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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 22:28:22 UTC

Update Date

2021-09-26 23:17:22 UTC

HMDB ID

HMDB0259676

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Ioflupane

Description

Ioflupane, also known as 123i-FP-cit or FPCIT, belongs to the class of organic compounds known as phenyltropanes. Phenyltropanes are compounds containing a phenyl group linked to a tropane moiety. Tropane is an organonitrogenous [3.2.1] bicyclic organic compound. Based on a literature review a significant number of articles have been published on Ioflupane. This compound has been identified in human blood as reported by (PMID: 31557052 ). Ioflupane is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Ioflupane 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

HMDB0259676
     RDKit          3D
Ioflupane
 46 48  0  0  0  0  0  0  0  0999 V2000
    0.8981    4.1891    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5736    2.8487   -0.1952 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    1.8934    0.7553 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    2.2908    1.9620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0026    0.4838    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -0.2683   -0.2842 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3239   -0.4172    0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4020   -0.7020   -0.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -0.8536   -0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9678   -0.7258    1.2788 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9507   -0.9656    1.9557 I   0  0  0  0  0  0  0  0  0  0  0  0
    3.9171   -0.4437    2.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6110   -0.2902    1.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -1.7008   -0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -1.5343   -1.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8182   -0.5823   -2.3480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    0.7429   -1.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3440    0.4262   -0.2325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8077   -0.9258   -0.2678 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -1.1043   -0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603   -0.5723    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0270   -1.2667    1.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2313   -2.6301    1.5517 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.1259    4.9004   -0.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688    4.4676    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8068    4.4128   -0.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1490   -0.0475    1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1622    0.0821   -1.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2269   -0.8145   -1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5146   -1.0816   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1415   -0.3418    3.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7974   -0.0696    2.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2399   -2.1075    0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1388   -2.3043   -1.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3062   -2.4901   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1069   -0.5738   -2.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6236   -0.8850   -3.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333    1.5425   -1.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425    1.1362   -2.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0339    1.1435    0.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3780   -2.1791   -0.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -0.5501   -1.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9741    0.4980    0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1860   -0.7212   -0.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0369   -1.0447    2.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7936   -0.8641    2.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
  6 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 18  5  1  0
 13  7  1  0
 19 15  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  5 27  1  0
  6 28  1  0
  8 29  1  0
  9 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 22 46  1  0
M  END

  Mrv1652309122100282D          

 23 25  0  0  0  0            999 V2000
    3.1574    2.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6430    2.3449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9444    1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.4540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257    1.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    0.6012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -0.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3940    0.1887    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5690    0.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1565   -0.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -0.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0810   -1.2403    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300   -0.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    0.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130    0.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255    0.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8505    0.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2630    0.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8505   -0.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255   -0.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0880    0.1887    0.0000 I   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  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  1  0  0  0  0
  6 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  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259676

> <DATABASE_NAME>
hmdb

> <SMILES>
COC(=O)C1C2CCC(CC1C1=CC=C(I)C=C1)N2CCCF

> <INCHI_IDENTIFIER>
InChI=1S/C18H23FINO2/c1-23-18(22)17-15(12-3-5-13(20)6-4-12)11-14-7-8-16(17)21(14)10-2-9-19/h3-6,14-17H,2,7-11H2,1H3

> <INCHI_KEY>
HXWLAJVUJSVENX-UHFFFAOYSA-N

> <FORMULA>
C18H23FINO2

> <MOLECULAR_WEIGHT>
431.29

> <EXACT_MASS>
431.07575

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
38.728396904165685

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 8-(3-fluoropropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylate

> <ALOGPS_LOGP>
4.24

> <JCHEM_LOGP>
3.701130281666666

> <ALOGPS_LOGS>
-4.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.455009222707973

