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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:37:59 UTC

Update Date

2021-09-26 22:52:15 UTC

HMDB ID

HMDB0244479

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Methyl-N-2-propynyl-1-indanamine, (S)-

Description

N-Methyl-N-2-propynyl-1-indanamine, (S)- belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring. Based on a literature review very few articles have been published on N-Methyl-N-2-propynyl-1-indanamine, (S)-. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-methyl-n-2-propynyl-1-indanamine, (s)- is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-Methyl-N-2-propynyl-1-indanamine, (S)- 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

HMDB0244479
     RDKit          3D
N-Methyl-N-2-propynyl-1-indanamine, (S)-
 29 30  0  0  0  0  0  0  0  0999 V2000
    2.9175   -0.1786    2.2630 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2654   -0.6981    1.3889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -1.3423    0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3286   -0.6160   -0.8301 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4918   -0.4433   -1.6241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553    0.3950   -0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5870    1.5655    0.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    2.1874    0.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292    0.9506    0.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8750    0.7355    0.7035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4926   -0.5153    0.7053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7763   -1.5259    0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511   -1.3685   -0.4356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9602   -0.1077   -0.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4851    0.2699    3.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9669   -2.3317    0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5228   -1.6618    0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371   -0.6680   -2.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9154    0.5834   -1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2948   -1.1731   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1954    0.7765   -1.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7669    1.2583    1.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    2.2826   -0.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9578    2.9174    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9904    2.5693   -0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4498    1.5494    1.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4550   -0.6882    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1974   -2.5314    0.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9932   -2.1909   -0.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14  6  1  0
 14  9  1  0
  1 15  1  0
  3 16  1  0
  3 17  1  0
  5 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
M  END


  Mrv1652309102123382D          

 14 15  0  0  0  0            999 V2000
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4331   -3.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  3  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  6 14  1  0  0  0  0
  9 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0244479

> <DATABASE_NAME>
hmdb

> <SMILES>
CN(CC#C)C1CCC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C13H15N/c1-3-10-14(2)13-9-8-11-6-4-5-7-12(11)13/h1,4-7,13H,8-10H2,2H3

> <INCHI_KEY>
CSVGVHNFFZWQJU-UHFFFAOYSA-N

> <FORMULA>
C13H15N

> <MOLECULAR_WEIGHT>
185.27

> <EXACT_MASS>
185.120449487

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
21.70157754439245

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-methyl-N-(prop-2-yn-1-yl)-2,3-dihydro-1H-inden-1-amine

> <ALOGPS_LOGP>
2.59

> <JCHEM_LOGP>
2.6869498703333328

> <ALOGPS_LOGS>
-3.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.460249719663542

> <JCHEM_POLAR_SURFACE_AREA>
3.24

> <JCHEM_REFRACTIVITY>
59.76170000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
indanamin

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0244479
     RDKit          3D
N-Methyl-N-2-propynyl-1-indanamine, (S)-
 29 30  0  0  0  0  0  0  0  0999 V2000
    2.9175   -0.1786    2.2630 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2654   -0.6981    1.3889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -1.3423    0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3286   -0.6160   -0.8301 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4918   -0.4433   -1.6241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553    0.3950   -0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5870    1.5655    0.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    2.1874    0.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292    0.9506    0.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8750    0.7355    0.7035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4926   -0.5153    0.7053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7763   -1.5259    0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511   -1.3685   -0.4356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9602   -0.1077   -0.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4851    0.2699    3.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9669   -2.3317    0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5228   -1.6618    0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371   -0.6680   -2.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9154    0.5834   -1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2948   -1.1731   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1954    0.7765   -1.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7669    1.2583    1.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    2.2826   -0.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9578    2.9174    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9904    2.5693   -0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4498    1.5494    1.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4550   -0.6882    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1974   -2.5314    0.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9932   -2.1909   -0.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14  6  1  0
 14  9  1  0
  1 15  1  0
  3 16  1  0
  3 17  1  0
  5 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       1.650  -4.013   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.808  -7.263   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    6    9                                                  
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

COMPND    HMDB0244479
HETATM    1  C1  UNL     1       2.918  -0.179   2.263  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.265  -0.698   1.389  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.479  -1.342   0.361  1.00  0.00           C  
HETATM    4  N1  UNL     1       1.329  -0.616  -0.830  1.00  0.00           N  
HETATM    5  C4  UNL     1       2.492  -0.443  -1.624  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.355   0.395  -0.915  1.00  0.00           C  
HETATM    7  C6  UNL     1       0.587   1.565   0.028  1.00  0.00           C  
HETATM    8  C7  UNL     1      -0.807   2.187   0.043  1.00  0.00           C  
HETATM    9  C8  UNL     1      -1.629   0.951   0.154  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.875   0.735   0.703  1.00  0.00           C  
HETATM   11  C10 UNL     1      -3.493  -0.515   0.705  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.776  -1.526   0.119  1.00  0.00           C  
HETATM   13  C12 UNL     1      -1.551  -1.369  -0.436  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.960  -0.108  -0.419  1.00  0.00           C  
HETATM   15  H1  UNL     1       3.485   0.270   3.030  1.00  0.00           H  
HETATM   16  H2  UNL     1       1.967  -2.332   0.095  1.00  0.00           H  
HETATM   17  H3  UNL     1       0.523  -1.662   0.838  1.00  0.00           H  
HETATM   18  H4  UNL     1       2.237  -0.668  -2.688  1.00  0.00           H  
HETATM   19  H5  UNL     1       2.915   0.583  -1.625  1.00  0.00           H  
HETATM   20  H6  UNL     1       3.295  -1.173  -1.310  1.00  0.00           H  
HETATM   21  H7  UNL     1       0.195   0.777  -1.914  1.00  0.00           H  
HETATM   22  H8  UNL     1       0.767   1.258   1.073  1.00  0.00           H  
HETATM   23  H9  UNL     1       1.326   2.283  -0.374  1.00  0.00           H  
HETATM   24  H10 UNL     1      -0.958   2.917   0.827  1.00  0.00           H  
HETATM   25  H11 UNL     1      -0.990   2.569  -0.987  1.00  0.00           H  
HETATM   26  H12 UNL     1      -3.450   1.549   1.182  1.00  0.00           H  
HETATM   27  H13 UNL     1      -4.455  -0.688   1.132  1.00  0.00           H  
HETATM   28  H14 UNL     1      -3.197  -2.531   0.086  1.00  0.00           H  
HETATM   29  H15 UNL     1      -0.993  -2.191  -0.907  1.00  0.00           H  
CONECT    1    2    2    2   15
CONECT    2    3
CONECT    3    4   16   17
CONECT    4    5    6
CONECT    5   18   19   20
CONECT    6    7   14   21
CONECT    7    8   22   23
CONECT    8    9   24   25
CONECT    9   10   10   14
CONECT   10   11   26
CONECT   11   12   12   27
CONECT   12   13   28
CONECT   13   14   14   29
END

HMDB0244479
     RDKit          3D
N-Methyl-N-2-propynyl-1-indanamine, (S)-
 29 30  0  0  0  0  0  0  0  0999 V2000
    2.9175   -0.1786    2.2630 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2654   -0.6981    1.3889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -1.3423    0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3286   -0.6160   -0.8301 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4918   -0.4433   -1.6241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553    0.3950   -0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5870    1.5655    0.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    2.1874    0.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292    0.9506    0.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8750    0.7355    0.7035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4926   -0.5153    0.7053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7763   -1.5259    0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511   -1.3685   -0.4356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9602   -0.1077   -0.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4851    0.2699    3.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9669   -2.3317    0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5228   -1.6618    0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371   -0.6680   -2.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9154    0.5834   -1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2948   -1.1731   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1954    0.7765   -1.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7669    1.2583    1.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    2.2826   -0.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9578    2.9174    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9904    2.5693   -0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4498    1.5494    1.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4550   -0.6882    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1974   -2.5314    0.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9932   -2.1909   -0.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14  6  1  0
 14  9  1  0
  1 15  1  0
  3 16  1  0
  3 17  1  0
  5 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₃H₁₅N

Average Molecular Weight

185.27

Monoisotopic Molecular Weight

185.120449487

IUPAC Name

N-methyl-N-(prop-2-yn-1-yl)-2,3-dihydro-1H-inden-1-amine

Traditional Name

indanamin

CAS Registry Number

Not Available

SMILES

CN(CC#C)C1CCC2=CC=CC=C12

InChI Identifier

InChI=1S/C13H15N/c1-3-10-14(2)13-9-8-11-6-4-5-7-12(11)13/h1,4-7,13H,8-10H2,2H3

InChI Key

CSVGVHNFFZWQJU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Indanes

Sub Class

Not Available

Direct Parent

Indanes

Alternative Parents

Substituents

Indane
Aralkylamine
Tertiary aliphatic amine
Tertiary amine
Acetylide
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Amine
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (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	2.59	ALOGPS
logP	2.69	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Basic)	8.46	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	3.24 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	59.76 m³·mol⁻¹	ChemAxon
Polarizability	21.7 Å³	ChemAxon
Number of Rings	2	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]-	171.588	30932474
DeepCCS	[M+Na]+	147.126	30932474
AllCCS	[M+H]+	142.6	32859911
AllCCS	[M+H-H2O]+	138.4	32859911
AllCCS	[M+NH4]+	146.5	32859911
AllCCS	[M+Na]+	147.6	32859911
AllCCS	[M-H]-	146.5	32859911
AllCCS	[M+Na-2H]-	146.9	32859911
AllCCS	[M+HCOO]-	147.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Methyl-N-2-propynyl-1-indanamine, (S)-	CN(CC#C)C1CCC2=CC=CC=C12	2062.1	Standard polar	33892256
N-Methyl-N-2-propynyl-1-indanamine, (S)-	CN(CC#C)C1CCC2=CC=CC=C12	1501.5	Standard non polar	33892256
N-Methyl-N-2-propynyl-1-indanamine, (S)-	CN(CC#C)C1CCC2=CC=CC=C12	1499.7	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 - N-Methyl-N-2-propynyl-1-indanamine, (S)- GC-MS (Non-derivatized) - 70eV, Positive	splash10-014i-3900000000-e301ad1cbeda935c4348	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 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 - N-Methyl-N-2-propynyl-1-indanamine, (S)- 10V, Positive-QTOF	splash10-00kr-2900000000-481504f715209f4e5253	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 20V, Positive-QTOF	splash10-014u-9700000000-78d6f5d5692b53a12080	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 40V, Positive-QTOF	splash10-0006-9600000000-fe63e1c711a87d6fbd6a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 10V, Negative-QTOF	splash10-001i-1900000000-161c7a51c76c245cd6b9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 20V, Negative-QTOF	splash10-00lr-2900000000-e5ba64d1e8c0bec2431d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Methyl-N-2-propynyl-1-indanamine, (S)- 40V, Negative-QTOF	splash10-0uxr-9200000000-d02b178d1f950a15286b	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

14447

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15179

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 N-Methyl-N-2-propynyl-1-indanamine, (S)- (HMDB0244479)

MOL for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

3D MOL for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

3D SDF for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

3D-SDF for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

PDB for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

3D PDB for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

SMILES for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

INCHI for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

Structure for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

3D Structure for HMDB0244479 (N-Methyl-N-2-propynyl-1-indanamine, (S)-)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra