ChemFOnt: Showing chemical card for 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid (CFc000021582)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 19:13:26 UTC

Chemfont ID

CFc000021582

Molecule Identification

Common Name

16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid

Definition

16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid is found in alcoholic beverages. 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid is a constituent of Vitis vinifera (wine grape).

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
16b-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16b-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oic acid	Generator
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16Β-16-hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16Β-16-hydroxy-3-oxo-1,12-oleanadien-28-Oic acid	Generator
5-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,12a,12b,13,14b-octadecahydropicene-4a-carboxylate	HMDB

Chemical Formula

C₃₀H₄₄O₄

Average Molecular Weight

468.668

Monoisotopic Molecular Weight

468.323959896

IUPAC Name

5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,12a,12b,13,14b-octadecahydropicene-4a-carboxylic acid

Traditional Name

5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,7,8,8a,12b,13,14b-decahydro-1H-picene-4a-carboxylic acid

CAS Registry Number

77625-72-0

SMILES

CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O

InChI Identifier

InChI=1S/C30H44O4/c1-25(2)14-15-30(24(33)34)19(16-25)18-8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-28(21,6)29(18,7)17-23(30)32/h8,11-12,19-21,23,32H,9-10,13-17H2,1-7H3,(H,33,34)

InChI Key

DFSIQVYXMRYQGI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Beta-hydroxy acid
Cyclohexenone
Hydroxy acid
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0040711)

Source

Endogenous

Endogenous (HMDB: HMDB0040711)

Plant

Plant (HMDB: HMDB0040711)

Animal

Animal (HMDB: HMDB0040711)

Exogenous

Food

Food (HMDB: HMDB0040711)

Fruit

Fruits (FooDB: FOOD00871)

Beverage

Alcoholic beverage

Alcoholic beverages (FooDB: FOOD00854)

Exogenous (HMDB: HMDB0040711)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0040711)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0040711)

Lipid metabolism pathway (HMDB: HMDB0040711)

Cellular process

Cell signaling (HMDB: HMDB0040711)

Biochemical process

Lipid transport (HMDB: HMDB0040711)

Role

Biological role

Energy source (HMDB: HMDB0040711)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0040711)

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.0013 g/L	ALOGPS
logP	5.79	ALOGPS
logP	5.93	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.62	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	135.41 m³·mol⁻¹	ChemAxon
Polarizability	54.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0040711

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB020515

KNApSAcK ID

Not Available

Chemspider ID

35015009

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752914

PDB ID

Not Available

ChEBI ID

168172

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid (CFc000021582)

MOL for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D MOL for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D SDF for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D-SDF for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

PDB for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D PDB for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

SMILES for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

INCHI for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

Structure for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D Structure for CFc000021582 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)