NP-MRD: Showing NP-Card for (13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one (NP0251484)

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Record Information

Version

2.0

Created at

2022-09-07 14:41:53 UTC

Updated at

2022-09-07 14:41:54 UTC

NP-MRD ID

NP0251484

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one

Description

Tacamonidine belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17. (13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one is found in Tabernaemontana corymbosa. (13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one was first documented in 2015 (PMID: 25919190). Based on a literature review very few articles have been published on Tacamonidine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -5.0169   -0.9526    0.3574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2090   -0.0116   -0.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8947    0.2731    0.1796 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1590    0.8634    1.4110 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0572    1.2335   -0.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8130    1.5219    0.1996 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0020    2.5037   -0.5955 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508    2.4398   -0.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2196    3.4479   -0.3043 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0466    1.1533   -0.2588 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2700    0.1880    0.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9885   -0.9585    0.2789 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2398   -0.7244   -0.1929 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3667   -1.4899   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5303   -0.9291   -0.8987 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5043    0.4176   -1.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3889    1.2195   -1.0491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2574    0.6295   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3365   -2.1932    0.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1404   -2.0953    0.8511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7605   -0.9176    0.4090 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1406   -0.9973    0.2922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1289    0.3118    0.6767 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7234   -2.0178    0.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0922   -0.8825    0.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8531   -0.7422    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8159    0.9035   -0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0165   -0.5545   -1.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4583    1.7793    1.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8122    0.8505   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6249    2.1819   -0.7081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2275    2.1224    1.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3053    3.5689   -0.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2423    2.4127   -1.6979 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -2.5405   -0.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4003   -1.5427   -1.0353 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4024    0.8451   -1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3553    2.2594   -1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6808   -3.0199    0.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639   -2.4572    1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4846   -2.3051    1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5718   -2.9553    0.2580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5636   -1.5822    1.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4062   -1.6289   -0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0684    0.3720    1.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  1
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 23  1  0
 23 21  1  0
 21 20  1  0
 20 19  1  0
 21 22  1  0
 22  3  1  0
 23  6  1  0
 11 10  1  0
 13 18  1  0
 19 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 17 38  1  0
 16 37  1  0
 15 36  1  0
 14 35  1  0
 23 45  1  1
 20 41  1  0
 20 42  1  0
 19 39  1  0
 19 40  1  0
 22 43  1  0
 22 44  1  0
M  END


  Mrv1652309072216412D          

 23 27  0  0  1  0            999 V2000
   -0.0994    0.5327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6585    0.8587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3198    0.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7191   -0.2002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6908    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5144    1.1494    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8854    1.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7091    1.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0801    2.6703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1617    1.2437    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2434   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0392    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7333   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4665   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5058    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8117    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0784    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8724   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0487   -0.9670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5961   -0.2772    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7724   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9671    0.4596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  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  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 10 18  1  0  0  0  0
 12 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
  3 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 11  1  6  0  0  0
  6 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251484

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@]1(O)C[C@@H]2CC(=O)N3C4=CC=CC=C4C4=C3[C@@H]2N(CC4)C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O2/c1-2-19(23)10-12-9-16(22)21-15-6-4-3-5-13(15)14-7-8-20(11-19)17(12)18(14)21/h3-6,12,17,23H,2,7-11H2,1H3/t12-,17+,19-/m0/s1

> <INCHI_KEY>
AEVSWHAHLKOISK-WILYLXEWSA-N

> <FORMULA>
C19H22N2O2

> <MOLECULAR_WEIGHT>
310.397

> <EXACT_MASS>
310.168127956

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.44662728577187

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(13S,15R,19R)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

> <JCHEM_LOGP>
1.6440774139999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.771943048055345

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.407317566263995

> <JCHEM_PKA_STRONGEST_BASIC>
6.340095661435357

> <JCHEM_POLAR_SURFACE_AREA>
45.47

> <JCHEM_REFRACTIVITY>
88.57480000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(13S,15R,19R)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.185   0.994   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.229   1.603   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.464   0.682   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.342  -0.374   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.156   2.057   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.694   2.146   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.386   3.521   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.924   3.609   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.616   4.985   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       7.769   2.322   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       7.076   0.946   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.921  -0.341   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.407   0.064   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.702  -0.768   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.071  -0.063   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.144   1.476   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.849   2.308   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.480   1.603   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.228  -1.717   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.691  -1.805   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       4.846  -0.517   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.309  -0.606   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.539   0.858   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   22                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12   23                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13   10                                                  
CONECT   19   12   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21    3                                                       
CONECT   23   21   11    6                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂N₂O₂

Average Mass

310.3970 Da

Monoisotopic Mass

310.16813 Da

IUPAC Name

(13S,15R,19R)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

Traditional Name

(13S,15R,19R)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

CAS Registry Number

Not Available

SMILES

CC[C@]1(O)C[C@@H]2CC(=O)N3C4=CC=CC=C4C4=C3[C@@H]2N(CC4)C1

InChI Identifier

InChI=1S/C19H22N2O2/c1-2-19(23)10-12-9-16(22)21-15-6-4-3-5-13(15)14-7-8-20(11-19)17(12)18(14)21/h3-6,12,17,23H,2,7-11H2,1H3/t12-,17+,19-/m0/s1

InChI Key

AEVSWHAHLKOISK-WILYLXEWSA-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
Tabernaemontana corymbosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tacaman alkaloids

Sub Class

Not Available

Direct Parent

Tacaman alkaloids

Alternative Parents

Substituents

Tacaman alkaloid
Indolo[3,2-1de][1,5]naphthyridine
Beta-carboline
Pyridoindole
Diazanaphthalene
Naphthyridine
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
Piperidine
Benzenoid
Heteroaromatic compound
Pyrrole
Tertiary alcohol
1,2-aminoalcohol
Lactam
Tertiary amine
Tertiary aliphatic amine
Azacycle
Organoheterocyclic compound
Amine
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen 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	1.64	ChemAxon
pKa (Strongest Acidic)	14.41	ChemAxon
pKa (Strongest Basic)	6.34	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.47 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.57 m³·mol⁻¹	ChemAxon
Polarizability	34.45 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

59006980

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122179181

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lim KH, Raja VJ, Bradshaw TD, Lim SH, Low YY, Kam TS: Ibogan, tacaman, and cytotoxic bisindole alkaloids from tabernaemontana. Cononusine, an iboga alkaloid with unusual incorporation of a pyrrolidone moiety. J Nat Prod. 2015 May 22;78(5):1129-38. doi: 10.1021/acs.jnatprod.5b00117. Epub 2015 Apr 28. [PubMed:25919190 ]
LOTUS database [Link]

Showing NP-Card for (13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one (NP0251484)

MOL for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

3D MOL for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

3D SDF for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

3D-SDF for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

PDB for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

3D PDB for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

SMILES for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

INCHI for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

Structure for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)

3D Structure for NP0251484 ((13s,15r,19r)-13-ethyl-13-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]nonadeca-2,4,6,8(18)-tetraen-17-one)