ChemFOnt: Showing chemical card for 5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid (CFc000161554)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:50:55 UTC

Chemfont ID

CFc000161554

Molecule Identification

Common Name

5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid

Definition

5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on 5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
5-[(6-Carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylate	Generator

Chemical Formula

C₁₉H₂₀N₂O₁₁

Average Molecular Weight

452.372

Monoisotopic Molecular Weight

452.106709472

IUPAC Name

5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid

Traditional Name

5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC2=CC=CC3=C2C2=C(N3)C(NC(C2)C(O)=O)C(O)=O)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C19H20N2O11/c22-12-13(23)15(18(29)30)32-19(14(12)24)31-8-3-1-2-6-9(8)5-4-7(16(25)26)21-11(17(27)28)10(5)20-6/h1-3,7,11-15,19-24H,4H2,(H,25,26)(H,27,28)(H,29,30)

InChI Key

CRPPOOINPNDEMP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
O-glucuronide
1-o-glucuronide
Harman
Pyridoindole
Glucuronic acid or derivatives
Beta-carboline
O-glycosyl compound
3-alkylindole
Alpha-amino acid or derivatives
Alpha-amino acid
Alkaloid or derivatives
Tricarboxylic acid or derivatives
Indole or derivatives
Indole
Aralkylamine
Beta-hydroxy acid
Benzenoid
Pyran
Oxane
Monosaccharide
Hydroxy acid
Heteroaromatic compound
Pyrrole
Amino acid
Secondary alcohol
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Polyol
Secondary aliphatic amine
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	11.9 g/L	ALOGPS
logP	-0.63	ALOGPS
logP	-3.9	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	2.22	ChemAxon
pKa (Strongest Basic)	6.87	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	218.87 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	99.23 m³·mol⁻¹	ChemAxon
Polarizability	42.21 Å³	ChemAxon
Number of Rings	4	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

HMDB0181146

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 5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid (CFc000161554)

MOL for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

3D MOL for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

3D SDF for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

3D-SDF for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

PDB for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

3D PDB for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

SMILES for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

INCHI for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

Structure for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)

3D Structure for CFc000161554 (5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-1,3-dicarboxylic acid)