ChemFOnt: Showing chemical card for PIP(18:1(9Z)/18:3(6Z,9Z,12Z)) (CFc000006024)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 18:51:53 UTC

Chemfont ID

CFc000006024

Molecule Identification

Common Name

PIP(18:1(9Z)/18:3(6Z,9Z,12Z))

Definition

PIP(18:1(9Z)/18:3(6Z,9Z,12Z)) is a phosphatidylinositol phosphate. Phosphatidylinositol phosphates are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to a phosphorylated inositol (hexahydroxycyclohexane). Phosphatidylinositol phosphates are generated from phosphatidylinositols, which are phosphorylated by a number of different kinases that place the phosphate moiety on positions 4 and 5 of the inositol ring, although position 3 can also be phosphorylated. Phosphatidylinositols phosphates can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 18 and 20 carbons are the most common. PIP(18:1(9Z)/18:3(6Z,9Z,12Z)), in particular, consists of one chain of oleic acid at the C-1 position and one chain of g-linolenic acid at the C-2 position. The oleic acid moiety is derived from vegetable oils, especially olive and canola oil, while the g-linolenic acid moiety is derived from animal fats. The most important phosphatidylinositol phosphate in both quantitative and biological terms is phosphatidylinositol 4-phosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main source of diacylglycerols that serve as signaling molecules, via the action of phospholipase C enzymes. Phosphatidylinositols phosphates are usually present at low levels only in tissues, typically at about 1 to 3% of the concentration of phosphatidylinositol.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Chemical Formula

C₄₈H₈₆O₁₈P₂

Average Molecular Weight

1013.1332

Monoisotopic Molecular Weight

1012.528938972

IUPAC Name

{[(1R,5S)-2,3,4,6-tetrahydroxy-5-({hydroxy[(2R)-2-hydroxy-3-[(2S)-3-(octadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propoxy]propoxy]phosphoryl}oxy)cyclohexyl]oxy}phosphonic acid

Traditional Name

[(1R,5S)-2,3,4,6-tetrahydroxy-5-{[hydroxy(2R)-2-hydroxy-3-[(2S)-3-(octadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propoxy]propoxyphosphoryl]oxy}cyclohexyl]oxyphosphonic acid

CAS Registry Number

None

SMILES

[H][C@@](O)(COC[C@@]([H])(COC(=O)CCCCCCCC=CCCCCCCCC)OC(=O)CCCCC=CCC=CCC=CCCCCC)COP(O)(=O)O[C@@]1([H])C(O)C(O)C(O)[C@@]([H])(OP(O)(O)=O)C1O

InChI Identifier

InChI=1S/C48H86O18P2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-41(50)62-38-40(64-42(51)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)37-61-35-39(49)36-63-68(59,60)66-48-45(54)43(52)44(53)47(46(48)55)65-67(56,57)58/h12,14,17-20,24,26,39-40,43-49,52-55H,3-11,13,15-16,21-23,25,27-38H2,1-2H3,(H,59,60)(H2,56,57,58)/t39-,40+,43?,44?,45?,46?,47-,48+/m1/s1

InChI Key

DUFSYGTYTBEWOA-YDCSQBCJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycerophosphoinositol phosphates. These are lipids containing a common glycerophosphate skeleton linked to at least one fatty acyl chain and an inositol-5-phosphate moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoinositol phosphates

Direct Parent

Glycerophosphoinositol phosphates

Alternative Parents

Substituents

Glycerophosphoinositol phosphate
Monoalkylglycerophosphoinositol
Glycerophosphoinositol
Inositol phosphate
Alkyldiacylglycerol
Cyclohexanol
Fatty acid ester
Glycerol ether
Monoalkyl phosphate
Dialkyl phosphate
Glycerolipid
Alkyl phosphate
Cyclitol or derivatives
Fatty acyl
Phosphoric acid ester
Organic phosphoric acid derivative
Dicarboxylic acid or derivatives
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Dialkyl ether
Ether
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Alcohol
Organic oxide
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

All cells and tissues (HMDB: HMDB0009982)

Tissue

All Tissues (HMDB: HMDB0009982)

Organ

Brain (HMDB: HMDB0009982)

Cellular substructure

Membrane (HMDB: HMDB0009982)
Extracellular (HMDB: HMDB0009982)
Golgi apparatus membrane (PMID: 20519312)
Cell membrane (PMID: 20519312)

Organelle

Endoplasmic reticulum (PMID: 20519312)

Source

Exogenous

Exogenous (HMDB: HMDB0009982)

Food

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Endogenous

Endogenous (HMDB: HMDB0009982)

Process

Naturally occurring process

Biological process

Cellular process

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.0089 g/L	ALOGPS
logP	6.16	ALOGPS
logP	8.52	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	1.08	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	285.5 Å²	ChemAxon
Rotatable Bond Count	44	ChemAxon
Refractivity	261.32 m³·mol⁻¹	ChemAxon
Polarizability	110.86 Å³	ChemAxon
Number of Rings	1	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB027168

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 PIP(18:1(9Z)/18:3(6Z,9Z,12Z)) (CFc000006024)

MOL for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

3D MOL for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

3D SDF for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

3D-SDF for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

PDB for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

3D PDB for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

SMILES for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

INCHI for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

Structure for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))

3D Structure for CFc000006024 (PIP(18:1(9Z)/18:3(6Z,9Z,12Z)))