NP-MRD: Showing NP-Card for (+)-Leueantine B (NP0079984)

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Record Information

Version

1.0

Created at

2022-04-29 01:02:33 UTC

Updated at

2022-04-29 01:02:33 UTC

NP-MRD ID

NP0079984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Leueantine B

Description

(1S,2R,3R,4S,5R,6S,8S,9R,10R,13S,16S,17R,18S)-4-(acetyloxy)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-8-yl (2E)-3-phenylprop-2-enoate belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom. (+)-Leueantine B is found in Aconitum hemsleyanum and Aconitum hemsleyanum var.leucanthus. Based on a literature review very few articles have been published on (1S,2R,3R,4S,5R,6S,8S,9R,10R,13S,16S,17R,18S)-4-(acetyloxy)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-8-yl (2E)-3-phenylprop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203022D          

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M  END

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M  END


  Mrv1652304292203022D          

 45 51  0  0  1  0            999 V2000
   -0.3558   -0.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9140   -0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6138   -1.7742    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2009   -1.7085    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8077   -1.4449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4745   -0.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2245    0.2906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1942    1.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -0.7834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0963   -1.1216    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3031   -1.9438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1388   -1.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5372   -1.1688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9980   -0.4617    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5019   -0.2213    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7884    0.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2158    1.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8080    2.0836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0408    1.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9961   -0.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4310   -1.0622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8505   -0.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5610   -2.4846    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9650   -2.4748    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2896   -2.9691    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5425   -3.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3027   -4.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5578   -2.6212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5081   -2.5591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0813   -3.4517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9459   -3.7971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6390   -2.8057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693   -3.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0832   -4.1979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0584   -3.1534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2444   -2.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0335   -2.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2196   -1.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0087   -1.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6117   -1.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4257   -2.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6366   -2.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5473   -1.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2340   -1.2209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9965   -1.5360    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  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  5  9  1  1  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  6  0  0  0
  9 20  1  6  0  0  0
 13 21  1  1  0  0  0
 21 22  1  0  0  0  0
 11 23  1  0  0  0  0
 23 24  1  6  0  0  0
  5 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
  3 28  1  0  0  0  0
 23 29  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 11 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 37 42  1  0  0  0  0
  3 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0079984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1C[C@]2(COC)CC[C@H](OC)[C@@]34[C@@H]5C[C@H]6[C@H](OC(C)=O)[C@@H]5[C@](C[C@@H]6OC)(OC(=O)\C=C\C5=CC=CC=C5)[C@@H]([C@@H](OC)[C@H]23)[C@@H]14

> <INCHI_IDENTIFIER>
InChI=1S/C36H49NO8/c1-7-37-19-34(20-40-3)16-15-26(42-5)36-24-17-23-25(41-4)18-35(28(24)30(23)44-21(2)38,29(33(36)37)31(43-6)32(34)36)45-27(39)14-13-22-11-9-8-10-12-22/h8-14,23-26,28-33H,7,15-20H2,1-6H3/b14-13+/t23-,24-,25+,26+,28-,29+,30+,31-,32-,33-,34+,35+,36+/m1/s1

> <INCHI_KEY>
PTWXOFVEMDDRDD-IGNBUWPESA-N

> <FORMULA>
C36H49NO8

> <MOLECULAR_WEIGHT>
623.787

> <EXACT_MASS>
623.345817542

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -0.664  -0.649   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.706  -1.817   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.146  -3.312   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.375  -3.189   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.508  -2.697   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.886  -1.083   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.419   0.542   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.363   2.164   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.702  -1.462   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.913  -2.094   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.299  -3.628   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.859  -3.569   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.603  -2.182   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.596  -0.862   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.670  -0.413   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.205   1.190   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.003   2.551   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.242   3.889   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.543   2.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.726  -0.065   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.271  -1.983   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.054  -0.546   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.914  -4.638   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.801  -4.620   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       0.541  -5.542   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       1.013  -7.197   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.432  -8.138   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.041  -4.893   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.949  -4.777   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.152  -6.443   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.766  -7.088   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.926  -5.237   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.103  -6.336   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.755  -7.836   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       7.576  -5.886   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.923  -4.386   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.396  -3.937   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.743  -2.436   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.216  -1.987   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.342  -3.038   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.995  -4.538   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.522  -4.988   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -2.888  -3.264   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -4.170  -2.279   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -5.593  -2.867   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   28   43                                             
CONECT    4    3    5   29                                                  
CONECT    5    4    6    9   24                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10   20                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12   23   32                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   10   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14    9                                                       
CONECT   21   13   22                                                       
CONECT   22   21                                                            
CONECT   23   11   24   29                                                  
CONECT   24   23    5   25                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25    3                                                       
CONECT   29   23    4   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   11   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   37                                                       
CONECT   43    3   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3R,4S,5R,6S,8S,9R,10R,13S,16S,17R,18S)-4-(Acetyloxy)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1,.0,.0,.0,]nonadecan-8-yl (2E)-3-phenylprop-2-enoic acid	Generator

Chemical Formula

C₃₆H₄₉NO₈

Average Mass

623.7870 Da

Monoisotopic Mass

623.34582 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCN1C[C@]2(COC)CC[C@H](OC)[C@@]34[C@@H]5C[C@H]6[C@H](OC(C)=O)[C@@H]5[C@](C[C@@H]6OC)(OC(=O)\C=C\C5=CC=CC=C5)[C@@H]([C@@H](OC)[C@H]23)[C@@H]14

InChI Identifier

InChI=1S/C36H49NO8/c1-7-37-19-34(20-40-3)16-15-26(42-5)36-24-17-23-25(41-4)18-35(28(24)30(23)44-21(2)38,29(33(36)37)31(43-6)32(34)36)45-27(39)14-13-22-11-9-8-10-12-22/h8-14,23-26,28-33H,7,15-20H2,1-6H3/b14-13+/t23-,24-,25+,26+,28-,29+,30+,31-,32-,33-,34+,35+,36+/m1/s1

InChI Key

PTWXOFVEMDDRDD-IGNBUWPESA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aconitum hemsleyanum	LOTUS Database	35616633
Aconitum hemsleyanum var.leucanthus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Aconitane-type diterpenoid alkaloids

Alternative Parents

Substituents

Aconitane-type diterpenoid alkaloid
Cinnamic acid ester
Cinnamic acid or derivatives
Quinolidine
Alkaloid or derivatives
Styrene
Fatty acid ester
Azepane
Fatty acyl
Benzenoid
Piperidine
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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

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

162872160

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Leueantine B (NP0079984)

MOL for NP0079984 ((+)-Leueantine B)

3D MOL for NP0079984 ((+)-Leueantine B)

3D SDF for NP0079984 ((+)-Leueantine B)

3D-SDF for NP0079984 ((+)-Leueantine B)

PDB for NP0079984 ((+)-Leueantine B)

3D PDB for NP0079984 ((+)-Leueantine B)

SMILES for NP0079984 ((+)-Leueantine B)

INCHI for NP0079984 ((+)-Leueantine B)

Structure for NP0079984 ((+)-Leueantine B)

3D Structure for NP0079984 ((+)-Leueantine B)