Bovine Metabolome Database: Showing metabocard for Heptadecanoyl CoA (BMDB0006497)

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

Record Information

Version

1.0

Creation Date

2016-09-30 23:22:34 UTC

Update Date

2020-05-21 16:29:09 UTC

BMDB ID

BMDB0006497

Secondary Accession Numbers

BMDB06497

Metabolite Identification

Common Name

Heptadecanoyl CoA

Description

Heptadecanoyl CoA, also known as heptadecanoyl coa or heptadecyl-CoA, belongs to the class of organic compounds known as long-chain fatty acyl coas. These are acyl CoAs where the group acylated to the coenzyme A moiety is a long aliphatic chain of 13 to 21 carbon atoms. Thus, heptadecanoyl CoA is considered to be a fatty ester lipid molecule. Heptadecanoyl CoA is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. In cattle, heptadecanoyl CoA is involved in the metabolic pathway called de novo triacylglycerol biosynthesis TG(8:0/17:0/17:0) pathway.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
Heptadecanoyl-coenzyme A	ChEBI
Heptadecanoate	HMDB
Heptadecanoic acid	HMDB
Heptadecanoic acid CoA	HMDB
Heptadecanoyl coenzyme A	HMDB
Heptadecanoyl-CoA	HMDB
Heptadecyl-CoA	HMDB
Heptadecyl-coenzyme A	HMDB
Margaric acid CoA	HMDB
Margaroyl coenzyme A	HMDB
N-Heptadecanoate	HMDB
N-Heptadecanoic acid	HMDB
N-Heptadecanoic acid coenzyme A	HMDB
S-Heptadecanoate	HMDB
S-Heptadecanoate coenzyme A	HMDB
S-Heptadecanoate-coenzyme A	HMDB
S-Heptadecanoic acid	HMDB
S-Heptadecanoyl CoA	HMDB
S-Heptadecanoyl coenzyme A	HMDB

Chemical Formula

C₃₈H₆₈N₇O₁₇P₃S

Average Molecular Weight

1019.97

Monoisotopic Molecular Weight

1019.360524011

IUPAC Name

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-2-({[({[(3R)-3-[(2-{[2-(heptadecanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]-3-hydroxy-2,2-dimethylpropoxy](hydroxy)phosphoryl}oxy)(hydroxy)phosphoryl]oxy}methyl)-4-hydroxyoxolan-3-yl]oxy}phosphonic acid

Traditional Name

[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-2-[({[(3R)-3-[(2-{[2-(heptadecanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]-3-hydroxy-2,2-dimethylpropoxy(hydroxy)phosphoryl]oxy(hydroxy)phosphoryl}oxy)methyl]-4-hydroxyoxolan-3-yl]oxyphosphonic acid

CAS Registry Number

3546-17-6

SMILES

CCCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C(N)N=CN=C12

InChI Identifier

InChI=1S/C38H68N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-29(47)66-22-21-40-28(46)19-20-41-36(50)33(49)38(2,3)24-59-65(56,57)62-64(54,55)58-23-27-32(61-63(51,52)53)31(48)37(60-27)45-26-44-30-34(39)42-25-43-35(30)45/h25-27,31-33,37,48-49H,4-24H2,1-3H3,(H,40,46)(H,41,50)(H,54,55)(H,56,57)(H2,39,42,43)(H2,51,52,53)/t27-,31-,32-,33+,37-/m1/s1

InChI Key

DRABUZIHHACUPI-DUPKZGIXSA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as long-chain fatty acyl coas. These are acyl CoAs where the group acylated to the coenzyme A moiety is a long aliphatic chain of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl thioesters

Direct Parent

Long-chain fatty acyl CoAs

Alternative Parents

Substituents

Coenzyme a or derivatives
Purine ribonucleoside 3',5'-bisphosphate
Purine ribonucleoside bisphosphate
Purine ribonucleoside diphosphate
Ribonucleoside 3'-phosphate
Pentose phosphate
Pentose-5-phosphate
Beta amino acid or derivatives
Glycosyl compound
N-glycosyl compound
6-aminopurine
Monosaccharide phosphate
Organic pyrophosphate
Pentose monosaccharide
Imidazopyrimidine
Purine
Monoalkyl phosphate
Aminopyrimidine
Imidolactam
N-acyl-amine
N-substituted imidazole
Organic phosphoric acid derivative
Monosaccharide
Pyrimidine
Alkyl phosphate
Fatty amide
Phosphoric acid ester
Tetrahydrofuran
Imidazole
Azole
Heteroaromatic compound
Carbothioic s-ester
Secondary alcohol
Thiocarboxylic acid ester
Carboxamide group
Secondary carboxylic acid amide
Amino acid or derivatives
Sulfenyl compound
Thiocarboxylic acid or derivatives
Organoheterocyclic compound
Azacycle
Oxacycle
Carboxylic acid derivative
Organosulfur compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Primary amine
Organopnictogen compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Alcohol
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

long-chain fatty acyl-CoA (CHEBI:74397 )
11,12-saturated fatty acyl-CoA (CHEBI:74397 )

Ontology

Status

Expected but not Quantified

Origin

Endogenous

Exogenous

Biofunction

Not Available

Application

Not Available

Cellular locations

Cell membrane
Cytoplasm
Membrane
Mitochondria

Physical Properties

State

Solid

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	2.61	ALOGPS
logP	-0.051	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	0.83	ChemAxon
pKa (Strongest Basic)	4.95	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	363.63 Å²	ChemAxon
Rotatable Bond Count	35	ChemAxon
Refractivity	241.25 m³·mol⁻¹	ChemAxon
Polarizability	102.54 Å³	ChemAxon
Number of Rings	3	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	splash10-000i-4902110200-db5443e07e150b0ec7d1	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-000i-1913130000-a3c3e7ad6d370a0d9ab8	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-000i-1900010000-be853ba709390a162e5f	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0lgi-9761332400-df46f923c788e4633547	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-001i-4921201000-103592f0573f96ddf6a4	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-057i-5900000000-f863779e788bb009e57b	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-9000000000-b60e8c6845a544b99284	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-016r-9010201300-38edd61504f16ec953af	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004r-8103401309-d69730a7d790b0b5c65a	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-9000000000-94bf02cb6c8de72ec588	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0uxr-7000200629-c0856e9611760f88f172	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-03di-0100590000-4ba435930803a1cdd95a	View in MoNA
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Not Available	View in JSpectraViewer

Biological Properties

Cellular Locations

Cell membrane
Cytoplasm
Membrane
Mitochondria

Biospecimen Locations

Not Available

Pathways

Name	SMPDB/Pathwhiz	KEGG
De Novo Triacylglycerol Biosynthesis TG(20:0/17:0/14:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(20:0/17:0/17:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(20:0/17:0/19:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(20:0/18:0/17:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(20:0/17:0/21:0)		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

External Links

HMDB ID

HMDB0006497

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB023941

KNApSAcK ID

Not Available

Chemspider ID

2339497

KEGG Compound ID

Not Available

BioCyc ID

CPD-14723

BiGG ID

2415330

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3082004

PDB ID

Not Available

ChEBI ID

74397

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(20:0/17:0/0:0) + Heptadecanoyl CoA → TG(20:0/17:0/17:0) + Coenzyme A	details
DG(20:0/18:0/0:0) + Heptadecanoyl CoA → TG(20:0/18:0/17:0) + Coenzyme A	details
DG(20:0/15:0/0:0) + Heptadecanoyl CoA → TG(20:0/15:0/17:0) + Coenzyme A	details
DG(19:0/21:0/0:0) + Heptadecanoyl CoA → TG(19:0/21:0/17:0) + Coenzyme A	details
DG(20:0/20:0/0:0) + Heptadecanoyl CoA → TG(20:0/20:0/17:0) + Coenzyme A	details
DG(20:0/12:0/0:0) + Heptadecanoyl CoA → TG(20:0/12:0/17:0) + Coenzyme A	details
DG(19:0/22:0/0:0) + Heptadecanoyl CoA → TG(19:0/22:0/17:0) + Coenzyme A	details
DG(20:0/10:0/0:0) + Heptadecanoyl CoA → TG(20:0/10:0/17:0) + Coenzyme A	details
DG(21:0/13:0/0:0) + Heptadecanoyl CoA → TG(21:0/13:0/17:0) + Coenzyme A	details
DG(21:0/10:0/0:0) + Heptadecanoyl CoA → TG(21:0/10:0/17:0) + Coenzyme A	details
DG(21:0/14:0/0:0) + Heptadecanoyl CoA → TG(21:0/14:0/17:0) + Coenzyme A	details
DG(21:0/16:0/0:0) + Heptadecanoyl CoA → TG(21:0/16:0/17:0) + Coenzyme A	details
DG(21:0/15:0/0:0) + Heptadecanoyl CoA → TG(21:0/15:0/17:0) + Coenzyme A	details
DG(21:0/17:0/0:0) + Heptadecanoyl CoA → TG(21:0/17:0/17:0) + Coenzyme A	details
DG(21:0/22:0/0:0) + Heptadecanoyl CoA → TG(21:0/22:0/17:0) + Coenzyme A	details
DG(21:0/18:0/0:0) + Heptadecanoyl CoA → TG(21:0/18:0/17:0) + Coenzyme A	details
DG(22:0/18:0/0:0) + Heptadecanoyl CoA → TG(22:0/18:0/17:0) + Coenzyme A	details
DG(22:0/13:0/0:0) + Heptadecanoyl CoA → TG(22:0/13:0/17:0) + Coenzyme A	details
DG(22:0/17:0/0:0) + Heptadecanoyl CoA → TG(22:0/17:0/17:0) + Coenzyme A	details
DG(22:0/22:0/0:0) + Heptadecanoyl CoA → TG(22:0/22:0/17:0) + Coenzyme A	details
DG(10:0/18:0/0:0) + Heptadecanoyl CoA → TG(10:0/18:0/17:0) + Coenzyme A	details
DG(8:0/18:0/0:0) + Heptadecanoyl CoA → TG(8:0/18:0/17:0) + Coenzyme A	details
DG(10:0/8:0/0:0) + Heptadecanoyl CoA → TG(10:0/8:0/17:0) + Coenzyme A	details
DG(10:0/16:0/0:0) + Heptadecanoyl CoA → TG(10:0/16:0/17:0) + Coenzyme A	details
DG(10:0/15:0/0:0) + Heptadecanoyl CoA → TG(10:0/15:0/17:0) + Coenzyme A	details
DG(8:0/13:0/0:0) + Heptadecanoyl CoA → TG(8:0/13:0/17:0) + Coenzyme A	details
DG(8:0/19:0/0:0) + Heptadecanoyl CoA → TG(8:0/19:0/17:0) + Coenzyme A	details
DG(10:0/14:0/0:0) + Heptadecanoyl CoA → TG(10:0/14:0/17:0) + Coenzyme A	details
DG(8:0/14:0/0:0) + Heptadecanoyl CoA → TG(8:0/14:0/17:0) + Coenzyme A	details
DG(8:0/15:0/0:0) + Heptadecanoyl CoA → TG(8:0/15:0/17:0) + Coenzyme A	details
DG(10:0/17:0/0:0) + Heptadecanoyl CoA → TG(10:0/17:0/17:0) + Coenzyme A	details
DG(8:0/17:0/0:0) + Heptadecanoyl CoA → TG(8:0/17:0/17:0) + Coenzyme A	details
DG(10:0/19:0/0:0) + Heptadecanoyl CoA → TG(10:0/19:0/17:0) + Coenzyme A	details
DG(19:0/a-21:0/0:0) + Heptadecanoyl CoA → TG(19:0/a-21:0/17:0) + Coenzyme A	details
DG(19:0/a-25:0/0:0) + Heptadecanoyl CoA → TG(19:0/a-25:0/17:0) + Coenzyme A	details
DG(19:0/i-21:0/0:0) + Heptadecanoyl CoA → TG(19:0/i-21:0/17:0) + Coenzyme A	details
DG(19:0/i-22:0/0:0) + Heptadecanoyl CoA → TG(19:0/i-22:0/17:0) + Coenzyme A	details
DG(19:0/i-24:0/0:0) + Heptadecanoyl CoA → TG(19:0/i-24:0/17:0) + Coenzyme A	details
DG(a-21:0/12:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/12:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/13:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/13:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/14:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/14:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/15:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/15:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/16:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/16:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/17:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/17:0/17:0)[rac] + Coenzyme A	details
DG(a-21:0/a-21:0/0:0) + Heptadecanoyl CoA → TG(a-21:0/a-21:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/12:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/12:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/13:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/13:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/14:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/14:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/15:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/15:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/16:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/16:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/17:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/17:0/17:0)[rac] + Coenzyme A	details
DG(a-25:0/a-25:0/0:0) + Heptadecanoyl CoA → TG(a-25:0/a-25:0/17:0)[rac] + Coenzyme A	details
DG(i-19:0/i-21:0/0:0) + Heptadecanoyl CoA → TG(i-19:0/i-21:0/17:0) + Coenzyme A	details
DG(i-19:0/i-22:0/0:0) + Heptadecanoyl CoA → TG(i-19:0/i-22:0/17:0) + Coenzyme A	details
DG(i-19:0/i-24:0/0:0) + Heptadecanoyl CoA → TG(i-19:0/i-24:0/17:0) + Coenzyme A	details
DG(i-20:0/12:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/12:0/17:0) + Coenzyme A	details
DG(i-20:0/13:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/13:0/17:0) + Coenzyme A	details
DG(i-20:0/14:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/14:0/17:0) + Coenzyme A	details
DG(i-20:0/15:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/15:0/17:0) + Coenzyme A	details
DG(i-20:0/16:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/16:0/17:0) + Coenzyme A	details
DG(i-20:0/17:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/17:0/17:0) + Coenzyme A	details
DG(i-20:0/i-20:0/0:0) + Heptadecanoyl CoA → TG(i-20:0/i-20:0/17:0) + Coenzyme A	details
DG(i-21:0/12:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/12:0/17:0) + Coenzyme A	details
DG(i-21:0/13:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/13:0/17:0) + Coenzyme A	details
DG(i-21:0/14:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/14:0/17:0) + Coenzyme A	details
DG(i-21:0/15:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/15:0/17:0) + Coenzyme A	details
DG(i-21:0/16:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/16:0/17:0) + Coenzyme A	details
DG(i-21:0/17:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/17:0/17:0) + Coenzyme A	details
DG(i-21:0/i-21:0/0:0) + Heptadecanoyl CoA → TG(i-21:0/i-21:0/17:0) + Coenzyme A	details
DG(i-22:0/12:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/12:0/17:0) + Coenzyme A	details
DG(i-22:0/13:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/13:0/17:0) + Coenzyme A	details
DG(i-22:0/14:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/14:0/17:0) + Coenzyme A	details
DG(i-22:0/15:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/15:0/17:0) + Coenzyme A	details
DG(i-22:0/16:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/16:0/17:0) + Coenzyme A	details
DG(i-22:0/17:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/17:0/17:0) + Coenzyme A	details
DG(i-22:0/i-22:0/0:0) + Heptadecanoyl CoA → TG(i-22:0/i-22:0/17:0) + Coenzyme A	details
DG(i-24:0/12:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/12:0/17:0) + Coenzyme A	details
DG(i-24:0/13:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/13:0/17:0) + Coenzyme A	details
DG(i-24:0/14:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/14:0/17:0) + Coenzyme A	details
DG(i-24:0/15:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/15:0/17:0) + Coenzyme A	details
DG(i-24:0/16:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/16:0/17:0) + Coenzyme A	details
DG(i-24:0/17:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/17:0/17:0) + Coenzyme A	details
DG(i-24:0/i-24:0/0:0) + Heptadecanoyl CoA → TG(i-24:0/i-24:0/17:0) + Coenzyme A	details

Showing metabocard for Heptadecanoyl CoA (BMDB0006497)

Structure for BMDB0006497 (Heptadecanoyl CoA)

Enzymes

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