ChemFOnt: Showing chemical card for 5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid (CFc000164822)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:56:47 UTC

Chemfont ID

CFc000164822

Molecule Identification

Common Name

5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid

Definition

5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton. Based on a literature review very few articles have been published on 5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0,.0,]heptadecan-14-yl]pentanoate	Generator
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulphooxy)tetracyclo[8.7.0.0,.0,]heptadecan-14-yl]pentanoate	Generator
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulphooxy)tetracyclo[8.7.0.0,.0,]heptadecan-14-yl]pentanoic acid	Generator
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate	Generator
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulphooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate	Generator
5-Hydroxy-4-[(2S)-2-methyl-5,16-bis(sulphooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid	Generator

Chemical Formula

C₂₃H₃₈O₁₁S₂

Average Molecular Weight

554.67

Monoisotopic Molecular Weight

554.185554392

IUPAC Name

5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

Traditional Name

5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

CAS Registry Number

Not Available

SMILES

[H]C(CO)(CCC(O)=O)C1([H])CCC2([H])C1([H])C([H])(CC1([H])C2([H])CCC2([H])CC([H])(CC[C@]12C)OS(O)(=O)=O)OS(O)(=O)=O

InChI Identifier

InChI=1S/C23H38O11S2/c1-23-9-8-15(33-35(27,28)29)10-14(23)3-4-17-18-6-5-16(13(12-24)2-7-21(25)26)22(18)20(11-19(17)23)34-36(30,31)32/h13-20,22,24H,2-12H2,1H3,(H,25,26)(H,27,28,29)(H,30,31,32)/t13?,14?,15?,16?,17?,18?,19?,20?,22?,23-/m0/s1

InChI Key

XGIWKJLCWQKZMY-GJWXMLOZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Sulfated steroids

Direct Parent

Sulfated steroids

Alternative Parents

Substituents

21-hydroxysteroid
Sulfated steroid skeleton
Hydroxysteroid
Sulfated fatty acid
Hydroxy fatty acid
Fatty acyl
Fatty acid
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Organic sulfuric acid or derivatives
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.099 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-0.56	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	-1.9	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	184.73 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	126.63 m³·mol⁻¹	ChemAxon
Polarizability	56.36 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0184540

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-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid (CFc000164822)

MOL for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

3D MOL for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

3D SDF for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

3D-SDF for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

PDB for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

3D PDB for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

SMILES for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

INCHI for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

Structure for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)

3D Structure for CFc000164822 (5-hydroxy-4-[(2S)-2-methyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid)