NP-MRD: Showing NP-Card for (1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one (NP0308670)

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Record Information

Version

2.0

Created at

2022-09-11 02:37:49 UTC

Updated at

2022-09-11 02:37:50 UTC

NP-MRD ID

NP0308670

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one

Description

Dihydrosongorine belongs to the class of organic compounds known as napelline-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the napelline skeleton, which is a hexacyclic compound, with an additional C-20-C-7 bond in the kaurane-type. (1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one is found in Aconitum karakolicum. Based on a literature review very few articles have been published on dihydrosongorine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112204372D          

 26 31  0  0  1  0            999 V2000
    1.2942    2.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178    1.6462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    0.8361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9778    0.4852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7495   -0.3516    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0330   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4299   -1.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9348   -1.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7679   -1.6576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2875   -2.2984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1355   -0.8277    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3833    0.1948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307   -0.0464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8812    0.1801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -0.5643    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4706   -0.7374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9211   -1.2802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4630   -1.8127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8733   -2.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0959   -3.2350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0537   -2.2136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8925   -1.0734    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7133   -0.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.4213    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5078    0.3798    0.0000 O   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  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 15 14  1  6  0  0  0
  5 15  1  0  0  0  0
 11 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 11 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          2D

 59 64  0  0  0  0  0  0  0  0999 V2000
   -4.8476   -0.3425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3498   -0.4244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8520   -0.5062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1740   -1.8442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -2.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328   -3.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086   -3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470   -1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9419   -0.4816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9206    4.0858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9243    5.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0429    4.5032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9294   -1.8403    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5593   -3.6078    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1785   -0.6653    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8612    0.9834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9280    6.3153    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1531    4.3402    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7273    2.7656    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5429    4.5032    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  1  1
 17 18  1  0
 18 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 12  3  1  0
 25 16  1  0
 15  5  1  0
 22 16  1  0
 15 11  1  0
 11 22  1  1
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  4 32  1  0
  4 33  1  0
  6 34  1  0
  6 35  1  0
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  7 37  1  0
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  9 41  1  1
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 24 56  1  0
 24 57  1  0
 25 58  1  6
 26 59  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
M  END


  Mrv1652309112204372D          

 26 31  0  0  1  0            999 V2000
    1.2942    2.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178    1.6462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    0.8361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9778    0.4852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7495   -0.3516    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0330   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4299   -1.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9348   -1.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7679   -1.6576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2875   -2.2984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1355   -0.8277    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3833    0.1948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307   -0.0464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8812    0.1801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -0.5643    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4706   -0.7374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9211   -1.2802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4630   -1.8127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8733   -2.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0959   -3.2350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0537   -2.2136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8925   -1.0734    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7133   -0.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.4213    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5078    0.3798    0.0000 O   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  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 15 14  1  6  0  0  0
  5 15  1  0  0  0  0
 11 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 11 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0308670

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1C[C@]2(C)CC[C@H](O)[C@]34C1[C@H](C[C@@H]23)[C@@]12C[C@H]([C@@H](C)[C@H]1O)C(=O)CC42

> <INCHI_IDENTIFIER>
InChI=1S/C22H33NO3/c1-4-23-10-20(3)6-5-17(25)22-15(20)7-13(18(22)23)21-9-12(11(2)19(21)26)14(24)8-16(21)22/h11-13,15-19,25-26H,4-10H2,1-3H3/t11-,12-,13+,15+,16?,17+,18?,19-,20+,21-,22+/m1/s1

> <INCHI_KEY>
HLVOECRPUBDISK-ZFMPVUFUSA-N

> <FORMULA>
C22H33NO3

> <MOLECULAR_WEIGHT>
359.51

> <EXACT_MASS>
359.246043927

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       2.416   4.081   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.580   3.073   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       3.289   1.561   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       1.825   0.906   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.399  -0.656   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.062  -0.168   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.803  -2.155   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.745  -3.424   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.300  -3.094   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.270  -4.290   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.986  -1.545   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.449   0.364   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.471  -0.087   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.512   0.336   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.799  -1.053   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.478  -1.376   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.319  -2.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.331  -3.384   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.230  -4.556   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.646  -6.039   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.700  -4.132   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.296  -2.496   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.133  -2.004   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.665  -1.848   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.047  -0.787   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.415   0.709   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   15                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   15   22                                             
CONECT   12   11    3   13                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14    5   11                                                  
CONECT   16   13   17   22   25                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16   11                                                  
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₃NO₃

Average Mass

359.5100 Da

Monoisotopic Mass

359.24604 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCN1C[C@]2(C)CC[C@H](O)[C@]34C1[C@H](C[C@@H]23)[C@@]12C[C@H]([C@@H](C)[C@H]1O)C(=O)CC42

InChI Identifier

InChI=1S/C22H33NO3/c1-4-23-10-20(3)6-5-17(25)22-15(20)7-13(18(22)23)21-9-12(11(2)19(21)26)14(24)8-16(21)22/h11-13,15-19,25-26H,4-10H2,1-3H3/t11-,12-,13+,15+,16?,17+,18?,19-,20+,21-,22+/m1/s1

InChI Key

HLVOECRPUBDISK-ZFMPVUFUSA-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
Aconitum karakolicum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as napelline-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the napelline skeleton, which is a hexacyclic compound, with an additional C-20-C-7 bond in the kaurane-type.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Napelline-type diterpenoid alkaloids

Alternative Parents

Substituents

Napelline-type diterpenoid alkaloid
Alkaloid or derivatives
Azepane
Piperidine
Cyclic alcohol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

129777956

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one (NP0308670)

MOL for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

3D MOL for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

3D SDF for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

3D-SDF for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

PDB for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

3D PDB for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

SMILES for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

INCHI for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

Structure for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)

3D Structure for NP0308670 ((1r,5r,6r,7r,8s,9r,13r,16s,17s)-11-ethyl-7,16-dihydroxy-6,13-dimethyl-11-azahexacyclo[7.7.2.1⁵,⁸.0¹,¹⁰.0²,⁸.0¹³,¹⁷]nonadecan-4-one)