NP-MRD: Showing NP-Card for methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0223547)

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Record Information

Version

2.0

Created at

2022-09-06 01:40:15 UTC

Updated at

2022-09-06 01:40:15 UTC

NP-MRD ID

NP0223547

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

Description

Tubotaiwin belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate is found in Strempeliopsis strempelioides. Based on a literature review very few articles have been published on Tubotaiwin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062203402D          

 24 28  0  0  1  0            999 V2000
   -0.8444   -0.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0879   -0.5242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6117    0.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2167    0.6033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3744   -0.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1406   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7036   -1.1615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4126   -1.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0960   -1.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9012   -0.2782    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8249    0.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0211    1.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9958    1.8952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5454    2.5367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377    2.4152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4570    3.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5848    0.9629    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1712    0.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9959    0.4013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4273   -0.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340   -1.0271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2093   -1.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7779   -0.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192   -0.4837    0.0000 C   0  0  1  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  1  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
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 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
 18 23  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24  7  1  6  0  0  0
M  END

     RDKit          2D

 48 52  0  0  0  0  0  0  0  0999 V2000
   -4.2597    3.7981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2955    2.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3313    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6304    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9896    2.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4994    2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3694    0.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2686    0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3313   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6304   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9294   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2284   -0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9294   -3.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2284   -3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0195   -2.9672    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5277   -3.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3540   -4.3375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8458   -4.1807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4559   -2.8104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5742   -1.5969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0824   -1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2239    4.9472    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1106    4.7623    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4088    2.8340    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2725    3.7461    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5535    1.8321    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2343    2.5230    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0111    1.3361    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7180    3.7218    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3209    2.9377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8422    3.0892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9272    3.8559    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3907    1.0037    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5047   -0.8603    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8362   -1.6269    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1339   -2.6908    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5275   -4.5000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4784   -5.0490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9784   -2.4510    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0232   -4.0819    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2561   -5.7079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -5.3943    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9477   -2.6536    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3468   -0.3112    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0585    2.2498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 24  1  0
 24  7  1  0
  7  8  1  0
  8  9  1  0
 10  9  1  1
 10 11  1  0
 11 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 11 12  2  0
 12  4  1  0
  4  5  1  0
  5  6  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
  4  3  1  0
 10 24  1  0
 23 10  1  0
  6  7  1  0
 23 18  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
 24 48  1  6
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 17 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
  4 31  1  1
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END


  Mrv1652309062203402D          

 24 28  0  0  1  0            999 V2000
   -0.8444   -0.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0879   -0.5242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6117    0.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2167    0.6033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3744   -0.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1406   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7036   -1.1615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4126   -1.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0960   -1.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9012   -0.2782    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8249    0.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0211    1.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9958    1.8952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5454    2.5367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377    2.4152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4570    3.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5848    0.9629    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1712    0.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9959    0.4013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4273   -0.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340   -1.0271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2093   -1.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7779   -0.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192   -0.4837    0.0000 C   0  0  1  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  1  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
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 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
 18 23  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24  7  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0223547

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1[C@H]2N3CC[C@@]22C(NC4=CC=CC=C24)=C([C@@H]1CC3)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N2O2/c1-3-12-13-8-10-22-11-9-20(18(12)22)14-6-4-5-7-15(14)21-17(20)16(13)19(23)24-2/h4-7,12-13,18,21H,3,8-11H2,1-2H3/t12?,13-,18-,20-/m1/s1

> <INCHI_KEY>
RLAKWLFUMAABBE-UOFCVENLSA-N

> <FORMULA>
C20H24N2O2

> <MOLECULAR_WEIGHT>
324.424

> <EXACT_MASS>
324.183778021

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
40.695318888426165

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,11R,17R)-18-ethyl-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

> <JCHEM_LOGP>
2.2582812539999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.980956252562393

> <JCHEM_PKA_STRONGEST_BASIC>
10.270074203598881

> <JCHEM_POLAR_SURFACE_AREA>
41.57

> <JCHEM_REFRACTIVITY>
95.83470000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,11R,17R)-18-ethyl-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

> <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      -1.576  -1.122   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.164  -0.979   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.142   0.247   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.404   1.126   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.699  -0.163   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.263  -1.766   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       1.313  -2.168   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       2.637  -3.090   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.913  -2.149   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.549  -0.519   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.406   1.134   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.906   1.909   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.859   3.538   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.885   4.735   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       0.630   4.508   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.853   6.032   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.825   1.797   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       5.920   0.708   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.459   0.749   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.530  -1.917   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.991  -1.958   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.185  -0.646   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.089  -0.903   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   23   24                                             
CONECT   11   10   12   17                                                  
CONECT   12   11    4   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17   11   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18   10                                                  
CONECT   24   10    3    7                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   56    0
END

View in JSmol

Synonyms

Value	Source
Condyfolan-16-carboxylic acid, 2,16-didehydro-, methyl ester	MeSH
Dihydrocondylocarpine	MeSH
Tubotaiwine	MeSH

Chemical Formula

C₂₀H₂₄N₂O₂

Average Mass

324.4240 Da

Monoisotopic Mass

324.18378 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCC1[C@H]2N3CC[C@@]22C(NC4=CC=CC=C24)=C([C@@H]1CC3)C(=O)OC

InChI Identifier

InChI=1S/C20H24N2O2/c1-3-12-13-8-10-22-11-9-20(18(12)22)14-6-4-5-7-15(14)21-17(20)16(13)19(23)24-2/h4-7,12-13,18,21H,3,8-11H2,1-2H3/t12?,13-,18-,20-/m1/s1

InChI Key

RLAKWLFUMAABBE-UOFCVENLSA-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
Strempeliopsis strempelioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Aspidosperma alkaloid
Stemmadenine-skeleton
Carbazole
Indole or derivatives
Dihydroindole
Indolizidine
Aralkylamine
Secondary aliphatic/aromatic amine
Piperidine
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Vinylogous amide
Alpha,beta-unsaturated carboxylic ester
Methyl ester
Enoate ester
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Secondary amine
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Azacycle
Enamine
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Organooxygen 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00025216

Chemspider ID

114724729

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78358510

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0223547)

MOL for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D MOL for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D SDF for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D-SDF for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

PDB for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D PDB for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

SMILES for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

INCHI for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

Structure for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D Structure for NP0223547 (methyl (1s,11r,17r)-18-ethyl-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)