039 -13.301   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.134 -12.055   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.669 -12.531   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.669 -14.071   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       9.336 -14.841   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       9.336 -16.381   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.002 -14.071   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668 -14.841   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335 -14.071   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335 -12.531   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668 -11.761   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002 -12.531   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.336 -11.761   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.336 -10.221   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      12.134 -14.547   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   21                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   10   16                                                  
CONECT   22    2   23   36                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   34                                                  
CONECT   25   24   26   36                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   24   35                                                  
CONECT   35   34                                                            
CONECT   36   25   22                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₀N₂O₄

Average Mass

482.5800 Da

Monoisotopic Mass

482.22056 Da

IUPAC Name

(4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-2H,3H,4H,9H-furo[2,3-b]quinolin-2-ylidene]propyl}-2H,3H,4H,5H,6H-pyrano[3,2-c]quinolin-5-one

Traditional Name

(4R)-2,2,6-trimethyl-4-{2-[(2E)-9-methyl-4-oxo-3H-furo[2,3-b]quinolin-2-ylidene]propyl}-3H,4H-pyrano[3,2-c]quinolin-5-one

CAS Registry Number

Not Available

SMILES

CN1C2=C(C\C(O2)=C(\C)C[C@@H]2CC(C)(C)OC3=C2C(=O)N(C)C2=CC=CC=C32)C(=O)C2=CC=CC=C12

InChI Identifier

InChI=1S/C30H30N2O4/c1-17(24-15-21-26(33)19-10-6-8-12-22(19)32(5)29(21)35-24)14-18-16-30(2,3)36-27-20-11-7-9-13-23(20)31(4)28(34)25(18)27/h6-13,18H,14-16H2,1-5H3/b24-17+/t18-/m1/s1

InChI Key

YZAPTPVRHPBWGT-ZDSQJECRSA-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
Ptelea trifoliata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Pyranoquinolines

Alternative Parents

Substituents

Pyranoquinoline
Dihydrofuranoquinoline
Dihydroquinolone
Dihydroquinoline
Pyranopyridine
Alkyl aryl ether
Pyridinone
Pyran
Benzenoid
Pyridine
Heteroaromatic compound
Vinylogous ester
Vinylogous amide
Lactam
Oxacycle
Ether
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen 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	4.07	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	59.08 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	152.09 m³·mol⁻¹	ChemAxon
Polarizability	54.31 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

163195025

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one (NP0314755)

MOL for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

3D MOL for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

3D SDF for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

3D-SDF for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

PDB for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

3D PDB for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

SMILES for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

INCHI for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

Structure for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)

3D Structure for NP0314755 ((4r)-2,2,6-trimethyl-4-{2-[(2e)-9-methyl-4-oxo-3h-furo[2,3-b]quinolin-2-ylidene]propyl}-3h,4h-pyrano[3,2-c]quinolin-5-one)