NP-MRD: Showing NP-Card for Embellicine E (NP0331527)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2023-03-08 00:19:04 UTC

Updated at

2024-04-19 10:11:39 UTC

NP-MRD ID

NP0331527

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Embellicine E

Description

CHEMBL56717 belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group. Based on a literature review very few articles have been published on CHEMBL56717.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309282217262D          

 31 34  0  0  1  0            999 V2000
    6.3618   -0.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9909    0.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1672    0.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7145   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962    1.1022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2489    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8779    2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3305    3.2186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9595    3.9554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0542    2.5760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0725    1.7448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4435    1.0079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2672    0.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199    0.4596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8909   -0.2772    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    4.2619   -1.0141    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.4382   -0.9670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6146   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1489    1.1965    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6962    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4477    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7929   -1.2356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5262   -1.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4085    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1801    1.1504    0.0000 N   0  0  0  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  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  6 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 20  1  1  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 22  1  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  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 21 31  1  0  0  0  0
M  CHG  2  16   1  17  -1
M  END


  Mrv1652309282217262D          

 31 34  0  0  1  0            999 V2000
    6.3618   -0.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9909    0.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1672    0.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7145   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962    1.1022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2489    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8779    2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3305    3.2186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9595    3.9554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0542    2.5760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0725    1.7448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4435    1.0079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2672    0.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199    0.4596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8909   -0.2772    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    4.2619   -1.0141    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.4382   -0.9670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6146   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1489    1.1965    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6962    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4477    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7929   -1.2356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5262   -1.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4085    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1801    1.1504    0.0000 N   0  0  0  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  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  6 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 20  1  1  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 22  1  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  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 21 31  1  0  0  0  0
M  CHG  2  16   1  17  -1
M  END
> <DATABASE_ID>
NP0331527

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@@H]([C@H](CC)C[N+]1([O-])CCC1=C2NC2=CC=CC(OC)=C12)C(=C/OC)\C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H30N2O5/c1-5-14-12-25(27)10-9-15-21-18(7-6-8-20(21)29-3)24-22(15)19(25)11-16(14)17(13-28-2)23(26)30-4/h6-8,13-14,16,19,24H,5,9-12H2,1-4H3/b17-13+/t14-,16+,19+,25?/m1/s1

> <INCHI_KEY>
KXNRITUKNSFMGJ-CUKABGIGSA-N

> <FORMULA>
C23H30N2O5

> <MOLECULAR_WEIGHT>
414.502

> <EXACT_MASS>
414.215472074

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.23414865410081

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,12bS)-2-[(1E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-methoxy-1H,2H,3H,4H,5H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-5-ium-5-olate

> <ALOGPS_LOGP>
2.62

> <JCHEM_LOGP>
2.175218403333332

> <ALOGPS_LOGS>
-5.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.24989171243993

> <JCHEM_PKA_STRONGEST_BASIC>
3.2275381583195775

> <JCHEM_POLAR_SURFACE_AREA>
83.61000000000001

> <JCHEM_REFRACTIVITY>
114.9581

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,12bS)-2-[(1E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-methoxy-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-5-ium-5-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-SEP-22         0                                  
HETATM    1  C   UNK     0      11.875  -0.782   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.183   0.594   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.645   0.682   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.800  -0.606   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.953   2.057   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.798   3.345   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.105   4.720   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.950   6.008   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.258   7.383   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.568   4.809   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.335   3.257   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.028   1.881   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.565   1.793   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.415   2.146   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.570   0.858   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       7.263  -0.517   0.000  0.00  0.00           N+1
HETATM   17  O   UNK     0       7.956  -1.893   0.000  0.00  0.00           O-1
HETATM   18  C   UNK     0       6.418  -1.805   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.881  -1.717   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       5.878   2.234   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0       5.033   0.946   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.188  -0.341   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.702   0.064   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.407  -0.768   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.480  -2.307   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.849  -3.012   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.038  -0.063   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.035   1.476   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.260   2.308   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.629   1.603   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       4.070   2.147   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3   16                                                       
CONECT    5    3    6   14                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    5   15                                                       
CONECT   15   14   16   20   21                                             
CONECT   16   15    4   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   22                                                       
CONECT   20   15                                                            
CONECT   21   15   22   31                                                  
CONECT   22   21   19   23                                                  
CONECT   23   22   24   30                                                  
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   23   31                                                  
CONECT   31   30   21                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₄₅NO₅

Average Mass

559.7470 Da

Monoisotopic Mass

559.32977 Da

IUPAC Name

(2S,3S,12bS)-2-[(1E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-methoxy-1H,2H,3H,4H,5H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-5-ium-5-olate

Traditional Name

(2S,3S,12bS)-2-[(1E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-methoxy-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-5-ium-5-olate

CAS Registry Number

Not Available

SMILES

[H][C@@]12C[C@H](C)C[C@H](C)[C@@]1([H])[C@H]1OC3=CC=C(C[C@]4(O)NC(=O)\C([C@H]4OC)=C(O)\[C@H]4[C@]1([H])[C@]2([H])C(C)=C1[C@H](C)C(C)=C[C@@]41C)C=C3

InChI Identifier

InChI=1S/C35H45NO5/c1-16-12-17(2)24-23(13-16)25-20(5)28-19(4)18(3)14-34(28,6)29-26(25)31(24)41-22-10-8-21(9-11-22)15-35(39)32(40-7)27(30(29)37)33(38)36-35/h8-11,14,16-17,19,23-26,29,31-32,37,39H,12-13,15H2,1-7H3,(H,36,38)/b30-27-/t16-,17+,19-,23-,24-,25-,26+,29-,31-,32-,34-,35-/m1/s1

InChI Key

GLTWXUDIIDOBCT-NBNWVARQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2024-02-26	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2024-02-26	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Corynanthean-type alkaloids

Sub Class

Not Available

Direct Parent

Corynanthean-type alkaloids

Alternative Parents

Substituents

Corynanthean skeleton
Pyridoindole
Beta-carboline
Quinolizine
3-alkylindole
Indole or derivatives
Indole
Phenol ether
Anisole
Alkyl aryl ether
Benzenoid
Piperidine
Pyrrole
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Trialkyl amine oxide
Methyl ester
Heteroaromatic compound
Carboxylic acid ester
N-oxide
Carboxylic acid derivative
Azacycle
Ether
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Trisubstituted n-oxide
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organic salt
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic zwitterion
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	2.62	ALOGPS
logP	2.18	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	14.25	ChemAxon
pKa (Strongest Basic)	3.23	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.61 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	114.96 m³·mol⁻¹	ChemAxon
Polarizability	46.23 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	Yes	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

9233918

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11058760

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Embellicine E (NP0331527)

MOL for NP0331527 (Embellicine E)

3D MOL for NP0331527 (Embellicine E)

3D SDF for NP0331527 (Embellicine E)

3D-SDF for NP0331527 (Embellicine E)

PDB for NP0331527 (Embellicine E)

3D PDB for NP0331527 (Embellicine E)

SMILES for NP0331527 (Embellicine E)

INCHI for NP0331527 (Embellicine E)

Structure for NP0331527 (Embellicine E)

3D Structure for NP0331527 (Embellicine E)