NP-MRD: Showing NP-Card for huperminone A (NP0042272)

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Record Information

Version

2.0

Created at

2021-06-20 23:58:33 UTC

Updated at

2021-06-30 00:17:16 UTC

NP-MRD ID

NP0042272

Secondary Accession Numbers

None

Natural Product Identification

Common Name

huperminone A

Provided By

JEOL Database JEOL Logo

Description

Huperminone A belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring. huperminone A is found in Huperzia phlegmaria. huperminone A was first documented in 2013 (Hirasawa, Y., et al.). Based on a literature review very few articles have been published on Huperminone A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101583D          

 48 50  0  0  0  0            999 V2000
    5.0298    1.4805    0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745    1.5020    1.1494 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8624    0.2022    0.7520 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3784    0.1980    1.1901 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6751   -1.1588    0.8860 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6753   -1.5464   -0.6001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0358   -2.8778   -0.8416 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6193   -3.9951   -0.0372 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6193   -3.6844    1.4507 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2242   -2.3222    1.7233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0200   -2.1711    2.6491 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582    1.4434    0.5669 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.8445    4.2273    2.9116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3584    2.7725    0.9892 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8375    2.7063    0.5548 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0986    1.3989   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    5.0298    1.4805    0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745    1.5020    1.1494 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8624    0.2022    0.7520 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784    0.1980    1.1901 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306212101583D          

 48 50  0  0  0  0            999 V2000
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    3.5745    1.5020    1.1494 C   0  0  2  0  0  0  0  0  0  0  0  0
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 13 38  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  2 23  1  1  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  9 34  1  0  0  0  0
  9 35  1  0  0  0  0
  8 32  1  0  0  0  0
  8 33  1  0  0  0  0
  7 30  1  0  0  0  0
  7 31  1  0  0  0  0
  6 28  1  0  0  0  0
  6 29  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
 17 45  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042272

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])([H])N1C([H])([H])C([H])([H])C([H])([H])[C@@]2([H])[C@]1([H])C([H])([H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]2([H])[C@]1([H])C(=O)C([H])([H])C([H])([H])C([H])([H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H29NO/c1-12-10-15(14-6-3-4-8-17(14)19)13-7-5-9-18(2)16(13)11-12/h12-16H,3-11H2,1-2H3/t12-,13-,14-,15+,16+/m1/s1

> <INCHI_KEY>
UCHLTCVIJSLZTA-SUJAAXHWSA-N

> <FORMULA>
C17H29NO

> <MOLECULAR_WEIGHT>
263.425

> <EXACT_MASS>
263.224914558

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
31.956195836276386

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-[(4aR,5S,7R,8aS)-1,7-dimethyl-decahydroquinolin-5-yl]cyclohexan-1-one

> <ALOGPS_LOGP>
3.75

> <JCHEM_LOGP>
3.5778041086666668

> <ALOGPS_LOGS>
-4.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.451607752982154

> <JCHEM_POLAR_SURFACE_AREA>
20.310000000000002

> <JCHEM_REFRACTIVITY>
79.25819999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(4aR,5S,7R,8aS)-1,7-dimethyl-octahydro-2H-quinolin-5-yl]cyclohexan-1-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    5.0298    1.4805    0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745    1.5020    1.1494 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8624    0.2022    0.7520 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784    0.1980    1.1901 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6751   -1.1588    0.8860 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6753   -1.5464   -0.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0358   -2.8778   -0.8416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6193   -3.9951   -0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6193   -3.6844    1.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2242   -2.3222    1.7233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0200   -2.1711    2.6491 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582    1.4434    0.5669 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8392    1.5514    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0573    1.8791    2.3675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2773    3.1301    2.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1553    3.0242    2.4380 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8445    4.2273    2.9116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3584    2.7725    0.9892 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8375    2.7063    0.5548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0986    1.3989   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5652    0.6313    1.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3958    0.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5777    1.5823    2.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9319    0.0809   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3971   -0.6445    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3729    0.3142    2.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3662   -1.0817    1.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1789   -0.7730   -1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7011   -1.6370   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0941   -2.7902   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0016   -3.1242   -1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919   -4.9386   -0.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6513   -4.1323   -0.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1961   -4.4452    1.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4005   -3.6874    1.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360    1.3637   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3884    0.6477    0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752    2.3561    0.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537    1.0323    2.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1255    2.0404    2.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7194    4.0068    2.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4019    3.2705    3.8467 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5665    5.1155    2.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6100    4.4194    3.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9311    4.1052    2.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8987    3.5977    0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3628    3.6358    0.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    2.6421   -0.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 18  1  0
 14 15  1  0
 14 13  1  0
 15 16  1  0
 16 18  1  0
  5  6  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  4  5  1  0
 12 13  1  0
 16 17  1  0
 12  4  1  0
 10 11  2  0
 18 19  1  0
  4 26  1  1
 19  2  1  0
  5 27  1  1
  2  3  1  0
  2  1  1  0
  3  4  1  0
 18 46  1  6
  5 10  1  0
 12 36  1  6
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 13 37  1  0
 13 38  1  0
 19 47  1  0
 19 48  1  0
  2 23  1  1
  3 24  1  0
  3 25  1  0
  9 34  1  0
  9 35  1  0
  8 32  1  0
  8 33  1  0
  7 30  1  0
  7 31  1  0
  6 28  1  0
  6 29  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       5.030   1.480   0.682  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.575   1.502   1.149  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.862   0.202   0.752  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.378   0.198   1.190  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.675  -1.159   0.886  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.675  -1.546  -0.600  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.036  -2.878  -0.842  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.619  -3.995  -0.037  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.619  -3.684   1.451  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.224  -2.322   1.723  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.020  -2.171   2.649  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.658   1.443   0.567  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.839   1.551   0.898  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.057   1.879   2.368  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.277   3.130   2.766  0.00  0.00           C+0
HETATM   16  N   UNK     0       1.155   3.024   2.438  0.00  0.00           N+0
HETATM   17  C   UNK     0       1.845   4.227   2.912  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.358   2.773   0.989  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.837   2.706   0.555  0.00  0.00           C+0
HETATM   20  H   UNK     0       5.099   1.399  -0.408  0.00  0.00           H+0
HETATM   21  H   UNK     0       5.565   0.631   1.120  0.00  0.00           H+0
HETATM   22  H   UNK     0       5.548   2.396   0.987  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.578   1.582   2.244  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.932   0.081  -0.336  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.397  -0.645   1.195  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.373   0.314   2.283  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.366  -1.082   1.222  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.179  -0.773  -1.196  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.701  -1.637  -0.975  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.094  -2.790  -0.568  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.002  -3.124  -1.909  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.092  -4.939  -0.217  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.651  -4.132  -0.384  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.196  -4.445   1.987  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.401  -3.687   1.851  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.736   1.364  -0.526  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.388   0.648   0.620  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.275   2.356   0.291  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.754   1.032   2.994  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.126   2.040   2.553  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.719   4.007   2.274  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.402   3.271   3.847  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.567   5.115   2.333  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.610   4.419   3.965  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.931   4.105   2.874  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.899   3.598   0.426  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.363   3.636   0.801  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.871   2.642  -0.542  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2   19    3    1   23                                             
CONECT    3    2    4   24   25                                             
CONECT    4    5   12   26    3                                             
CONECT    5    6    4   27   10                                             
CONECT    6    5    7   28   29                                             
CONECT    7    8    6   30   31                                             
CONECT    8    9    7   32   33                                             
CONECT    9   10    8   34   35                                             
CONECT   10    9   11    5                                                  
CONECT   11   10                                                            
CONECT   12   18   13    4   36                                             
CONECT   13   14   12   37   38                                             
CONECT   14   15   13   39   40                                             
CONECT   15   14   16   41   42                                             
CONECT   16   15   18   17                                                  
CONECT   17   16   43   44   45                                             
CONECT   18   12   16   19   46                                             
CONECT   19   18    2   47   48                                             
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    2                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28    6                                                            
CONECT   29    6                                                            
CONECT   30    7                                                            
CONECT   31    7                                                            
CONECT   32    8                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35    9                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   14                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

RDKit          3D

48 50  0  0  0  0  0  0  0  0999 V2000
    5.0298    1.4805    0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745    1.5020    1.1494 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8624    0.2022    0.7520 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784    0.1980    1.1901 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6751   -1.1588    0.8860 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6753   -1.5464   -0.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0358   -2.8778   -0.8416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6193   -3.9951   -0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6193   -3.6844    1.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2242   -2.3222    1.7233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0200   -2.1711    2.6491 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582    1.4434    0.5669 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8392    1.5514    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0573    1.8791    2.3675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2773    3.1301    2.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1553    3.0242    2.4380 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8445    4.2273    2.9116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3584    2.7725    0.9892 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8375    2.7063    0.5548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0986    1.3989   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5652    0.6313    1.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3958    0.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5777    1.5823    2.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9319    0.0809   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3971   -0.6445    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3729    0.3142    2.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3662   -1.0817    1.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1789   -0.7730   -1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7011   -1.6370   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0941   -2.7902   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0016   -3.1242   -1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919   -4.9386   -0.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6513   -4.1323   -0.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1961   -4.4452    1.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4005   -3.6874    1.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360    1.3637   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3884    0.6477    0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752    2.3561    0.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537    1.0323    2.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1255    2.0404    2.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7194    4.0068    2.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4019    3.2705    3.8467 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5665    5.1155    2.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6100    4.4194    3.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9311    4.1052    2.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8987    3.5977    0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3628    3.6358    0.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    2.6421   -0.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 18  1  0
 14 15  1  0
 14 13  1  0
 15 16  1  0
 16 18  1  0
  5  6  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  4  5  1  0
 12 13  1  0
 16 17  1  0
 12  4  1  0
 10 11  2  0
 18 19  1  0
  4 26  1  1
 19  2  1  0
  5 27  1  1
  2  3  1  0
  2  1  1  0
  3  4  1  0
 18 46  1  6
  5 10  1  0
 12 36  1  6
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 13 37  1  0
 13 38  1  0
 19 47  1  0
 19 48  1  0
  2 23  1  1
  3 24  1  0
  3 25  1  0
  9 34  1  0
  9 35  1  0
  8 32  1  0
  8 33  1  0
  7 30  1  0
  7 31  1  0
  6 28  1  0
  6 29  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₉NO

Average Mass

263.4250 Da

Monoisotopic Mass

263.22491 Da

IUPAC Name

(2R)-2-[(4aR,5S,7R,8aS)-1,7-dimethyl-decahydroquinolin-5-yl]cyclohexan-1-one

Traditional Name

(2R)-2-[(4aR,5S,7R,8aS)-1,7-dimethyl-octahydro-2H-quinolin-5-yl]cyclohexan-1-one

CAS Registry Number

Not Available

SMILES

[H]C([H])([H])N1C([H])([H])C([H])([H])C([H])([H])[C@@]2([H])[C@]1([H])C([H])([H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]2([H])[C@]1([H])C(=O)C([H])([H])C([H])([H])C([H])([H])C1([H])[H]

InChI Identifier

InChI=1S/C17H29NO/c1-12-10-15(14-6-3-4-8-17(14)19)13-7-5-9-18(2)16(13)11-12/h12-16H,3-11H2,1-2H3/t12-,13-,14-,15+,16+/m1/s1

InChI Key

UCHLTCVIJSLZTA-SUJAAXHWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Phlegmariurus phlegmaria	JEOL database	Hirasawa, Y., et al, Tetrahedron Lett. 54, 1593 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolidines

Sub Class

Not Available

Direct Parent

Quinolidines

Alternative Parents

Substituents

Quinolidine
Piperidine
Ketone
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Azacycle
Amine
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
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	3.75	ALOGPS
logP	3.58	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Basic)	9.45	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	20.31 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	79.26 m³·mol⁻¹	ChemAxon
Polarizability	31.96 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

28945575

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71578357

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hirasawa, Y., et al. (2013). Hirasawa, Y., et al, Tetrahedron Lett. 54, 1593 (2013). Tetrahedron Lett.

Showing NP-Card for huperminone A (NP0042272)

MOL for NP0042272 (huperminone A)

3D MOL for NP0042272 (huperminone A)

3D SDF for NP0042272 (huperminone A)

3D-SDF for NP0042272 (huperminone A)

PDB for NP0042272 (huperminone A)

3D PDB for NP0042272 (huperminone A)

SMILES for NP0042272 (huperminone A)

INCHI for NP0042272 (huperminone A)

Structure for NP0042272 (huperminone A)

3D Structure for NP0042272 (huperminone A)