NP-MRD: Showing NP-Card for 2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde (NP0267891)

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Record Information

Version

2.0

Created at

2022-09-08 12:49:18 UTC

Updated at

2022-09-08 12:49:18 UTC

NP-MRD ID

NP0267891

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde

Description

10-O-Demethylprotoemetine belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. 2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde is found in Alangium longiflorum. Based on a literature review very few articles have been published on 10-O-Demethylprotoemetine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -3.8574   -0.1739   -2.1970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4677    0.4647   -0.8832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7261   -0.5337    0.0011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4837   -0.9385   -0.8061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6476    0.2093   -0.8573 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0819    0.4278   -2.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5137    0.0374   -2.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1318    0.1703   -0.6722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5093    0.0078   -0.5523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1658    0.1128    0.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5493   -0.0523    0.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3630   -0.3337   -0.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4169    0.3891    1.7787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0556    0.4981    2.9987 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    0.5508    1.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3838    0.4462    0.4485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0692    0.6226    0.3621 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8029   -0.0679    1.4979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2872    0.1175    1.2881 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0824   -0.3926    2.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5309   -0.1198    2.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2700   -0.8105    1.6169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1619    0.1107   -3.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8874    0.1541   -2.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8427   -1.2837   -2.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3305    0.8836   -0.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8087    1.3427   -1.1129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3814   -1.3821    0.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0652   -1.8242   -0.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7925   -1.1800   -1.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4348   -0.1155   -2.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0159    1.5272   -2.2952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0942    0.7439   -2.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7218   -0.9758   -2.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1257   -0.2130   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0974    0.3630   -1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2244   -1.3533   -0.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4263   -0.1239   -0.0894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0545    0.3731    3.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4895    0.7662    2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2898    1.7214    0.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5105    0.3799    2.4791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -1.1512    1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4528    1.2120    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9577   -1.4645    2.6379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7281    0.1323    3.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0186    0.7256    2.8124 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  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 19  3  1  0
 17  5  1  0
 16  8  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  1
  4 29  1  0
  4 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  9 35  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  1
 18 42  1  0
 18 43  1  0
 19 44  1  6
 20 45  1  0
 20 46  1  0
 21 47  1  0
M  END


  Mrv1652309082214492D          

 22 24  0  0  1  0            999 V2000
    0.7954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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
 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
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17  5  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0267891

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1CN2CCC3=CC(OC)=C(O)C=C3[C@@H]2C[C@@H]1CC=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H25NO3/c1-3-12-11-19-6-4-14-9-18(22-2)17(21)10-15(14)16(19)8-13(12)5-7-20/h7,9-10,12-13,16,21H,3-6,8,11H2,1-2H3/t12-,13-,16-/m0/s1

> <INCHI_KEY>
ZMIUDPUOTLDSHP-XEZPLFJOSA-N

> <FORMULA>
C18H25NO3

> <MOLECULAR_WEIGHT>
303.402

> <EXACT_MASS>
303.183443669

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.54948945692905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(2R,3R,11bS)-3-ethyl-10-hydroxy-9-methoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde

> <JCHEM_LOGP>
2.465698939000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
17.55543772933858

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.120722989814341

> <JCHEM_PKA_STRONGEST_BASIC>
7.7069334093741135

> <JCHEM_POLAR_SURFACE_AREA>
49.77

> <JCHEM_REFRACTIVITY>
87.12879999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2R,3R,11bS)-3-ethyl-10-hydroxy-9-methoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.485  -2.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.255  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       6.105  -0.206   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      13.035  -1.540   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      13.805  -0.206   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.495  -4.207   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.795  -4.207   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.565  -5.541   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.795  -6.875   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    8   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₅NO₃

Average Mass

303.4020 Da

Monoisotopic Mass

303.18344 Da

IUPAC Name

2-[(2R,3R,11bS)-3-ethyl-10-hydroxy-9-methoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde

Traditional Name

2-[(2R,3R,11bS)-3-ethyl-10-hydroxy-9-methoxy-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde

CAS Registry Number

Not Available

SMILES

CC[C@H]1CN2CCC3=CC(OC)=C(O)C=C3[C@@H]2C[C@@H]1CC=O

InChI Identifier

InChI=1S/C18H25NO3/c1-3-12-11-19-6-4-14-9-18(22-2)17(21)10-15(14)16(19)8-13(12)5-7-20/h7,9-10,12-13,16,21H,3-6,8,11H2,1-2H3/t12-,13-,16-/m0/s1

InChI Key

ZMIUDPUOTLDSHP-XEZPLFJOSA-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
Alangium longiflorum	LOTUS Database	35616633

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

Quinolizidine
Tetrahydroisoquinoline
Anisole
Phenol ether
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Piperidine
Benzenoid
Alpha-hydrogen aldehyde
Tertiary amine
Tertiary aliphatic amine
Azacycle
Ether
Aldehyde
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic oxygen compound
Amine
Organic nitrogen 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	2.47	ChemAxon
pKa (Strongest Acidic)	10.12	ChemAxon
pKa (Strongest Basic)	7.71	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	87.13 m³·mol⁻¹	ChemAxon
Polarizability	34.55 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00051864

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

101718137

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde (NP0267891)

MOL for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

3D MOL for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

3D SDF for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

3D-SDF for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

PDB for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

3D PDB for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

SMILES for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

INCHI for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

Structure for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)

3D Structure for NP0267891 (2-[(2r,3r,11bs)-3-ethyl-10-hydroxy-9-methoxy-1h,2h,3h,4h,6h,7h,11bh-pyrido[2,1-a]isoquinolin-2-yl]acetaldehyde)