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Showing NP-Card for Condelphine (NP0050778)

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Record Information
Version2.0
Created at2022-04-27 22:06:32 UTC
Updated at2022-04-27 22:06:32 UTC
NP-MRD IDNP0050778
Secondary Accession NumbersNone
Natural Product Identification
Common NameCondelphine
DescriptionCONDELPHINE 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. Condelphine is found in Aconitum balfourii, Aconitum coreanum, Aconitum deiphinifolium, Aconitum delphinifolium, Aconitum sanyoense, Delphinium bicolor, Delphinium confusum, Delphinium denudatum , Delphinium nuttallianum Pritz., Delphinium pyramidale, Delphinium pyrimadale and Delphinium uncinatum Hook f.and Thomas . Condelphine was first documented in 2006 (PMID: 16724552). Based on a literature review a small amount of articles have been published on CONDELPHINE (PMID: 32566879) (PMID: 29698893) (PMID: 27514662) (PMID: 24040959).
Structure
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MOLSDFPDBSMILESInChI

MOL for NP0050778 (Condelphine)


  Mrv1652304282200062D          

 32 37  0  0  1  0            999 V2000
   -1.4203   -1.9481    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  2  0  0  0  0  0  0  0  0  0
   -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
    1.0296    0.0303    0.0000 O   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
    1.5610   -2.4846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5081   -2.5591    0.0000 C   0  0  0  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
    0.1926   -3.0339    0.0000 N   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
    0.2436   -3.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4440   -4.3132    0.0000 C   0  0  0  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
    2.2205    0.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515    1.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4701    1.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638    1.0417    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
    4.3596   -1.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7139   -0.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5736   -2.7232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9741   -1.3367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7806   -1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  6  0  0  0
  4  9  1  0  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  1  0  0  0
  3 13  1  6  0  0  0
 12 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 27  1  6  0  0  0
  9 27  1  6  0  0  0
 20 28  1  1  0  0  0
 28 29  1  0  0  0  0
 11 30  1  1  0  0  0
  1 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
Download

3D MOL for NP0050778 (Condelphine)

Download
3D SDF for NP0050778 (Condelphine)

  Mrv1652304282200062D          

 32 37  0  0  1  0            999 V2000
   -1.4203   -1.9481    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  2  0  0  0  0  0  0  0  0  0
   -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
    1.0296    0.0303    0.0000 O   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
    1.5610   -2.4846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5081   -2.5591    0.0000 C   0  0  0  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
    0.1926   -3.0339    0.0000 N   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
    0.2436   -3.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4440   -4.3132    0.0000 C   0  0  0  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
    2.2205    0.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515    1.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4701    1.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638    1.0417    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
    4.3596   -1.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7139   -0.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5736   -2.7232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9741   -1.3367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7806   -1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  6  0  0  0
  4  9  1  0  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  1  0  0  0
  3 13  1  6  0  0  0
 12 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 27  1  6  0  0  0
  9 27  1  6  0  0  0
 20 28  1  1  0  0  0
 28 29  1  0  0  0  0
 11 30  1  1  0  0  0
  1 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0050778

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C25H39NO6/c1-5-26-11-23(12-30-3)7-6-19(28)25-15-8-14-17(31-4)10-24(29,16(22(25)26)9-18(23)25)20(15)21(14)32-13(2)27/h14-22,28-29H,5-12H2,1-4H3/t14-,15-,16+,17+,18-,19+,20-,21+,22-,23+,24+,25-/m1/s1

> <INCHI_KEY>
ZEBMMHUDQRRILP-YNLINXDKSA-N

> <FORMULA>
C25H39NO6

> <MOLECULAR_WEIGHT>
449.588

> <EXACT_MASS>
449.27773798

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
49.94217953878684

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8,16-dihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-4-yl acetate

> <ALOGPS_LOGP>
0.77

> <JCHEM_LOGP>
-0.4721000010000011

> <ALOGPS_LOGS>
-2.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.752661453550434

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.00798355132332

> <JCHEM_PKA_STRONGEST_BASIC>
9.842202932618891

> <JCHEM_POLAR_SURFACE_AREA>
88.46000000000001

> <JCHEM_REFRACTIVITY>
117.4377

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8,16-dihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0050778 (Condelphine)
Download
PDB for NP0050778 (Condelphine)
HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -2.651  -3.636   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.146  -3.312   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.375  -3.189   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.508  -2.697   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.886  -1.083   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.664  -0.649   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.706  -1.817   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.922   0.057   0.000  0.00  0.00           O+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       2.914  -4.638   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.949  -4.777   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.801  -4.620   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       0.360  -5.663   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -1.041  -4.893   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.455  -7.200   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.829  -8.051   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.859  -3.569   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.603  -2.182   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.596  -0.862   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.670  -0.413   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.145   1.035   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.136   2.213   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.611   3.661   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.652   1.944   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.726  -0.065   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.138  -2.059   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.799  -0.668   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.804  -5.083   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -3.685  -2.495   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -5.190  -2.820   0.000  0.00  0.00           C+0
CONECT    1    2   31                                                       
CONECT    2    1    3    7   16                                             
CONECT    3    2    4   13                                                  
CONECT    4    3    5    9   14                                             
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5                                                            
CONECT    9    4   10   27                                                  
CONECT   10    9   11   22                                                  
CONECT   11   10   12   19   30                                             
CONECT   12   11   13   14                                                  
CONECT   13   12    3                                                       
CONECT   14   12    4   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15    2                                                       
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   11   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   10   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21    9                                                       
CONECT   28   20   29                                                       
CONECT   29   28                                                            
CONECT   30   11                                                            
CONECT   31    1   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

Download
3D PDB for NP0050778 (Condelphine)
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SMILES for NP0050778 (Condelphine)
CCN1C[C@]2(COC)CC[C@H](O)[C@@]34[C@@H]5C[C@H]6[C@H](OC(C)=O)[C@@H]5[C@](O)(C[C@@H]6OC)[C@@H](C[C@H]23)[C@@H]14
Download
INCHI for NP0050778 (Condelphine)
InChI=1S/C25H39NO6/c1-5-26-11-23(12-30-3)7-6-19(28)25-15-8-14-17(31-4)10-24(29,16(22(25)26)9-18(23)25)20(15)21(14)32-13(2)27/h14-22,28-29H,5-12H2,1-4H3/t14-,15-,16+,17+,18-,19+,20-,21+,22-,23+,24+,25-/m1/s1
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SynonymsNot Available
Chemical FormulaC25H39NO6
Average Mass449.5880 Da
Monoisotopic Mass449.27774 Da
IUPAC Name(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8,16-dihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-4-yl acetate
Traditional Name(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8,16-dihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-4-yl acetate
CAS Registry NumberNot Available
SMILES
CCN1C[C@]2(COC)CC[C@H](O)[C@@]34[C@@H]5C[C@H]6[C@H](OC(C)=O)[C@@H]5[C@](O)(C[C@@H]6OC)[C@@H](C[C@H]23)[C@@H]14
InChI Identifier
InChI=1S/C25H39NO6/c1-5-26-11-23(12-30-3)7-6-19(28)25-15-8-14-17(31-4)10-24(29,16(22(25)26)9-18(23)25)20(15)21(14)32-13(2)27/h14-22,28-29H,5-12H2,1-4H3/t14-,15-,16+,17+,18-,19+,20-,21+,22-,23+,24+,25-/m1/s1
InChI KeyZEBMMHUDQRRILP-YNLINXDKSA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Aconitum balfouriiLOTUS Database
Aconitum coreanumLOTUS Database
Aconitum deiphinifoliumPlant
Aconitum delphinifoliumPlant
Aconitum sanyoenseLOTUS Database
Delphinium bicolorLOTUS Database
Delphinium confusumPlant
Delphinium denudatumPlant
Delphinium nuttallianumPlant
Delphinium pyramidaleLOTUS Database
Delphinium pyrimadalePlant
Delphinium uncinatum Hook f.and ThomasPlant
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.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassPrenol lipids  
Sub ClassDiterpenoids  
Direct ParentAconitane-type diterpenoid alkaloids  
Alternative Parents
Substituents
  • Aconitane-type diterpenoid alkaloid
    • 

  • Quinolidine
    • 

  • Alkaloid or derivatives
    • 

  • Azepane
    • 

  • Piperidine
    • 

  • Cyclic alcohol
    • 

  • Tertiary alcohol
    • 

  • Amino acid or derivatives
    • 

  • Carboxylic acid ester
    • 

  • Secondary alcohol
    • 

  • Tertiary amine
    • 

  • Tertiary aliphatic amine
    • 

  • Organoheterocyclic compound
    • 

  • Azacycle
    • 

  • Carboxylic acid derivative
    • 

  • Dialkyl ether
    • 

  • Ether
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Organic oxide
    • 

  • Organonitrogen compound
    • 

  • Organooxygen compound
    • 

  • Organic oxygen compound
    • 

  • Organopnictogen compound
    • 

  • Carbonyl group
    • 

  • Alcohol
    • 

  • Organic nitrogen compound
    • 

  • Hydrocarbon derivative
    • 

  • Amine
    • 

  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External Descriptors
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP0.77ALOGPS
logP-0.47ChemAxon
logS-2.5ALOGPS
pKa (Strongest Acidic)14.01ChemAxon
pKa (Strongest Basic)9.84ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area88.46 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity117.44 m³·mol⁻¹ChemAxon
Polarizability49.94 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDC00001627  
Chemspider ID21179607  
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound92854546  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. Zeng Z, Qasem AMA, Woodman TJ, Rowan MG, Blagbrough IS: Impacts of Steric Compression, Protonation, and Intramolecular Hydrogen Bonding on the (15)N NMR Spectroscopy of Norditerpenoid Alkaloids and Their Piperidine-Ring Analogues. ACS Omega. 2020 Jun 8;5(23):14116-14122. doi: 10.1021/acsomega.0c01648. eCollection 2020 Jun 16. [PubMed:32566879  ] 
  2. Ahmad H, Ahmad S, Ali M, Latif A, Shah SAA, Naz H, Ur Rahman N, Shaheen F, Wadood A, Khan HU, Ahmad M: Norditerpenoid alkaloids of Delphinium denudatum as cholinesterase inhibitors. Bioorg Chem. 2018 Aug;78:427-435. doi: 10.1016/j.bioorg.2018.04.008. Epub 2018 Apr 17. [PubMed:29698893  ] 
  3. Salgado VL: Antagonist pharmacology of desensitizing and non-desensitizing nicotinic acetylcholine receptors in cockroach neurons. Neurotoxicology. 2016 Sep;56:188-195. doi: 10.1016/j.neuro.2016.08.003. Epub 2016 Aug 8. [PubMed:27514662  ] 
  4. Shi Y, Wilmot JT, Nordstrom LU, Tan DS, Gin DY: Total synthesis, relay synthesis, and structural confirmation of the C18-norditerpenoid alkaloid neofinaconitine. J Am Chem Soc. 2013 Sep 25;135(38):14313-20. doi: 10.1021/ja4064958. Epub 2013 Sep 16. [PubMed:24040959  ] 
  5. Mericli AH, Suzgec S, Bitis L, Mericli F, Ozcelik H, Zapp J, Becker H: Diterpenoid alkaloids from the roots of Aconitum cochleare. Pharmazie. 2006 May;61(5):483-5. [PubMed:16724552  ]