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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 11:10:12 UTC

Update Date

2021-09-26 23:05:58 UTC

HMDB ID

HMDB0253003

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane

Description

(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane, also known as (4-methoxyphenyl)(morpholin-4-yl)sulphanyl--phosphanethione or morpholin-4-ium-4-methoxyphenyl(morpholino)phosphinodithioate, belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. Based on a literature review very few articles have been published on (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane. This compound has been identified in human blood as reported by (PMID: 31557052 ). (4-methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 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

HMDB0253003
     RDKit          3D
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.3006    1.0284    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7173    0.4749   -0.2153 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4024    0.0446   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8663   -0.4879   -1.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.9043   -1.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7749   -0.8037   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -1.3421   -0.1644 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.4086   -1.7536   -1.7733 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0381   -3.0456    1.0702 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8855   -0.0243    0.4590 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8995    1.0294   -0.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0818    1.9253   -0.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2880    1.3259   -0.3009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3231    0.0423    0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1723   -0.4269    0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3226   -0.2704    0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6558    0.1571    0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3997    1.1078    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106    1.9820    1.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0415    0.3263    1.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4409   -0.5861   -2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0868   -1.3295   -2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0288   -3.9489    0.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7801    0.5945   -1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9841    1.6588   -0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0973    2.5331   -1.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    2.6920    0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2521   -0.0867    0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4816   -0.6720   -0.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382   -1.5436    1.0075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2907   -0.0646    1.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7050   -0.1969    1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0176    0.5651    1.8516 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  6 16  1  0
 16 17  2  0
 17  3  1  0
 15 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  5 22  1  0
  9 23  1  0
 11 24  1  0
 11 25  1  0
 12 26  1  0
 12 27  1  0
 14 28  1  0
 14 29  1  0
 15 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
M  END

  Mrv1652309112113102D          

 17 18  0  0  0  0            999 V2000
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    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   -3.3000    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
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -4.5375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.5375    0.0000 S   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0253003

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC=C(C=C1)P(S)(=S)N1CCOCC1

> <INCHI_IDENTIFIER>
InChI=1S/C11H16NO2PS2/c1-13-10-2-4-11(5-3-10)15(16,17)12-6-8-14-9-7-12/h2-5H,6-9H2,1H3,(H,16,17)

> <INCHI_KEY>
QDSAKNAFJWRQIV-UHFFFAOYSA-N

> <FORMULA>
C11H16NO2PS2

> <MOLECULAR_WEIGHT>
289.35

> <EXACT_MASS>
289.036008105

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
28.892759400481594

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4-methoxyphenyl)(morpholin-4-yl)sulfanyl-lambda5-phosphanethione

> <ALOGPS_LOGP>
3.36

> <JCHEM_LOGP>
1.8787000000000003

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.1949703640125

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0609647220196186

> <JCHEM_POLAR_SURFACE_AREA>
21.700000000000003

> <JCHEM_REFRACTIVITY>
76.09500000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4-methoxyphenyl)(morpholin-4-yl)sulfanyl-lambda5-phosphanethione

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0253003
     RDKit          3D
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.3006    1.0284    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7173    0.4749   -0.2153 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4024    0.0446   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8663   -0.4879   -1.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.9043   -1.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7749   -0.8037   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -1.3421   -0.1644 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.4086   -1.7536   -1.7733 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0381   -3.0456    1.0702 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8855   -0.0243    0.4590 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8995    1.0294   -0.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0818    1.9253   -0.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2880    1.3259   -0.3009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3231    0.0423    0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1723   -0.4269    0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3226   -0.2704    0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6558    0.1571    0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3997    1.1078    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106    1.9820    1.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0415    0.3263    1.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4409   -0.5861   -2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0868   -1.3295   -2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0288   -3.9489    0.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7801    0.5945   -1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9841    1.6588   -0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0973    2.5331   -1.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    2.6920    0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2521   -0.0867    0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4816   -0.6720   -0.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382   -1.5436    1.0075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2907   -0.0646    1.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7050   -0.1969    1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0176    0.5651    1.8516 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  6 16  1  0
 16 17  2  0
 17  3  1  0
 15 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  5 22  1  0
  9 23  1  0
 11 24  1  0
 11 25  1  0
 12 26  1  0
 12 27  1  0
 14 28  1  0
 14 29  1  0
 15 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -3.850   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  -6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    9  P   UNK     0       1.334  -8.470   0.000  0.00  0.00           P+0
HETATM   10  S   UNK     0      -0.206  -8.470   0.000  0.00  0.00           S+0
HETATM   11  N   UNK     0       1.334 -10.010   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334 -13.090   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.000 -10.780   0.000  0.00  0.00           C+0
HETATM   17  S   UNK     0       2.874  -8.470   0.000  0.00  0.00           S+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   11   17                                             
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    9                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0253003
HETATM    1  C1  UNL     1       5.301   1.028   0.958  1.00  0.00           C  
HETATM    2  O1  UNL     1       4.717   0.475  -0.215  1.00  0.00           O  
HETATM    3  C2  UNL     1       3.402   0.045  -0.227  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.866  -0.488  -1.380  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.551  -0.904  -1.346  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.775  -0.804  -0.211  1.00  0.00           C  
HETATM    7  P1  UNL     1      -0.928  -1.342  -0.164  1.00  0.00           P  
HETATM    8  S1  UNL     1      -1.409  -1.754  -1.773  1.00  0.00           S  
HETATM    9  S2  UNL     1      -1.038  -3.046   1.070  1.00  0.00           S  
HETATM   10  N1  UNL     1      -1.885  -0.024   0.459  1.00  0.00           N  
HETATM   11  C6  UNL     1      -1.900   1.029  -0.501  1.00  0.00           C  
HETATM   12  C7  UNL     1      -3.082   1.925  -0.431  1.00  0.00           C  
HETATM   13  O2  UNL     1      -4.288   1.326  -0.301  1.00  0.00           O  
HETATM   14  C8  UNL     1      -4.323   0.042   0.122  1.00  0.00           C  
HETATM   15  C9  UNL     1      -3.172  -0.427   0.932  1.00  0.00           C  
HETATM   16  C10 UNL     1       1.323  -0.270   0.933  1.00  0.00           C  
HETATM   17  C11 UNL     1       2.656   0.157   0.916  1.00  0.00           C  
HETATM   18  H1  UNL     1       6.400   1.108   0.862  1.00  0.00           H  
HETATM   19  H2  UNL     1       4.811   1.982   1.155  1.00  0.00           H  
HETATM   20  H3  UNL     1       5.042   0.326   1.795  1.00  0.00           H  
HETATM   21  H4  UNL     1       3.441  -0.586  -2.298  1.00  0.00           H  
HETATM   22  H5  UNL     1       1.087  -1.330  -2.231  1.00  0.00           H  
HETATM   23  H6  UNL     1      -0.029  -3.949   0.637  1.00  0.00           H  
HETATM   24  H7  UNL     1      -1.780   0.595  -1.510  1.00  0.00           H  
HETATM   25  H8  UNL     1      -0.984   1.659  -0.320  1.00  0.00           H  
HETATM   26  H9  UNL     1      -3.097   2.533  -1.383  1.00  0.00           H  
HETATM   27  H10 UNL     1      -2.914   2.692   0.373  1.00  0.00           H  
HETATM   28  H11 UNL     1      -5.252  -0.087   0.754  1.00  0.00           H  
HETATM   29  H12 UNL     1      -4.482  -0.672  -0.731  1.00  0.00           H  
HETATM   30  H13 UNL     1      -3.238  -1.544   1.007  1.00  0.00           H  
HETATM   31  H14 UNL     1      -3.291  -0.065   1.993  1.00  0.00           H  
HETATM   32  H15 UNL     1       0.705  -0.197   1.815  1.00  0.00           H  
HETATM   33  H16 UNL     1       3.018   0.565   1.852  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3
CONECT    3    4    4   17
CONECT    4    5   21
CONECT    5    6    6   22
CONECT    6    7   16
CONECT    7    8    8    9   10
CONECT    9   23
CONECT   10   11   15
CONECT   11   12   24   25
CONECT   12   13   26   27
CONECT   13   14
CONECT   14   15   28   29
CONECT   15   30   31
CONECT   16   17   17   32
CONECT   17   33
END

HMDB0253003
     RDKit          3D
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.3006    1.0284    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7173    0.4749   -0.2153 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4024    0.0446   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8663   -0.4879   -1.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.9043   -1.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7749   -0.8037   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -1.3421   -0.1644 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.4086   -1.7536   -1.7733 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0381   -3.0456    1.0702 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8855   -0.0243    0.4590 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8995    1.0294   -0.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0818    1.9253   -0.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2880    1.3259   -0.3009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3231    0.0423    0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1723   -0.4269    0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3226   -0.2704    0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6558    0.1571    0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3997    1.1078    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106    1.9820    1.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0415    0.3263    1.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4409   -0.5861   -2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0868   -1.3295   -2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0288   -3.9489    0.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7801    0.5945   -1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9841    1.6588   -0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0973    2.5331   -1.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    2.6920    0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2521   -0.0867    0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4816   -0.6720   -0.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382   -1.5436    1.0075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2907   -0.0646    1.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7050   -0.1969    1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0176    0.5651    1.8516 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  6 16  1  0
 16 17  2  0
 17  3  1  0
 15 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  5 22  1  0
  9 23  1  0
 11 24  1  0
 11 25  1  0
 12 26  1  0
 12 27  1  0
 14 28  1  0
 14 29  1  0
 15 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(4-Methoxyphenyl)-morpholin-4-yl-sulphanyl-sulphanylidene-$l^{5}-phosphane	Generator
(4-Methoxyphenyl)(morpholin-4-yl)sulphanyl--phosphanethione	HMDB
Morpholin-4-ium-4-methoxyphenyl(morpholino)phosphinodithioate	HMDB

Chemical Formula

C₁₁H₁₆NO₂PS₂

Average Molecular Weight

289.35

Monoisotopic Molecular Weight

289.036008105

IUPAC Name

(4-methoxyphenyl)(morpholin-4-yl)sulfanyl-lambda5-phosphanethione

Traditional Name

(4-methoxyphenyl)(morpholin-4-yl)sulfanyl-lambda5-phosphanethione

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)P(S)(=S)N1CCOCC1

InChI Identifier

InChI=1S/C11H16NO2PS2/c1-13-10-2-4-11(5-3-10)15(16,17)12-6-8-14-9-7-12/h2-5H,6-9H2,1H3,(H,16,17)

InChI Key

QDSAKNAFJWRQIV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Morpholine
Oxazinane
Dialkyl ether
Ether
Organothiophosphorus compound
Oxacycle
Organoheterocyclic compound
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organophosphorus compound
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	3.36	ALOGPS
logP	1.88	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	9.19	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	21.7 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	76.1 m³·mol⁻¹	ChemAxon
Polarizability	28.89 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+H]+	157.752	30932474
DeepCCS	[M-H]-	155.36	30932474
DeepCCS	[M-2H]-	188.315	30932474
DeepCCS	[M+Na]+	163.811	30932474
AllCCS	[M+H]+	159.0	32859911
AllCCS	[M+H-H2O]+	156.0	32859911
AllCCS	[M+NH4]+	161.8	32859911
AllCCS	[M+Na]+	162.6	32859911
AllCCS	[M-H]-	160.2	32859911
AllCCS	[M+Na-2H]-	160.4	32859911
AllCCS	[M+HCOO]-	160.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane	COC1=CC=C(C=C1)P(S)(=S)N1CCOCC1	3313.8	Standard polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane	COC1=CC=C(C=C1)P(S)(=S)N1CCOCC1	2225.8	Standard non polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane	COC1=CC=C(C=C1)P(S)(=S)N1CCOCC1	2543.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C)N2CCOCC2)C=C1	2491.1	Semi standard non polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C)N2CCOCC2)C=C1	2279.7	Standard non polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C)N2CCOCC2)C=C1	3040.2	Standard polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TBDMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C(C)(C)C)N2CCOCC2)C=C1	2747.9	Semi standard non polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TBDMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C(C)(C)C)N2CCOCC2)C=C1	2494.3	Standard non polar	33892256
(4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane,1TBDMS,isomer #1	COC1=CC=C(P(=S)(S[Si](C)(C)C(C)(C)C)N2CCOCC2)C=C1	3162.1	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4s-2290000000-7458cc24058ff24c9a6a	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 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 - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 10V, Positive-QTOF	splash10-000i-9020000000-74bcd0fd8d5972c71397	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 20V, Positive-QTOF	splash10-000i-9020000000-309464c42645befc773e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 40V, Positive-QTOF	splash10-000i-9210000000-7f351420051b967e9e56	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 10V, Negative-QTOF	splash10-000i-0090000000-0f2a4872e945ca8e9faa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 20V, Negative-QTOF	splash10-0f79-0190000000-6d1b14121e30d09519d3	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane 40V, Negative-QTOF	splash10-000l-7900000000-9408267a76d9eb4f25d8	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

35033023

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46937262

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 (4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane (HMDB0253003)

MOL for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

3D MOL for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

3D SDF for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

3D-SDF for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

PDB for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

3D PDB for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

SMILES for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

INCHI for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

Structure for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

3D Structure for HMDB0253003 ((4-Methoxyphenyl)-morpholin-4-yl-sulfanyl-sulfanylidene-$l^{5}-phosphane)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra