MiMeDB: Showing metabocard for 1,3,7-trimethyl-5-hydroxyisouric acid (MMDBc0032848)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 22:02:24 UTC

Update Date

2022-08-31 21:44:26 UTC

Metabolite ID

MMDBc0032848

Metabolite Identification

Common Name

1,3,7-trimethyl-5-hydroxyisouric acid

Description

A member of the class of oxopurines that is 5-hydroxyisouric acid carrying three additional methyl substituents at positions 1, 3 and 7.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652311182123022D          

 16 17  0  0  0  0            999 V2000
    1.3556    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5549   -1.9309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  4  1  0  0  0  0
  8  5  1  0  0  0  0
  9  4  2  0  0  0  0
  9  6  1  0  0  0  0
 10  1  1  0  0  0  0
 10  4  1  0  0  0  0
 10  7  1  0  0  0  0
 11  2  1  0  0  0  0
 11  5  1  0  0  0  0
 11  7  1  0  0  0  0
 12  3  1  0  0  0  0
 12  6  1  0  0  0  0
 12  8  1  0  0  0  0
 13  5  2  0  0  0  0
 14  6  2  0  0  0  0
 15  7  2  0  0  0  0
 16  8  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0032848

> <DATABASE_NAME>
MIME

> <SMILES>
CN1C(=O)N=C2N(C)C(=O)N(C)C(=O)C12O

> <INCHI_IDENTIFIER>
InChI=1S/C8H10N4O4/c1-10-4-8(16,12(3)6(14)9-4)5(13)11(2)7(10)15/h16H,1-3H3

> <INCHI_KEY>
XNXQVRHXDIDGDT-UHFFFAOYSA-N

> <FORMULA>
C8H10N4O4

> <MOLECULAR_WEIGHT>
226.192

> <EXACT_MASS>
226.070204818

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
26

> <JCHEM_AVERAGE_POLARIZABILITY>
20.34611870874505

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-1,3,7-trimethyl-2,3,5,6,7,8-hexahydro-1H-purine-2,6,8-trione

> <ALOGPS_LOGP>
-0.67

> <JCHEM_LOGP>
-1.394794080666667

> <ALOGPS_LOGS>
-1.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.71806768299926

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1223491293457393

> <JCHEM_POLAR_SURFACE_AREA>
93.52

> <JCHEM_REFRACTIVITY>
50.28060000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.52e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-1,3,7-trimethylpurine-2,6,8-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-NOV-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-NOV-21         0                                  
HETATM    1  C   UNK     0       2.530   1.777   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.198  -2.843   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.744  -4.013   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0       2.530   0.237   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       3.864  -2.073   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       2.530  -4.383   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -2.713  -1.303   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       5.198   0.237   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.036  -3.604   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   11                                                            
CONECT    3   12                                                            
CONECT    4    8    9   10                                                  
CONECT    5    8   11   13                                                  
CONECT    6    9   12   14                                                  
CONECT    7   10   11   15                                                  
CONECT    8    4    5   12   16                                             
CONECT    9    4    6                                                       
CONECT   10    1    4    7                                                  
CONECT   11    2    5    7                                                  
CONECT   12    3    6    8                                                  
CONECT   13    5                                                            
CONECT   14    6                                                            
CONECT   15    7                                                            
CONECT   16    8                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

Synonyms

Value	Source
1,3,7-Trimethyl-5-hydroxyisourate	ChEBI
1,3,7-Trimethyl-5-hydroxyisoate	Generator
1,3,7-Trimethyl-5-hydroxyisoic acid	Generator
1,3,7-Trimethyl-5-hydroxyisouric acid	Generator

Molecular Formula

C₈H₁₀N₄O₄

Average Mass

226.192

Monoisotopic Mass

226.070204818

IUPAC Name

5-hydroxy-1,3,7-trimethyl-2,3,5,6,7,8-hexahydro-1H-purine-2,6,8-trione

Traditional Name

5-hydroxy-1,3,7-trimethylpurine-2,6,8-trione

CAS Registry Number

Not Available

SMILES

CN1C(=O)N=C2N(C)C(=O)N(C)C(=O)C12O

InChI Identifier

InChI=1S/C8H10N4O4/c1-10-4-8(16,12(3)6(14)9-4)5(13)11(2)7(10)15/h16H,1-3H3

InChI Key

XNXQVRHXDIDGDT-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Imidazopyrimidines

Sub Class

Purines and purine derivatives

Direct Parent

Xanthines

Alternative Parents

Substituents

Xanthine
Alpha-amino acid or derivatives
Purinone
Alkaloid or derivatives
N-acyl urea
Pyrimidone
Ureide
1,3-diazinane
Pyrimidine
Dicarboximide
3-imidazoline
Carbonic acid derivative
Urea
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Amidine
Carboxylic acid amidine
Carboxylic acid derivative
Carboximidamide
Azacycle
Alkanolamine
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	15.2 g/L	ALOGPS
logP	-0.67	ALOGPS
logP	-1.4	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	9.72	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	93.52 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	50.28 m³·mol⁻¹	ChemAxon
Polarizability	20.35 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

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	1	Human	Unknown

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58827362

KEGG Compound ID

Not Available

BioCyc ID

CPD-16697

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118796883

PDB ID

Not Available

ChEBI ID

90885

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Huang W, Brewer LK, Jones JW, Nguyen AT, Marcu A, Wishart DS, Oglesby-Sherrouse AG, Kane MA, Wilks A: PAMDB: a comprehensive Pseudomonas aeruginosa metabolome database. Nucleic Acids Res. 2018 Jan 4;46(D1):D575-D580. doi: 10.1093/nar/gkx1061. [PubMed:29106626 ]

Showing metabocard for 1,3,7-trimethyl-5-hydroxyisouric acid (MMDBc0032848)

MOL for #<Metabolite:0x0000560be1c4b308>

3D MOL for #<Metabolite:0x0000560be1c4b308>

3D SDF for #<Metabolite:0x0000560be1c4b308>

3D-SDF for #<Metabolite:0x0000560be1c4b308>

PDB for #<Metabolite:0x0000560be1c4b308>

3D PDB for #<Metabolite:0x0000560be1c4b308>

SMILES for #<Metabolite:0x0000560be1c4b308>

INCHI for #<Metabolite:0x0000560be1c4b308>

Structure for #<Metabolite:0x0000560be1c4b308>

3D Structure for #<Metabolite:0x0000560be1c4b308>