NP-MRD: Showing NP-Card for methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0286673)

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Record Information

Version

2.0

Created at

2022-09-09 15:21:08 UTC

Updated at

2022-09-09 15:21:08 UTC

NP-MRD ID

NP0286673

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

Description

Lagumicine 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 (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate is found in Alstonia angustifolia. methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate was first documented in 2004 (PMID: 15003424). Based on a literature review very few articles have been published on Lagumicine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092217212D          

 26 30  0  0  1  0            999 V2000
    1.4781    3.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4797    3.0533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1949    2.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9086    3.0560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965    1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0003    1.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.7571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3466    1.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1713    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6027    0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533    0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766    0.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2714   -0.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881   -0.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -0.3673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0636    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927    1.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5242    1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6011    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7871    0.9265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2946    0.3105    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 26 25  1  1  0  0  0
 17 26  1  0  0  0  0
 14 26  1  0  0  0  0
M  END

     RDKit          3D

 48 52  0  0  0  0  0  0  0  0999 V2000
   -2.5666    4.2087    0.1642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1013    2.9643   -0.3267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9141    2.3716    0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2779    3.0811    0.9331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3930    1.1118   -0.4036 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8106    0.7186    0.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9724    1.4514    0.4321 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0976    0.5686    0.5216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4333    0.8402    0.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3142   -0.2095    0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8674   -1.4836    0.3118 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5238   -1.7371    0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312   -0.6973    0.2519 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1244   -0.7162    0.2603 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6577   -1.2750    1.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0459   -2.5775    1.1608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5700   -2.2590   -0.1526 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097   -1.4542    0.1776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1418   -0.6552   -0.9983 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1779   -1.6056   -2.0928 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5050   -0.1291   -0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0731    0.6464    0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2862   -0.3478   -1.8364 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0698    0.2864   -1.4112 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0574   -0.6651   -1.9294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5106   -1.5580   -0.7976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3842    4.1096    0.8783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7032    4.7543    0.6339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8357    4.8267   -0.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0219    2.4800    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8258    1.8162    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3860   -0.0120    0.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6151   -2.2708    0.2355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2241   -2.7577   -0.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0432   -0.6149    2.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5700   -1.5244    2.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403   -3.3343    1.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7226   -2.8854    1.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5597   -0.8352    1.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5399   -2.1978    0.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7018   -2.3667   -1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9197    0.0589    0.6739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3044    0.8779    0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4830    1.6060   -0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3806    0.8956   -2.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8978    0.0203   -2.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3335   -1.2152   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1841   -2.3098   -1.2310 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 24  1  0
 24 25  1  0
 25 26  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 24  5  1  0
 14  6  1  0
 26 14  1  0
 13  8  1  0
 26 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  7 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 15 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  1  0
 18 39  1  0
 18 40  1  0
 20 41  1  0
 24 45  1  6
 25 46  1  0
 25 47  1  0
 26 48  1  6
 22 42  1  0
 22 43  1  0
 22 44  1  0
M  END


  Mrv1652309092217212D          

 26 30  0  0  1  0            999 V2000
    1.4781    3.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4797    3.0533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1949    2.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9086    3.0560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965    1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0003    1.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.7571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3466    1.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1713    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6027    0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533    0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766    0.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2714   -0.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881   -0.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -0.3673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0636    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927    1.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5242    1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6011    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7871    0.9265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2946    0.3105    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 26 25  1  1  0  0  0
 17 26  1  0  0  0  0
 14 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286673

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C2NC3=CC=CC=C3C22CCN3C[C@](O)([C@@H]1C[C@@H]23)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N2O4/c1-11(23)20(25)10-22-8-7-19-12-5-3-4-6-14(12)21-17(19)16(18(24)26-2)13(20)9-15(19)22/h3-6,13,15,21,25H,7-10H2,1-2H3/t13-,15+,19?,20-/m1/s1

> <INCHI_KEY>
KTEDEOXQNICGRJ-LSTICJSWSA-N

> <FORMULA>
C20H22N2O4

> <MOLECULAR_WEIGHT>
354.406

> <EXACT_MASS>
354.157957196

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
36.99539178595156

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (11R,12R,17S)-12-acetyl-12-hydroxy-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>
0.487545865666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.004372416018427

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.382688649581954

> <JCHEM_PKA_STRONGEST_BASIC>
8.829471007187752

> <JCHEM_POLAR_SURFACE_AREA>
78.87

> <JCHEM_REFRACTIVITY>
97.72210000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (11R,12R,17S)-12-acetyl-12-hydroxy-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                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.759   7.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.762   5.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.097   4.932   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.429   5.705   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.100   3.392   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.601   2.616   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.019   3.280   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.114   2.191   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.653   2.232   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.458   0.919   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.724  -0.435   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.185  -0.476   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.379   0.837   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.743   0.963   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.107  -0.666   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.831  -1.608   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.508  -0.686   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.932  -0.284   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.495   1.319   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.119   0.629   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.546   2.532   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.979   2.316   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.122   3.960   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.599   2.609   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.336   1.729   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.283   0.580   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   24                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13    6   15   26                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21   24                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19    5   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   17   14                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂N₂O₄

Average Mass

354.4060 Da

Monoisotopic Mass

354.15796 Da

IUPAC Name

methyl (11R,12R,17S)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

Traditional Name

methyl (11R,12R,17S)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C2NC3=CC=CC=C3C22CCN3C[C@](O)([C@@H]1C[C@@H]23)C(C)=O

InChI Identifier

InChI=1S/C20H22N2O4/c1-11(23)20(25)10-22-8-7-19-12-5-3-4-6-14(12)21-17(19)16(18(24)26-2)13(20)9-15(19)22/h3-6,13,15,21,25H,7-10H2,1-2H3/t13-,15+,19?,20-/m1/s1

InChI Key

KTEDEOXQNICGRJ-LSTICJSWSA-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 angustifolia	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

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Carbazole
Indole or derivatives
Dihydroindole
Indolizidine
Aralkylamine
Secondary aliphatic/aromatic amine
Beta-aminoketone
Piperidine
Benzenoid
N-alkylpyrrolidine
Alpha-hydroxy ketone
Pyrrolidine
Vinylogous amide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Carboxylic acid ester
Ketone
Organoheterocyclic compound
Secondary amine
Carboxylic acid derivative
Enamine
Azacycle
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Carbonyl group
Alcohol
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Amine
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	0.49	ChemAxon
pKa (Strongest Acidic)	12.38	ChemAxon
pKa (Strongest Basic)	8.83	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	78.87 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	97.72 m³·mol⁻¹	ChemAxon
Polarizability	37 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00027061

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

101288221

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kam TS, Choo YM: Alkaloids from Alstonia angustifolia. Phytochemistry. 2004 Mar;65(5):603-8. doi: 10.1016/j.phytochem.2003.12.014. [PubMed:15003424 ]
LOTUS database [Link]

Showing NP-Card for methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0286673)

MOL for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D MOL for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D SDF for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D-SDF for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

PDB for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D PDB for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

SMILES for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

INCHI for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

Structure for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D Structure for NP0286673 (methyl (11r,12r,17s)-12-acetyl-12-hydroxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)