NP-MRD: Showing NP-Card for alstoniaphylline C (NP0043351)

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Record Information

Version

1.0

Created at

2021-06-21 00:46:58 UTC

Updated at

2021-06-30 00:18:59 UTC

NP-MRD ID

NP0043351

Secondary Accession Numbers

None

Natural Product Identification

Common Name

alstoniaphylline C

Provided By

JEOL Database JEOL Logo

Description

alstoniaphylline C is found in Alstonia macrophylla. It was first documented in 2013 (Cheenpracha, S., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102463D          

 50 54  0  0  0  0            999 V2000
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    1.0324   -2.7122   -1.8961 C   0  0  2  0  0  0  0  0  0  0  0  0
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 20 21  1  0  0  0  0
 12 11  2  0  0  0  0
 21 22  1  0  0  0  0
 14 37  1  0  0  0  0
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 12 35  1  0  0  0  0
 15 38  1  0  0  0  0
  7 34  1  0  0  0  0
 18 40  1  0  0  0  0
 18 41  1  0  0  0  0
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  2 29  1  1  0  0  0
  4 30  1  0  0  0  0
  4 31  1  0  0  0  0
  1 26  1  0  0  0  0
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 25 50  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 22 46  1  0  0  0  0
M  CHG  1  23   1
M  END

     RDKit          3D

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    1.0324   -2.7122   -1.8961 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  CHG  1  23   1
M  END


  Mrv1652306212102463D          

 50 54  0  0  0  0            999 V2000
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   -0.6385   -3.2868    0.3587 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 23 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  5 19  1  0  0  0  0
 10  9  2  0  0  0  0
 16 15  2  0  0  0  0
 15 14  1  0  0  0  0
  8  9  1  0  0  0  0
  8 16  1  0  0  0  0
  5  4  1  0  0  0  0
 19 20  1  0  0  0  0
 20  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
 16 11  1  0  0  0  0
  2  1  1  0  0  0  0
  8  7  2  0  0  0  0
 19 42  1  1  0  0  0
  9 17  1  0  0  0  0
  5 32  1  6  0  0  0
  6  7  1  0  0  0  0
  6 33  1  6  0  0  0
  6 23  1  0  0  0  0
 17 39  1  1  0  0  0
 14 13  2  0  0  0  0
 23 24  1  0  0  0  0
 11 10  1  0  0  0  0
 23 25  1  6  0  0  0
 13 12  1  0  0  0  0
 20 21  1  0  0  0  0
 12 11  2  0  0  0  0
 21 22  1  0  0  0  0
 14 37  1  0  0  0  0
 13 36  1  0  0  0  0
 12 35  1  0  0  0  0
 15 38  1  0  0  0  0
  7 34  1  0  0  0  0
 18 40  1  0  0  0  0
 18 41  1  0  0  0  0
 20 43  1  1  0  0  0
  2 29  1  1  0  0  0
  4 30  1  0  0  0  0
  4 31  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
 24 47  1  0  0  0  0
 24 48  1  0  0  0  0
 24 49  1  0  0  0  0
 25 50  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 22 46  1  0  0  0  0
M  CHG  1  23   1
M  END
> <DATABASE_ID>
NP0043351

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]1([H])[C@@]([H])(OC([H])([H])[C@@]2([H])[C@]3([H])C([H])=C4C5=C([H])C([H])=C([H])C([H])=C5N=C4[C@]([H])(C([H])([H])[C@@]12[H])[N@@+]3(O[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H25N2O3/c1-11-15(9-23)13-7-19-20-14(12-5-3-4-6-17(12)21-20)8-18(22(19,2)24)16(13)10-25-11/h3-6,8,11,13,15-16,18-19,23-24H,7,9-10H2,1-2H3/q+1/t11-,13-,15+,16+,18-,19-,22+/m0/s1

> <INCHI_KEY>
GIZQKPKADDVEKS-SAKOKNRDSA-N

> <FORMULA>
C20H25N2O3

> <MOLECULAR_WEIGHT>
341.43

> <EXACT_MASS>
341.185969093

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
37.622273791944764

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,12S,13R,16S,17R,18R,20R)-20-hydroxy-17-(hydroxymethyl)-16,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2,4,6,8,10-pentaen-20-ium

> <ALOGPS_LOGP>
-0.13

> <JCHEM_LOGP>
0.9601571451949211

> <ALOGPS_LOGS>
-4.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.380154909317216

> <JCHEM_PKA_STRONGEST_BASIC>
2.894038031017403

> <JCHEM_POLAR_SURFACE_AREA>
62.05

> <JCHEM_REFRACTIVITY>
99.9122

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.51e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,12S,13R,16S,17R,18R,20R)-20-hydroxy-17-(hydroxymethyl)-16,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2,4,6,8,10-pentaen-20-ium

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 50 54  0  0  0  0  0  0  0  0999 V2000
    1.3227   -3.3382   -3.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0324   -2.7122   -1.8961 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1426   -3.3098   -1.2999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3474   -2.7108   -1.7737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4796   -1.3257   -1.1301 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4607   -1.3324    0.0691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9488    0.0878    0.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426    0.9124    1.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1626    0.4464    1.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6840    1.3619    2.7363 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5219    2.4928    2.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013    3.7139    3.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3181    4.7195    2.8446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3356    4.4939    1.8981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4585    3.2589    1.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5458    2.2780    1.5877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6389   -0.9568    1.7415 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4281   -0.9662    0.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0866   -0.6981   -0.7972 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0035   -1.1567   -1.8128 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9048   -0.4096   -3.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3491   -0.6087   -3.7838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7811   -1.9101    1.3310 N   0  0  1  0  0  4  0  0  0  0  0  0
   -2.7851   -2.0769    2.4813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2693   -3.2766    1.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3484   -4.4301   -3.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5481   -3.1109   -3.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2887   -3.0049   -3.6473 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489   -3.0424   -1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1814   -3.3653   -1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519   -2.6670   -2.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559   -0.7010   -1.8994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3281   -1.9737   -0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    0.4301   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6163    3.8872    3.8970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437    5.6911    3.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    5.2969    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441    3.0931    0.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2305   -1.3298    2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9609   -1.9227    0.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1905   -0.2097    0.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1938    0.3925   -0.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9844   -0.8529   -1.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0251    0.6665   -2.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6994   -0.7229   -3.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3008   -0.1748   -4.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2478   -2.5067    3.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2169   -1.1131    2.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5661   -2.7637    2.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385   -3.2868    0.3587 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
 23 17  1  0
 17 18  1  0
 18 19  1  0
  5 19  1  0
 10  9  2  0
 16 15  2  0
 15 14  1  0
  8  9  1  0
  8 16  1  0
  5  4  1  0
 19 20  1  0
 20  2  1  0
  2  3  1  0
  3  4  1  0
 16 11  1  0
  2  1  1  0
  8  7  2  0
 19 42  1  1
  9 17  1  0
  5 32  1  6
  6  7  1  0
  6 33  1  6
  6 23  1  0
 17 39  1  1
 14 13  2  0
 23 24  1  0
 11 10  1  0
 23 25  1  6
 13 12  1  0
 20 21  1  0
 12 11  2  0
 21 22  1  0
 14 37  1  0
 13 36  1  0
 12 35  1  0
 15 38  1  0
  7 34  1  0
 18 40  1  0
 18 41  1  0
 20 43  1  1
  2 29  1  1
  4 30  1  0
  4 31  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
 25 50  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
M  CHG  1  23   1
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  C   UNK     0       1.323  -3.338  -3.256  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.032  -2.712  -1.896  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.143  -3.310  -1.300  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.347  -2.711  -1.774  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.480  -1.326  -1.130  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.461  -1.332   0.069  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.949   0.088   0.302  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.343   0.912   1.162  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.163   0.446   1.936  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.684   1.362   2.736  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.522   2.493   2.534  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.401   3.714   3.168  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.318   4.720   2.845  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.336   4.494   1.898  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.458   3.259   1.256  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.546   2.278   1.588  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.639  -0.957   1.742  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.428  -0.966   0.647  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.087  -0.698  -0.797  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.004  -1.157  -1.813  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.905  -0.410  -3.156  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.349  -0.609  -3.784  0.00  0.00           O+0
HETATM   23  N   UNK     0      -1.781  -1.910   1.331  0.00  0.00           N+1
HETATM   24  C   UNK     0      -2.785  -2.077   2.481  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.269  -3.277   1.115  0.00  0.00           O+0
HETATM   26  H   UNK     0       1.348  -4.430  -3.168  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.548  -3.111  -3.994  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.289  -3.005  -3.647  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.849  -3.042  -1.240  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.181  -3.365  -1.499  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.352  -2.667  -2.866  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.956  -0.701  -1.899  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.328  -1.974  -0.128  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.802   0.430  -0.279  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.616   3.887   3.897  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.244   5.691   3.331  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.034   5.297   1.666  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.244   3.093   0.527  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.231  -1.330   2.688  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.961  -1.923   0.697  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.190  -0.210   0.879  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.194   0.393  -0.882  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.984  -0.853  -1.418  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.025   0.667  -2.988  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.699  -0.723  -3.841  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.301  -0.175  -4.657  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.248  -2.507   3.332  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.217  -1.113   2.755  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.566  -2.764   2.143  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.639  -3.287   0.359  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2   20    3    1   29                                             
CONECT    3    2    4                                                       
CONECT    4    5    3   30   31                                             
CONECT    5    6   19    4   32                                             
CONECT    6    5    7   33   23                                             
CONECT    7    8    6   34                                                  
CONECT    8    9   16    7                                                  
CONECT    9   10    8   17                                                  
CONECT   10    9   11                                                       
CONECT   11   16   10   12                                                  
CONECT   12   13   11   35                                                  
CONECT   13   14   12   36                                                  
CONECT   14   15   13   37                                                  
CONECT   15   16   14   38                                                  
CONECT   16   15    8   11                                                  
CONECT   17   23   18    9   39                                             
CONECT   18   17   19   40   41                                             
CONECT   19   18    5   20   42                                             
CONECT   20   19    2   21   43                                             
CONECT   21   20   22   44   45                                             
CONECT   22   21   46                                                       
CONECT   23   17    6   24   25                                             
CONECT   24   23   47   48   49                                             
CONECT   25   23   50                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    4                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   18                                                            
CONECT   42   19                                                            
CONECT   43   20                                                            
CONECT   44   21                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
CONECT   47   24                                                            
CONECT   48   24                                                            
CONECT   49   24                                                            
CONECT   50   25                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  108    0
END

RDKit          3D

50 54  0  0  0  0  0  0  0  0999 V2000
    1.3227   -3.3382   -3.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0324   -2.7122   -1.8961 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1426   -3.3098   -1.2999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3474   -2.7108   -1.7737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4796   -1.3257   -1.1301 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4607   -1.3324    0.0691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9488    0.0878    0.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426    0.9124    1.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1626    0.4464    1.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6840    1.3619    2.7363 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5219    2.4928    2.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013    3.7139    3.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3181    4.7195    2.8446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3356    4.4939    1.8981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4585    3.2589    1.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5458    2.2780    1.5877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6389   -0.9568    1.7415 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4281   -0.9662    0.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0866   -0.6981   -0.7972 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0035   -1.1567   -1.8128 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9048   -0.4096   -3.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3491   -0.6087   -3.7838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7811   -1.9101    1.3310 N   0  0  1  0  0  4  0  0  0  0  0  0
   -2.7851   -2.0769    2.4813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2693   -3.2766    1.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3484   -4.4301   -3.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5481   -3.1109   -3.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2887   -3.0049   -3.6473 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489   -3.0424   -1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1814   -3.3653   -1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519   -2.6670   -2.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559   -0.7010   -1.8994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3281   -1.9737   -0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    0.4301   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6163    3.8872    3.8970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437    5.6911    3.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    5.2969    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441    3.0931    0.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2305   -1.3298    2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9609   -1.9227    0.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1905   -0.2097    0.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1938    0.3925   -0.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9844   -0.8529   -1.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0251    0.6665   -2.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6994   -0.7229   -3.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3008   -0.1748   -4.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2478   -2.5067    3.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2169   -1.1131    2.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5661   -2.7637    2.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385   -3.2868    0.3587 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
 23 17  1  0
 17 18  1  0
 18 19  1  0
  5 19  1  0
 10  9  2  0
 16 15  2  0
 15 14  1  0
  8  9  1  0
  8 16  1  0
  5  4  1  0
 19 20  1  0
 20  2  1  0
  2  3  1  0
  3  4  1  0
 16 11  1  0
  2  1  1  0
  8  7  2  0
 19 42  1  1
  9 17  1  0
  5 32  1  6
  6  7  1  0
  6 33  1  6
  6 23  1  0
 17 39  1  1
 14 13  2  0
 23 24  1  0
 11 10  1  0
 23 25  1  6
 13 12  1  0
 20 21  1  0
 12 11  2  0
 21 22  1  0
 14 37  1  0
 13 36  1  0
 12 35  1  0
 15 38  1  0
  7 34  1  0
 18 40  1  0
 18 41  1  0
 20 43  1  1
  2 29  1  1
  4 30  1  0
  4 31  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
 25 50  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
M  CHG  1  23   1
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₅N₂O₃

Average Mass

341.4300 Da

Monoisotopic Mass

341.18597 Da

IUPAC Name

(1S,12S,13R,16S,17R,18R,20R)-20-hydroxy-17-(hydroxymethyl)-16,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2,4,6,8,10-pentaen-20-ium

Traditional Name

(1S,12S,13R,16S,17R,18R,20R)-20-hydroxy-17-(hydroxymethyl)-16,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2,4,6,8,10-pentaen-20-ium

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]1([H])[C@@]([H])(OC([H])([H])[C@@]2([H])[C@]3([H])C([H])=C4C5=C([H])C([H])=C([H])C([H])=C5N=C4[C@]([H])(C([H])([H])[C@@]12[H])[N@@+]3(O[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H25N2O3/c1-11-15(9-23)13-7-19-20-14(12-5-3-4-6-17(12)21-20)8-18(22(19,2)24)16(13)10-25-11/h3-6,8,11,13,15-16,18-19,23-24H,7,9-10H2,1-2H3/q+1/t11-,13-,15+,16+,18-,19-,22+/m0/s1

InChI Key

GIZQKPKADDVEKS-SAKOKNRDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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
Alstonia macrophylla	JEOL database	Cheenpracha, S., et al, J. Nat. Prod. 76, 723 (2013)

Chemical Taxonomy

Classification

Not classified

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	-0.13	ALOGPS
logP	0.96	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	15.38	ChemAxon
pKa (Strongest Basic)	2.89	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.05 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	99.91 m³·mol⁻¹	ChemAxon
Polarizability	37.62 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Cheenpracha, S., et al. (2013). Cheenpracha, S., et al, J. Nat. Prod. 76, 723 (2013). J. Nat. Prod..

Showing NP-Card for alstoniaphylline C (NP0043351)

MOL for NP0043351 (alstoniaphylline C)

3D MOL for NP0043351 (alstoniaphylline C)

3D SDF for NP0043351 (alstoniaphylline C)

3D-SDF for NP0043351 (alstoniaphylline C)

PDB for NP0043351 (alstoniaphylline C)

3D PDB for NP0043351 (alstoniaphylline C)

SMILES for NP0043351 (alstoniaphylline C)

INCHI for NP0043351 (alstoniaphylline C)

Structure for NP0043351 (alstoniaphylline C)

3D Structure for NP0043351 (alstoniaphylline C)