NP-MRD: Showing NP-Card for methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate (NP0266536)

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Record Information

Version

2.0

Created at

2022-09-08 10:54:33 UTC

Updated at

2022-09-08 10:54:33 UTC

NP-MRD ID

NP0266536

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate

Description

Methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]Nonadeca-3,5,7-triene-19-carboxylate belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group. methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate is found in Alstonia macrophylla. Methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]Nonadeca-3,5,7-triene-19-carboxylate is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231514442D          

 46 52  0  0  0  0            999 V2000
    0.4266   -1.9123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5149   -1.0921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2694   -0.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9356   -1.2450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3578    0.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1423   -0.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3134   -1.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0979   -1.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7113   -0.7040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2691   -2.0629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0536   -2.3181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0093   -3.3805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5754    1.3811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5653    2.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5442    1.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322    2.2240    0.0000 O   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  2  0  0  0  0
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 33 42  1  0  0  0  0
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 32 45  1  0  0  0  0
 45 46  1  0  0  0  0
 30 46  1  0  0  0  0
M  END

     RDKit          3D

 86 92  0  0  0  0  0  0  0  0999 V2000
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 20 65  1  0
 20 66  1  0
M  END


  Mrv1533004231514442D          

 46 52  0  0  0  0            999 V2000
    0.4266   -1.9123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5149   -1.0921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2694   -0.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9356   -1.2450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3578    0.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1423   -0.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3134   -1.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0979   -1.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7113   -0.7040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2691   -2.0629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0536   -2.3181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2248   -3.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0093   -3.3805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1804   -4.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6114   -3.6769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7826   -4.4840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1693   -5.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8269   -3.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2136   -3.9734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4291   -3.7181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6558   -2.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4584   -0.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5605    0.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5754    1.3811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0021    1.6148    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7098    1.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280    0.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9983   -0.3705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7671   -1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0343    1.2669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427    1.4846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7982    0.8276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6310    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0938    0.0632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9167    0.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3795   -0.5604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2024   -0.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0996    0.9242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4597    1.6665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8139    1.5478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9911    1.4885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3960    2.1024    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5653    2.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5442    1.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322    2.2240    0.0000 O   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  2  0  0  0  0
  3  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
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 10 21  1  0  0  0  0
  5 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  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  2  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 24 45  1  0  0  0  0
 32 45  1  0  0  0  0
 45 46  1  0  0  0  0
 30 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266536

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(COC(=O)C2=CC(OC)=C(OC)C(OC)=C2)C2CC3N(C\C2=C\C)C2CC11C4=CC(OC)=C(OC)C=C4N(C)C31O2

> <INCHI_IDENTIFIER>
InChI=1S/C34H40N2O10/c1-9-18-16-36-27-13-20(18)32(31(38)44-8,17-45-30(37)19-10-25(41-5)29(43-7)26(11-19)42-6)33-15-28(36)46-34(27,33)35(2)22-14-24(40-4)23(39-3)12-21(22)33/h9-12,14,20,27-28H,13,15-17H2,1-8H3/b18-9-

> <INCHI_KEY>
XMPQOOTZKXFCNH-NVMNQCDNSA-N

> <FORMULA>
C34H40N2O10

> <MOLECULAR_WEIGHT>
636.698

> <EXACT_MASS>
636.268295496

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
66.07652682282992

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate

> <ALOGPS_LOGP>
3.21

> <JCHEM_LOGP>
3.969723394999999

> <ALOGPS_LOGS>
-4.03

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
4.766624243087886

> <JCHEM_POLAR_SURFACE_AREA>
114.46000000000001

> <JCHEM_REFRACTIVITY>
166.94699999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.90e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       0.796  -3.570   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.961  -2.039   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.370  -1.416   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.613  -2.324   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.534   0.115   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.999  -0.361   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.318  -1.868   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.783  -2.344   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.928  -1.314   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.102  -3.851   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.567  -4.327   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.886  -5.834   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.351  -6.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.670  -7.817   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.741  -6.864   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.061  -8.370   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.916  -9.400   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.277  -6.387   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.132  -7.417   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.668  -6.941   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.957  -4.881   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.856  -0.053   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.046   1.071   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.074   2.578   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       0.004   3.014   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -1.325   1.990   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.799   0.421   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.863  -0.692   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.432  -2.170   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.931   2.365   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.813   2.771   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.357   1.545   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.911   1.393   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.775   0.118   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.311   0.229   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.175  -1.046   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       9.711  -0.935   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.983   1.614   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.519   1.725   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.191   3.111   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.119   2.889   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.583   2.778   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0       4.472   3.925   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0       4.789   5.432   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.883   3.276   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       1.927   4.152   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   22   32                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   21                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   10                                                       
CONECT   22    5   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   45                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   22   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   25   31   46                                                  
CONECT   31   30   32                                                       
CONECT   32   31    5   33   45                                             
CONECT   33   32   34   42                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42                                                       
CONECT   42   41   33   43                                                  
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   24   32   46                                             
CONECT   46   45   30                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Value	Source
Methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1,.0,.0,.0,]nonadeca-3,5,7-triene-19-carboxylic acid	Generator
Methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylic acid	Generator

Chemical Formula

C₃₄H₄₀N₂O₁₀

Average Mass

636.6980 Da

Monoisotopic Mass

636.26830 Da

IUPAC Name

methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate

Traditional Name

methyl (14E)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1(COC(=O)C2=CC(OC)=C(OC)C(OC)=C2)C2CC3N(C\C2=C\C)C2CC11C4=CC(OC)=C(OC)C=C4N(C)C31O2

InChI Identifier

InChI=1S/C34H40N2O10/c1-9-18-16-36-27-13-20(18)32(31(38)44-8,17-45-30(37)19-10-25(41-5)29(43-7)26(11-19)42-6)33-15-28(36)46-34(27,33)35(2)22-14-24(40-4)23(39-3)12-21(22)33/h9-12,14,20,27-28H,13,15-17H2,1-8H3/b18-9-

InChI Key

XMPQOOTZKXFCNH-NVMNQCDNSA-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
Alstonia macrophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Corynanthean-type alkaloids

Sub Class

Not Available

Direct Parent

Corynanthean-type alkaloids

Alternative Parents

Substituents

Corynanthean skeleton
Pyridoindole
Carbazole
Beta-carboline
Gallic acid or derivatives
P-methoxybenzoic acid or derivatives
M-methoxybenzoic acid or derivatives
Quinolizidine
Benzoate ester
Indole or derivatives
Benzoic acid or derivatives
Phenoxy compound
Methoxybenzene
Dialkylarylamine
Phenol ether
Benzoyl
Anisole
Alkyl aryl ether
Benzenoid
Piperidine
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Methyl ester
Tetrahydrofuran
Oxazolidine
Hemiaminal
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	3.21	ALOGPS
logP	3.97	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Basic)	4.77	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.46 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	166.95 m³·mol⁻¹	ChemAxon
Polarizability	66.08 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate (NP0266536)

MOL for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

3D MOL for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

3D SDF for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

3D-SDF for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

PDB for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

3D PDB for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

SMILES for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

INCHI for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

Structure for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)

3D Structure for NP0266536 (methyl (14e)-14-ethylidene-5,6-dimethoxy-2-methyl-19-[(3,4,5-trimethoxybenzoyloxy)methyl]-18-oxa-2,12-diazahexacyclo[9.6.1.1⁹,¹⁵.0¹,⁹.0³,⁸.0¹²,¹⁷]nonadeca-3,5,7-triene-19-carboxylate)