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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:19:53 UTC

Update Date

2021-09-26 22:51:42 UTC

HMDB ID

HMDB0244146

Secondary Accession Numbers

None

Metabolite Identification

Common Name

1,2,4,5-Tetramethoxybenzene

Description

1,2,4,5-Tetramethoxybenzene, also known as 1,2,4,5-TMB, 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 a significant number of articles have been published on 1,2,4,5-Tetramethoxybenzene. This compound has been identified in human blood as reported by (PMID: 31557052 ). 1,2,4,5-tetramethoxybenzene is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 1,2,4,5-Tetramethoxybenzene 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

HMDB0244146
     RDKit          3D
1,2,4,5-Tetramethoxybenzene
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7445   -0.9981   -2.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656   -0.3108   -1.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -0.1637   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1772   -0.6634   -1.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1020   -0.4874   -0.6542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1729   -1.0058   -1.3577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9324   -1.6800   -2.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2627    0.1840    0.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5411    0.3349    1.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8836    0.9823    2.2217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1672    0.6808    1.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1117    0.5047    0.6619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2393    0.9922    1.3014 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0729    1.6786    2.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0919   -0.5567   -3.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4255   -2.0756   -2.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053   -1.0270   -2.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348   -1.1866   -2.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -2.5005   -2.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9025   -2.0748   -2.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949   -0.9674   -3.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1101    0.9052    3.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0878    2.0680    2.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8229    0.5410    2.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2156    2.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    1.1089    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6074    2.6660    2.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0568    1.8356    3.0384 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  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 12  3  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  7 19  1  0
  7 20  1  0
  7 21  1  0
 10 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 14 28  1  0
M  END

HMDB0244146
     RDKit          3D
1,2,4,5-Tetramethoxybenzene
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7445   -0.9981   -2.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656   -0.3108   -1.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -0.1637   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1772   -0.6634   -1.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1020   -0.4874   -0.6542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1729   -1.0058   -1.3577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9324   -1.6800   -2.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2627    0.1840    0.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5411    0.3349    1.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8836    0.9823    2.2217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1672    0.6808    1.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1117    0.5047    0.6619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2393    0.9922    1.3014 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0729    1.6786    2.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0919   -0.5567   -3.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4255   -2.0756   -2.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053   -1.0270   -2.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348   -1.1866   -2.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -2.5005   -2.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9025   -2.0748   -2.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949   -0.9674   -3.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1101    0.9052    3.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0878    2.0680    2.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8229    0.5410    2.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2156    2.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    1.1089    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6074    2.6660    2.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0568    1.8356    3.0384 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  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 12  3  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  7 19  1  0
  7 20  1  0
  7 21  1  0
 10 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 14 28  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12                                                       
CONECT   12   11                                                            
CONECT   13    5   14                                                       
CONECT   14   13                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0244146
HETATM    1  C1  UNL     1       2.745  -0.998  -2.244  1.00  0.00           C  
HETATM    2  O1  UNL     1       2.566  -0.311  -1.019  1.00  0.00           O  
HETATM    3  C2  UNL     1       1.278  -0.164  -0.528  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.177  -0.663  -1.194  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.102  -0.487  -0.654  1.00  0.00           C  
HETATM    6  O2  UNL     1      -2.173  -1.006  -1.358  1.00  0.00           O  
HETATM    7  C5  UNL     1      -1.932  -1.680  -2.571  1.00  0.00           C  
HETATM    8  C6  UNL     1      -1.263   0.184   0.540  1.00  0.00           C  
HETATM    9  O3  UNL     1      -2.541   0.335   1.036  1.00  0.00           O  
HETATM   10  C7  UNL     1      -2.884   0.982   2.222  1.00  0.00           C  
HETATM   11  C8  UNL     1      -0.167   0.681   1.201  1.00  0.00           C  
HETATM   12  C9  UNL     1       1.112   0.505   0.662  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.239   0.992   1.301  1.00  0.00           O  
HETATM   14  C10 UNL     1       2.073   1.679   2.523  1.00  0.00           C  
HETATM   15  H1  UNL     1       2.092  -0.557  -3.032  1.00  0.00           H  
HETATM   16  H2  UNL     1       2.425  -2.076  -2.157  1.00  0.00           H  
HETATM   17  H3  UNL     1       3.805  -1.027  -2.543  1.00  0.00           H  
HETATM   18  H4  UNL     1       0.335  -1.187  -2.130  1.00  0.00           H  
HETATM   19  H5  UNL     1      -1.211  -2.500  -2.352  1.00  0.00           H  
HETATM   20  H6  UNL     1      -2.902  -2.075  -2.945  1.00  0.00           H  
HETATM   21  H7  UNL     1      -1.495  -0.967  -3.294  1.00  0.00           H  
HETATM   22  H8  UNL     1      -2.110   0.905   3.021  1.00  0.00           H  
HETATM   23  H9  UNL     1      -3.088   2.068   2.042  1.00  0.00           H  
HETATM   24  H10 UNL     1      -3.823   0.541   2.632  1.00  0.00           H  
HETATM   25  H11 UNL     1      -0.266   1.216   2.148  1.00  0.00           H  
HETATM   26  H12 UNL     1       1.447   1.109   3.251  1.00  0.00           H  
HETATM   27  H13 UNL     1       1.607   2.666   2.405  1.00  0.00           H  
HETATM   28  H14 UNL     1       3.057   1.836   3.038  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3
CONECT    3    4    4   12
CONECT    4    5   18
CONECT    5    6    8    8
CONECT    6    7
CONECT    7   19   20   21
CONECT    8    9   11
CONECT    9   10
CONECT   10   22   23   24
CONECT   11   12   12   25
CONECT   12   13
CONECT   13   14
CONECT   14   26   27   28
END

HMDB0244146
     RDKit          3D
1,2,4,5-Tetramethoxybenzene
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7445   -0.9981   -2.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656   -0.3108   -1.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -0.1637   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1772   -0.6634   -1.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1020   -0.4874   -0.6542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1729   -1.0058   -1.3577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9324   -1.6800   -2.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2627    0.1840    0.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5411    0.3349    1.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8836    0.9823    2.2217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1672    0.6808    1.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1117    0.5047    0.6619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2393    0.9922    1.3014 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0729    1.6786    2.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0919   -0.5567   -3.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4255   -2.0756   -2.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053   -1.0270   -2.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348   -1.1866   -2.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -2.5005   -2.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9025   -2.0748   -2.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949   -0.9674   -3.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1101    0.9052    3.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0878    2.0680    2.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8229    0.5410    2.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2156    2.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    1.1089    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6074    2.6660    2.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0568    1.8356    3.0384 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  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 12  3  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  7 19  1  0
  7 20  1  0
  7 21  1  0
 10 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 14 28  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1,2,4,5-TMB	HMDB

Chemical Formula

C₁₀H₁₄O₄

Average Molecular Weight

198.218

Monoisotopic Molecular Weight

198.089208931

IUPAC Name

1,2,4,5-tetramethoxybenzene

Traditional Name

1,2,4,5-tetramethoxybenzene

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(OC)C=C1OC

InChI Identifier

InChI=1S/C10H14O4/c1-11-7-5-9(13-3)10(14-4)6-8(7)12-2/h5-6H,1-4H3

InChI Key

JUVJUCAKSWHQEE-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
Methoxybenzene
Anisole
Alkyl aryl ether
Monocyclic benzene moiety
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

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	1.69	ALOGPS
logP	1.34	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	36.92 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	51.91 m³·mol⁻¹	ChemAxon
Polarizability	20.61 Å³	ChemAxon
Number of Rings	1	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]+	141.196	30932474
DeepCCS	[M-H]-	137.483	30932474
DeepCCS	[M-2H]-	174.93	30932474
DeepCCS	[M+Na]+	150.468	30932474
AllCCS	[M+H]+	143.7	32859911
AllCCS	[M+H-H2O]+	139.7	32859911
AllCCS	[M+NH4]+	147.5	32859911
AllCCS	[M+Na]+	148.6	32859911
AllCCS	[M-H]-	144.3	32859911
AllCCS	[M+Na-2H]-	145.2	32859911
AllCCS	[M+HCOO]-	146.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1,2,4,5-Tetramethoxybenzene	COC1=CC(OC)=C(OC)C=C1OC	2417.9	Standard polar	33892256
1,2,4,5-Tetramethoxybenzene	COC1=CC(OC)=C(OC)C=C1OC	1521.7	Standard non polar	33892256
1,2,4,5-Tetramethoxybenzene	COC1=CC(OC)=C(OC)C=C1OC	1507.5	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 - 1,2,4,5-Tetramethoxybenzene GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-0900000000-7bf56a69d1329f885c12	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1,2,4,5-Tetramethoxybenzene 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 - 1,2,4,5-Tetramethoxybenzene 10V, Positive-QTOF	splash10-0002-0900000000-ec7a975138638045b7e1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,2,4,5-Tetramethoxybenzene 20V, Positive-QTOF	splash10-0002-0900000000-ec7a975138638045b7e1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,2,4,5-Tetramethoxybenzene 40V, Positive-QTOF	splash10-0532-9600000000-beb5a078a9a104b0f527	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,2,4,5-Tetramethoxybenzene 10V, Negative-QTOF	splash10-0002-0900000000-a5b29b9811d2efb8c73c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,2,4,5-Tetramethoxybenzene 20V, Negative-QTOF	splash10-0002-0900000000-b23af1e1ce2a19f89b07	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,2,4,5-Tetramethoxybenzene 40V, Negative-QTOF	splash10-0a4i-9400000000-4e806c2cdc310d0959bd	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

88165

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

97686

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 1,2,4,5-Tetramethoxybenzene (HMDB0244146)

MOL for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

3D MOL for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

3D SDF for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

3D-SDF for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

PDB for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

3D PDB for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

SMILES for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

INCHI for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

Structure for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

3D Structure for HMDB0244146 (1,2,4,5-Tetramethoxybenzene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra