NP-MRD: Showing NP-Card for 5-oxopseudostrychnine (NP0041376)

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Record Information

Version

2.0

Created at

2021-06-20 23:18:14 UTC

Updated at

2021-06-30 00:15:51 UTC

NP-MRD ID

NP0041376

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-oxopseudostrychnine

Provided By

JEOL Database JEOL Logo

Description

5-Oxopseudostrychnine 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. 5-oxopseudostrychnine is found in Strychnos nux-vomica. 5-oxopseudostrychnine was first documented in 2012 (Zhao, N., et al.). Based on a literature review very few articles have been published on 5-Oxopseudostrychnine.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101183D          

 47 53  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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  Mrv1652306212101183D          

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 23 22  1  0  0  0  0
 22 42  1  1  0  0  0
 26 10  1  0  0  0  0
 11 12  2  0  0  0  0
  4  5  1  0  0  0  0
 18 19  1  0  0  0  0
  4 30  1  6  0  0  0
 19 20  2  0  0  0  0
 23 43  1  6  0  0  0
 20 21  1  0  0  0  0
 26 27  1  6  0  0  0
 17 39  1  0  0  0  0
 18 40  1  0  0  0  0
 19 41  1  0  0  0  0
 16 38  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
 13 36  1  0  0  0  0
 13 37  1  0  0  0  0
  9 34  1  0  0  0  0
  9 35  1  0  0  0  0
  7 33  1  0  0  0  0
  6 31  1  0  0  0  0
  6 32  1  0  0  0  0
 27 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0041376

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]12N3C(=O)C([H])([H])[C@@]11C4=C([H])C([H])=C([H])C([H])=C4N4C(=O)C([H])([H])[C@]5([H])OC([H])([H])C([H])=C(C3([H])[H])[C@]([H])(C2([H])[H])[C@]5([H])[C@@]14[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H20N2O4/c24-16-7-15-18-12-8-21(26)20(9-17(25)22(21)10-11(12)5-6-27-15)13-3-1-2-4-14(13)23(16)19(18)20/h1-5,12,15,18-19,26H,6-10H2/t12-,15-,18-,19-,20-,21+/m0/s1

> <INCHI_KEY>
CBNUTWOIYIEZGH-PMTQKSLQSA-N

> <FORMULA>
C21H20N2O4

> <MOLECULAR_WEIGHT>
364.401

> <EXACT_MASS>
364.142307132

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.812570414498936

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,11S,18R,20R,21R,22S)-18-hydroxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraene-9,24-dione

> <ALOGPS_LOGP>
0.64

> <JCHEM_LOGP>
-0.4437643370000004

> <ALOGPS_LOGS>
-1.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.239998244180804

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.527467541313221

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2129811305068996

> <JCHEM_POLAR_SURFACE_AREA>
70.08

> <JCHEM_REFRACTIVITY>
95.7109

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.10e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11S,18R,20R,21R,22S)-18-hydroxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraene-9,24-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 53  0  0  0  0  0  0  0  0999 V2000
   -1.6637    2.7500    0.0104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2431    1.6294    0.2876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8033    0.8680    1.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -0.6702    1.3212 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4493   -1.2123    2.5603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963   -2.5986    2.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -3.3364    2.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428   -3.3835    0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767   -3.9849    0.5211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8027   -2.9594   -0.2865 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457   -2.0866    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4824   -2.3011    1.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6528   -0.7909   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120   -0.8666   -1.0819 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0205    0.1780   -2.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5658    0.2205   -3.4284 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3038    1.3302   -4.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5112    2.3844   -3.7613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0355    2.3407   -2.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2286    1.2357   -1.6863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.9463   -0.4059 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1616   -0.4040   -0.0132 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1612   -1.1897    0.0762 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9871   -2.7070   -0.1116 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3303   -2.8975   -1.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0935   -2.3667   -1.3947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8203   -2.7495   -2.5438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009    1.2713    1.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1747    1.1254    2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9860   -0.9254    1.2229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6278   -2.9282    2.2773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008   -2.7692    3.8272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1419   -3.7761    3.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0213   -4.8801   -0.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -4.2430    1.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4211   -0.7889   -1.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8061    0.0643    0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1961   -0.5812   -3.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7243    1.3812   -5.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3177    3.2439   -4.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6533    3.1607   -2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236   -0.3391    0.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7912   -0.8792   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9743   -3.1863   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8857   -2.3825   -2.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3351   -3.9580   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2976   -3.5552   -2.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  1  0
 23  4  1  0
 21  2  1  0
  2  3  1  0
  3  4  1  0
 14 15  1  0
  2  1  2  0
 14 22  1  0
 14 13  1  1
 17 18  2  0
 13 11  1  0
 15 16  2  0
 16 17  1  0
 11 10  1  0
  9 10  1  0
 15 20  1  0
  9  8  1  0
 14 26  1  0
  8  7  2  0
 23 24  1  0
  7  6  1  0
 24 25  1  0
  6  5  1  0
 25 26  1  0
 24 44  1  6
  8 24  1  0
 23 22  1  0
 22 42  1  1
 26 10  1  0
 11 12  2  0
  4  5  1  0
 18 19  1  0
  4 30  1  6
 19 20  2  0
 23 43  1  6
 20 21  1  0
 26 27  1  6
 17 39  1  0
 18 40  1  0
 19 41  1  0
 16 38  1  0
 25 45  1  0
 25 46  1  0
  3 28  1  0
  3 29  1  0
 13 36  1  0
 13 37  1  0
  9 34  1  0
  9 35  1  0
  7 33  1  0
  6 31  1  0
  6 32  1  0
 27 47  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  O   UNK     0      -1.664   2.750   0.010  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.243   1.629   0.288  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.803   0.868   1.483  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.923  -0.670   1.321  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.449  -1.212   2.560  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.696  -2.599   2.751  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.499  -3.336   2.259  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.143  -3.384   0.963  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.177  -3.985   0.521  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.803  -2.959  -0.287  0.00  0.00           N+0
HETATM   11  C   UNK     0       2.746  -2.087   0.247  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.482  -2.301   1.194  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.653  -0.791  -0.520  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.212  -0.867  -1.082  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.020   0.178  -2.152  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.566   0.221  -3.428  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.304   1.330  -4.235  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.511   2.384  -3.761  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.036   2.341  -2.477  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.229   1.236  -1.686  0.00  0.00           C+0
HETATM   21  N   UNK     0      -0.262   0.946  -0.406  0.00  0.00           N+0
HETATM   22  C   UNK     0       0.162  -0.404  -0.013  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.161  -1.190   0.076  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.987  -2.707  -0.112  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.330  -2.898  -1.488  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.093  -2.367  -1.395  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.820  -2.749  -2.544  0.00  0.00           O+0
HETATM   28  H   UNK     0      -2.801   1.271   1.697  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.175   1.125   2.345  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.986  -0.925   1.223  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.628  -2.928   2.277  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.801  -2.769   3.827  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.142  -3.776   3.020  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.021  -4.880  -0.089  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.819  -4.243   1.369  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.421  -0.789  -1.301  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.806   0.064   0.145  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.196  -0.581  -3.802  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.724   1.381  -5.237  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.318   3.244  -4.399  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.653   3.161  -2.126  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.624  -0.339   0.981  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.791  -0.879  -0.775  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.974  -3.186  -0.140  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.886  -2.382  -2.282  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.335  -3.958  -1.774  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.298  -3.555  -2.280  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2   21    3    1                                                  
CONECT    3    2    4   28   29                                             
CONECT    4   23    3    5   30                                             
CONECT    5    6    4                                                       
CONECT    6    7    5   31   32                                             
CONECT    7    8    6   33                                                  
CONECT    8    9    7   24                                                  
CONECT    9   10    8   34   35                                             
CONECT   10   11    9   26                                                  
CONECT   11   13   10   12                                                  
CONECT   12   11                                                            
CONECT   13   14   11   36   37                                             
CONECT   14   15   22   13   26                                             
CONECT   15   14   16   20                                                  
CONECT   16   15   17   38                                                  
CONECT   17   18   16   39                                                  
CONECT   18   17   19   40                                                  
CONECT   19   18   20   41                                                  
CONECT   20   15   19   21                                                  
CONECT   21   22    2   20                                                  
CONECT   22   21   14   23   42                                             
CONECT   23    4   24   22   43                                             
CONECT   24   23   25   44    8                                             
CONECT   25   24   26   45   46                                             
CONECT   26   14   25   10   27                                             
CONECT   27   26   47                                                       
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    4                                                            
CONECT   31    6                                                            
CONECT   32    6                                                            
CONECT   33    7                                                            
CONECT   34    9                                                            
CONECT   35    9                                                            
CONECT   36   13                                                            
CONECT   37   13                                                            
CONECT   38   16                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
CONECT   46   25                                                            
CONECT   47   27                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  106    0
END

RDKit          3D

47 53  0  0  0  0  0  0  0  0999 V2000
   -1.6637    2.7500    0.0104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2431    1.6294    0.2876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8033    0.8680    1.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -0.6702    1.3212 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4493   -1.2123    2.5603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963   -2.5986    2.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -3.3364    2.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428   -3.3835    0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767   -3.9849    0.5211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8027   -2.9594   -0.2865 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457   -2.0866    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4824   -2.3011    1.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6528   -0.7909   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120   -0.8666   -1.0819 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0205    0.1780   -2.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5658    0.2205   -3.4284 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3038    1.3302   -4.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5112    2.3844   -3.7613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0355    2.3407   -2.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2286    1.2357   -1.6863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.9463   -0.4059 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1616   -0.4040   -0.0132 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1612   -1.1897    0.0762 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9871   -2.7070   -0.1116 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3303   -2.8975   -1.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0935   -2.3667   -1.3947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8203   -2.7495   -2.5438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009    1.2713    1.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1747    1.1254    2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9860   -0.9254    1.2229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6278   -2.9282    2.2773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008   -2.7692    3.8272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1419   -3.7761    3.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0213   -4.8801   -0.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -4.2430    1.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4211   -0.7889   -1.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8061    0.0643    0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1961   -0.5812   -3.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7243    1.3812   -5.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3177    3.2439   -4.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6533    3.1607   -2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236   -0.3391    0.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7912   -0.8792   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9743   -3.1863   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8857   -2.3825   -2.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3351   -3.9580   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2976   -3.5552   -2.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  1  0
 23  4  1  0
 21  2  1  0
  2  3  1  0
  3  4  1  0
 14 15  1  0
  2  1  2  0
 14 22  1  0
 14 13  1  1
 17 18  2  0
 13 11  1  0
 15 16  2  0
 16 17  1  0
 11 10  1  0
  9 10  1  0
 15 20  1  0
  9  8  1  0
 14 26  1  0
  8  7  2  0
 23 24  1  0
  7  6  1  0
 24 25  1  0
  6  5  1  0
 25 26  1  0
 24 44  1  6
  8 24  1  0
 23 22  1  0
 22 42  1  1
 26 10  1  0
 11 12  2  0
  4  5  1  0
 18 19  1  0
  4 30  1  6
 19 20  2  0
 23 43  1  6
 20 21  1  0
 26 27  1  6
 17 39  1  0
 18 40  1  0
 19 41  1  0
 16 38  1  0
 25 45  1  0
 25 46  1  0
  3 28  1  0
  3 29  1  0
 13 36  1  0
 13 37  1  0
  9 34  1  0
  9 35  1  0
  7 33  1  0
  6 31  1  0
  6 32  1  0
 27 47  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀N₂O₄

Average Mass

364.4010 Da

Monoisotopic Mass

364.14231 Da

IUPAC Name

(1S,11S,18R,20R,21R,22S)-18-hydroxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraene-9,24-dione

Traditional Name

(1S,11S,18R,20R,21R,22S)-18-hydroxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraene-9,24-dione

CAS Registry Number

Not Available

SMILES

[H]O[C@@]12N3C(=O)C([H])([H])[C@@]11C4=C([H])C([H])=C([H])C([H])=C4N4C(=O)C([H])([H])[C@]5([H])OC([H])([H])C([H])=C(C3([H])[H])[C@]([H])(C2([H])[H])[C@]5([H])[C@@]14[H]

InChI Identifier

InChI=1S/C21H20N2O4/c24-16-7-15-18-12-8-21(26)20(9-17(25)22(21)10-11(12)5-6-27-15)13-3-1-2-4-14(13)23(16)19(18)20/h1-5,12,15,18-19,26H,6-10H2/t12-,15-,18-,19-,20-,21+/m0/s1

InChI Key

CBNUTWOIYIEZGH-PMTQKSLQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Strychnos nux-vomica L.	JEOL database	Zhao, N., et al, Tetrahedron 68, 3288 (2012)

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

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Carbazole
Quinolidine
Indole or derivatives
Indolizidine
Delta-lactam
Piperidinone
Piperidine
Pyrrolidone
2-pyrrolidone
Benzenoid
N-alkylpyrrolidine
Cyclic alcohol
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Alkanolamine
Dialkyl ether
Ether
Oxacycle
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Carbonyl group
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
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	0.64	ALOGPS
logP	-0.44	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	12.53	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.08 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	95.71 m³·mol⁻¹	ChemAxon
Polarizability	36.81 Å³	ChemAxon
Number of Rings	7	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

57412269

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhao, N., et al. (2012). Zhao, N., et al, Tetrahedron 68, 3288 (2012). Tetrahedron.

Showing NP-Card for 5-oxopseudostrychnine (NP0041376)

MOL for NP0041376 (5-oxopseudostrychnine)

3D MOL for NP0041376 (5-oxopseudostrychnine)

3D SDF for NP0041376 (5-oxopseudostrychnine)

3D-SDF for NP0041376 (5-oxopseudostrychnine)

PDB for NP0041376 (5-oxopseudostrychnine)

3D PDB for NP0041376 (5-oxopseudostrychnine)

SMILES for NP0041376 (5-oxopseudostrychnine)

INCHI for NP0041376 (5-oxopseudostrychnine)

Structure for NP0041376 (5-oxopseudostrychnine)

3D Structure for NP0041376 (5-oxopseudostrychnine)