NP-MRD: Showing NP-Card for 12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol (NP0231237)

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Record Information

Version

2.0

Created at

2022-09-06 12:00:05 UTC

Updated at

2022-09-06 12:00:05 UTC

NP-MRD ID

NP0231237

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol

Description

12-Ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]Nonadecane-4,7,17-triol belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. 12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol is found in Aconitum karakolicum. Based on a literature review very few articles have been published on 12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]Nonadecane-4,7,17-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214002D          

 26 31  0  0  0  0            999 V2000
    5.3367    1.4341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5534    1.1751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2449    0.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5688    0.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9763    1.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0640    1.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2435    0.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0337    0.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5729    0.7588    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3692    0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5807   -0.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4598    1.6999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5548    1.8588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5645    2.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2180    0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6253    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1747   -0.4685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4537    0.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4642    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5985    0.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1249   -0.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9439   -0.3901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4699   -1.0256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806    2.4637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 13 20  1  0  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
  5 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
    4.4726    0.0133    1.7123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7270    0.3990    0.6873 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7782   -0.2522   -0.6604 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8808    0.6601   -1.4778 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7907    0.9550   -0.4355 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8319    1.9659   -0.9400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6146    1.5499   -0.8365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8389    1.0709    0.5774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2010    0.8529    0.9053 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7942    1.6782    1.8814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7567    0.8339    2.7145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0343    0.3627   -0.1314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2987   -0.2259   -1.2850 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9549    0.2350   -2.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3859   -1.7509   -1.3063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7052   -2.3585   -0.1126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9889   -1.4012    0.7602 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0314   -2.1202    1.5171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2973   -0.2812    0.0911 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2047   -0.3076    0.0784 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6356   -1.4943   -0.7805 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1570   -1.6096   -0.6043 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3444   -2.2034    0.6582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8314    0.1048   -1.2593 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7180    1.5143    0.6596 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3922    2.6348    0.2061 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066    0.5135    2.6754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1645   -0.8134    1.6333 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8222   -0.2623   -1.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926    0.2152   -2.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4355    1.5986   -1.6169 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9360    2.8822   -0.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1023    2.3343   -1.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3053    2.2827   -1.2340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2547    1.5453    1.3531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1063    2.2651    2.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4374    2.4384    1.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3878    0.7489    3.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8134   -0.2129    2.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7867    1.2285    2.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6686   -0.4658    0.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7953    1.1088   -0.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7406   -0.4897   -2.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4246    1.2050   -2.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1907    0.3595   -3.3765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8047   -2.0729   -2.2118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186   -2.0600   -1.4542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0458   -3.2204   -0.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5219   -2.8492    0.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7061   -1.0322    1.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -3.0892    1.4486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5328   -0.5729    1.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3560   -1.3832   -1.8331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2257   -2.4413   -0.4213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5188   -2.3028   -1.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1779   -3.1627    0.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2625   -0.1883   -2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2050    1.6483    1.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2568    3.4191    0.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 19 17  1  1
 19  8  1  0
  8  7  1  0
  7  6  1  0
  5  6  1  6
  5  4  1  0
  4  3  1  0
  3 22  1  0
 22 23  1  0
 22 21  1  0
 21 20  1  0
  3  2  1  0
  2  1  2  3
  2 25  1  0
 25 26  1  0
  7 24  1  0
  8  9  1  0
 20  5  1  0
 24 13  1  0
 20 19  1  0
 24 19  1  0
 25  5  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
 10 36  1  0
 10 37  1  0
 12 41  1  0
 12 42  1  0
 14 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  1
 18 51  1  0
  8 35  1  1
  7 34  1  6
  6 32  1  0
  6 33  1  0
  4 30  1  0
  4 31  1  0
  3 29  1  6
 22 55  1  6
 23 56  1  0
 21 53  1  0
 21 54  1  0
 20 52  1  1
  1 27  1  0
  1 28  1  0
 25 58  1  1
 26 59  1  0
 24 57  1  6
M  END


  Mrv1652309062214002D          

 26 31  0  0  0  0            999 V2000
    5.3367    1.4341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5534    1.1751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2449    0.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5688    0.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9763    1.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0640    1.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2435    0.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0337    0.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5729    0.7588    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3692    0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5807   -0.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4598    1.6999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5548    1.8588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5645    2.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2180    0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6253    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1747   -0.4685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4537    0.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4642    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5985    0.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1249   -0.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9439   -0.3901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4699   -1.0256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806    2.4637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 13 20  1  0  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
  5 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231237

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(C)CCC(O)C34C1C(CC15CC(C(O)CC31)C(=C)C5O)C24

> <INCHI_IDENTIFIER>
InChI=1S/C22H33NO3/c1-4-23-10-20(3)6-5-16(25)22-15-7-14(24)12-8-21(15,19(26)11(12)2)9-13(17(20)22)18(22)23/h12-19,24-26H,2,4-10H2,1,3H3

> <INCHI_KEY>
IZUTYRYPLISYDD-UHFFFAOYSA-N

> <FORMULA>
C22H33NO3

> <MOLECULAR_WEIGHT>
359.51

> <EXACT_MASS>
359.246043927

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.85256010095233

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1^{5,8}.0^{1,11}.0^{2,8}.0^{14,18}]nonadecane-4,7,17-triol

> <JCHEM_LOGP>
0.5308862870000011

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.567441095822094

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.961223475203074

> <JCHEM_PKA_STRONGEST_BASIC>
8.277286692385044

> <JCHEM_POLAR_SURFACE_AREA>
63.93000000000001

> <JCHEM_REFRACTIVITY>
99.6886

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1^{5,8}.0^{1,11}.0^{2,8}.0^{14,18}]nonadecane-4,7,17-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.962   2.677   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.500   2.193   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.924   0.743   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.662   1.533   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.556   1.980   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.853   2.324   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.321   1.189   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.796   0.088   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       4.803   1.416   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       6.289   1.014   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.684  -0.475   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.592   3.173   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.902   3.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.920   5.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.273   3.223   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.407   1.811   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.167   0.415   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.326  -0.875   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.714   0.285   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.733   2.206   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.851   0.250   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.833  -1.001   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.362  -0.728   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.344  -1.914   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.100   3.060   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.057   4.599   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   21   25                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9   19                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   15   20                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    8   20   21                                             
CONECT   20   19    7   13                                                  
CONECT   21   19    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23                                                            
CONECT   25    5    2   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

CCN1CC2(C)CCC(O)C34C1C(CC15CC(C(O)CC31)C(=C)C5O)C24

InChI Identifier

InChI=1S/C22H33NO3/c1-4-23-10-20(3)6-5-16(25)22-15-7-14(24)12-8-21(15,19(26)11(12)2)9-13(17(20)22)18(22)23/h12-19,24-26H,2,4-10H2,1,3H3

InChI Key

IZUTYRYPLISYDD-UHFFFAOYSA-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 kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Quinolidine
Piperidine
Cyclic alcohol
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Polyol
Azacycle
Organoheterocyclic compound
Organopnictogen compound
Alcohol
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Amine
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

163017575

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol (NP0231237)

MOL for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

3D MOL for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

3D SDF for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

3D-SDF for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

PDB for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

3D PDB for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

SMILES for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

INCHI for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

Structure for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)

3D Structure for NP0231237 (12-ethyl-14-methyl-6-methylidene-12-azahexacyclo[8.7.1.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]nonadecane-4,7,17-triol)