NP-MRD: Showing NP-Card for 3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate (NP0202276)

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Record Information

Version

2.0

Created at

2022-09-04 21:28:15 UTC

Updated at

2022-09-04 21:28:15 UTC

NP-MRD ID

NP0202276

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate

Description

3-(3,7-Dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methyl-1λ⁵-quinolin-1-one belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. Based on a literature review very few articles have been published on 3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methyl-1λ⁵-quinolin-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
    2.9329    3.0630   -1.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1064    2.3646   -0.2178 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1837    0.9968   -0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0621    0.1988    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7884    0.8737    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4293    0.1605   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211   -0.0396    0.8144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2608    0.4839    2.1993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6632   -0.7565    0.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.0937    0.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1253   -0.7015    0.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0037   -0.4076   -0.5748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1940   -1.2719   -0.8381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7974    0.8262   -1.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -1.1428    0.4235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0916   -2.0115    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5008   -1.7062    0.3227 N   0  0  0  0  0  4  0  0  0  0  0  0
    3.6098   -3.0782    0.5023 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.5886   -0.9701    0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8189   -1.5838   -0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9222   -0.8080   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7648    0.5544   -0.4678 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    1.1819   -0.3890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4196    0.3933   -0.1198 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3966    2.5813   -2.2909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9115    3.3559   -1.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4823    4.0538   -1.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6911    1.3680    1.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223    1.7708   -0.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5066   -0.1917   -1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3202    0.1840    2.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2879    1.6114    2.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0698    0.1447    2.8854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.5848    1.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6561   -1.2308   -0.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8422    0.8984   -0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9469    0.5853    1.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2873   -1.6086    0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0116   -2.2549   -0.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1467   -0.8240   -0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2539   -1.4974   -1.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6263    1.6671   -0.6569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7392    1.0894   -1.9486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9412    0.7394   -2.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877   -3.0735    0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6223   -1.7973    1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3833   -2.1419   -0.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9437   -2.6428    0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8658   -1.3108   -0.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6159    1.1609   -0.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3972    2.2350   -0.5176 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 24  2  0
 24 23  1  0
 23 22  2  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 15  1  0
 15 16  1  0
 15  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  3
 12 13  1  0
 12 14  1  0
  4  3  1  0
 19 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 23 51  1  0
 22 50  1  0
 21 49  1  0
 20 48  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  8 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 14 44  1  0
M  CHG  2  17   1  18  -1
M  END


  Mrv1652309042223282D          

 24 25  0  0  0  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  5  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
    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  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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  4 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
  3 24  2  0  0  0  0
 19 24  1  0  0  0  0
M  CHG  2  17   1  18  -1
M  END
> <DATABASE_ID>
NP0202276

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=CC=CC2=[N+]([O-])C(C)=C1CC=C(C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C21H27NO2/c1-15(2)9-8-10-16(3)13-14-18-17(4)22(23)20-12-7-6-11-19(20)21(18)24-5/h6-7,9,11-13H,8,10,14H2,1-5H3

> <INCHI_KEY>
HWBJYDDVFLLLIR-UHFFFAOYSA-N

> <FORMULA>
C21H27NO2

> <MOLECULAR_WEIGHT>
325.452

> <EXACT_MASS>
325.204179113

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.942548534031246

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate

> <JCHEM_LOGP>
4.445599245333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.4065605815144564

> <JCHEM_POLAR_SURFACE_AREA>
36.17

> <JCHEM_REFRACTIVITY>
102.89070000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       2.667   0.000   0.000  0.00  0.00           N+1
HETATM   18  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O-1
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   0.000   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                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    4   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    3   19                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₇NO₂

Average Mass

325.4520 Da

Monoisotopic Mass

325.20418 Da

IUPAC Name

3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate

Traditional Name

3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate

CAS Registry Number

Not Available

SMILES

COC1=C2C=CC=CC2=[N+]([O-])C(C)=C1CC=C(C)CCC=C(C)C

InChI Identifier

InChI=1S/C21H27NO2/c1-15(2)9-8-10-16(3)13-14-18-17(4)22(23)20-12-7-6-11-19(20)21(18)24-5/h6-7,9,11-13H,8,10,14H2,1-5H3

InChI Key

HWBJYDDVFLLLIR-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Not Available

Direct Parent

Quinolines and derivatives

Alternative Parents

Substituents

Quinoline
Monoterpenoid
Bicyclic monoterpenoid
Aromatic monoterpenoid
Methylpyridine
Alkyl aryl ether
Benzenoid
Pyridinium
Pyridine
Heteroaromatic compound
Azacycle
Ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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	4.45	ChemAxon
pKa (Strongest Basic)	3.41	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	36.17 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	102.89 m³·mol⁻¹	ChemAxon
Polarizability	37.94 Å³	ChemAxon
Number of Rings	2	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

163187635

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate (NP0202276)

MOL for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

3D MOL for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

3D SDF for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

3D-SDF for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

PDB for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

3D PDB for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

SMILES for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

INCHI for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

Structure for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)

3D Structure for NP0202276 (3-(3,7-dimethylocta-2,6-dien-1-yl)-4-methoxy-2-methylquinolin-1-ium-1-olate)