ChemFOnt: Showing chemical card for 2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid (CFc000140464)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:16:31 UTC

Chemfont ID

CFc000140464

Molecule Identification

Common Name

2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid

Definition

2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid belongs to the class of organic compounds known as purine nucleosides. Purine nucleosides are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety. Based on a literature review very few articles have been published on 2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioate	Generator
2-[(9-{3,4-dihydroxy-5-[(sulphooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioate	Generator
2-[(9-{3,4-dihydroxy-5-[(sulphooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid	Generator

Chemical Formula

C₁₄H₁₇N₅O₁₁S

Average Molecular Weight

463.37

Monoisotopic Molecular Weight

463.064527561

IUPAC Name

2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid

Traditional Name

2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}purin-6-yl)amino]butanedioic acid

CAS Registry Number

Not Available

SMILES

OC1C(COS(O)(=O)=O)OC(C1O)N1C=NC2=C(NC(CC(O)=O)C(O)=O)N=CN=C12

InChI Identifier

InChI=1S/C14H17N5O11S/c20-7(21)1-5(14(24)25)18-11-8-12(16-3-15-11)19(4-17-8)13-10(23)9(22)6(30-13)2-29-31(26,27)28/h3-6,9-10,13,22-23H,1-2H2,(H,20,21)(H,24,25)(H,15,16,18)(H,26,27,28)

InChI Key

AGKPPGRGTFBOEC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine nucleosides. Purine nucleosides are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Sub Class

Not Available

Direct Parent

Purine nucleosides

Alternative Parents

Substituents

Purine nucleoside
Aspartic acid or derivatives
Glycosyl compound
N-glycosyl compound
6-alkylaminopurine
6-aminopurine
Alpha-amino acid or derivatives
Pentose monosaccharide
Monosaccharide sulfate
Imidazopyrimidine
Purine
Aminopyrimidine
Secondary aliphatic/aromatic amine
Dicarboxylic acid or derivatives
Monosaccharide
N-substituted imidazole
Pyrimidine
Sulfuric acid monoester
Sulfate-ester
Imidolactam
Sulfuric acid ester
Alkyl sulfate
Azole
Tetrahydrofuran
Heteroaromatic compound
Organic sulfuric acid or derivatives
Imidazole
Amino acid or derivatives
Secondary alcohol
1,2-diol
Amino acid
Azacycle
Oxacycle
Secondary amine
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Amine
Organonitrogen compound
Organic oxide
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
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	4.85 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-5.5	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	-1.8	ChemAxon
pKa (Strongest Basic)	3.81	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	243.52 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	95.29 m³·mol⁻¹	ChemAxon
Polarizability	40.53 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0160056

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 2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid (CFc000140464)

MOL for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

3D MOL for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

3D SDF for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

3D-SDF for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

PDB for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

3D PDB for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

SMILES for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

INCHI for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

Structure for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)

3D Structure for CFc000140464 (2-[(9-{3,4-dihydroxy-5-[(sulfooxy)methyl]oxolan-2-yl}-9H-purin-6-yl)amino]butanedioic acid)