ChemFOnt: Showing chemical card for 1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid (CFc000162549)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:52:42 UTC

Chemfont ID

CFc000162549

Molecule Identification

Common Name

1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid

Definition

1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. Based on a literature review very few articles have been published on 1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
1,5-Dihydroxy-7-[(sulfooxy)methyl]-1H,4ah,5H,7ah-cyclopenta[c]pyran-4-carboxylate	Generator
1,5-Dihydroxy-7-[(sulphooxy)methyl]-1H,4ah,5H,7ah-cyclopenta[c]pyran-4-carboxylate	Generator
1,5-Dihydroxy-7-[(sulphooxy)methyl]-1H,4ah,5H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₁₀H₁₂O₉S

Average Molecular Weight

308.26

Monoisotopic Molecular Weight

308.02020314

IUPAC Name

1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid

Traditional Name

1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C=C(COS(O)(=O)=O)C2C1C(=COC2O)C(O)=O

InChI Identifier

InChI=1S/C10H12O9S/c11-6-1-4(2-19-20(15,16)17)7-8(6)5(9(12)13)3-18-10(7)14/h1,3,6-8,10-11,14H,2H2,(H,12,13)(H,15,16,17)

InChI Key

DWINWFNTVXMFHD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Iridoid-skeleton
Bicyclic monoterpenoid
Sulfuric acid ester
Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Vinylogous ester
Organic sulfuric acid or derivatives
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	15.9 g/L	ALOGPS
logP	-1.7	ALOGPS
logP	-3.7	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	-1.9	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	150.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	62.75 m³·mol⁻¹	ChemAxon
Polarizability	26.53 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

External Links

HMDB ID

HMDB0182141

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 1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid (CFc000162549)

MOL for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

3D MOL for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

3D SDF for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

3D-SDF for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

PDB for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

3D PDB for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

SMILES for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

INCHI for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

Structure for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)

3D Structure for CFc000162549 (1,5-dihydroxy-7-[(sulfooxy)methyl]-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylic acid)