> <JCHEM_POLAR_SURFACE_AREA>
29.54

> <JCHEM_REFRACTIVITY>
97.33820000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.66e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 8-(3-fluoropropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0259676
     RDKit          3D
Ioflupane
 46 48  0  0  0  0  0  0  0  0999 V2000
    0.8981    4.1891    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5736    2.8487   -0.1952 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    1.8934    0.7553 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    2.2908    1.9620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0026    0.4838    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -0.2683   -0.2842 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3239   -0.4172    0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4020   -0.7020   -0.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -0.8536   -0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9678   -0.7258    1.2788 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9507   -0.9656    1.9557 I   0  0  0  0  0  0  0  0  0  0  0  0
    3.9171   -0.4437    2.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6110   -0.2902    1.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -1.7008   -0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -1.5343   -1.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8182   -0.5823   -2.3480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    0.7429   -1.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3440    0.4262   -0.2325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8077   -0.9258   -0.2678 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -1.1043   -0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603   -0.5723    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0270   -1.2667    1.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2313   -2.6301    1.5517 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.1259    4.9004   -0.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688    4.4676    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8068    4.4128   -0.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1490   -0.0475    1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1622    0.0821   -1.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2269   -0.8145   -1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5146   -1.0816   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1415   -0.3418    3.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7974   -0.0696    2.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2399   -2.1075    0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1388   -2.3043   -1.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3062   -2.4901   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1069   -0.5738   -2.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6236   -0.8850   -3.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333    1.5425   -1.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425    1.1362   -2.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0339    1.1435    0.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3780   -2.1791   -0.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -0.5501   -1.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9741    0.4980    0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1860   -0.7212   -0.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0369   -1.0447    2.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7936   -0.8641    2.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
  6 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 18  5  1  0
 13  7  1  0
 19 15  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  5 27  1  0
  6 28  1  0
  8 29  1  0
  9 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 22 46  1  0
M  END

HEADER    PROTEIN                                 12-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-21         0                                  
HETATM    1  C   UNK     0       5.894   5.581   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.934   4.377   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.496   2.944   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.019   2.714   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.536   1.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.035   2.082   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.831   1.122   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.831  -0.418   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.035  -1.378   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       2.602   0.352   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.062   0.352   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.292  -0.982   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.248  -0.982   0.000  0.00  0.00           C+0
HETATM   14  F   UNK     0      -2.018  -2.315   0.000  0.00  0.00           F+0
HETATM   15  C   UNK     0       4.536  -1.035   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.204   0.352   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.744   0.352   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.514   1.686   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.054   1.686   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.824   0.352   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.054  -0.982   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.514  -0.982   0.000  0.00  0.00           C+0
HETATM   23  I   UNK     0      11.364   0.352   0.000  0.00  0.00           I+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   16                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9    6   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    9   16                                                       
CONECT   16   15    5   17                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   20                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

COMPND    HMDB0259676
HETATM    1  C1  UNL     1       0.898   4.189   0.017  1.00  0.00           C  
HETATM    2  O1  UNL     1       0.574   2.849  -0.195  1.00  0.00           O  
HETATM    3  C2  UNL     1       0.340   1.893   0.755  1.00  0.00           C  
HETATM    4  O2  UNL     1       0.434   2.291   1.962  1.00  0.00           O  
HETATM    5  C3  UNL     1      -0.003   0.484   0.503  1.00  0.00           C  
HETATM    6  C4  UNL     1       0.999  -0.268  -0.284  1.00  0.00           C  
HETATM    7  C5  UNL     1       2.324  -0.417   0.344  1.00  0.00           C  
HETATM    8  C6  UNL     1       3.402  -0.702  -0.500  1.00  0.00           C  
HETATM    9  C7  UNL     1       4.678  -0.854  -0.067  1.00  0.00           C  
HETATM   10  C8  UNL     1       4.968  -0.726   1.279  1.00  0.00           C  
HETATM   11  I1  UNL     1       6.951  -0.966   1.956  1.00  0.00           I  
HETATM   12  C9  UNL     1       3.917  -0.444   2.132  1.00  0.00           C  
HETATM   13  C10 UNL     1       2.611  -0.290   1.674  1.00  0.00           C  
HETATM   14  C11 UNL     1       0.454  -1.701  -0.475  1.00  0.00           C  
HETATM   15  C12 UNL     1      -0.877  -1.534  -1.199  1.00  0.00           C  
HETATM   16  C13 UNL     1      -0.818  -0.582  -2.348  1.00  0.00           C  
HETATM   17  C14 UNL     1      -1.158   0.743  -1.718  1.00  0.00           C  
HETATM   18  C15 UNL     1      -1.344   0.426  -0.233  1.00  0.00           C  
HETATM   19  N1  UNL     1      -1.808  -0.926  -0.268  1.00  0.00           N  
HETATM   20  C16 UNL     1      -3.155  -1.104  -0.690  1.00  0.00           C  
HETATM   21  C17 UNL     1      -4.160  -0.572   0.307  1.00  0.00           C  
HETATM   22  C18 UNL     1      -4.027  -1.267   1.649  1.00  0.00           C  
HETATM   23  F1  UNL     1      -4.231  -2.630   1.552  1.00  0.00           F  
HETATM   24  H1  UNL     1       0.126   4.900  -0.391  1.00  0.00           H  
HETATM   25  H2  UNL     1       1.169   4.468   1.034  1.00  0.00           H  
HETATM   26  H3  UNL     1       1.807   4.413  -0.615  1.00  0.00           H  
HETATM   27  H4  UNL     1      -0.149  -0.048   1.466  1.00  0.00           H  
HETATM   28  H5  UNL     1       1.162   0.082  -1.330  1.00  0.00           H  
HETATM   29  H6  UNL     1       3.227  -0.814  -1.584  1.00  0.00           H  
HETATM   30  H7  UNL     1       5.515  -1.082  -0.729  1.00  0.00           H  
HETATM   31  H8  UNL     1       4.141  -0.342   3.178  1.00  0.00           H  
HETATM   32  H9  UNL     1       1.797  -0.070   2.341  1.00  0.00           H  
HETATM   33  H10 UNL     1       0.240  -2.107   0.530  1.00  0.00           H  
HETATM   34  H11 UNL     1       1.139  -2.304  -1.083  1.00  0.00           H  
HETATM   35  H12 UNL     1      -1.306  -2.490  -1.535  1.00  0.00           H  
HETATM   36  H13 UNL     1       0.107  -0.574  -2.925  1.00  0.00           H  
HETATM   37  H14 UNL     1      -1.624  -0.885  -3.077  1.00  0.00           H  
HETATM   38  H15 UNL     1      -0.433   1.543  -1.901  1.00  0.00           H  
HETATM   39  H16 UNL     1      -2.143   1.136  -2.097  1.00  0.00           H  
HETATM   40  H17 UNL     1      -2.034   1.143   0.235  1.00  0.00           H  
HETATM   41  H18 UNL     1      -3.378  -2.179  -0.851  1.00  0.00           H  
HETATM   42  H19 UNL     1      -3.341  -0.550  -1.649  1.00  0.00           H  
HETATM   43  H20 UNL     1      -3.974   0.498   0.481  1.00  0.00           H  
HETATM   44  H21 UNL     1      -5.186  -0.721  -0.093  1.00  0.00           H  
HETATM   45  H22 UNL     1      -3.037  -1.045   2.093  1.00  0.00           H  
HETATM   46  H23 UNL     1      -4.794  -0.864   2.346  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3
CONECT    3    4    4    5
CONECT    5    6   18   27
CONECT    6    7   14   28
CONECT    7    8    8   13
CONECT    8    9   29
CONECT    9   10   10   30
CONECT   10   11   12
CONECT   12   13   13   31
CONECT   13   32
CONECT   14   15   33   34
CONECT   15   16   19   35
CONECT   16   17   36   37
CONECT   17   18   38   39
CONECT   18   19   40
CONECT   19   20
CONECT   20   21   41   42
CONECT   21   22   43   44
CONECT   22   23   45   46
END

HMDB0259676
     RDKit          3D
Ioflupane
 46 48  0  0  0  0  0  0  0  0999 V2000
    0.8981    4.1891    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5736    2.8487   -0.1952 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    1.8934    0.7553 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    2.2908    1.9620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0026    0.4838    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -0.2683   -0.2842 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3239   -0.4172    0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4020   -0.7020   -0.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -0.8536   -0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9678   -0.7258    1.2788 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9507   -0.9656    1.9557 I   0  0  0  0  0  0  0  0  0  0  0  0
    3.9171   -0.4437    2.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6110   -0.2902    1.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -1.7008   -0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -1.5343   -1.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8182   -0.5823   -2.3480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    0.7429   -1.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3440    0.4262   -0.2325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8077   -0.9258   -0.2678 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -1.1043   -0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603   -0.5723    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0270   -1.2667    1.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2313   -2.6301    1.5517 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.1259    4.9004   -0.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688    4.4676    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8068    4.4128   -0.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1490   -0.0475    1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1622    0.0821   -1.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2269   -0.8145   -1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5146   -1.0816   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1415   -0.3418    3.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7974   -0.0696    2.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2399   -2.1075    0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1388   -2.3043   -1.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3062   -2.4901   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1069   -0.5738   -2.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6236   -0.8850   -3.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333    1.5425   -1.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425    1.1362   -2.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0339    1.1435    0.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3780   -2.1791   -0.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -0.5501   -1.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9741    0.4980    0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1860   -0.7212   -0.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0369   -1.0447    2.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7936   -0.8641    2.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
  6 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 18  5  1  0
 13  7  1  0
 19 15  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  5 27  1  0
  6 28  1  0
  8 29  1  0
  9 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 22 46  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Methyl 8-(3-fluoropropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylic acid	HMDB
(O-Methyl-11C)beta-cit-FP	HMDB
2-Carbomethoxy-8-(3-fluoropropyl)-3-(4-iodophenyl)tropane	HMDB
I(123)-N-fluoropropyl-2-beta-carbomethoxy-3-(4-iodophenyl)nortropane	HMDB
N-Omega-fluoropropyl-2beta-carbomethoxy-3beta-(4-iodophenyl)tropane	HMDB
Fluoropropylcarbomethoxyiodophenylnortropane	HMDB
123I-FP-cit	HMDB
FPCIT	HMDB
beta-CIT-FP	HMDB
(18F)FP-CIT	HMDB
FP-CIT	HMDB
I(123)-N-omega-fluoropropyl-2-beta-carbomethoxy-3-beta(4-iodophenyl)nortropane	HMDB

Chemical Formula

C₁₈H₂₃FINO₂

Average Molecular Weight

431.29

Monoisotopic Molecular Weight

431.07575

IUPAC Name

methyl 8-(3-fluoropropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylate

Traditional Name

methyl 8-(3-fluoropropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1C2CCC(CC1C1=CC=C(I)C=C1)N2CCCF

InChI Identifier

InChI=1S/C18H23FINO2/c1-23-18(22)17-15(12-3-5-13(20)6-4-12)11-14-7-8-16(17)21(14)10-2-9-19/h3-6,14-17H,2,7-11H2,1H3

InChI Key

HXWLAJVUJSVENX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenyltropanes. Phenyltropanes are compounds containing a phenyl group linked to a tropane moiety. Tropane is an organonitrogenous [3.2.1] Bicyclic organic compound.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tropane alkaloids

Sub Class

Phenyltropanes

Direct Parent

Phenyltropanes

Alternative Parents

Substituents

Phenyltropane
Phenylpiperidine
Piperidinecarboxylic acid
Halobenzene
Aralkylamine
Iodobenzene
Aryl halide
Aryl iodide
Monocyclic benzene moiety
Benzenoid
N-alkylpyrrolidine
Piperidine
Methyl ester
Pyrrolidine
Tertiary aliphatic amine
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organohalogen compound
Organic nitrogen compound
Amine
Alkyl halide
Hydrocarbon derivative
Alkyl fluoride
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organofluoride
Organoiodide
Organonitrogen compound
Organooxygen compound
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	4.24	ALOGPS
logP	3.7	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	9.46	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.54 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	97.34 m³·mol⁻¹	ChemAxon
Polarizability	38.73 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	185.339	30932474
DeepCCS	[M-H]-	182.981	30932474
DeepCCS	[M-2H]-	216.662	30932474
DeepCCS	[M+Na]+	191.889	30932474
AllCCS	[M+H]+	190.7	32859911
AllCCS	[M+H-H2O]+	188.3	32859911
AllCCS	[M+NH4]+	192.9	32859911
AllCCS	[M+Na]+	193.5	32859911
AllCCS	[M-H]-	187.3	32859911
AllCCS	[M+Na-2H]-	188.1	32859911
AllCCS	[M+HCOO]-	189.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ioflupane	COC(=O)C1C2CCC(CC1C1=CC=C(I)C=C1)N2CCCF	3077.0	Standard polar	33892256
Ioflupane	COC(=O)C1C2CCC(CC1C1=CC=C(I)C=C1)N2CCCF	2538.2	Standard non polar	33892256
Ioflupane	COC(=O)C1C2CCC(CC1C1=CC=C(I)C=C1)N2CCCF	2638.2	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 - Ioflupane GC-MS (Non-derivatized) - 70eV, Positive	splash10-002g-6958300000-9018392f49218c55f0bb	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ioflupane GC-MS (Non-derivatized) - 70eV, Positive	Not Available	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

19116969

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ioflupane (123I)

METLIN ID

Not Available

PubChem Compound

22896913

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 Ioflupane (HMDB0259676)

MOL for HMDB0259676 (Ioflupane)

3D MOL for HMDB0259676 (Ioflupane)

3D SDF for HMDB0259676 (Ioflupane)

3D-SDF for HMDB0259676 (Ioflupane)

PDB for HMDB0259676 (Ioflupane)

3D PDB for HMDB0259676 (Ioflupane)

SMILES for HMDB0259676 (Ioflupane)

INCHI for HMDB0259676 (Ioflupane)

Structure for HMDB0259676 (Ioflupane)

3D Structure for HMDB0259676 (Ioflupane)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra