MiMeDB: Showing metabocard for Pyrraline (MMDBc0000481)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:38:44 UTC

Update Date

2024-04-30 19:32:34 UTC

Metabolite ID

MMDBc0000481

Metabolite Identification

Common Name

Pyrraline

Description

Pyrraline is Maillard produced, obtained by reaction between BCS47-B and HHS42-T.

Structure

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

HMDB0033143
     RDKit          3D
Pyrraline
 36 36  0  0  0  0  0  0  0  0999 V2000
    3.7920    0.0437    1.2875 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1493    0.0163   -0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9150   -0.8678    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097   -0.3839    0.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3504   -1.1277    1.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3135   -1.1460   -0.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8441    0.1549   -0.3875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4871    0.9481   -1.3902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6278    0.7057   -2.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0978   -0.3781   -2.8276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220    2.1351   -1.2108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045    1.9984   -0.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7636    0.7465    0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3938    0.1599    1.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7600    0.5352    1.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0820   -0.4842   -1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2402   -0.8072   -0.7072 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -0.5850   -2.3389 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197   -0.8535    1.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7390    0.4300    1.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8117    1.0533   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2808   -1.8993    0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4928   -1.0022   -0.9657 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4255   -0.4289    2.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7775    0.7137    0.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9278   -0.7645    2.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1466   -2.2358    1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394   -1.8343    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7835   -1.6239   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4164    1.5176   -3.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1497    2.9871   -1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6905    2.7366    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3290   -0.9260    1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8757    0.4877    2.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3135   -0.2060    1.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450    0.1843   -2.9786 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  8 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 13  7  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  9 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 18 36  1  0
M  END


  Mrv1652309121709232D          

 18 18  0  0  0  0            999 V2000
   -3.3159    1.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    2.4660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0101    2.1304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9034    1.1384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4833    0.7579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6548   -0.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2957    2.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1333    2.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8477    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5622    2.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9912    2.5429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767    1.3054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5622    3.3679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9353    3.2729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3223    3.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  3  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000481

> <DATABASE_NAME>
MIME

> <SMILES>
NC(CCCCN1C(CO)=CC=C1C=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H18N2O4/c13-11(12(17)18)3-1-2-6-14-9(7-15)4-5-10(14)8-16/h4-5,7,11,16H,1-3,6,8,13H2,(H,17,18)

> <INCHI_KEY>
VTYFITADLSVOAS-UHFFFAOYSA-N

> <FORMULA>
C12H18N2O4

> <MOLECULAR_WEIGHT>
254.2823

> <EXACT_MASS>
254.126657074

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
26.658317639728928

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-6-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]hexanoic acid

> <ALOGPS_LOGP>
-1.59

> <JCHEM_LOGP>
-2.2856380641666174

> <ALOGPS_LOGS>
-2.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.630287988067721

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.025976806842895

> <JCHEM_PKA_STRONGEST_BASIC>
9.326523050009708

> <JCHEM_POLAR_SURFACE_AREA>
105.55

> <JCHEM_REFRACTIVITY>
66.75909999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.16e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-6-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0033143
     RDKit          3D
Pyrraline
 36 36  0  0  0  0  0  0  0  0999 V2000
    3.7920    0.0437    1.2875 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1493    0.0163   -0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9150   -0.8678    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097   -0.3839    0.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3504   -1.1277    1.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3135   -1.1460   -0.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8441    0.1549   -0.3875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4871    0.9481   -1.3902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6278    0.7057   -2.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0978   -0.3781   -2.8276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220    2.1351   -1.2108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045    1.9984   -0.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7636    0.7465    0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3938    0.1599    1.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7600    0.5352    1.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0820   -0.4842   -1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2402   -0.8072   -0.7072 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -0.5850   -2.3389 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197   -0.8535    1.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7390    0.4300    1.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8117    1.0533   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2808   -1.8993    0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4928   -1.0022   -0.9657 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4255   -0.4289    2.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7775    0.7137    0.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9278   -0.7645    2.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1466   -2.2358    1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394   -1.8343    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7835   -1.6239   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4164    1.5176   -3.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1497    2.9871   -1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6905    2.7366    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3290   -0.9260    1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8757    0.4877    2.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3135   -0.2060    1.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450    0.1843   -2.9786 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  8 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 13  7  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  9 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 18 36  1  0
M  END

HEADER    PROTEIN                                 12-SEP-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-17         0                                  
HETATM    1  C   UNK     0      -6.190   3.459   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.159   4.603   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -3.752   3.977   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -3.913   2.445   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.420   2.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.769   1.415   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.089  -0.092   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.419   4.747   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.085   3.977   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.249   4.747   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.582   3.977   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.916   4.747   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.250   3.977   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.583   4.747   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.250   2.437   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       2.916   6.287   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -5.479   6.109   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.335   7.140   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6                                                            
CONECT    8    3    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12                                                            
CONECT   17    2   18                                                       
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0033143
HETATM    1  N1  UNL     1       3.792   0.044   1.288  1.00  0.00           N  
HETATM    2  C1  UNL     1       3.149   0.016  -0.006  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.915  -0.868   0.008  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.910  -0.384   0.998  1.00  0.00           C  
HETATM    5  C4  UNL     1      -0.350  -1.128   1.112  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.313  -1.146  -0.033  1.00  0.00           C  
HETATM    7  N2  UNL     1      -1.844   0.155  -0.387  1.00  0.00           N  
HETATM    8  C6  UNL     1      -1.487   0.948  -1.390  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.628   0.706  -2.543  1.00  0.00           C  
HETATM   10  O1  UNL     1      -0.098  -0.378  -2.828  1.00  0.00           O  
HETATM   11  C8  UNL     1      -2.222   2.135  -1.211  1.00  0.00           C  
HETATM   12  C9  UNL     1      -3.004   1.998  -0.092  1.00  0.00           C  
HETATM   13  C10 UNL     1      -2.764   0.746   0.425  1.00  0.00           C  
HETATM   14  C11 UNL     1      -3.394   0.160   1.641  1.00  0.00           C  
HETATM   15  O2  UNL     1      -4.760   0.535   1.692  1.00  0.00           O  
HETATM   16  C12 UNL     1       4.082  -0.484  -1.036  1.00  0.00           C  
HETATM   17  O3  UNL     1       5.240  -0.807  -0.707  1.00  0.00           O  
HETATM   18  O4  UNL     1       3.656  -0.585  -2.339  1.00  0.00           O  
HETATM   19  H1  UNL     1       3.720  -0.854   1.796  1.00  0.00           H  
HETATM   20  H2  UNL     1       4.739   0.430   1.223  1.00  0.00           H  
HETATM   21  H3  UNL     1       2.812   1.053  -0.221  1.00  0.00           H  
HETATM   22  H4  UNL     1       2.281  -1.899   0.337  1.00  0.00           H  
HETATM   23  H5  UNL     1       1.493  -1.002  -0.966  1.00  0.00           H  
HETATM   24  H6  UNL     1       1.426  -0.429   2.007  1.00  0.00           H  
HETATM   25  H7  UNL     1       0.777   0.714   0.835  1.00  0.00           H  
HETATM   26  H8  UNL     1      -0.928  -0.764   2.030  1.00  0.00           H  
HETATM   27  H9  UNL     1      -0.147  -2.236   1.332  1.00  0.00           H  
HETATM   28  H10 UNL     1      -2.139  -1.834   0.218  1.00  0.00           H  
HETATM   29  H11 UNL     1      -0.783  -1.624  -0.884  1.00  0.00           H  
HETATM   30  H12 UNL     1      -0.416   1.518  -3.224  1.00  0.00           H  
HETATM   31  H13 UNL     1      -2.150   2.987  -1.870  1.00  0.00           H  
HETATM   32  H14 UNL     1      -3.691   2.737   0.319  1.00  0.00           H  
HETATM   33  H15 UNL     1      -3.329  -0.926   1.568  1.00  0.00           H  
HETATM   34  H16 UNL     1      -2.876   0.488   2.569  1.00  0.00           H  
HETATM   35  H17 UNL     1      -5.313  -0.206   1.319  1.00  0.00           H  
HETATM   36  H18 UNL     1       3.645   0.184  -2.979  1.00  0.00           H  
CONECT    1    2   19   20
CONECT    2    3   16   21
CONECT    3    4   22   23
CONECT    4    5   24   25
CONECT    5    6   26   27
CONECT    6    7   28   29
CONECT    7    8   13
CONECT    8    9   11   11
CONECT    9   10   10   30
CONECT   11   12   31
CONECT   12   13   13   32
CONECT   13   14
CONECT   14   15   33   34
CONECT   15   35
CONECT   16   17   17   18
CONECT   18   36
END

HMDB0033143
     RDKit          3D
Pyrraline
 36 36  0  0  0  0  0  0  0  0999 V2000
    3.7920    0.0437    1.2875 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1493    0.0163   -0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9150   -0.8678    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097   -0.3839    0.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3504   -1.1277    1.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3135   -1.1460   -0.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8441    0.1549   -0.3875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4871    0.9481   -1.3902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6278    0.7057   -2.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0978   -0.3781   -2.8276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220    2.1351   -1.2108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045    1.9984   -0.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7636    0.7465    0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3938    0.1599    1.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7600    0.5352    1.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0820   -0.4842   -1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2402   -0.8072   -0.7072 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -0.5850   -2.3389 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197   -0.8535    1.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7390    0.4300    1.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8117    1.0533   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2808   -1.8993    0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4928   -1.0022   -0.9657 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4255   -0.4289    2.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7775    0.7137    0.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9278   -0.7645    2.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1466   -2.2358    1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394   -1.8343    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7835   -1.6239   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4164    1.5176   -3.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1497    2.9871   -1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6905    2.7366    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3290   -0.9260    1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8757    0.4877    2.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3135   -0.2060    1.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450    0.1843   -2.9786 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  8 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 13  7  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  9 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 18 36  1  0
M  END

Synonyms

Value	Source
2-Amino-6-(2-formyl-5-hydroxymethylpyrrol-1-yl)hexanoic acid	MeSH
2-Formyl-5-(hydroxymethyl)pyrrole-1-norleucine	MeSH
2-FHMPN	MeSH
2-Amino-6-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]hexanoate	Generator
Pyrraline	MeSH

Molecular Formula

C₁₂H₁₈N₂O₄

Average Mass

254.2823

Monoisotopic Mass

254.126657074

IUPAC Name

2-amino-6-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]hexanoic acid

Traditional Name

2-amino-6-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]hexanoic acid

CAS Registry Number

Not Available

SMILES

NC(CCCCN1C(CO)=CC=C1C=O)C(O)=O

InChI Identifier

InChI=1S/C12H18N2O4/c13-11(12(17)18)3-1-2-6-14-9(7-15)4-5-10(14)8-16/h4-5,7,11,16H,1-3,6,8,13H2,(H,17,18)

InChI Key

VTYFITADLSVOAS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids

Alternative Parents

Substituents

Alpha-amino acid
Medium-chain fatty acid
Amino fatty acid
Heterocyclic fatty acid
Hydroxy fatty acid
Aryl-aldehyde
Substituted pyrrole
Fatty acid
Fatty acyl
Pyrrole
Heteroaromatic compound
Amino acid
Azacycle
Organoheterocyclic compound
Carboxylic acid
Monocarboxylic acid or derivatives
Aldehyde
Primary amine
Primary alcohol
Organooxygen compound
Organonitrogen compound
Alcohol
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Aromatic alcohol
Carbonyl group
Organic oxygen compound
Amine
Organic nitrogen compound
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	2.16 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-2.3	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	2.03	ChemAxon
pKa (Strongest Basic)	9.33	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.55 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	66.76 m³·mol⁻¹	ChemAxon
Polarizability	26.66 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Verrucomicrobia	1	Human feces; Human stool; Human ; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Firmicutes	7	Human stool; Human ; Human feces; Human urine; Human sputum; Human saliva; Human subgingival plaque; Human vaginal fluid; Human supragingival plaque	Indirect association between microbiota composition and metabolites measured in host biospecimen
Archaea	Euryarchaeota	1	Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen
Archaea	Euryarchaeota	1	Human feces; Human	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	27543620
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0033143

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB011144

KNApSAcK ID

Not Available

Chemspider ID

19980286

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14274616

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

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

Showing metabocard for Pyrraline (MMDBc0000481)

MOL for #<Metabolite:0x00007f923000dc90>

3D MOL for #<Metabolite:0x00007f923000dc90>

3D SDF for #<Metabolite:0x00007f923000dc90>

3D-SDF for #<Metabolite:0x00007f923000dc90>

PDB for #<Metabolite:0x00007f923000dc90>

3D PDB for #<Metabolite:0x00007f923000dc90>

SMILES for #<Metabolite:0x00007f923000dc90>

INCHI for #<Metabolite:0x00007f923000dc90>

Structure for #<Metabolite:0x00007f923000dc90>

3D Structure for #<Metabolite:0x00007f923000dc90>