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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 15:32:06 UTC

Update Date

2021-09-26 23:10:48 UTC

HMDB ID

HMDB0255722

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Norathyriol

Description

Norathyriol belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Norathyriol is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a significant number of articles have been published on Norathyriol. This compound has been identified in human blood as reported by (PMID: 31557052 ). Norathyriol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Norathyriol 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

 
  Mrv0541 02271201352D          
 
 19 21  0  0  0  0            999 V2000
   13.9225   -8.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9156   -9.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6360   -8.3506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2091   -8.3471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6292  -10.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2091   -9.9971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3495   -8.7690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4921   -8.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3838   -9.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6292  -10.8271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4921   -9.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2091  -10.8237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0664   -8.3608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7821   -8.3471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0527  -10.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7764   -8.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7696   -9.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4900   -8.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4762  -10.0210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  2  0  0  0  0
  5  9  1  0  0  0  0
  5 10  2  0  0  0  0
  6 11  2  0  0  0  0
  6 12  1  0  0  0  0
  7 13  1  0  0  0  0
  8 14  1  0  0  0  0
  9 15  1  0  0  0  0
 13 16  2  0  0  0  0
 15 17  2  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
  7  9  2  0  0  0  0
  8 11  1  0  0  0  0
 16 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255722

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1=CC2=C(C(O)=C1)C(=O)C1=C(O2)C=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H8O6/c14-5-1-9(17)12-11(2-5)19-10-4-8(16)7(15)3-6(10)13(12)18/h1-4,14-17H

> <INCHI_KEY>
ZHTQCPCDXKMMLU-UHFFFAOYSA-N

> <FORMULA>
C13H8O6

> <MOLECULAR_WEIGHT>
260.199

> <EXACT_MASS>
260.032087988

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
24.276432794964343

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3,6,7-tetrahydroxy-9H-xanthen-9-one

> <ALOGPS_LOGP>
2.10

> <JCHEM_LOGP>
2.3953789336666667

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.889587676579917

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.277816682827577

> <JCHEM_PKA_STRONGEST_BASIC>
-4.179342222399989

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
64.7399

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.45e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3,6,7-tetrahydroxyxanthone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  C   UNK     0      25.989 -16.356   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.976 -17.899   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      27.321 -15.588   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      24.657 -15.581   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      27.308 -18.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.657 -18.661   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      28.652 -16.369   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      23.319 -16.356   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      28.716 -17.906   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      27.308 -20.211   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      23.319 -17.899   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      24.657 -20.204   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      29.991 -15.607   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      21.993 -15.581   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      29.965 -18.680   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.316 -16.395   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      31.303 -17.931   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      32.648 -15.632   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      32.622 -18.706   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8                                                       
CONECT    5    2    9   10                                                  
CONECT    6    2   11   12                                                  
CONECT    7    3   13    9                                                  
CONECT    8    4   14   11                                                  
CONECT    9    5   15    7                                                  
CONECT   10    5                                                            
CONECT   11    6    8                                                       
CONECT   12    6                                                            
CONECT   13    7   16                                                       
CONECT   14    8                                                            
CONECT   15    9   17                                                       
CONECT   16   13   18   17                                                  
CONECT   17   15   19   16                                                  
CONECT   18   16                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

COMPND    HMDB0255722
HETATM    1  O1  UNL     1      -0.067  -1.872  -1.521  1.00  0.00           O  
HETATM    2  C1  UNL     1      -0.117  -0.922  -0.729  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.091  -0.400  -0.286  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.299  -0.922  -0.713  1.00  0.00           C  
HETATM    5  C4  UNL     1       3.494  -0.399  -0.269  1.00  0.00           C  
HETATM    6  O2  UNL     1       4.726  -0.910  -0.687  1.00  0.00           O  
HETATM    7  C5  UNL     1       3.423   0.658   0.611  1.00  0.00           C  
HETATM    8  O3  UNL     1       4.591   1.221   1.089  1.00  0.00           O  
HETATM    9  C6  UNL     1       2.219   1.179   1.038  1.00  0.00           C  
HETATM   10  C7  UNL     1       1.015   0.659   0.596  1.00  0.00           C  
HETATM   11  O4  UNL     1      -0.145   1.133   0.984  1.00  0.00           O  
HETATM   12  C8  UNL     1      -1.309   0.651   0.574  1.00  0.00           C  
HETATM   13  C9  UNL     1      -2.504   1.196   1.021  1.00  0.00           C  
HETATM   14  C10 UNL     1      -3.732   0.716   0.613  1.00  0.00           C  
HETATM   15  O5  UNL     1      -4.925   1.276   1.071  1.00  0.00           O  
HETATM   16  C11 UNL     1      -3.738  -0.340  -0.268  1.00  0.00           C  
HETATM   17  C12 UNL     1      -2.535  -0.899  -0.726  1.00  0.00           C  
HETATM   18  O6  UNL     1      -2.646  -1.939  -1.594  1.00  0.00           O  
HETATM   19  C13 UNL     1      -1.322  -0.407  -0.308  1.00  0.00           C  
HETATM   20  H1  UNL     1       2.325  -1.751  -1.404  1.00  0.00           H  
HETATM   21  H2  UNL     1       4.813  -1.673  -1.322  1.00  0.00           H  
HETATM   22  H3  UNL     1       5.512   0.904   0.831  1.00  0.00           H  
HETATM   23  H4  UNL     1       2.157   2.015   1.734  1.00  0.00           H  
HETATM   24  H5  UNL     1      -2.468   2.033   1.719  1.00  0.00           H  
HETATM   25  H6  UNL     1      -5.399   2.035   0.613  1.00  0.00           H  
HETATM   26  H7  UNL     1      -4.699  -0.714  -0.587  1.00  0.00           H  
HETATM   27  H8  UNL     1      -2.058  -2.528  -2.080  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   19
CONECT    3    4    4   10
CONECT    4    5   20
CONECT    5    6    7    7
CONECT    6   21
CONECT    7    8    9
CONECT    8   22
CONECT    9   10   10   23
CONECT   10   11
CONECT   11   12
CONECT   12   13   13   19
CONECT   13   14   24
CONECT   14   15   16   16
CONECT   15   25
CONECT   16   17   26
CONECT   17   18   19   19
CONECT   18   27
END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1,3,6,7-Tetrahydroxyxanthone	ChEBI

Chemical Formula

C₁₃H₈O₆

Average Molecular Weight

260.199

Monoisotopic Molecular Weight

260.032087988

IUPAC Name

1,3,6,7-tetrahydroxy-9H-xanthen-9-one

Traditional Name

1,3,6,7-tetrahydroxyxanthone

CAS Registry Number

Not Available

SMILES

OC1=CC2=C(C(O)=C1)C(=O)C1=C(O2)C=C(O)C(O)=C1

InChI Identifier

InChI=1S/C13H8O6/c14-5-1-9(17)12-11(2-5)19-10-4-8(16)7(15)3-6(10)13(12)18/h1-4,14-17H

InChI Key

ZHTQCPCDXKMMLU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Chromone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Polyol
Oxacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

polyphenol (CHEBI:7622 )
xanthones (CHEBI:7622 )
xanthenes (C10086 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	2.1	ALOGPS
logP	2.4	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	7.28	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	64.74 m³·mol⁻¹	ChemAxon
Polarizability	24.28 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	162.544	30932474
DeepCCS	[M-H]-	160.185	30932474
DeepCCS	[M-2H]-	193.251	30932474
DeepCCS	[M+Na]+	168.637	30932474
AllCCS	[M+H]+	156.7	32859911
AllCCS	[M+H-H2O]+	152.7	32859911
AllCCS	[M+NH4]+	160.3	32859911
AllCCS	[M+Na]+	161.4	32859911
AllCCS	[M-H]-	155.9	32859911
AllCCS	[M+Na-2H]-	155.2	32859911
AllCCS	[M+HCOO]-	154.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Norathyriol	OC1=CC2=C(C(O)=C1)C(=O)C1=C(O2)C=C(O)C(O)=C1	4486.6	Standard polar	33892256
Norathyriol	OC1=CC2=C(C(O)=C1)C(=O)C1=C(O2)C=C(O)C(O)=C1	2756.4	Standard non polar	33892256
Norathyriol	OC1=CC2=C(C(O)=C1)C(=O)C1=C(O2)C=C(O)C(O)=C1	2893.9	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 - Norathyriol GC-MS (Non-derivatized) - 70eV, Positive	splash10-001i-0590000000-e2acd4c6d283fe465345	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TMS_4_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Norathyriol GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-04	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 - Norathyriol 10V, Positive-QTOF	splash10-03di-0090000000-f65f946e50c604010287	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Norathyriol 20V, Positive-QTOF	splash10-03di-0090000000-7c54b120090b415ecfc8	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Norathyriol 40V, Positive-QTOF	splash10-0uy3-2690000000-ae05ac4e70e33e677e97	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Norathyriol 10V, Negative-QTOF	splash10-0a4i-0090000000-664ffee71e42e409f57d	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Norathyriol 20V, Negative-QTOF	splash10-0a4i-0090000000-af88dcc4d98dd1553530	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Norathyriol 40V, Negative-QTOF	splash10-00ll-1970000000-f6495ddf390e42dd5997	2019-02-23	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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

7622

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1911321

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 Norathyriol (HMDB0255722)

MOL for HMDB0255722 (Norathyriol)

3D MOL for HMDB0255722 (Norathyriol)

3D SDF for HMDB0255722 (Norathyriol)

3D-SDF for HMDB0255722 (Norathyriol)

PDB for HMDB0255722 (Norathyriol)

3D PDB for HMDB0255722 (Norathyriol)

SMILES for HMDB0255722 (Norathyriol)

INCHI for HMDB0255722 (Norathyriol)

Structure for HMDB0255722 (Norathyriol)

3D Structure for HMDB0255722 (Norathyriol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra