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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-07 06:34:13 UTC

Update Date

2021-09-26 22:50:25 UTC

HMDB ID

HMDB0242710

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid

Description

(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group. Based on a literature review very few articles have been published on (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). (2r)-2-(diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 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

HMDB0242710
     RDKit          3D
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid
 35 36  0  0  0  0  0  0  0  0999 V2000
   -5.7899    1.8547   -0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3333    0.7932    0.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1283    0.0637    1.0760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773    0.3514   -0.2207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1979   -1.4662   -1.3681 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1710    0.1002    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -0.3659    0.7336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7275    0.5025    0.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5750    0.0537    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289   -1.2890    0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1124   -1.7758   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -0.9259   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408   -0.5746    0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0092    0.2870    0.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3126    0.7928   -0.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3873    1.6567   -0.6214 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5650    0.4527   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -0.4055   -1.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2423   -2.1442    0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5305   -1.7289    0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4463    1.3183   -1.1443 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5396    1.3431   -2.9234 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4411    3.2459   -0.3873 I   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049   -0.8189    0.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6216   -0.7219    1.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1149    0.9628    1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077    1.5526    0.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3658    0.7849    0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7238   -0.9560    1.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160    0.5734    1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9671    1.9403    0.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8579    0.8836   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071   -0.6829   -2.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405   -3.2072    0.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3511   -2.4506    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 10 19  1  0
 19 20  2  0
  4 21  1  0
 21 22  1  0
 21 23  1  0
 20  7  1  0
 18 12  1  0
  3 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 13 29  1  0
 14 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
M  END


  Mrv1652309072108442D          

 23 24  0  0  0  0            999 V2000
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 I   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 I   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.7145    0.0000 I   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  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
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  8 15  1  0  0  0  0
  3 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>
HMDB0242710

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)C(I)(CC1=CC=C(OC2=CC=C(O)C=C2)C=C1)N(I)I

> <INCHI_IDENTIFIER>
InChI=1S/C15H12I3NO4/c16-15(14(21)22,19(17)18)9-10-1-5-12(6-2-10)23-13-7-3-11(20)4-8-13/h1-8,20H,9H2,(H,21,22)

> <INCHI_KEY>
HGTMNBCXVHLDTM-UHFFFAOYSA-N

> <FORMULA>
C15H12I3NO4

> <MOLECULAR_WEIGHT>
650.977

> <EXACT_MASS>
650.79004

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
42.77551018641649

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid

> <ALOGPS_LOGP>
5.29

> <JCHEM_LOGP>
4.955849421999999

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.696096700599664

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2192288606145576

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5904224480272675

> <JCHEM_POLAR_SURFACE_AREA>
70.0

> <JCHEM_REFRACTIVITY>
111.83280000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.72e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242710
     RDKit          3D
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid
 35 36  0  0  0  0  0  0  0  0999 V2000
   -5.7899    1.8547   -0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3333    0.7932    0.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1283    0.0637    1.0760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773    0.3514   -0.2207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1979   -1.4662   -1.3681 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1710    0.1002    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -0.3659    0.7336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7275    0.5025    0.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5750    0.0537    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289   -1.2890    0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1124   -1.7758   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -0.9259   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408   -0.5746    0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0092    0.2870    0.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3126    0.7928   -0.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3873    1.6567   -0.6214 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5650    0.4527   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -0.4055   -1.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2423   -2.1442    0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5305   -1.7289    0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4463    1.3183   -1.1443 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5396    1.3431   -2.9234 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4411    3.2459   -0.3873 I   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049   -0.8189    0.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6216   -0.7219    1.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1149    0.9628    1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077    1.5526    0.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3658    0.7849    0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7238   -0.9560    1.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160    0.5734    1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9671    1.9403    0.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8579    0.8836   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071   -0.6829   -2.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405   -3.2072    0.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3511   -2.4506    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 10 19  1  0
 19 20  2  0
  4 21  1  0
 21 22  1  0
 21 23  1  0
 20  7  1  0
 18 12  1  0
  3 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 13 29  1  0
 14 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
M  END

HEADER    PROTEIN                                 07-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-21         0                                  
HETATM    1  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.437   1.334   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.977   1.334   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.667   2.667   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0       1.334   0.770   0.000  0.00  0.00           N+0
HETATM   13  I   UNK     0       1.334   2.310   0.000  0.00  0.00           I+0
HETATM   14  I   UNK     0       0.000  -0.000   0.000  0.00  0.00           I+0
HETATM   15  I   UNK     0       1.897  -1.334   0.000  0.00  0.00           I+0
HETATM   16  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   12   15                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    8                                                            
CONECT   16    3   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   48    0
END

COMPND    HMDB0242710
HETATM    1  O1  UNL     1      -5.790   1.855  -0.304  1.00  0.00           O  
HETATM    2  C1  UNL     1      -5.333   0.793   0.177  1.00  0.00           C  
HETATM    3  O2  UNL     1      -6.128   0.064   1.076  1.00  0.00           O  
HETATM    4  C2  UNL     1      -3.977   0.351  -0.221  1.00  0.00           C  
HETATM    5  I1  UNL     1      -4.198  -1.466  -1.368  1.00  0.00           I  
HETATM    6  C3  UNL     1      -3.171   0.100   1.002  1.00  0.00           C  
HETATM    7  C4  UNL     1      -1.785  -0.366   0.734  1.00  0.00           C  
HETATM    8  C5  UNL     1      -0.728   0.503   0.626  1.00  0.00           C  
HETATM    9  C6  UNL     1       0.575   0.054   0.367  1.00  0.00           C  
HETATM   10  C7  UNL     1       0.829  -1.289   0.211  1.00  0.00           C  
HETATM   11  O3  UNL     1       2.112  -1.776  -0.048  1.00  0.00           O  
HETATM   12  C8  UNL     1       3.180  -0.926  -0.159  1.00  0.00           C  
HETATM   13  C9  UNL     1       3.941  -0.575   0.946  1.00  0.00           C  
HETATM   14  C10 UNL     1       5.009   0.287   0.785  1.00  0.00           C  
HETATM   15  C11 UNL     1       5.313   0.793  -0.473  1.00  0.00           C  
HETATM   16  O4  UNL     1       6.387   1.657  -0.621  1.00  0.00           O  
HETATM   17  C12 UNL     1       4.565   0.453  -1.580  1.00  0.00           C  
HETATM   18  C13 UNL     1       3.502  -0.406  -1.415  1.00  0.00           C  
HETATM   19  C14 UNL     1      -0.242  -2.144   0.323  1.00  0.00           C  
HETATM   20  C15 UNL     1      -1.530  -1.729   0.577  1.00  0.00           C  
HETATM   21  N1  UNL     1      -3.446   1.318  -1.144  1.00  0.00           N  
HETATM   22  I2  UNL     1      -4.540   1.343  -2.923  1.00  0.00           I  
HETATM   23  I3  UNL     1      -3.441   3.246  -0.387  1.00  0.00           I  
HETATM   24  H1  UNL     1      -6.505  -0.819   0.701  1.00  0.00           H  
HETATM   25  H2  UNL     1      -3.622  -0.722   1.635  1.00  0.00           H  
HETATM   26  H3  UNL     1      -3.115   0.963   1.688  1.00  0.00           H  
HETATM   27  H4  UNL     1      -0.908   1.553   0.750  1.00  0.00           H  
HETATM   28  H5  UNL     1       1.366   0.785   0.293  1.00  0.00           H  
HETATM   29  H6  UNL     1       3.724  -0.956   1.936  1.00  0.00           H  
HETATM   30  H7  UNL     1       5.616   0.573   1.636  1.00  0.00           H  
HETATM   31  H8  UNL     1       6.967   1.940   0.145  1.00  0.00           H  
HETATM   32  H9  UNL     1       4.858   0.884  -2.528  1.00  0.00           H  
HETATM   33  H10 UNL     1       2.907  -0.683  -2.265  1.00  0.00           H  
HETATM   34  H11 UNL     1      -0.041  -3.207   0.200  1.00  0.00           H  
HETATM   35  H12 UNL     1      -2.351  -2.451   0.656  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   24
CONECT    4    5    6   21
CONECT    6    7   25   26
CONECT    7    8    8   20
CONECT    8    9   27
CONECT    9   10   10   28
CONECT   10   11   19
CONECT   11   12
CONECT   12   13   13   18
CONECT   13   14   29
CONECT   14   15   15   30
CONECT   15   16   17
CONECT   16   31
CONECT   17   18   18   32
CONECT   18   33
CONECT   19   20   20   34
CONECT   20   35
CONECT   21   22   23
END

HMDB0242710
     RDKit          3D
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid
 35 36  0  0  0  0  0  0  0  0999 V2000
   -5.7899    1.8547   -0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3333    0.7932    0.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1283    0.0637    1.0760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773    0.3514   -0.2207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1979   -1.4662   -1.3681 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1710    0.1002    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -0.3659    0.7336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7275    0.5025    0.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5750    0.0537    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289   -1.2890    0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1124   -1.7758   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -0.9259   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408   -0.5746    0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0092    0.2870    0.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3126    0.7928   -0.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3873    1.6567   -0.6214 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5650    0.4527   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -0.4055   -1.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2423   -2.1442    0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5305   -1.7289    0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4463    1.3183   -1.1443 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5396    1.3431   -2.9234 I   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4411    3.2459   -0.3873 I   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049   -0.8189    0.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6216   -0.7219    1.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1149    0.9628    1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077    1.5526    0.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3658    0.7849    0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7238   -0.9560    1.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160    0.5734    1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9671    1.9403    0.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8579    0.8836   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071   -0.6829   -2.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405   -3.2072    0.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3511   -2.4506    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 10 19  1  0
 19 20  2  0
  4 21  1  0
 21 22  1  0
 21 23  1  0
 20  7  1  0
 18 12  1  0
  3 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 13 29  1  0
 14 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoate	Generator

Chemical Formula

C₁₅H₁₂I₃NO₄

Average Molecular Weight

650.977

Monoisotopic Molecular Weight

650.79004

IUPAC Name

2-(diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid

Traditional Name

2-(diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)C(I)(CC1=CC=C(OC2=CC=C(O)C=C2)C=C1)N(I)I

InChI Identifier

InChI=1S/C15H12I3NO4/c16-15(14(21)22,19(17)18)9-10-1-5-12(6-2-10)23-13-7-3-11(20)4-8-13/h1-8,20H,9H2,(H,21,22)

InChI Key

HGTMNBCXVHLDTM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Diphenylethers

Direct Parent

Diphenylethers

Alternative Parents

Substituents

Diphenylether
3-phenylpropanoic-acid
Diaryl ether
Amphetamine or derivatives
Alpha-amino acid or derivatives
Phenoxy compound
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alpha-halocarboxylic acid or derivatives
Alpha-halocarboxylic acid
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organoiodide
Organohalogen compound
Carbonyl group
Alkyl iodide
Alkyl halide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	5.29	ALOGPS
logP	4.96	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	1.22	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	70 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	111.83 m³·mol⁻¹	ChemAxon
Polarizability	42.78 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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
DeepCCS	[M+H]+	197.524	30932474
DeepCCS	[M-H]-	195.166	30932474
DeepCCS	[M-2H]-	229.126	30932474
DeepCCS	[M+Na]+	204.479	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	13.1489 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.3 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1988.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	344.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	162.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	196.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	232.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	515.7 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	517.6 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	110.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1143.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	486.3 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1255.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	343.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	393.8 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	345.1 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	136.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	80.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid	OC(=O)C(I)(CC1=CC=C(OC2=CC=C(O)C=C2)C=C1)N(I)I	4702.8	Standard polar	33892256
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid	OC(=O)C(I)(CC1=CC=C(OC2=CC=C(O)C=C2)C=C1)N(I)I	3293.3	Standard non polar	33892256
(2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid	OC(=O)C(I)(CC1=CC=C(OC2=CC=C(O)C=C2)C=C1)N(I)I	3674.3	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 - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-03	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 - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 10V, Positive-QTOF	splash10-0udi-0000009000-8c931e9783af99739916	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 20V, Positive-QTOF	splash10-0udi-0001009000-f68f4d25d3f31181216b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 40V, Positive-QTOF	splash10-0006-9702020000-605a94e2702adbd4849c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 10V, Negative-QTOF	splash10-0002-0000009000-f8e74b77f02e17e351b1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 20V, Negative-QTOF	splash10-0002-0202209000-2441665b5efb682db6f8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid 40V, Negative-QTOF	splash10-003r-1900150000-6b165d62cd2d0617c293	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

15319560

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

20392096

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 (2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid (HMDB0242710)

MOL for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

3D MOL for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

3D SDF for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

3D-SDF for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

PDB for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

3D PDB for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

SMILES for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

INCHI for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

Structure for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

3D Structure for HMDB0242710 ((2R)-2-(Diiodoamino)-3-[4-(4-hydroxyphenoxy)phenyl]-2-iodopropanoic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra