NP-MRD: Showing NP-Card for Scholaricine (NP0137339)

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Record Information

Version

2.0

Created at

2022-05-30 16:49:26 UTC

Updated at

2022-05-30 16:49:26 UTC

NP-MRD ID

NP0137339

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Scholaricine

Description

Methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2(7),3,5,9-tetraene-10-carboxylate 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. Scholaricine is found in Alstonia scholaris. Methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2(7),3,5,9-tetraene-10-carboxylate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171508102D          

 26 30  0  0  0  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
    5.5646    1.9207    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
   -0.0039    0.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2497    1.6750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  0  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  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  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
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 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  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  0  0  0  0
 18 26  1  0  0  0  0
M  END

     RDKit          3D

 50 54  0  0  0  0  0  0  0  0999 V2000
   -1.0578    4.4950    1.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3949    3.3247    1.1345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1266    2.4585    0.3119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3044    2.7629    0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5565    1.2318   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6976    0.8586    0.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8271    1.6115    0.4500 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9821    0.7932    0.3940 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974    1.1707    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119    2.4539    1.0038 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2763    0.2246    0.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9413   -1.0483   -0.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6290   -1.4025   -0.2033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6082   -0.4513    0.0034 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450   -0.5313   -0.0380 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7162   -1.3752    1.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0482   -2.5801    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2411   -2.3274   -0.7956 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6377   -2.1100   -0.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0546   -0.7442   -0.3500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -0.6925   -0.6140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2379   -1.8795    0.0749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1687    0.4591   -0.1781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3318    0.3314   -1.0660 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2906   -0.2525   -2.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5578   -1.2242   -1.2269 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7438    4.8566    0.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7091    4.3196    2.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3470    5.3365    1.7394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8010    2.6414    0.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8758    3.1209    1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3327    0.4897    0.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7122   -1.7788   -0.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2949   -2.3747   -0.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6244   -1.7317    1.6839 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1310   -0.8050    1.8913 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6447   -3.5035    0.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927   -2.7616    1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9972   -2.0869   -1.9992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1676   -2.9239   -0.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9391   -0.7304    0.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6876   -0.7662   -1.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2600   -1.6093    0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3852   -2.7196   -0.6329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5971   -2.2426    0.8999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9799    0.6165   -0.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0641    0.8943   -1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7530   -0.7500   -2.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860    0.5621   -2.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3574   -1.6102   -1.8813 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
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  1
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 20 24  1  0
 24 25  1  0
 25 26  1  0
 24  5  1  0
 15  6  1  0
 26 15  1  0
 14  8  1  0
 26 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  7 30  1  0
 10 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  0
 16 35  1  0
 16 36  1  0
 17 37  1  0
 17 38  1  0
 19 39  1  0
 19 40  1  0
 20 41  1  1
 21 42  1  6
 22 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  6
 25 48  1  0
 25 49  1  0
 26 50  1  6
M  END


  Mrv1533004171508102D          

 26 30  0  0  0  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
    5.5646    1.9207    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
   -0.0039    0.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2497    1.6750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  0  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  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  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
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 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  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  0  0  0  0
 18 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137339

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C2NC3=C(O)C=CC=C3C22CCN3CC(C(C)O)C1CC23

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N2O4/c1-10(23)12-9-22-7-6-20-13-4-3-5-14(24)17(13)21-18(20)16(19(25)26-2)11(12)8-15(20)22/h3-5,10-12,15,21,23-24H,6-9H2,1-2H3

> <INCHI_KEY>
GNCUCBQZLQLSOF-UHFFFAOYSA-N

> <FORMULA>
C20H24N2O4

> <MOLECULAR_WEIGHT>
356.422

> <EXACT_MASS>
356.173607261

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
38.110053301294975

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

> <ALOGPS_LOGP>
1.94

> <JCHEM_LOGP>
-0.03663980511035001

> <ALOGPS_LOGS>
-2.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.858540651070001

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.99468236703362

> <JCHEM_PKA_STRONGEST_BASIC>
9.359215179526664

> <JCHEM_POLAR_SURFACE_AREA>
82.03

> <JCHEM_REFRACTIVITY>
99.4633

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.28e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         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  O   UNK     0      10.387   3.585   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.458   0.919   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.724  -0.435   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.185  -0.476   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.379   0.837   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.743   0.963   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.107  -0.666   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.831  -1.608   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       3.508  -0.686   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       1.932  -0.284   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.495   1.319   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.007   1.657   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.051   0.524   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.466   3.127   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   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    6   16   26                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   20    5   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   15   18                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0,.0,.0,]octadeca-2(7),3,5,9-tetraene-10-carboxylic acid	Generator

Chemical Formula

C₂₀H₂₄N₂O₄

Average Mass

356.4220 Da

Monoisotopic Mass

356.17361 Da

IUPAC Name

methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

Traditional Name

methyl 6-hydroxy-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C2NC3=C(O)C=CC=C3C22CCN3CC(C(C)O)C1CC23

InChI Identifier

InChI=1S/C20H24N2O4/c1-10(23)12-9-22-7-6-20-13-4-3-5-14(24)17(13)21-18(20)16(19(25)26-2)11(12)8-15(20)22/h3-5,10-12,15,21,23-24H,6-9H2,1-2H3

InChI Key

GNCUCBQZLQLSOF-UHFFFAOYSA-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 Alstonia scholaris	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
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Secondary aliphatic/aromatic amine
Piperidine
Benzenoid
N-alkylpyrrolidine
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Vinylogous amide
Methyl ester
Pyrrolidine
1,3-aminoalcohol
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Secondary alcohol
Carboxylic acid ester
Secondary amine
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Enamine
Monocarboxylic acid or derivatives
Amine
Alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.94	ALOGPS
logP	-0.037	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.99	ChemAxon
pKa (Strongest Basic)	9.36	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	82.03 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	99.46 m³·mol⁻¹	ChemAxon
Polarizability	38.11 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

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

14707744

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Scholaricine (NP0137339)

MOL for NP0137339 (Scholaricine)

3D MOL for NP0137339 (Scholaricine)

3D SDF for NP0137339 (Scholaricine)

3D-SDF for NP0137339 (Scholaricine)

PDB for NP0137339 (Scholaricine)

3D PDB for NP0137339 (Scholaricine)

SMILES for NP0137339 (Scholaricine)

INCHI for NP0137339 (Scholaricine)

Structure for NP0137339 (Scholaricine)

3D Structure for NP0137339 (Scholaricine)