ChemFOnt: Showing chemical card for {[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid (CFc000139701)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:15:26 UTC

Chemfont ID

CFc000139701

Molecule Identification

Common Name

{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid

Definition

{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid belongs to the class of organic compounds known as biopterins and derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland. Based on a literature review very few articles have been published on {[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonate	Generator
{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulphonate	Generator
{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulphonic acid	Generator

Chemical Formula

C₉H₁₁N₅O₇S

Average Molecular Weight

333.28

Monoisotopic Molecular Weight

333.037918888

IUPAC Name

{[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid

Traditional Name

[1,3-dihydroxy-1-(4-hydroxy-2-imino-1H-pteridin-6-yl)propan-2-yl]oxysulfonic acid

CAS Registry Number

Not Available

SMILES

OCC(OS(O)(=O)=O)C(O)C1=NC2=C(NC(=N)N=C2O)N=C1

InChI Identifier

InChI=1S/C9H11N5O7S/c10-9-13-7-5(8(17)14-9)12-3(1-11-7)6(16)4(2-15)21-22(18,19)20/h1,4,6,15-16H,2H2,(H,18,19,20)(H3,10,11,13,14,17)

InChI Key

XPPCWNGWSRQNEX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biopterins and derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Pterins and derivatives

Direct Parent

Biopterins and derivatives

Alternative Parents

Substituents

Biopterin
Hydroxypyrimidine
Pyrazine
Pyrimidine
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Organic sulfuric acid or derivatives
Heteroaromatic compound
Secondary alcohol
Azacycle
Aromatic alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Primary alcohol
Organooxygen compound
Organonitrogen compound
Alcohol
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	1.55 g/L	ALOGPS
logP	-1.9	ALOGPS
logP	-4.1	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	-2.6	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	198.31 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	80.68 m³·mol⁻¹	ChemAxon
Polarizability	28.48 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0159293

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

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

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for {[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid (CFc000139701)

MOL for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

3D MOL for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

3D SDF for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

3D-SDF for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

PDB for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

3D PDB for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

SMILES for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

INCHI for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

Structure for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)

3D Structure for CFc000139701 ({[1,3-dihydroxy-1-(4-hydroxy-2-imino-1,2-dihydropteridin-6-yl)propan-2-yl]oxy}sulfonic acid)