NP-MRD: Showing NP-Card for (2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine (NP0226463)

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Record Information

Version

2.0

Created at

2022-09-06 05:30:36 UTC

Updated at

2022-09-06 05:30:36 UTC

NP-MRD ID

NP0226463

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine

Description

(2R,4S,5R)-5-ethyl-13-methoxy-4-{[(1R)-6-methoxy-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-1-yl]methyl}-7,17-diazatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),11(16),12,14-tetraene 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. (2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine is found in Cinchona calisaya. Based on a literature review very few articles have been published on (2R,4S,5R)-5-ethyl-13-methoxy-4-{[(1R)-6-methoxy-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-1-yl]methyl}-7,17-diazatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),11(16),12,14-tetraene.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062207302D          

 37 43  0  0  1  0            999 V2000
    2.5089   -9.6730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3159   -9.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8679   -9.2314    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6749   -9.4030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2269   -8.7899    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0339   -8.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5859   -8.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3310   -7.5637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5240   -7.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4378   -6.5717    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1914   -6.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4464   -5.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2533   -5.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8054   -5.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6123   -5.7215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8673   -4.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5504   -6.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7435   -6.8492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9720   -8.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1650   -7.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130   -8.4468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8060   -8.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5510   -7.4907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1031   -6.8776    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8481   -6.0930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0412   -5.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4891   -6.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7441   -7.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0766   -7.8041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4092   -7.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3978   -7.4907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9498   -6.8776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949   -6.0930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2469   -5.4799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0539   -5.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1121   -5.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6641   -6.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 18  1  0  0  0  0
 11 18  1  0  0  0  0
 19  9  1  6  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  1  0  0  0
 23 22  1  6  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  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  2  0  0  0  0
 27 37  1  0  0  0  0
 30 37  1  0  0  0  0
M  END


  Mrv1652309062207302D          

 37 43  0  0  1  0            999 V2000
    2.5089   -9.6730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3159   -9.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8679   -9.2314    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6749   -9.4030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2269   -8.7899    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0339   -8.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5859   -8.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3310   -7.5637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5240   -7.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4378   -6.5717    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1914   -6.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4464   -5.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2533   -5.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8054   -5.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6123   -5.7215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8673   -4.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5504   -6.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7435   -6.8492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9720   -8.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1650   -7.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130   -8.4468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8060   -8.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5510   -7.4907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1031   -6.8776    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8481   -6.0930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0412   -5.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4891   -6.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7441   -7.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0766   -7.8041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4092   -7.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3978   -7.4907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9498   -6.8776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949   -6.0930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2469   -5.4799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0539   -5.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1121   -5.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6641   -6.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 18  1  0  0  0  0
 11 18  1  0  0  0  0
 19  9  1  6  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  1  0  0  0
 23 22  1  6  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  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  2  0  0  0  0
 27 37  1  0  0  0  0
 30 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226463

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1CN2CCC3=C(NC4=CC=C(OC)C=C34)[C@H]2C[C@@H]1C[C@H]1NCCC2=C1NC1=CC=C(OC)C=C21

> <INCHI_IDENTIFIER>
InChI=1S/C31H38N4O2/c1-4-18-17-35-12-10-23-25-16-21(37-3)6-8-27(25)34-31(23)29(35)14-19(18)13-28-30-22(9-11-32-28)24-15-20(36-2)5-7-26(24)33-30/h5-8,15-16,18-19,28-29,32-34H,4,9-14,17H2,1-3H3/t18-,19-,28+,29+/m0/s1

> <INCHI_KEY>
RPRJNENQRCTMRQ-PITNESRCSA-N

> <FORMULA>
C31H38N4O2

> <MOLECULAR_WEIGHT>
498.671

> <EXACT_MASS>
498.29947648

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
59.57195261801324

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,12bR)-3-ethyl-9-methoxy-2-{[(1R)-6-methoxy-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-1-yl]methyl}-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine

> <JCHEM_LOGP>
4.841125919666669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
16.955544704290123

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.353450376499396

> <JCHEM_PKA_STRONGEST_BASIC>
9.342644935250135

> <JCHEM_POLAR_SURFACE_AREA>
65.31

> <JCHEM_REFRACTIVITY>
148.75229999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,12bR)-3-ethyl-9-methoxy-2-{[(1R)-6-methoxy-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-1-yl]methyl}-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.683 -18.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.190 -18.376   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.220 -17.232   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.726 -17.552   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.757 -16.408   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      11.263 -16.728   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.294 -15.584   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.818 -14.119   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.311 -13.799   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      10.150 -12.267   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      11.557 -11.641   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.033 -10.176   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.540  -9.856   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.570 -11.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.076 -10.680   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.552  -9.216   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.094 -12.465   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.588 -12.785   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.281 -14.943   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.775 -14.623   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.744 -15.767   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.238 -15.447   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.762 -13.983   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       5.792 -12.838   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       5.317 -11.374   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.810 -11.053   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.780 -12.198   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.256 -13.662   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       2.010 -14.568   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       0.764 -13.662   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.743 -13.983   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.773 -12.838   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.297 -11.374   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.328 -10.229   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.834 -10.549   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.209 -11.053   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.240 -12.198   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17    8   11                                                  
CONECT   19    9    5   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20    3   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   37                                                  
CONECT   28   27   23   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   37                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   33   37                                                       
CONECT   37   36   27   30                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₃₈N₄O₂

Average Mass

498.6710 Da

Monoisotopic Mass

498.29948 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@H]1CN2CCC3=C(NC4=CC=C(OC)C=C34)[C@H]2C[C@@H]1C[C@H]1NCCC2=C1NC1=CC=C(OC)C=C21

InChI Identifier

InChI=1S/C31H38N4O2/c1-4-18-17-35-12-10-23-25-16-21(37-3)6-8-27(25)34-31(23)29(35)14-19(18)13-28-30-22(9-11-32-28)24-15-20(36-2)5-7-26(24)33-30/h5-8,15-16,18-19,28-29,32-34H,4,9-14,17H2,1-3H3/t18-,19-,28+,29+/m0/s1

InChI Key

RPRJNENQRCTMRQ-PITNESRCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cinchona calisaya	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
Beta-carboline
Pyridoindole
3-alkylindole
Quinolizine
Indole
Indole or derivatives
Anisole
Alkyl aryl ether
Aralkylamine
Piperidine
Benzenoid
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Azacycle
Ether
Secondary aliphatic amine
Secondary amine
Amine
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
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

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

163185643

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine (NP0226463)

MOL for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

3D MOL for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

3D SDF for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

3D-SDF for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

PDB for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

3D PDB for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

SMILES for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

INCHI for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

Structure for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)

3D Structure for NP0226463 ((2s,3r,12br)-3-ethyl-9-methoxy-2-{[(1r)-6-methoxy-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]methyl}-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine)