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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-08-30 00:20:54 UTC

Update Date

2021-09-26 22:48:56 UTC

HMDB ID

HMDB0242345

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one

Description

7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4-dien-6-one belongs to the class of organic compounds known as anagyrine-type alkaloids. These are lupin alkaloids with a structure based on the anagyrine skeleton. Anagyrine is a tetracyclic ketone containing a quinolizidine, and two pyridine rings fused together to form dipyrido[1,2-a:1',2'-e][1,5]diazocin-4-one. Based on a literature review very few articles have been published on 7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4-dien-6-one. This compound has been identified in human blood as reported by (PMID: 31557052 ). (1r,9s,10s)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0248379
     RDKit          3D
3,4,5,6-Tetradehydrospartein-2-one
 38 41  0  0  0  0  0  0  0  0999 V2000
    3.0970    0.0630    2.6935 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0865    0.3403    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    1.0265    0.9645 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1760    1.3397   -0.3713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892    0.9450   -1.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0295    0.2631   -0.6209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233   -0.0404    0.6820 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.7568    1.2823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0507   -1.5095    0.3508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6152   -1.6014   -1.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8996   -0.1481   -1.4667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376    0.7202   -1.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4334   -0.1639   -0.9949 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7135    0.3447   -1.2924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5393    0.8064   -0.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2476    0.1754    1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7439   -0.0657    1.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409   -0.9430    0.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0078    1.3259    1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0239    1.8789   -0.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1169    1.1978   -2.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.5101    1.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3561   -0.0897    1.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0904   -2.5847    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1666   -2.0051   -1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5663   -2.1385   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0947   -0.1095   -2.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1658    1.4017   -0.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5753    1.3543   -2.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5969    1.2171   -2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -0.4246   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5071    1.9259   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6235    0.5960   -0.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6564    0.8018    1.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7344   -0.8237    1.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5977   -0.5462    2.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2770    0.9444    1.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871   -1.7556    0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 18  9  1  0
 11  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
M  END

  Mrv1533004161502292D          

 18 21  0  0  0  0            999 V2000
    6.1269   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8413    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8413    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040    1.4084    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
  2 11  1  0  0  0  0
  6 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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242345

> <DATABASE_NAME>
hmdb

> <SMILES>
O=C1C=CC=C2C3CC(CN12)C1CCCCN1C3

> <INCHI_IDENTIFIER>
InChI=1S/C15H20N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h3,5-6,11-13H,1-2,4,7-10H2

> <INCHI_KEY>
FQEQMASDZFXSJI-UHFFFAOYSA-N

> <FORMULA>
C15H20N2O

> <MOLECULAR_WEIGHT>
244.338

> <EXACT_MASS>
244.157563272

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
27.280644343459137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4-dien-6-one

> <ALOGPS_LOGP>
2.58

> <JCHEM_LOGP>
1.0133275319999986

> <ALOGPS_LOGS>
-1.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.196367600103125

> <JCHEM_POLAR_SURFACE_AREA>
23.550000000000004

> <JCHEM_REFRACTIVITY>
74.03519999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.02e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
anagyrine

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0248379
     RDKit          3D
3,4,5,6-Tetradehydrospartein-2-one
 38 41  0  0  0  0  0  0  0  0999 V2000
    3.0970    0.0630    2.6935 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0865    0.3403    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    1.0265    0.9645 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1760    1.3397   -0.3713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892    0.9450   -1.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0295    0.2631   -0.6209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233   -0.0404    0.6820 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.7568    1.2823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0507   -1.5095    0.3508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6152   -1.6014   -1.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8996   -0.1481   -1.4667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376    0.7202   -1.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4334   -0.1639   -0.9949 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7135    0.3447   -1.2924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5393    0.8064   -0.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2476    0.1754    1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7439   -0.0657    1.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409   -0.9430    0.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0078    1.3259    1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0239    1.8789   -0.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1169    1.1978   -2.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.5101    1.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3561   -0.0897    1.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0904   -2.5847    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1666   -2.0051   -1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5663   -2.1385   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0947   -0.1095   -2.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1658    1.4017   -0.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5753    1.3543   -2.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5969    1.2171   -2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -0.4246   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5071    1.9259   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6235    0.5960   -0.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6564    0.8018    1.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7344   -0.8237    1.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5977   -0.5462    2.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2770    0.9444    1.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871   -1.7556    0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 18  9  1  0
 11  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
M  END

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  O   UNK     0      11.437  -2.310   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      11.437  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.770   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.770   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.437   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.103   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.014   2.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.709   0.577   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.474  -1.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.014  -1.089   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      10.103  -0.000   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.385  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.052  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.718   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.718   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.052   2.310   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.385   1.540   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       7.474   2.629   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    2    6                                                  
CONECT   12    9   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17    7                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   42    0
END

COMPND    HMDB0248380
HETATM    1  O1  UNL     1      -3.370   2.582  -0.303  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.272   1.324  -0.224  1.00  0.00           C  
HETATM    3  C2  UNL     1      -4.403   0.607  -0.546  1.00  0.00           C  
HETATM    4  C3  UNL     1      -4.325  -0.767  -0.469  1.00  0.00           C  
HETATM    5  C4  UNL     1      -3.137  -1.357  -0.077  1.00  0.00           C  
HETATM    6  C5  UNL     1      -2.017  -0.619   0.241  1.00  0.00           C  
HETATM    7  N1  UNL     1      -2.107   0.719   0.161  1.00  0.00           N  
HETATM    8  C6  UNL     1      -1.025   1.637   0.461  1.00  0.00           C  
HETATM    9  C7  UNL     1       0.277   0.918   0.740  1.00  0.00           C  
HETATM   10  C8  UNL     1      -0.068  -0.288   1.574  1.00  0.00           C  
HETATM   11  C9  UNL     1      -0.746  -1.266   0.660  1.00  0.00           C  
HETATM   12  C10 UNL     1       0.096  -1.613  -0.544  1.00  0.00           C  
HETATM   13  N2  UNL     1       1.261  -0.833  -0.684  1.00  0.00           N  
HETATM   14  C11 UNL     1       2.474  -1.368  -0.233  1.00  0.00           C  
HETATM   15  C12 UNL     1       3.652  -0.554  -0.690  1.00  0.00           C  
HETATM   16  C13 UNL     1       3.486   0.852  -0.154  1.00  0.00           C  
HETATM   17  C14 UNL     1       2.235   1.420  -0.728  1.00  0.00           C  
HETATM   18  C15 UNL     1       1.019   0.547  -0.532  1.00  0.00           C  
HETATM   19  H1  UNL     1      -5.332   1.080  -0.853  1.00  0.00           H  
HETATM   20  H2  UNL     1      -5.196  -1.368  -0.715  1.00  0.00           H  
HETATM   21  H3  UNL     1      -3.069  -2.452  -0.013  1.00  0.00           H  
HETATM   22  H4  UNL     1      -1.245   2.291   1.327  1.00  0.00           H  
HETATM   23  H5  UNL     1      -0.860   2.298  -0.431  1.00  0.00           H  
HETATM   24  H6  UNL     1       0.958   1.548   1.347  1.00  0.00           H  
HETATM   25  H7  UNL     1      -0.860   0.060   2.303  1.00  0.00           H  
HETATM   26  H8  UNL     1       0.741  -0.685   2.169  1.00  0.00           H  
HETATM   27  H9  UNL     1      -0.920  -2.195   1.237  1.00  0.00           H  
HETATM   28  H10 UNL     1       0.342  -2.703  -0.561  1.00  0.00           H  
HETATM   29  H11 UNL     1      -0.541  -1.460  -1.463  1.00  0.00           H  
HETATM   30  H12 UNL     1       2.607  -2.387  -0.708  1.00  0.00           H  
HETATM   31  H13 UNL     1       2.545  -1.572   0.862  1.00  0.00           H  
HETATM   32  H14 UNL     1       3.666  -0.529  -1.791  1.00  0.00           H  
HETATM   33  H15 UNL     1       4.571  -1.000  -0.296  1.00  0.00           H  
HETATM   34  H16 UNL     1       4.338   1.453  -0.513  1.00  0.00           H  
HETATM   35  H17 UNL     1       3.507   0.839   0.953  1.00  0.00           H  
HETATM   36  H18 UNL     1       2.404   1.575  -1.821  1.00  0.00           H  
HETATM   37  H19 UNL     1       1.993   2.426  -0.323  1.00  0.00           H  
HETATM   38  H20 UNL     1       0.320   0.840  -1.376  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    7
CONECT    3    4    4   19
CONECT    4    5   20
CONECT    5    6    6   21
CONECT    6    7   11
CONECT    7    8
CONECT    8    9   22   23
CONECT    9   10   18   24
CONECT   10   11   25   26
CONECT   11   12   27
CONECT   12   13   28   29
CONECT   13   14   18
CONECT   14   15   30   31
CONECT   15   16   32   33
CONECT   16   17   34   35
CONECT   17   18   36   37
CONECT   18   38
END

