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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:18:35 UTC

Update Date

2023-02-21 17:26:48 UTC

HMDB ID

HMDB0038963

Secondary Accession Numbers

HMDB38963

Metabolite Identification

Common Name

4,6-Heptadiyne-1,3-diol

Description

4,6-Heptadiyne-1,3-diol belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. Based on a literature review a significant number of articles have been published on 4,6-Heptadiyne-1,3-diol.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₇H₈O₂

Average Molecular Weight

124.1372

Monoisotopic Molecular Weight

124.0524295

IUPAC Name

hepta-4,6-diyne-1,3-diol

Traditional Name

hepta-4,6-diyne-1,3-diol

CAS Registry Number

Not Available

SMILES

OCCC(O)C#CC#C

InChI Identifier

InChI=1S/C7H8O2/c1-2-3-4-7(9)5-6-8/h1,7-9H,5-6H2

InChI Key

VTFRDZFVCKUXNE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Secondary alcohol
Acetylide
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0038963)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038963)

Source

Endogenous

Endogenous (HMDB: HMDB0038963)

Plant

Plant (HMDB: HMDB0038963)

Animal

Animal (HMDB: HMDB0038963)

Exogenous

Food

Food (HMDB: HMDB0038963)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0038963)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0038963)

Lipid metabolism pathway (HMDB: HMDB0038963)

Cellular process

Cell signaling (HMDB: HMDB0038963)

Biochemical process

Lipid transport (HMDB: HMDB0038963)

Role

Biological role

Energy source (HMDB: HMDB0038963)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038963)

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.28 g/L	ALOGPS
logP	-0.12	ALOGPS
logP	-0.39	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	13.38	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	35.23 m³·mol⁻¹	ChemAxon
Polarizability	13.41 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	129.222	31661259
DarkChem	[M-H]-	123.62	31661259
DeepCCS	[M+H]+	127.766	30932474
DeepCCS	[M-H]-	125.128	30932474
DeepCCS	[M-2H]-	161.454	30932474
DeepCCS	[M+Na]+	135.872	30932474
AllCCS	[M+H]+	129.4	32859911
AllCCS	[M+H-H2O]+	125.1	32859911
AllCCS	[M+NH4]+	133.5	32859911
AllCCS	[M+Na]+	134.6	32859911
AllCCS	[M-H]-	126.9	32859911
AllCCS	[M+Na-2H]-	129.4	32859911
AllCCS	[M+HCOO]-	132.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4,6-Heptadiyne-1,3-diol	OCCC(O)C#CC#C	2166.7	Standard polar	33892256
4,6-Heptadiyne-1,3-diol	OCCC(O)C#CC#C	1139.4	Standard non polar	33892256
4,6-Heptadiyne-1,3-diol	OCCC(O)C#CC#C	1228.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4,6-Heptadiyne-1,3-diol,1TMS,isomer #1	C#CC#CC(O)CCO[Si](C)(C)C	1294.0	Semi standard non polar	33892256
4,6-Heptadiyne-1,3-diol,1TMS,isomer #2	C#CC#CC(CCO)O[Si](C)(C)C	1318.9	Semi standard non polar	33892256
4,6-Heptadiyne-1,3-diol,2TMS,isomer #1	C#CC#CC(CCO[Si](C)(C)C)O[Si](C)(C)C	1406.5	Semi standard non polar	33892256
4,6-Heptadiyne-1,3-diol,1TBDMS,isomer #1	C#CC#CC(O)CCO[Si](C)(C)C(C)(C)C	1522.7	Semi standard non polar	33892256
4,6-Heptadiyne-1,3-diol,1TBDMS,isomer #2	C#CC#CC(CCO)O[Si](C)(C)C(C)(C)C	1541.1	Semi standard non polar	33892256
4,6-Heptadiyne-1,3-diol,2TBDMS,isomer #1	C#CC#CC(CCO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	1821.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4,6-Heptadiyne-1,3-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-9100000000-b354429ef675e7730436	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,6-Heptadiyne-1,3-diol GC-MS (2 TMS) - 70eV, Positive	splash10-0umi-9720000000-3cdac3befc1eec560220	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,6-Heptadiyne-1,3-diol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 10V, Positive-QTOF	splash10-0a6r-2900000000-507fdf38150a579f6597	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 20V, Positive-QTOF	splash10-0a6r-8900000000-4380b24a1bcf38b5187c	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 40V, Positive-QTOF	splash10-0a70-9000000000-00ddad0d48a1f52064af	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 10V, Negative-QTOF	splash10-00di-4900000000-548eb8549c72c5bc59ab	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 20V, Negative-QTOF	splash10-0097-9300000000-98b93c6c72686d9cce45	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 40V, Negative-QTOF	splash10-002g-9000000000-f9b9251617b78876a4ce	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 10V, Negative-QTOF	splash10-004l-9300000000-4e941cae2afeeab704c9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 20V, Negative-QTOF	splash10-004i-9100000000-a7a97dca34936088dfe6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 40V, Negative-QTOF	splash10-004j-9000000000-60c10a05c8a824f32263	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 10V, Positive-QTOF	splash10-0bvr-9100000000-f8c2cbb97d06d2a2cfc0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 20V, Positive-QTOF	splash10-01ri-9000000000-72bf2b2dee9215b5136b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Heptadiyne-1,3-diol 40V, Positive-QTOF	splash10-002k-9000000000-e5ce89f52a62f51df0e2	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB018449

KNApSAcK ID

Not Available

Chemspider ID

35014701

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85627657

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 4,6-Heptadiyne-1,3-diol (HMDB0038963)

MOL for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

3D MOL for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

3D SDF for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

3D-SDF for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

PDB for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

3D PDB for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

SMILES for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

INCHI for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

Structure for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

3D Structure for HMDB0038963 (4,6-Heptadiyne-1,3-diol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

IR Spectra