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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:49:48 UTC

Update Date

2021-09-26 22:56:07 UTC

HMDB ID

HMDB0246816

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Dendrid

Description

4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2-dihydropyrimidin-2-one belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. Pyrimidine 2'-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2. Based on a literature review very few articles have been published on 4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2-dihydropyrimidin-2-one. This compound has been identified in human blood as reported by (PMID: 31557052 ). Dendrid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Dendrid 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


  Mrv1533004261506382D          

 17 18  0  0  0  0            999 V2000
    1.3819   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 N   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
    2.1434   -0.4125    0.0000 O   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
   -0.1830   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -3.9282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  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
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 14  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246816

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(CC1O)N1C=C(I)C(=O)NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H11IN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)

> <INCHI_KEY>
XQFRJNBWHJMXHO-UHFFFAOYSA-N

> <FORMULA>
C9H11IN2O5

> <MOLECULAR_WEIGHT>
354.1

> <EXACT_MASS>
353.97127

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
26.459415580137772

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2,3,4-tetrahydropyrimidine-2,4-dione

> <ALOGPS_LOGP>
-0.70

> <JCHEM_LOGP>
-0.5289186266666662

> <ALOGPS_LOGS>
-1.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.907879720516654

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.4560818072529

> <JCHEM_PKA_STRONGEST_BASIC>
-2.978083591952415

> <JCHEM_POLAR_SURFACE_AREA>
99.10000000000001

> <JCHEM_REFRACTIVITY>
64.4039

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.34e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
iododeoxyuridine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       2.580  -3.215   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.564  -4.680   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.088  -3.215   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       1.334  -0.770   0.000  0.00  0.00           N+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  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       2.667   1.540   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.667   0.000   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  I   UNK     0      -1.334   2.310   0.000  0.00  0.00           I+0
HETATM   15  C   UNK     0      -0.342  -5.926   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.285  -7.333   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.009  -5.926   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    1    6                                                  
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12                                                            
CONECT   14    8                                                            
CONECT   15    3   16                                                       
CONECT   16   15                                                            
CONECT   17    2                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0246816
HETATM    1  O1  UNL     1       5.165   0.140   0.944  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.933   0.102   0.706  1.00  0.00           C  
HETATM    3  N1  UNL     1       3.088  -0.717   1.337  1.00  0.00           N  
HETATM    4  C2  UNL     1       1.754  -0.728   1.050  1.00  0.00           C  
HETATM    5  O2  UNL     1       0.945  -1.494   1.635  1.00  0.00           O  
HETATM    6  N2  UNL     1       1.276   0.095   0.119  1.00  0.00           N  
HETATM    7  C3  UNL     1      -0.118   0.103  -0.200  1.00  0.00           C  
HETATM    8  C4  UNL     1      -0.565  -1.223  -0.833  1.00  0.00           C  
HETATM    9  C5  UNL     1      -2.070  -0.910  -0.871  1.00  0.00           C  
HETATM   10  O3  UNL     1      -2.831  -2.049  -0.928  1.00  0.00           O  
HETATM   11  C6  UNL     1      -2.210  -0.157   0.430  1.00  0.00           C  
HETATM   12  C7  UNL     1      -2.988   1.137   0.275  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.381   1.999  -0.624  1.00  0.00           O  
HETATM   14  O5  UNL     1      -0.950   0.153   0.889  1.00  0.00           O  
HETATM   15  C8  UNL     1       2.096   0.936  -0.538  1.00  0.00           C  
HETATM   16  C9  UNL     1       3.458   0.965  -0.263  1.00  0.00           C  
HETATM   17  I1  UNL     1       4.706   2.294  -1.312  1.00  0.00           I  
HETATM   18  H1  UNL     1       3.456  -1.358   2.060  1.00  0.00           H  
HETATM   19  H2  UNL     1      -0.369   0.875  -0.965  1.00  0.00           H  
HETATM   20  H3  UNL     1      -0.452  -2.066  -0.150  1.00  0.00           H  
HETATM   21  H4  UNL     1      -0.156  -1.360  -1.835  1.00  0.00           H  
HETATM   22  H5  UNL     1      -2.207  -0.224  -1.714  1.00  0.00           H  
HETATM   23  H6  UNL     1      -2.722  -2.539  -0.077  1.00  0.00           H  
HETATM   24  H7  UNL     1      -2.739  -0.846   1.130  1.00  0.00           H  
HETATM   25  H8  UNL     1      -4.046   0.927  -0.017  1.00  0.00           H  
HETATM   26  H9  UNL     1      -2.976   1.638   1.262  1.00  0.00           H  
HETATM   27  H10 UNL     1      -1.824   2.686  -0.206  1.00  0.00           H  
HETATM   28  H11 UNL     1       1.727   1.618  -1.303  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   16
CONECT    3    4   18
CONECT    4    5    5    6
CONECT    6    7   15
CONECT    7    8   14   19
CONECT    8    9   20   21
CONECT    9   10   11   22
CONECT   10   23
CONECT   11   12   14   24
CONECT   12   13   25   26
CONECT   13   27
CONECT   15   16   16   28
CONECT   16   17
END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
125I-labeled idoxuridine	MeSH, HMDB
5-Iododeoxyuridine	MeSH, HMDB
IUdR	MeSH, HMDB
Idoxuridine, 125I-labeled	MeSH, HMDB
Idoxuridine, 3H-labeled	MeSH, HMDB
Iododeoxyuridine	MeSH, HMDB
Oftan idu	MeSH, HMDB
Oftan-idu	MeSH, HMDB
OftanIDU	MeSH, HMDB
SK And F-14287	MeSH, HMDB
131I-labeled idoxuridine	MeSH, HMDB
3H-Labeled idoxuridine	MeSH, HMDB
5 Iododeoxyuridine	MeSH, HMDB
Idoxuridine, 125I labeled	MeSH, HMDB
Kerecide	MeSH, HMDB
Stoxil	MeSH, HMDB
123I-labeled idoxuridine	MeSH, HMDB
Allergan 211	MeSH, HMDB
Idoxuridine, 123I labeled	MeSH, HMDB
Idoxuridine, 131I labeled	MeSH, HMDB
Idoxuridine, 131I-labeled	MeSH, HMDB
Idoxuridine, radical ion (1-)	MeSH, HMDB
5 Iodo 2' deoxyuridine	MeSH, HMDB
5-Iodo-2'-deoxyuridine	MeSH, HMDB
Herplex liquifilm	MeSH, HMDB
Idoxuridine	MeSH, HMDB
Idoxuridine, 123I-labeled	MeSH, HMDB
Idoxuridine, 3H labeled	MeSH, HMDB
Idoxuridine, radical ion (+1)	MeSH, HMDB
Liquifilm, herplex	MeSH, HMDB

Chemical Formula

C₉H₁₁IN₂O₅

Average Molecular Weight

354.1

Monoisotopic Molecular Weight

353.97127

IUPAC Name

1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2,3,4-tetrahydropyrimidine-2,4-dione

Traditional Name

iododeoxyuridine

CAS Registry Number

Not Available

SMILES

OCC1OC(CC1O)N1C=C(I)C(=O)NC1=O

InChI Identifier

InChI=1S/C9H11IN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)

InChI Key

XQFRJNBWHJMXHO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. Pyrimidine 2'-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Sub Class

Pyrimidine 2'-deoxyribonucleosides

Direct Parent

Pyrimidine 2'-deoxyribonucleosides

Alternative Parents

Substituents

Pyrimidine 2'-deoxyribonucleoside
Halopyrimidine
Pyrimidone
Aryl halide
Aryl iodide
Hydropyrimidine
Pyrimidine
Heteroaromatic compound
Vinylogous amide
Tetrahydrofuran
Lactam
Urea
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Organonitrogen compound
Organoiodide
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Organic nitrogen 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)

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	-0.7	ALOGPS
logP	-0.53	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	8.46	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.1 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	64.4 m³·mol⁻¹	ChemAxon
Polarizability	26.46 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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]+	160.801	30932474
DeepCCS	[M-H]-	158.212	30932474
DeepCCS	[M-2H]-	193.236	30932474
DeepCCS	[M+Na]+	168.786	30932474
AllCCS	[M+H]+	171.6	32859911
AllCCS	[M+H-H2O]+	168.4	32859911
AllCCS	[M+NH4]+	174.5	32859911
AllCCS	[M+Na]+	175.4	32859911
AllCCS	[M-H]-	159.5	32859911
AllCCS	[M+Na-2H]-	160.1	32859911
AllCCS	[M+HCOO]-	160.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dendrid	OCC1OC(CC1O)N1C=C(I)C(=O)NC1=O	2053.8	Standard non polar	33892256
Dendrid	OCC1OC(CC1O)N1C=C(I)C(=O)NC1=O	2728.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dendrid,1TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	2583.5	Semi standard non polar	33892256
Dendrid,1TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	2479.9	Standard non polar	33892256
Dendrid,1TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	3466.2	Standard polar	33892256
Dendrid,2TMS,isomer #3	C[Si](C)(C)OC1CC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)OC1CO	2625.7	Semi standard non polar	33892256
Dendrid,2TMS,isomer #3	C[Si](C)(C)OC1CC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)OC1CO	2517.7	Standard non polar	33892256
Dendrid,2TMS,isomer #3	C[Si](C)(C)OC1CC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)OC1CO	3090.0	Standard polar	33892256
Dendrid,3TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)CC1O[Si](C)(C)C	2609.5	Semi standard non polar	33892256
Dendrid,3TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)CC1O[Si](C)(C)C	2531.0	Standard non polar	33892256
Dendrid,3TMS,isomer #1	C[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C)C2=O)CC1O[Si](C)(C)C	2679.3	Standard polar	33892256
Dendrid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	2844.8	Semi standard non polar	33892256
Dendrid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	2778.6	Standard non polar	33892256
Dendrid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O	3497.6	Standard polar	33892256
Dendrid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O[Si](C)(C)C(C)(C)C	3064.6	Semi standard non polar	33892256
Dendrid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O[Si](C)(C)C(C)(C)C	2976.9	Standard non polar	33892256
Dendrid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)[NH]C2=O)CC1O[Si](C)(C)C(C)(C)C	3079.3	Standard polar	33892256
Dendrid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C(C)(C)C)C2=O)CC1O[Si](C)(C)C(C)(C)C	3299.4	Semi standard non polar	33892256
Dendrid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C(C)(C)C)C2=O)CC1O[Si](C)(C)C(C)(C)C	3168.9	Standard non polar	33892256
Dendrid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2C=C(I)C(=O)N([Si](C)(C)C(C)(C)C)C2=O)CC1O[Si](C)(C)C(C)(C)C	2964.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9044000000-bccd33421cbd5827f9e3	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dendrid GC-MS (TBDMS_2_3) - 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 - Dendrid 10V, Positive-QTOF	splash10-0udr-0059000000-86cefb7305f6f5493731	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dendrid 20V, Positive-QTOF	splash10-000l-2491000000-4255679ae8c5451c203b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dendrid 40V, Positive-QTOF	splash10-052r-2190000000-5aa7750d1b5c22b471c8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dendrid 10V, Negative-QTOF	splash10-0udi-0039000000-3de48ce6c73f3678a325	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dendrid 20V, Negative-QTOF	splash10-01p6-4192000000-bb1a34efb9165855507d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dendrid 40V, Negative-QTOF	splash10-0006-9210000000-0a1094a1f73c776fb40d	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	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

3559

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3687

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 Dendrid (HMDB0246816)

MOL for HMDB0246816 (Dendrid)

3D MOL for HMDB0246816 (Dendrid)

3D SDF for HMDB0246816 (Dendrid)

3D-SDF for HMDB0246816 (Dendrid)

PDB for HMDB0246816 (Dendrid)

3D PDB for HMDB0246816 (Dendrid)

SMILES for HMDB0246816 (Dendrid)

INCHI for HMDB0246816 (Dendrid)

Structure for HMDB0246816 (Dendrid)

3D Structure for HMDB0246816 (Dendrid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra