NP-MRD: Showing NP-Card for 3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one (NP0205648)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 01:36:22 UTC

Updated at

2022-09-05 01:36:22 UTC

NP-MRD ID

NP0205648

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one

Description

10-Chloro-7-hexyl-dodecahydropyrido[2,1-዆]quinolin-5-one belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. 10-Chloro-7-hexyl-dodecahydropyrido[2,1-዆]quinolin-5-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    6.4944    1.2102    0.2499 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1408   -0.1866    0.6673 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8929   -0.6966    0.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6818    0.1338    0.3181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5029   -0.4895   -0.4015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    0.3367   -0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0562   -0.3003   -0.8413 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0196   -1.6846   -0.2738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3682   -2.2138   -0.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5356   -3.1580    0.6651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -1.4834   -0.7658 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7797   -2.1065   -0.6352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8377   -1.3208    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7898    0.1454   -0.1673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5533    0.6443   -0.8816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3206   -0.0573   -0.3594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1654    0.1600    1.1313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0797    1.6207    1.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3052    2.4602    0.4908 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0131    4.0872    0.2965 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.0297    1.8651   -0.8543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1039    0.4559   -0.9241 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3284    1.2806   -0.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8397    1.9213    0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5765    1.3876    0.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9753   -0.8506    0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0838   -0.2726    1.7866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0489   -0.7073   -1.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7137   -1.7238    0.3829 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4243    0.0872    1.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8108    1.1974    0.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7453   -0.4687   -1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4077   -1.5221   -0.0078 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0672    0.2279    0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4842    1.3394   -0.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4488   -0.4207   -1.9011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5073   -2.4396   -0.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5229   -1.7976    0.7113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1495   -1.5297   -1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6551   -3.0692   -0.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1775   -2.4702   -1.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8392   -1.6809   -0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8750   -1.6009    1.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6627    0.5238   -0.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9258    0.6416    0.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5280    1.7421   -0.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6745    0.3893   -1.9533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2159   -0.3188    1.4364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9623   -0.2772    1.7289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1155    2.0657    1.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6796    1.7082    2.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3042    2.6689    0.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0712    2.2572   -1.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7907    2.2896   -1.5777 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 16 15  1  6
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22  7  1  0
 16 11  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
 11 39  1  6
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 17 48  1  0
 17 49  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  1
 21 53  1  0
 21 54  1  0
M  END


  Mrv1533004161514142D          

 22 24  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0068   -5.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3537   -5.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6973   -6.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1345   -5.9151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 N   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 16 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205648

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC1CC(=O)C2CCCCC22CCC(Cl)CN12

> <INCHI_IDENTIFIER>
InChI=1S/C19H32ClNO/c1-2-3-4-5-8-16-13-18(22)17-9-6-7-11-19(17)12-10-15(20)14-21(16)19/h15-17H,2-14H2,1H3

> <INCHI_KEY>
GMYMXBPMBUGRPG-UHFFFAOYSA-N

> <FORMULA>
C19H32ClNO

> <MOLECULAR_WEIGHT>
325.92

> <EXACT_MASS>
325.2172424

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.89412500418442

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-chloro-7-hexyl-dodecahydropyrido[2,1-዆]quinolin-5-one

> <ALOGPS_LOGP>
5.07

> <JCHEM_LOGP>
5.407254426333333

> <ALOGPS_LOGS>
-5.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.333787509220308

> <JCHEM_PKA_STRONGEST_BASIC>
7.612649513785588

> <JCHEM_POLAR_SURFACE_AREA>
20.310000000000002

> <JCHEM_REFRACTIVITY>
92.57049999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-chloro-7-hexyl-decahydro-1H-pyrido[2,1-዆]quinolin-5-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      14.670  -6.930   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.946  -9.708   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.594 -11.169   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.368 -12.203   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.318 -11.041   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   20 Cl   UNK     0       8.002 -12.320   0.000  0.00  0.00          Cl+0
HETATM   21  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      10.669  -9.240   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   22                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17   22                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    7   16                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₃₂ClNO

Average Mass

325.9200 Da

Monoisotopic Mass

325.21724 Da

IUPAC Name

10-chloro-7-hexyl-dodecahydropyrido[2,1-዆]quinolin-5-one

Traditional Name

10-chloro-7-hexyl-decahydro-1H-pyrido[2,1-዆]quinolin-5-one

CAS Registry Number

Not Available

SMILES

CCCCCCC1CC(=O)C2CCCCC22CCC(Cl)CN12

InChI Identifier

InChI=1S/C19H32ClNO/c1-2-3-4-5-8-16-13-18(22)17-9-6-7-11-19(17)12-10-15(20)14-21(16)19/h15-17H,2-14H2,1H3

InChI Key

GMYMXBPMBUGRPG-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 quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Azaspirodecane
Quinolizidine
Quinolidine
Piperidinone
Hydropyridine
Piperidine
Tertiary aliphatic amine
Tertiary amine
Ketone
Azacycle
Hydrocarbon derivative
Organic oxygen compound
Alkyl chloride
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Amine
Alkyl halide
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	5.07	ALOGPS
logP	5.41	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	18.33	ChemAxon
pKa (Strongest Basic)	7.61	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	20.31 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	92.57 m³·mol⁻¹	ChemAxon
Polarizability	38.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

74000122

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one (NP0205648)

MOL for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

3D MOL for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

3D SDF for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

3D-SDF for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

PDB for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

3D PDB for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

SMILES for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

INCHI for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

Structure for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)

3D Structure for NP0205648 (3-chloro-6-hexyl-decahydro-1h-pyrido[2,1-j]quinolin-8-one)