NP-MRD: Showing NP-Card for Polyneurine E (NP0332061)

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Record Information

Version

1.0

Created at

2023-10-31 20:09:54 UTC

Updated at

2024-05-11 13:24:21 UTC

NP-MRD ID

NP0332061

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Polyneurine E

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 10312320092D          

 33 37  0  0  1  0            999 V2000
   -0.6427    0.9118    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1720    0.7820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1299   -0.0603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9911   -0.1073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5601   -0.8108    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052   -0.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3527    0.0024    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -1.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4337    0.7756    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2567    1.6451    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961    1.6048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4116    1.4369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1200    2.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9354    2.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    2.7670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8725    2.2598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    1.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9377    1.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5765    0.4275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1704   -0.1452    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8985    0.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6740   -0.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3056    0.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1618    1.3040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    1.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548    1.0550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2158    1.0381    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7764    0.0606    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7696   -0.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806   -1.1828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -2.0077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4278   -1.5153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9371    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  9  4  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 18 26  1  0  0  0  0
  9 27  1  1  0  0  0
  9 28  1  0  0  0  0
 28 19  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  2  0  0  0  0
 28 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END


  Mrv2104 10312320092D          

 33 37  0  0  1  0            999 V2000
   -0.6427    0.9118    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1720    0.7820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1299   -0.0603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9911   -0.1073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5601   -0.8108    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052   -0.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3527    0.0024    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -1.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4337    0.7756    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2567    1.6451    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961    1.6048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4116    1.4369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1200    2.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9354    2.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    2.7670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8725    2.2598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    1.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9377    1.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5765    0.4275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1704   -0.1452    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8985    0.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6740   -0.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3056    0.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1618    1.3040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    1.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548    1.0550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2158    1.0381    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7764    0.0606    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7696   -0.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806   -1.1828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -2.0077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4278   -1.5153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9371    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  9  4  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 18 26  1  0  0  0  0
  9 27  1  1  0  0  0
  9 28  1  0  0  0  0
 28 19  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  2  0  0  0  0
 28 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332061

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(C)[C@@]1([H])C[C@]2([H])C[C@@]3(C(=O)OC)C4=C(CCN([C@]2([H])CC=O)[C@@]13[H])C1=CC=CC=C1N4

> <INCHI_IDENTIFIER>
InChI=1S/C23H28N2O3/c1-3-14-12-15-13-23(22(27)28-2)20-17(16-6-4-5-7-18(16)24-20)8-10-25(21(14)23)19(15)9-11-26/h4-7,11,14-15,19,21,24H,3,8-10,12-13H2,1-2H3/t14-,15+,19+,21-,23+/m0/s1

> <INCHI_KEY>
GHHJOFLCEKAQTK-BBXHBCTKSA-N

> <FORMULA>
C23H28N2O3

> <MOLECULAR_WEIGHT>
380.488

> <EXACT_MASS>
380.20999277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.63782572173617

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,14R,15R,17S,18S)-17-ethyl-14-(2-oxoethyl)-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

> <JCHEM_LOGP>
3.1350155563333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
17.212143581483716

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.30946314907491

> <JCHEM_PKA_STRONGEST_BASIC>
8.085011500902127

> <JCHEM_POLAR_SURFACE_AREA>
62.4

> <JCHEM_REFRACTIVITY>
107.46730000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,14R,15R,17S,18S)-17-ethyl-14-(2-oxoethyl)-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-OCT-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-OCT-23         0                                  
HETATM    1  H   UNK     0      -1.200   1.702   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       0.321   1.460   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.242  -0.113   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.850  -0.200   0.000  0.00  0.00           C+0
HETATM    5  H   UNK     0       1.045  -1.513   0.000  0.00  0.00           H+0
HETATM    6  C   UNK     0       2.623  -1.532   0.000  0.00  0.00           C+0
HETATM    7  H   UNK     0       2.525   0.005   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0       1.856  -2.868   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.676   1.448   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       2.346   3.071   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       0.739   2.996   0.000  0.00  0.00           C+0
HETATM   12  H   UNK     0      -0.768   2.682   0.000  0.00  0.00           H+0
HETATM   13  C   UNK     0      -0.224   4.197   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.746   3.964   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.710   5.165   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.495   4.218   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.976   3.669   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.484   2.183   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.810   0.798   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       5.918  -0.271   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       7.277   0.453   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.725  -0.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.904   0.918   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.635   2.434   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.188   2.960   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.009   1.969   0.000  0.00  0.00           C+0
HETATM   27  H   UNK     0       4.136   1.938   0.000  0.00  0.00           H+0
HETATM   28  C   UNK     0       3.316   0.113   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.303  -1.427   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.631  -2.208   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.618  -3.748   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.665  -2.829   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.749   0.863   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11   33                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6    9                                             
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   27   28                                             
CONECT   10    9   11   16                                                  
CONECT   11   10    2   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   10   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21   18                                                  
CONECT   27    9                                                            
CONECT   28    9   19   29   33                                             
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29                                                            
CONECT   33   28    2                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₈N₂O₃

Average Mass

380.4880 Da

Monoisotopic Mass

380.20999 Da

IUPAC Name

methyl (1S,14R,15R,17S,18S)-17-ethyl-14-(2-oxoethyl)-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

Traditional Name

methyl (1S,14R,15R,17S,18S)-17-ethyl-14-(2-oxoethyl)-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

CAS Registry Number

Not Available

SMILES

[H]C(C)[C@@]1([H])C[C@]2([H])C[C@@]3(C(=O)OC)C4=C(CCN([C@]2([H])CC=O)[C@@]13[H])C1=CC=CC=C1N4

InChI Identifier

InChI=1S/C23H28N2O3/c1-3-14-12-15-13-23(22(27)28-2)20-17(16-6-4-5-7-18(16)24-20)8-10-25(21(14)23)19(15)9-11-26/h4-7,11,14-15,19,21,24H,3,8-10,12-13H2,1-2H3/t14-,15+,19+,21-,23+/m0/s1

InChI Key

GHHJOFLCEKAQTK-BBXHBCTKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D_DEPT NMR	¹³C NMR Spectrum (1D, 151 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-11	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 151 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2023-10-31	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
polyneura		Not Available

Chemical Taxonomy

Classification

Not classified

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	3.14	ChemAxon
pKa (Strongest Acidic)	16.31	ChemAxon
pKa (Strongest Basic)	8.09	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	62.4 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	107.47 m³·mol⁻¹	ChemAxon
Polarizability	42.64 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

Not Available

References

General References

Tang SY, Tan CH, Sim KS, Yong KT, Lim KH, Low YY, Lim SH: Polyneurines A-H, iboga alkaloids from Tabernaemontana polyneura. Phytochemistry. 2023 Apr;208:113587. doi: 10.1016/j.phytochem.2023.113587. Epub 2023 Jan 14. [PubMed:36646163 ]

Showing NP-Card for Polyneurine E (NP0332061)

MOL for NP0332061 (Polyneurine E)

3D MOL for NP0332061 (Polyneurine E)

3D SDF for NP0332061 (Polyneurine E)

3D-SDF for NP0332061 (Polyneurine E)

PDB for NP0332061 (Polyneurine E)

3D PDB for NP0332061 (Polyneurine E)

SMILES for NP0332061 (Polyneurine E)

INCHI for NP0332061 (Polyneurine E)

Structure for NP0332061 (Polyneurine E)

3D Structure for NP0332061 (Polyneurine E)