HMDB0248379
     RDKit          3D
3,4,5,6-Tetradehydrospartein-2-one
 38 41  0  0  0  0  0  0  0  0999 V2000
    3.0970    0.0630    2.6935 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0865    0.3403    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    1.0265    0.9645 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1760    1.3397   -0.3713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892    0.9450   -1.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0295    0.2631   -0.6209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233   -0.0404    0.6820 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.7568    1.2823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0507   -1.5095    0.3508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6152   -1.6014   -1.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8996   -0.1481   -1.4667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376    0.7202   -1.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4334   -0.1639   -0.9949 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7135    0.3447   -1.2924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5393    0.8064   -0.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2476    0.1754    1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7439   -0.0657    1.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409   -0.9430    0.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0078    1.3259    1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0239    1.8789   -0.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1169    1.1978   -2.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.5101    1.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3561   -0.0897    1.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0904   -2.5847    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1666   -2.0051   -1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5663   -2.1385   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0947   -0.1095   -2.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1658    1.4017   -0.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5753    1.3543   -2.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5969    1.2171   -2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -0.4246   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5071    1.9259   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6235    0.5960   -0.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6564    0.8018    1.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7344   -0.8237    1.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5977   -0.5462    2.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2770    0.9444    1.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871   -1.7556    0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 18  9  1  0
 11  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Thermospine	MeSH, HMDB

Chemical Formula

C₁₅H₂₀N₂O

Average Molecular Weight

244.338

Monoisotopic Molecular Weight

244.157563272

IUPAC Name

7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4-dien-6-one

Traditional Name

anagyrine

CAS Registry Number

Not Available

SMILES

O=C1C=CC=C2C3CC(CN12)C1CCCCN1C3

InChI Identifier

InChI=1S/C15H20N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h3,5-6,11-13H,1-2,4,7-10H2

InChI Key

FQEQMASDZFXSJI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anagyrine-type alkaloids. These are lupin alkaloids with a structure based on the anagyrine skeleton. Anagyrine is a tetracyclic ketone containing a quinolizidine, and two pyridine rings fused together to form dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Anagyrine-type alkaloids

Direct Parent

Anagyrine-type alkaloids

Alternative Parents

Substituents

Anagyrine-type alkaloid
Quinolizidine
Pyridinone
Aralkylamine
Piperidine
Pyridine
Heteroaromatic compound
Lactam
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	2.58	ALOGPS
logP	1.01	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Basic)	9.2	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	23.55 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	74.04 m³·mol⁻¹	ChemAxon
Polarizability	27.28 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	187.989	30932474
DeepCCS	[M+Na]+	162.945	30932474
AllCCS	[M+H]+	157.6	32859911
AllCCS	[M+H-H2O]+	153.8	32859911
AllCCS	[M+NH4]+	161.1	32859911
AllCCS	[M+Na]+	162.1	32859911
AllCCS	[M-H]-	166.3	32859911
AllCCS	[M+Na-2H]-	166.0	32859911
AllCCS	[M+HCOO]-	165.8	32859911

Predicted Kovats Retention Indices

Not Available

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	splash10-0i01-3690000000-d27409a84bd1631c83c3	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 10V, Positive-QTOF	splash10-0002-0090000000-86fa3d03df57c0c1ea3a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 20V, Positive-QTOF	splash10-0002-0090000000-86fa3d03df57c0c1ea3a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 40V, Positive-QTOF	splash10-0f6t-3940000000-a9354fd67a9cf899f06e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 10V, Negative-QTOF	splash10-0006-0090000000-ff3c196dd6debdf160f0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 20V, Negative-QTOF	splash10-0006-0090000000-cbbaf651715e6049de54	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 40V, Negative-QTOF	splash10-000x-3930000000-841c6aa1e4ef54369fa7	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

83746

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for (1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one (HMDB0242345)

MOL for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

3D MOL for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

3D SDF for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

3D-SDF for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

PDB for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

3D PDB for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

SMILES for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

INCHI for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

Structure for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

3D Structure for HMDB0242345 ((1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

GC-MS Spectra

MS/MS Spectra

NMR Spectra