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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:33:38 UTC

Update Date

2023-02-21 17:27:23 UTC

HMDB ID

HMDB0040010

Secondary Accession Numbers

HMDB40010

Metabolite Identification

Common Name

1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone

Description

1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone belongs to the class of organic compounds known as pyrrolizines. Pyrrolizines are compounds containing a pyrrolizine moiety, which consists of a pyrrole ring fused to a pyrrolidine ring. Based on a literature review very few articles have been published on 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone.

Structure

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

HMDB0040010
     RDKit          3D
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone
 32 33  0  0  0  0  0  0  0  0999 V2000
   -2.1348   -2.8367    0.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270   -1.6825    0.0658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0644   -1.6034   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5468   -2.7065   -1.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4387   -0.3229   -0.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6837    0.1724   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3150   -0.6802   -1.8556 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1957    1.5342   -0.9821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5340    1.7882    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4007    1.6260   -1.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4200    0.3431    0.2747 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242   -0.4489    0.6387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548    0.3396    1.5321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1069    1.7404    1.0251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5825    1.6742    0.8551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -3.6800   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1768   -2.5280   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1916   -3.1713    1.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2222   -3.4864   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126   -2.3547   -2.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4522   -3.0685   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    2.3343   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6338    1.8654    0.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1992    0.9453    1.1351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1033    2.7425    0.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7099    2.5583   -1.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9797    0.2686    2.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3908    0.0113    1.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5634    1.8456    0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4019    2.5258    1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3036    2.4916    0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0988    1.7633    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 12  2  2  0
 15 11  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  4 19  1  0
  4 20  1  0
  4 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 14 30  1  0
 15 31  1  0
 15 32  1  0
M  END


  Mrv0541 05061311342D          

 15 16  0  0  0  0            999 V2000
    1.8242    0.0404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8792    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8861    3.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312    3.1160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8242    2.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.9049    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1832    2.5029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2721    3.5576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  0  0  0  0
  8  7  1  0  0  0  0
  9  3  1  0  0  0  0
 10  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  8  2  0  0  0  0
 12  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 13 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14  9  1  0  0  0  0
 15 12  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040010

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)C(=O)C1=C(C)C(C)=C2CCCN12

> <INCHI_IDENTIFIER>
InChI=1S/C12H17NO2/c1-7-8(2)11(12(15)9(3)14)13-6-4-5-10(7)13/h9,14H,4-6H2,1-3H3

> <INCHI_KEY>
ZCNNVEPQSPOCJM-UHFFFAOYSA-N

> <FORMULA>
C12H17NO2

> <MOLECULAR_WEIGHT>
207.2689

> <EXACT_MASS>
207.125928793

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
23.64687899683378

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(6,7-dimethyl-2,3-dihydro-1H-pyrrolizin-5-yl)-2-hydroxypropan-1-one

> <ALOGPS_LOGP>
1.42

> <JCHEM_LOGP>
1.7813644466666672

> <ALOGPS_LOGS>
-2.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.737994842345234

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3507948146561857

> <JCHEM_POLAR_SURFACE_AREA>
42.230000000000004

> <JCHEM_REFRACTIVITY>
60.2144

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(1,2-dimethyl-6,7-dihydro-5H-pyrrolizin-3-yl)-2-hydroxypropan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040010
     RDKit          3D
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone
 32 33  0  0  0  0  0  0  0  0999 V2000
   -2.1348   -2.8367    0.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270   -1.6825    0.0658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0644   -1.6034   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5468   -2.7065   -1.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4387   -0.3229   -0.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6837    0.1724   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3150   -0.6802   -1.8556 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1957    1.5342   -0.9821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5340    1.7882    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4007    1.6260   -1.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4200    0.3431    0.2747 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242   -0.4489    0.6387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548    0.3396    1.5321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1069    1.7404    1.0251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5825    1.6742    0.8551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -3.6800   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1768   -2.5280   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1916   -3.1713    1.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2222   -3.4864   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126   -2.3547   -2.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4522   -3.0685   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    2.3343   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6338    1.8654    0.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1992    0.9453    1.1351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1033    2.7425    0.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7099    2.5583   -1.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9797    0.2686    2.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3908    0.0113    1.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5634    1.8456    0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4019    2.5258    1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3036    2.4916    0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0988    1.7633    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 12  2  2  0
 15 11  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  4 19  1  0
  4 20  1  0
  4 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 14 30  1  0
 15 31  1  0
 15 32  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       3.405   0.075   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.375   2.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.387   7.281   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.905   2.786   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   4.032   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.929   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.835   2.786   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.912   5.817   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.929   4.032   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.405   5.496   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       1.465   3.556   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0       5.942   4.672   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       2.375   6.641   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2    8                                                            
CONECT    3    9                                                            
CONECT    4    5    6                                                       
CONECT    5    4   10                                                       
CONECT    6    4   13                                                       
CONECT    7    1    8   10                                                  
CONECT    8    2    7   11                                                  
CONECT    9    3   12   14                                                  
CONECT   10    5    7   13                                                  
CONECT   11    8   12   13                                                  
CONECT   12    9   11   15                                                  
CONECT   13    6   10   11                                                  
CONECT   14    9                                                            
CONECT   15   12                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

COMPND    HMDB0040010
HETATM    1  C1  UNL     1      -2.135  -2.837   0.236  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.227  -1.683   0.066  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.064  -1.603  -0.658  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.547  -2.706  -1.451  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.439  -0.323  -0.521  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.684   0.172  -1.143  1.00  0.00           C  
HETATM    7  O1  UNL     1       2.315  -0.680  -1.856  1.00  0.00           O  
HETATM    8  C7  UNL     1       2.196   1.534  -0.982  1.00  0.00           C  
HETATM    9  C8  UNL     1       2.534   1.788   0.463  1.00  0.00           C  
HETATM   10  O2  UNL     1       3.401   1.626  -1.713  1.00  0.00           O  
HETATM   11  N1  UNL     1      -0.420   0.343   0.275  1.00  0.00           N  
HETATM   12  C9  UNL     1      -1.424  -0.449   0.639  1.00  0.00           C  
HETATM   13  C10 UNL     1      -2.355   0.340   1.532  1.00  0.00           C  
HETATM   14  C11 UNL     1      -2.107   1.740   1.025  1.00  0.00           C  
HETATM   15  C12 UNL     1      -0.583   1.674   0.855  1.00  0.00           C  
HETATM   16  H1  UNL     1      -1.884  -3.680  -0.433  1.00  0.00           H  
HETATM   17  H2  UNL     1      -3.177  -2.528  -0.026  1.00  0.00           H  
HETATM   18  H3  UNL     1      -2.192  -3.171   1.303  1.00  0.00           H  
HETATM   19  H4  UNL     1      -0.222  -3.486  -1.599  1.00  0.00           H  
HETATM   20  H5  UNL     1       0.813  -2.355  -2.481  1.00  0.00           H  
HETATM   21  H6  UNL     1       1.452  -3.069  -0.952  1.00  0.00           H  
HETATM   22  H7  UNL     1       1.502   2.334  -1.310  1.00  0.00           H  
HETATM   23  H8  UNL     1       3.634   1.865   0.606  1.00  0.00           H  
HETATM   24  H9  UNL     1       2.199   0.945   1.135  1.00  0.00           H  
HETATM   25  H10 UNL     1       2.103   2.742   0.833  1.00  0.00           H  
HETATM   26  H11 UNL     1       3.710   2.558  -1.588  1.00  0.00           H  
HETATM   27  H12 UNL     1      -1.980   0.269   2.572  1.00  0.00           H  
HETATM   28  H13 UNL     1      -3.391   0.011   1.413  1.00  0.00           H  
HETATM   29  H14 UNL     1      -2.563   1.846   0.010  1.00  0.00           H  
HETATM   30  H15 UNL     1      -2.402   2.526   1.725  1.00  0.00           H  
HETATM   31  H16 UNL     1      -0.304   2.492   0.196  1.00  0.00           H  
HETATM   32  H17 UNL     1      -0.099   1.763   1.827  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3   12   12
CONECT    3    4    5    5
CONECT    4   19   20   21
CONECT    5    6   11
CONECT    6    7    7    8
CONECT    8    9   10   22
CONECT    9   23   24   25
CONECT   10   26
CONECT   11   12   15
CONECT   12   13
CONECT   13   14   27   28
CONECT   14   15   29   30
CONECT   15   31   32
END

HMDB0040010
     RDKit          3D
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone
 32 33  0  0  0  0  0  0  0  0999 V2000
   -2.1348   -2.8367    0.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270   -1.6825    0.0658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0644   -1.6034   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5468   -2.7065   -1.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4387   -0.3229   -0.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6837    0.1724   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3150   -0.6802   -1.8556 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1957    1.5342   -0.9821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5340    1.7882    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4007    1.6260   -1.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4200    0.3431    0.2747 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242   -0.4489    0.6387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548    0.3396    1.5321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1069    1.7404    1.0251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5825    1.6742    0.8551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -3.6800   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1768   -2.5280   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1916   -3.1713    1.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2222   -3.4864   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126   -2.3547   -2.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4522   -3.0685   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    2.3343   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6338    1.8654    0.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1992    0.9453    1.1351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1033    2.7425    0.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7099    2.5583   -1.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9797    0.2686    2.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3908    0.0113    1.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5634    1.8456    0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4019    2.5258    1.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3036    2.4916    0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0988    1.7633    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 12  2  2  0
 15 11  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  4 19  1  0
  4 20  1  0
  4 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 14 30  1  0
 15 31  1  0
 15 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,3-dihydro-6,7-Dimethyl-5-(2-hydroxypropionyl)-1H-pyrrolizine	HMDB

Chemical Formula

C₁₂H₁₇NO₂

Average Molecular Weight

207.2689

Monoisotopic Molecular Weight

207.125928793

IUPAC Name

1-(6,7-dimethyl-2,3-dihydro-1H-pyrrolizin-5-yl)-2-hydroxypropan-1-one

Traditional Name

1-(1,2-dimethyl-6,7-dihydro-5H-pyrrolizin-3-yl)-2-hydroxypropan-1-one

CAS Registry Number

97073-12-6

SMILES

CC(O)C(=O)C1=C(C)C(C)=C2CCCN12

InChI Identifier

InChI=1S/C12H17NO2/c1-7-8(2)11(12(15)9(3)14)13-6-4-5-10(7)13/h9,14H,4-6H2,1-3H3

InChI Key

ZCNNVEPQSPOCJM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolizines. Pyrrolizines are compounds containing a pyrrolizine moiety, which consists of a pyrrole ring fused to a pyrrolidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolizines

Sub Class

Not Available

Direct Parent

Pyrrolizines

Alternative Parents

Substituents

Pyrrolizine
Aryl alkyl ketone
Aryl ketone
Acyloin
Substituted pyrrole
Alpha-hydroxy ketone
Pyrrole
Heteroaromatic compound
Ketone
Secondary alcohol
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0040010)
Cytoplasm (HMDB: HMDB0040010)

Source

Exogenous

Food

Food (HMDB: HMDB0040010)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0040010)

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	671.7 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.14 g/L	ALOGPS
logP	1.42	ALOGPS
logP	1.78	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	13.74	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	42.23 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	60.21 m³·mol⁻¹	ChemAxon
Polarizability	23.65 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	151.069	31661259
DarkChem	[M-H]-	146.059	31661259
DeepCCS	[M-2H]-	179.301	30932474
DeepCCS	[M+Na]+	154.179	30932474
AllCCS	[M+H]+	146.3	32859911
AllCCS	[M+H-H2O]+	142.1	32859911
AllCCS	[M+NH4]+	150.1	32859911
AllCCS	[M+Na]+	151.2	32859911
AllCCS	[M-H]-	152.2	32859911
AllCCS	[M+Na-2H]-	152.6	32859911
AllCCS	[M+HCOO]-	153.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone	CC(O)C(=O)C1=C(C)C(C)=C2CCCN12	2516.1	Standard polar	33892256
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone	CC(O)C(=O)C1=C(C)C(C)=C2CCCN12	1927.5	Standard non polar	33892256
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone	CC(O)C(=O)C1=C(C)C(C)=C2CCCN12	1869.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone,1TMS,isomer #1	CC1=C2CCCN2C(C(=O)C(C)O[Si](C)(C)C)=C1C	1879.6	Semi standard non polar	33892256
1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone,1TBDMS,isomer #1	CC1=C2CCCN2C(C(=O)C(C)O[Si](C)(C)C(C)(C)C)=C1C	2110.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone GC-MS (Non-derivatized) - 70eV, Positive	splash10-03di-3900000000-5cd525ad3f436001e2f5	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone GC-MS (1 TMS) - 70eV, Positive	splash10-0303-9520000000-52611f86125ed8f38f56	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 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 - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 10V, Positive-QTOF	splash10-0a4l-0980000000-7990059e971858d3005b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 20V, Positive-QTOF	splash10-001i-0910000000-dae1dbe16e8038721715	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 40V, Positive-QTOF	splash10-00lu-2900000000-992a241085071420ff67	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 10V, Negative-QTOF	splash10-0a4i-0290000000-52ed20c8245960e4e178	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 20V, Negative-QTOF	splash10-03di-0910000000-3a80de08cdd57bf63a24	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 40V, Negative-QTOF	splash10-02am-4900000000-113306d3090ccf0b5c4a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 10V, Negative-QTOF	splash10-0a4i-0090000000-bc1578d935014f0ac50f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 20V, Negative-QTOF	splash10-000x-7920000000-a06ed2c31a9d3173adba	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 40V, Negative-QTOF	splash10-0159-5900000000-7a67401476019497d1ba	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 10V, Positive-QTOF	splash10-0a4i-0390000000-f9e31a93a5425dac9875	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 20V, Positive-QTOF	splash10-0a4l-1960000000-df25a6f88765150facb0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone 40V, Positive-QTOF	splash10-0a59-5900000000-ead7227373b4ea5fdf07	2021-09-22	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB019692

KNApSAcK ID

Not Available

Chemspider ID

35014911

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

86127015

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1881441

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for 1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone (HMDB0040010)

MOL for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

3D MOL for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

3D SDF for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

3D-SDF for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

PDB for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

3D PDB for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

SMILES for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

INCHI for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

Structure for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

3D Structure for HMDB0040010 (1-(2,3-Dihydro-6,7-dimethyl-1H-pyrrolizin-5-yl)-2-hydroxy-1-propanone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra