Bovine Metabolome Database: Showing metabocard for TG(19:0/i-24:0/12:0) (BMDB0067791)

Identification Taxonomy Physical properties Pathways Spectra Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

1.0

Creation Date

2020-03-04 19:26:26 UTC

Update Date

2020-05-21 16:29:17 UTC

BMDB ID

BMDB0067791

Secondary Accession Numbers

BMDB67791

Metabolite Identification

Common Name

TG(19:0/i-24:0/12:0)

Description

TG(19:0/i-24:0/12:0) belongs to the family of triradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. Their general formula is [R1]OCC(CO[R2])O[R3]. TG(19:0/i-24:0/12:0) is made up of one nonadecanoyl(R1), one 22-methyltricosanoyl(R2), and one dodecanoyl(R3).

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
1-nonadecyloyl-2-isotetracosanoyl-3-lauroyl-glycerol	SMPDB, HMDB
TG(19:0/i-24:0/12:0)	SMPDB
TG(55:0)	SMPDB, HMDB
Tag(19:0/i-24:0/12:0)	SMPDB, HMDB
Tag(55:0)	SMPDB, HMDB
Triacylglycerol(19:0/i-24:0/12:0)	SMPDB, HMDB
Triacylglycerol(55:0)	SMPDB, HMDB
Triacylglycerol	SMPDB, HMDB
Triglyceride	SMPDB, HMDB
1-nonadecanoyl-2-isotetracosanoyl-3-dodecanoyl-glycerol	Lipid Annotator, HMDB
Tracylglycerol(55:0)	Lipid Annotator, HMDB
Tracylglycerol(19:0/i-24:0/12:0)	Lipid Annotator, HMDB

Chemical Formula

C₅₈H₁₁₂O₆

Average Molecular Weight

905.528

Monoisotopic Molecular Weight

904.845891326

IUPAC Name

(2R)-1-(dodecanoyloxy)-3-(nonadecanoyloxy)propan-2-yl 22-methyltricosanoate

Traditional Name

(2R)-1-(dodecanoyloxy)-3-(nonadecanoyloxy)propan-2-yl 22-methyltricosanoate

CAS Registry Number

Not Available

SMILES

[H][C@@](COC(=O)CCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCCC(C)C

InChI Identifier

InChI=1S/C58H112O6/c1-5-7-9-11-13-15-16-17-18-24-27-30-34-38-42-46-50-57(60)63-53-55(52-62-56(59)49-45-41-37-32-14-12-10-8-6-2)64-58(61)51-47-43-39-35-31-28-25-22-20-19-21-23-26-29-33-36-40-44-48-54(3)4/h54-55H,5-53H2,1-4H3/t55-/m1/s1

InChI Key

ARSSEUSIAGAKJH-KZRJWCEASA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Triradylcglycerols

Direct Parent

Triacylglycerols

Alternative Parents

Substituents

Triacyl-sn-glycerol
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Status

Expected but not Quantified

Origin

Endogenous

Biofunction

Not Available

Application

Not Available

Cellular locations

Adiposome
Cell membrane

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	10.59	ALOGPS
logP	21.88	ChemAxon
logS	-7.9	ALOGPS
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	56	ChemAxon
Refractivity	273.44 m³·mol⁻¹	ChemAxon
Polarizability	124.11 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0000000009-e70e5c7e6252f8ee8c86	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-0000000009-e70e5c7e6252f8ee8c86	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4i-0000099907-39d1bd977e96216a09a5	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0002-0893020002-2ca3c4d7b819aa842b3f	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0002-0892000000-9c7660f7e8a37aeff2f0	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0002-4986000000-f66671fad9294e6bc548	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0000000009-c705e8a6fbb38d1be275	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-0000000009-c705e8a6fbb38d1be275	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4i-0111099907-5d6b80c8150d0e4dd3a7	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-004i-0000000009-00c6dd835d7efaa7b0b6	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-004i-0000000009-00c6dd835d7efaa7b0b6	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-004i-0000000009-00c6dd835d7efaa7b0b6	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-03di-0000000009-03016e1fa888e42abf74	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-03di-0000000009-03016e1fa888e42abf74	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-08fu-0009090909-36f6b4f11aabef0d7730	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0udi-0332031209-d95932c429c6d8898f7e	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0002-0249000000-a10fbb1bdf2e59abe7e6	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0002-3669000000-1a9c528ea0b340fc1326	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0a4i-3215021139-324c0ce7d44d4b0952e5	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0pb9-7029100271-6cef3c308099ede8a5d5	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0zfu-4947300100-4f17afbf943eec750a4f	View in MoNA

Biological Properties

Cellular Locations

Adiposome
Cell membrane

Biospecimen Locations

Not Available

Pathways

Not Available

Name	SMPDB/Pathwhiz	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

External Links

HMDB ID

HMDB0064410

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB036442

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

131772039

PDB ID

Not Available

ChEBI ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Enzymes

Enzyme Details

1. Diacylglycerol O-acyltransferase 1

General function:: Not Available
Specific function:: Catalyzes the terminal and only committed step in triacylglycerol synthesis by using diacylglycerol and fatty acyl CoA as substrates. In contrast to DGAT2 it is not essential for survival. May be involved in VLDL (very low density lipoprotein) assembly. Functions as the major acyl-CoA retinol acyltransferase (ARAT) in the skin, where it acts to maintain retinoid homeostasis and prevent retinoid toxicity leading to skin and hair disorders. In liver, plays a role in esterifying exogenous fatty acids to glycerol.
Gene Name:: DGAT1
Uniprot ID:: Q8MK44
Molecular weight:: 55602.0

Reactions

DG(19:0/i-24:0/0:0) + Lauroyl-CoA → TG(19:0/i-24:0/12:0) + Coenzyme A	details

Showing metabocard for TG(19:0/i-24:0/12:0) (BMDB0067791)

Structure for BMDB0067791 (TG(19:0/i-24:0/12:0))

Enzymes

Reactions