NP-MRD: Showing NP-Card for 12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one (NP0310299)

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Record Information

Version

2.0

Created at

2022-09-11 05:31:20 UTC

Updated at

2022-09-11 05:31:20 UTC

NP-MRD ID

NP0310299

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one

Description

12-Ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]Nonadeca-1(18),2,4,6,8-pentaen-17-one belongs to the class of organic compounds known as rhazinilam alkaloids. These are alkaloids with a structure based on the rhazinilam skeleton, a tetracyclic compound with a complex tetracyclic carbon skeleton containing pyrrole ring embedded in its indolizine core. 12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one is found in Alstonia scholaris, Kopsia griffithii and Kopsia singapurensis. 12-Ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]Nonadeca-1(18),2,4,6,8-pentaen-17-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161503502D          

 24 27  0  0  0  0            999 V2000
    1.8692   -2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255   -1.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0031   -0.9818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2845   -1.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984   -0.4567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326    0.2975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9530    0.3852    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367    1.0535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804    1.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2218    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2232   -0.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9887   -0.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    0.3677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2492    0.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6378   -0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2018   -1.0878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3773   -1.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2072   -1.8678    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5580   -2.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8143   -3.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7334   -2.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194   -1.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4391   -0.2814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481   -0.9306    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  1  0  0  0  0
  4  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  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 11 23  1  0  0  0  0
  3 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -2.3296    0.5120    1.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3597    1.0869    0.9705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2162    0.2262   -0.2479 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5572    0.0044   -0.9230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2656   -1.2577   -0.7210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3929   -2.4356   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0496   -2.0375   -0.7236 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1473   -2.4435   -1.6958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3642   -3.2384   -2.6959 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1252   -1.8163   -1.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9868   -1.0335   -0.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1571   -0.2892    0.2367 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2474   -1.1926    0.5465 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4167   -0.8291    1.1120 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5838    0.4930    1.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5848    1.3679    1.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3229    1.0279    0.5329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255    2.1891    0.3760 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8199    2.8378   -0.6325 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2164    4.0042   -1.0997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4375    2.3955   -1.3403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4161    0.9328   -1.3046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4270   -1.0149    0.0743 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6688   -1.3376    1.3966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7711   -0.4351    1.7323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8918    0.4153    3.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2050    1.2156    2.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6724    2.1216    0.8012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3824    1.0004    1.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2251    0.8307   -0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5279    0.2340   -2.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1679   -1.1946   -0.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7657   -1.5834   -1.6896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6823   -3.3649   -0.9346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544   -2.6910    0.7156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9886   -2.0194   -2.0378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1409   -2.2649    0.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2198   -1.5043    1.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5107    0.8553    1.8782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7937    2.4090    1.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233    2.8040    1.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3741    2.7755   -2.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2666    2.9417   -0.9227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7836    0.5997   -2.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6448    0.5372   -1.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0936   -1.8345    1.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 11 23  1  0
 23 24  1  1
 22  3  1  0
 23  3  1  0
 23  7  1  0
 17 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
 10 36  1  0
 13 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 18 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 22 45  1  0
 24 46  1  0
M  END


  Mrv1533004161503502D          

 24 27  0  0  0  0            999 V2000
    1.8692   -2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255   -1.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0031   -0.9818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2845   -1.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984   -0.4567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326    0.2975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9530    0.3852    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367    1.0535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804    1.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2218    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2232   -0.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9887   -0.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    0.3677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2492    0.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6378   -0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2018   -1.0878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3773   -1.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2072   -1.8678    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5580   -2.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8143   -3.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7334   -2.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194   -1.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4391   -0.2814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481   -0.9306    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  1  0  0  0  0
  4  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  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 11 23  1  0  0  0  0
  3 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0310299

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC12CCCN3C(=O)C=C(C4=CC=CC=C4NC(=O)CC1)C23O

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O3/c1-2-18-9-5-11-21-17(23)12-14(19(18,21)24)13-6-3-4-7-15(13)20-16(22)8-10-18/h3-4,6-7,12,24H,2,5,8-11H2,1H3,(H,20,22)

> <INCHI_KEY>
OXDBJKLQCGAPQX-UHFFFAOYSA-N

> <FORMULA>
C19H22N2O3

> <MOLECULAR_WEIGHT>
326.396

> <EXACT_MASS>
326.163042576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.633378583325765

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-ethyl-19-hydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6-tetraene-9,17-dione

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
2.2516394426666677

> <ALOGPS_LOGS>
-2.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.531920395833474

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.03404070388259

> <JCHEM_PKA_STRONGEST_BASIC>
-0.45094219541009195

> <JCHEM_POLAR_SURFACE_AREA>
69.64

> <JCHEM_REFRACTIVITY>
92.30779999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.28e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-ethyl-19-hydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6-tetraene-9,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       3.489  -4.488   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.848  -3.088   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.739  -1.833   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.398  -2.097   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.490  -0.853   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.114   0.555   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       3.646   0.719   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       4.548   1.967   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.070   3.430   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.014   1.493   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.017  -0.047   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.446  -0.621   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.259   0.686   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.798   0.635   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.524  -0.723   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.710  -2.031   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.171  -1.980   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       7.853  -3.486   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       6.642  -4.437   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.120  -5.901   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.102  -4.386   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.956  -3.357   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.553  -0.525   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.503  -1.737   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22   23                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    3                                                       
CONECT   23   11    3    7   24                                             
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
Leuconolam sesquihydrate	MeSH
8a-Ethyl-7,8,8a,10,11,12a-hexahydro-12a-hydroxyindolizino(8,1-ef)(1)benzazonine-6,13-(5H,9H)-dione	MeSH

Chemical Formula

C₁₉H₂₂N₂O₃

Average Mass

326.3960 Da

Monoisotopic Mass

326.16304 Da

IUPAC Name

12-ethyl-19-hydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6-tetraene-9,17-dione

Traditional Name

12-ethyl-19-hydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6-tetraene-9,17-dione

CAS Registry Number

Not Available

SMILES

CCC12CCCN3C(=O)C=C(C4=CC=CC=C4NC(=O)CC1)C23O

InChI Identifier

InChI=1S/C19H22N2O3/c1-2-18-9-5-11-21-17(23)12-14(19(18,21)24)13-6-3-4-7-15(13)20-16(22)8-10-18/h3-4,6-7,12,24H,2,5,8-11H2,1H3,(H,20,22)

InChI Key

OXDBJKLQCGAPQX-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
Kopsia griffithii	LOTUS Database	35616633
Kopsia singapurensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rhazinilam alkaloids. These are alkaloids with a structure based on the rhazinilam skeleton, a tetracyclic compound with a complex tetracyclic carbon skeleton containing pyrrole ring embedded in its indolizine core.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Rhazinilam alkaloids

Sub Class

Not Available

Direct Parent

Rhazinilam alkaloids

Alternative Parents

Substituents

Rhazinilam skeleton
Piperidine
Benzenoid
Pyrroline
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Alkanolamine
Organoheterocyclic compound
Azacycle
Organic oxide
Carbonyl group
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.63	ALOGPS
logP	2.25	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	12.03	ChemAxon
pKa (Strongest Basic)	-0.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	69.64 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.31 m³·mol⁻¹	ChemAxon
Polarizability	34.63 Å³	ChemAxon
Number of Rings	4	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

125060

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one (NP0310299)

MOL for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

3D MOL for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

3D SDF for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

3D-SDF for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

PDB for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

3D PDB for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

SMILES for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

INCHI for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

Structure for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)

3D Structure for NP0310299 (12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one)