NP-MRD: Showing NP-Card for 1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol (NP0159822)

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Record Information

Version

2.0

Created at

2022-09-02 17:38:39 UTC

Updated at

2022-09-02 17:38:39 UTC

NP-MRD ID

NP0159822

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol

Description

1-({3-Ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol belongs to the class of organic compounds known as harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole. 1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol is found in Pogonopus speciosus. 1-({3-Ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514452D          

 35 40  0  0  0  0            999 V2000
   12.1332    1.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5811    0.4639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8361   -0.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6431   -0.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8980   -1.2769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.7050   -1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9599   -2.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4079   -2.8461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6628   -3.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1108   -4.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3657   -5.0284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8137   -5.6415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3038   -4.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7518   -4.6854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9448   -4.5139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0489   -3.2877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6009   -2.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3460   -1.8899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5390   -1.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2840   -0.9338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4771   -0.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2221    0.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.5192    1.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7123    1.5916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1602    0.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4152    0.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7477   -0.2910    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0803    0.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2733    0.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7213    0.6354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9762    1.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4242    2.0332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7832    1.5916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3352    0.9785    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
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 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
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 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 26 35  1  0  0  0  0
 29 35  1  0  0  0  0
M  END

     RDKit          3D

 72 77  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004251514452D          

 35 40  0  0  0  0            999 V2000
   12.1332    1.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.7050   -1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.7518   -4.6854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9448   -4.5139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4242    2.0332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3352    0.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 26 35  1  0  0  0  0
 29 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0159822

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1CN2CCC3=CC(OC)=C(OC)C=C3C2CC1CC1NCCC2=C1NC1=CC=C(O)C=C21

> <INCHI_IDENTIFIER>
InChI=1S/C29H37N3O3/c1-4-17-16-32-10-8-18-13-27(34-2)28(35-3)15-22(18)26(32)12-19(17)11-25-29-21(7-9-30-25)23-14-20(33)5-6-24(23)31-29/h5-6,13-15,17,19,25-26,30-31,33H,4,7-12,16H2,1-3H3

> <INCHI_KEY>
JRVWIILYWSBUMC-UHFFFAOYSA-N

> <FORMULA>
C29H37N3O3

> <MOLECULAR_WEIGHT>
475.633

> <EXACT_MASS>
475.283492063

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
56.019661800412536

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-({3-ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol

> <ALOGPS_LOGP>
4.46

> <JCHEM_LOGP>
4.095737021259536

> <ALOGPS_LOGS>
-4.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
17.434431601932445

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.665616589881294

> <JCHEM_PKA_STRONGEST_BASIC>
8.914296658309512

> <JCHEM_POLAR_SURFACE_AREA>
69.75

> <JCHEM_REFRACTIVITY>
139.7692

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.14e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-({3-ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      22.649   2.010   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.618   0.866   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      22.094  -0.599   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.600  -0.919   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      24.076  -2.383   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      25.583  -2.704   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      26.058  -4.168   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      25.028  -5.313   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.504  -6.777   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.473  -7.922   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      24.949  -9.386   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      23.919 -10.531   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.967  -7.602   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      21.937  -8.746   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      20.430  -8.426   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      22.491  -6.137   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.522  -4.993   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.046  -3.528   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.539  -3.208   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.064  -1.743   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.557  -1.423   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.081   0.042   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      20.112   1.186   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      19.636   2.651   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.130   2.971   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.099   1.827   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.575   0.362   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      16.329  -0.543   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0      15.083   0.362   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.577   0.042   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.546   1.186   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.022   2.651   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      11.992   3.795   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      14.529   2.971   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      15.559   1.827   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17                                                       
CONECT   17   16    8   18                                                  
CONECT   18   17    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   35                                                  
CONECT   27   26   22   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   26   29                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₇N₃O₃

Average Mass

475.6330 Da

Monoisotopic Mass

475.28349 Da

IUPAC Name

1-({3-ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol

Traditional Name

1-({3-ethyl-9,10-dimethoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-ol

CAS Registry Number

Not Available

SMILES

CCC1CN2CCC3=CC(OC)=C(OC)C=C3C2CC1CC1NCCC2=C1NC1=CC=C(O)C=C21

InChI Identifier

InChI=1S/C29H37N3O3/c1-4-17-16-32-10-8-18-13-27(34-2)28(35-3)15-22(18)26(32)12-19(17)11-25-29-21(7-9-30-25)23-14-20(33)5-6-24(23)31-29/h5-6,13-15,17,19,25-26,30-31,33H,4,7-12,16H2,1-3H3

InChI Key

JRVWIILYWSBUMC-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
Pogonopus speciosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Harmala alkaloids

Sub Class

Not Available

Direct Parent

Harmala alkaloids

Alternative Parents

Substituents

Harman
Pyridoindole
Beta-carboline
Quinolizidine
Tetrahydroisoquinoline
Hydroxyindole
3-alkylindole
Indole or derivatives
Indole
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Piperidine
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Secondary aliphatic amine
Ether
Azacycle
Organoheterocyclic compound
Secondary amine
Hydrocarbon derivative
Amine
Organic nitrogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen 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	4.46	ALOGPS
logP	4.1	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	9.67	ChemAxon
pKa (Strongest Basic)	8.91	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	69.75 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	139.77 m³·mol⁻¹	ChemAxon
Polarizability	56.02 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

604599

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol (NP0159822)

MOL for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

3D MOL for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

3D SDF for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

3D-SDF for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

PDB for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

3D PDB for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

SMILES for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

INCHI for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

Structure for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)

3D Structure for NP0159822 (1-({3-ethyl-9,10-dimethoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl}methyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol)