NP-MRD: Showing NP-Card for methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate (NP0199539)

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Record Information

Version

2.0

Created at

2022-09-04 18:12:02 UTC

Updated at

2022-09-04 18:12:02 UTC

NP-MRD ID

NP0199539

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate

Description

4429-63-4, Also known as tabersonine, belongs to the class of organic compounds known as plumeran-type alkaloids. These are alkaloids with a structure based on the plumeran skeleton. Plumeran is a pentacyclic compound that consists of a pyrrolidine ring shed to the quinoline moiety of pyrido[3,2-c]carbazole ring system. methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate is found in Catharanthus roseus, Rauvolfia serpentina and Tabernaemontana citrifolia. 4429-63-4 Is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201504592D          

 25 29  0  0  0  0            999 V2000
    0.1477    0.2147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9183    0.5096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5589   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6888    0.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4593    1.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0999    0.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9149    0.7076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2886   -0.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0853   -0.2423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2980   -1.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7140   -1.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9173   -1.4077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7047   -0.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9700   -0.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4885   -0.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0384   -1.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0695   -1.3449    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2990   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6584   -1.1198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7883   -0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1995   -0.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5892    1.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9486    2.4338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0785    3.2485    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  1  0  0  0  0
  4  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  2  0  0  0  0
  3 20  1  0  0  0  0
 17 21  1  0  0  0  0
  3 21  1  0  0  0  0
 14 21  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
    0.0712   -2.7727    2.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0850   -1.9358    1.3518 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7361   -1.6387   -0.1161 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7595   -2.9394   -0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2811   -3.5443   -1.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6005   -2.8464   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3915   -1.4636   -1.2523 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0023   -0.8277   -2.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5597    0.5415   -1.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5555    0.4869   -0.4455 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6299    1.1948    0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7983    0.5699   -0.1057 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0015    1.2340    0.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1443    0.6670    0.2229 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0229    2.4825    0.9105 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1537    3.1648    1.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8510   -0.7888   -0.7153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927    2.4427    0.5527 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2452    2.4513    0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1332    3.3999    0.9905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4856    3.1414    0.9269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9685    1.9557    0.4172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0506    1.0277   -0.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6945    1.2586    0.0171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5887   -0.9936   -0.1660 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6229   -3.3007    2.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7206   -2.1316    2.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4074   -3.5030    1.3782 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1535   -0.9575    1.9101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1121   -2.3731    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7224   -3.4442   -0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2659   -4.4963   -1.8626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3049   -3.2124   -2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0597   -3.1937   -0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8364   -0.7553   -3.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -1.3203   -2.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3556    1.2532   -2.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3905    0.8803   -2.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9766    3.2293    0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4946    2.8022    2.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8341    4.2316    1.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8000   -1.2615   -0.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074   -0.8272   -1.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8236    3.2119    0.8849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8265    4.3532    1.4034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2306    3.8637    1.2770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0479    1.7684    0.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4433    0.0905   -0.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1150   -1.1748    0.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3 17  1  0
 17 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 12 11  2  0
 11 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 10  1  0
 10  9  1  6
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  7 25  1  0
  4  3  1  0
 25  3  1  0
 10 11  1  0
 25 10  1  0
 24 19  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
 17 42  1  0
 17 43  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 18 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
  9 37  1  0
  9 38  1  0
  8 35  1  0
  8 36  1  0
  6 33  1  0
  6 34  1  0
  5 32  1  0
  4 31  1  0
 25 49  1  1
M  END


  Mrv1533004201504592D          

 25 29  0  0  0  0            999 V2000
    0.1477    0.2147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9183    0.5096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5589   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6888    0.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4593    1.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0999    0.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9149    0.7076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2886   -0.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0853   -0.2423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2980   -1.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7140   -1.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9173   -1.4077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7047   -0.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9700   -0.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4885   -0.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0384   -1.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0695   -1.3449    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2990   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6584   -1.1198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7883   -0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1995   -0.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5892    1.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9486    2.4338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0785    3.2485    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  1  0  0  0  0
  4  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  2  0  0  0  0
  3 20  1  0  0  0  0
 17 21  1  0  0  0  0
  3 21  1  0  0  0  0
 14 21  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC12CC(C(=O)OC)=C3NC4=CC=CC=C4C33CCN(CC=C1)C23

> <INCHI_IDENTIFIER>
InChI=1S/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3

> <INCHI_KEY>
FNGGIPWAZSFKCN-UHFFFAOYSA-N

> <FORMULA>
C21H24N2O2

> <MOLECULAR_WEIGHT>
336.435

> <EXACT_MASS>
336.183778021

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.330711806831545

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
2.5878174760000006

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.065459620419091

> <JCHEM_PKA_STRONGEST_BASIC>
9.083108599513523

> <JCHEM_POLAR_SURFACE_AREA>
41.57000000000001

> <JCHEM_REFRACTIVITY>
101.24779999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.90e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       0.276   0.401   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.714   0.951   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.910  -0.019   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.152   1.502   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.591   2.052   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.786   1.082   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.308   1.321   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.005  -0.052   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.493  -0.452   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.890  -1.940   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.799  -3.028   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.312  -2.628   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.915  -1.140   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.544  -0.439   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.512  -1.637   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.672  -2.928   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.863  -2.510   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       2.425  -3.061   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.229  -2.090   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.472  -0.570   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.106  -0.990   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.833   3.573   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.271   4.123   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.637   4.543   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.880   6.064   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20   21                                             
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
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   21                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    3                                                       
CONECT   21   17    3   14                                                  
CONECT   22    5   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Value	Source
Tabersonine	MeSH
Tabersonine monoacetate	MeSH

Chemical Formula

C₂₁H₂₄N₂O₂

Average Mass

336.4350 Da

Monoisotopic Mass

336.18378 Da

IUPAC Name

methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate

Traditional Name

methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate

CAS Registry Number

Not Available

SMILES

CCC12CC(C(=O)OC)=C3NC4=CC=CC=C4C33CCN(CC=C1)C23

InChI Identifier

InChI=1S/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3

InChI Key

FNGGIPWAZSFKCN-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
Catharanthus roseus	LOTUS Database	35616633
Rauvolfia serpentina	LOTUS Database	35616633
Tabernaemontana citrifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as plumeran-type alkaloids. These are alkaloids with a structure based on the plumeran skeleton. Plumeran is a pentacyclic compound that consists of a pyrrolidine ring shed to the quinoline moiety of pyrido[3,2-c]carbazole ring system.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Plumeran-type alkaloids

Sub Class

Not Available

Direct Parent

Plumeran-type alkaloids

Alternative Parents

Substituents

Plumeran-type alkaloid
Carbazole
Indole or derivatives
Dihydroindole
Secondary aliphatic/aromatic amine
Aralkylamine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Vinylogous amide
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Secondary amine
Enamine
Monocarboxylic acid or derivatives
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Amine
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	3.56	ALOGPS
logP	2.59	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	14.07	ChemAxon
pKa (Strongest Basic)	9.08	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	41.57 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	101.25 m³·mol⁻¹	ChemAxon
Polarizability	37.33 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

495253

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate (NP0199539)

MOL for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

3D MOL for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

3D SDF for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

3D-SDF for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

PDB for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

3D PDB for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

SMILES for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

INCHI for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

Structure for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)

3D Structure for NP0199539 (methyl 12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]nonadeca-2,4,6,9,13-pentaene-10-carboxylate)