NP-MRD: Showing NP-Card for 13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one (NP0237370)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 20:29:42 UTC

Updated at

2022-09-06 20:29:42 UTC

NP-MRD ID

NP0237370

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one

Description

13,19-Dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-16-one belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. 13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one is found in Aconitum sachalinense. 13,19-Dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-16-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231519572D          

 25 30  0  0  0  0            999 V2000
    2.9658   -0.2049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    0.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852    1.2463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5700    2.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3604    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0539    1.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5125    0.7423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6639    1.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2304    1.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0855    1.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3219    1.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7918    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0676    1.0570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3938    1.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2923    2.3485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3663    2.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9830    2.3330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4208    3.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2904    3.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    3.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7614    2.4203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1315    2.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2050    3.1947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3483    1.7460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1730    1.7711    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  0  0  0  0
  4  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
  2 10  1  0  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
 14 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
  9 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 54 59  0  0  0  0  0  0  0  0999 V2000
    4.7914    0.7458   -0.0810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5431    0.4223    0.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0089   -0.8626   -0.3850 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4446   -1.1160   -1.6576 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5202   -0.7192   -0.4046 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7756   -1.8323   -1.0447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5744   -2.1124   -0.5222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1318   -3.1133   -0.9415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3253   -1.2999    0.4632 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5917   -0.6764   -0.0140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4446   -1.7827   -0.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3361   -0.3024    1.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2969    0.1757    2.2630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.8418    1.5576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4001   -0.0801    0.6509 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3454    0.4209   -0.8036 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0906    0.6708   -0.9454 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5462    1.7838   -0.0804 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5862    1.2698    0.8917 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8287    0.2788    1.7955 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8551   -0.5613    2.3042 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9281   -0.5725    1.0102 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3712    1.3202   -0.8945 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3856    2.2484   -1.9632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5908    0.4879   -0.8693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5066    0.1542   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1730    1.6930    0.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2567   -1.7167    0.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0258   -0.3630   -1.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811   -2.7672   -0.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8132   -1.7626   -2.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4430   -1.8056    1.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0985   -2.0567   -1.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5674   -2.6392    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4599   -1.3311   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7798   -1.2354    1.7310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1243    0.4224    1.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7747    1.0093    2.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9780   -0.5776    2.9824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5771    1.7124    1.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    1.3024    2.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5551   -0.3915   -1.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4853    0.6976   -1.9815 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9556    2.5907   -0.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7296    2.2293    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0525    2.0512    1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4193    0.7807    2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5186   -1.0381    3.0983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8931   -1.6091    1.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6642    3.0756   -1.7261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3910    2.7567   -1.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1221    1.8561   -2.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7247    0.1761   -1.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4559    1.1510   -0.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  0
 25 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 15 14  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22  5  1  0
  5  6  1  6
  6  7  1  0
  7  8  2  0
  7  9  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
 16 23  1  0
  5 17  1  0
  9 10  1  0
 22 15  1  0
  9 15  1  0
  2 19  1  0
 24 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 25 54  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  6
 17 43  1  6
 18 44  1  0
 18 45  1  0
 19 46  1  1
 20 47  1  1
 21 48  1  0
 22 49  1  1
  6 30  1  0
  6 31  1  0
  9 32  1  1
  3 28  1  1
  4 29  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv1533004231519572D          

 25 30  0  0  0  0            999 V2000
    2.9658   -0.2049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    0.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852    1.2463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5700    2.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3604    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0539    1.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5125    0.7423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6639    1.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2304    1.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0855    1.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3219    1.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7918    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0676    1.0570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3938    1.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2923    2.3485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3663    2.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9830    2.3330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4208    3.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2904    3.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    3.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7614    2.4203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1315    2.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2050    3.1947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3483    1.7460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1730    1.7711    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  0  0  0  0
  4  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
  2 10  1  0  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
 14 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
  9 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0237370

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CC2(C)CCCC34C1C1CC5C(O)C3C1(CC(=O)C24)C(O)C5=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H29NO3/c1-10-11-7-12-17-20-6-4-5-19(2,9-22(17)3)15(20)13(23)8-21(12,18(10)25)16(20)14(11)24/h11-12,14-18,24-25H,1,4-9H2,2-3H3

> <INCHI_KEY>
MMQZPMWTIRWJLO-UHFFFAOYSA-N

> <FORMULA>
C21H29NO3

> <MOLECULAR_WEIGHT>
343.467

> <EXACT_MASS>
343.214743798

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.88710134096608

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one

> <ALOGPS_LOGP>
0.96

> <JCHEM_LOGP>
0.5595925860000004

> <ALOGPS_LOGS>
-1.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.715874314966637

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.975834396686373

> <JCHEM_PKA_STRONGEST_BASIC>
9.243148890708298

> <JCHEM_POLAR_SURFACE_AREA>
60.769999999999996

> <JCHEM_REFRACTIVITY>
94.01479999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.04e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       5.536  -0.382   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       5.327   1.143   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       6.506   2.326   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.664   3.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.273   5.420   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.567   2.644   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.557   1.386   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.973   2.069   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.163   3.420   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.893   1.956   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.468   2.429   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.478   1.393   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.126   1.973   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.735   3.529   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.546   4.384   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.550   3.781   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.835   4.355   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.652   5.825   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.275   5.885   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.988   7.251   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.155   4.518   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.245   4.557   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.383   5.963   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.650   3.259   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.190   3.306   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   21                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16   21                                             
CONECT   10    9    2   11                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   24                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16   11   18   22                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    4    9                                                  
CONECT   22   17   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   13   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₉NO₃

Average Mass

343.4670 Da

Monoisotopic Mass

343.21474 Da

IUPAC Name

13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one

Traditional Name

13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one

CAS Registry Number

Not Available

SMILES

CN1CC2(C)CCCC34C1C1CC5C(O)C3C1(CC(=O)C24)C(O)C5=C

InChI Identifier

InChI=1S/C21H29NO3/c1-10-11-7-12-17-20-6-4-5-19(2,9-22(17)3)15(20)13(23)8-21(12,18(10)25)16(20)14(11)24/h11-12,14-18,24-25H,1,4-9H2,2-3H3

InChI Key

MMQZPMWTIRWJLO-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 sachalinense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Alkaloid or derivatives
Piperidine
Cyclic alcohol
Ketone
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Organic nitrogen compound
Amine
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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
logP	0.96	ALOGPS
logP	0.56	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	13.98	ChemAxon
pKa (Strongest Basic)	9.24	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	60.77 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.01 m³·mol⁻¹	ChemAxon
Polarizability	37.89 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

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

14558186

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one (NP0237370)

MOL for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

3D MOL for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

3D SDF for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

3D-SDF for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

PDB for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

3D PDB for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

SMILES for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

INCHI for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

Structure for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)

3D Structure for NP0237370 (13,19-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-16-one)