ChemFOnt: Showing chemical card for 2-methyl-3-(sulfooxy)propanoic acid (CFc000106526)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:23:58 UTC

Chemfont ID

CFc000106526

Molecule Identification

Common Name

2-methyl-3-(sulfooxy)propanoic acid

Definition

2-methyl-3-(sulfooxy)propanoic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-hydroxy-2-methylpropanoic acid. It is generated by Sulfotransferase family cytosolic 2B member 1 (O00204) and Sulfotransferase enzymes via a sulfation-of-primary-alcohol reaction. This sulfation-of-primary-alcohol occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
2-Methyl-3-(sulfooxy)propanoate	Generator
2-Methyl-3-(sulphooxy)propanoate	Generator
2-Methyl-3-(sulphooxy)propanoic acid	Generator

Chemical Formula

C₄H₈O₆S

Average Molecular Weight

184.16

Monoisotopic Molecular Weight

184.004159152

IUPAC Name

2-methyl-3-(sulfooxy)propanoic acid

Traditional Name

2-methyl-3-(sulfooxy)propanoic acid

CAS Registry Number

None

SMILES

CC(COS(O)(=O)=O)C(O)=O

InChI Identifier

InChI=1S/C4H8O6S/c1-3(4(5)6)2-10-11(7,8)9/h3H,2H2,1H3,(H,5,6)(H,7,8,9)

InChI Key

PEQDTRJYAJYFLE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic sulfuric acids and derivatives

Sub Class

Sulfuric acid esters

Direct Parent

Sulfuric acid monoesters

Alternative Parents

Substituents

Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0126117)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	27 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-0.21	ChemAxon
logS	-0.83	ALOGPS
pKa (Strongest Acidic)	-2	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	33.61 m³·mol⁻¹	ChemAxon
Polarizability	15.3 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0126117

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB084992

KNApSAcK ID

Not Available

Chemspider ID

74851876

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131832561

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 2-methyl-3-(sulfooxy)propanoic acid (CFc000106526)

MOL for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

3D MOL for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

3D SDF for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

3D-SDF for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

PDB for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

3D PDB for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

SMILES for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

INCHI for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

Structure for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)

3D Structure for CFc000106526 (2-methyl-3-(sulfooxy)propanoic acid)