MiMeDB: Showing metabocard for Fucitol (MMDBc0000723)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:53:33 UTC

Update Date

2025-10-07 16:04:13 UTC

Metabolite ID

MMDBc0000723

Metabolite Identification

Common Name

Fucitol

Description

Fucitol is a sugar alcohol belonging to the chemical class of polyols. Its chemical structure features a fucose moiety, which can be modified through various pathways, including sulfation, as indicated by the detection of 1, 3, 5-tri-O-acetyl-2, 4-di-O-methyl-L-fucitol and 1, 4, 5-tri-O-acetyl-2, 3-di-O-methyl-L-fucitol (PMID:37182947 ). In biological contexts, fucitol has been shown to rapidly lyse Microcystis aeruginosa cells, highlighting its potential role in cellular interactions (PMID:35495711 ). Furthermore, fucitol derivatives, such as 1-deoxyfuconojirimycin, act as fucosidase inhibitors, which are relevant in cancer research (PMID:30554081 ). The synthesis of 3-deoxy-3-fluoro-L-fucitol involves enzymatic oxidation of its precursor, showcasing its synthetic versatility (PMID:32390019 ). Additionally, fucitol is implicated in the formation of O-linked fucose structures associated with epidermal growth factor, as evidenced by its detection in LC-MS/MS analyses (PMID:22422444 ). Structural studies have also revealed interactions between fucitol and enzymes, such as Bacillus pallidus d-arabinose isomerase, providing insights into its biochemical roles (PMID:20123133 ).

Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Molecular Formula

C₆H₁₄O₅

Average Mass

166.1724

Monoisotopic Mass

166.084123558

IUPAC Name

(2R,3S,4S,5S)-hexane-1,2,3,4,5-pentol

Traditional Name

fucitol

CAS Registry Number

Not Available

SMILES

C[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO

InChI Identifier

InChI=1S/C6H14O5/c1-3(8)5(10)6(11)4(9)2-7/h3-11H,2H2,1H3/t3-,4+,5-,6-/m0/s1

InChI Key

SKCKOFZKJLZSFA-FSIIMWSLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Hexoses

Alternative Parents

Substituents

Hexose monosaccharide
Fatty alcohol
Fatty acyl
Secondary alcohol
Polyol
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	476 g/L	ALOGPS
logP	-2.2	ALOGPS
logP	-2.7	ChemAxon
logS	0.46	ALOGPS
pKa (Strongest Acidic)	12.7	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	101.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	36.86 m³·mol⁻¹	ChemAxon
Polarizability	16.25 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

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-23	357.6
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-23	327.8
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-23	43.3
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-23	224.7
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-23	300.5
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-23	312.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (void)	2025-10-23	653.5
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-23	607.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-23	790.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	165.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	395.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	182.6
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	29.8
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	327.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	659.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-23	70.4
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-23	245.6
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-23	814.0
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-23	601.8

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	Fucitol_TMS_1	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H](O)CO	standard non polar	2025-10-23	2103.04
Gas Chromatography	Fucitol_TMS_2	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO	standard non polar	2025-10-23	2018.3
Gas Chromatography	Fucitol_TMS_3	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard non polar	2025-10-23	2251.89
Gas Chromatography	Fucitol_TMS_4	C[C@H](O)[C@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	2124.84
Gas Chromatography	Fucitol_TMS_5	C[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	1665.32
Gas Chromatography	Fucitol_TMS_6	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO	standard non polar	2025-10-23	2179.65
Gas Chromatography	Fucitol_TMS_7	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard non polar	2025-10-23	1739.46
Gas Chromatography	Fucitol_TMS_8	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	1720.56
Gas Chromatography	Fucitol_TMS_9	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	2106.72
Gas Chromatography	Fucitol_TMS_10	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard non polar	2025-10-23	1922.65
Gas Chromatography	Fucitol_TMS_11	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	2136.92
Gas Chromatography	Fucitol_TMS_12	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	2441.52
Gas Chromatography	Fucitol_TMS_13	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	2610.66
Gas Chromatography	Fucitol_TMS_14	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	1953.42
Gas Chromatography	Fucitol_TMS_15	C[C@H](O)[C@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1710.23
Gas Chromatography	Fucitol_TMS_16	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard non polar	2025-10-23	1614.0
Gas Chromatography	Fucitol_TMS_17	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	1990.24
Gas Chromatography	Fucitol_TMS_18	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	2341.03
Gas Chromatography	Fucitol_TMS_19	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	1970.51
Gas Chromatography	Fucitol_TMS_20	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	1548.73
Gas Chromatography	Fucitol_TMS_21	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2170.69
Gas Chromatography	Fucitol_TMS_22	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	2159.71
Gas Chromatography	Fucitol_TMS_23	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	1468.59
Gas Chromatography	Fucitol_TMS_24	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2032.64
Gas Chromatography	Fucitol_TMS_25	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2240.28
Gas Chromatography	Fucitol_TMS_26	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard non polar	2025-10-23	2233.19
Gas Chromatography	Fucitol_TMS_27	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard non polar	2025-10-23	1408.06
Gas Chromatography	Fucitol_TMS_28	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2049.27
Gas Chromatography	Fucitol_TMS_29	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1781.74
Gas Chromatography	Fucitol_TMS_30	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2496.31
Gas Chromatography	Fucitol_TMS_31	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2481.79
Gas Chromatography	Fucitol_TMS_1	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H](O)CO	standard polar	2025-10-23	2493.49
Gas Chromatography	Fucitol_TMS_2	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO	standard polar	2025-10-23	1994.99
Gas Chromatography	Fucitol_TMS_3	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard polar	2025-10-23	1944.49
Gas Chromatography	Fucitol_TMS_4	C[C@H](O)[C@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	1573.7
Gas Chromatography	Fucitol_TMS_5	C[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	2688.3
Gas Chromatography	Fucitol_TMS_6	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO	standard polar	2025-10-23	2588.6
Gas Chromatography	Fucitol_TMS_7	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard polar	2025-10-23	2185.72
Gas Chromatography	Fucitol_TMS_8	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	1739.86
Gas Chromatography	Fucitol_TMS_9	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	2143.4
Gas Chromatography	Fucitol_TMS_10	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard polar	2025-10-23	2419.58
Gas Chromatography	Fucitol_TMS_11	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	1959.35
Gas Chromatography	Fucitol_TMS_12	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	1800.48
Gas Chromatography	Fucitol_TMS_13	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	2072.58
Gas Chromatography	Fucitol_TMS_14	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	2363.79
Gas Chromatography	Fucitol_TMS_15	C[C@H](O)[C@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1985.37
Gas Chromatography	Fucitol_TMS_16	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO	standard polar	2025-10-23	2276.62
Gas Chromatography	Fucitol_TMS_17	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	2022.96
Gas Chromatography	Fucitol_TMS_18	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	1848.27
Gas Chromatography	Fucitol_TMS_19	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	2611.98
Gas Chromatography	Fucitol_TMS_20	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	1380.81
Gas Chromatography	Fucitol_TMS_21	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2871.53
Gas Chromatography	Fucitol_TMS_22	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	1868.42
Gas Chromatography	Fucitol_TMS_23	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	2906.32
Gas Chromatography	Fucitol_TMS_24	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1465.34
Gas Chromatography	Fucitol_TMS_25	C[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1804.42
Gas Chromatography	Fucitol_TMS_26	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C	standard polar	2025-10-23	2047.82
Gas Chromatography	Fucitol_TMS_27	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C	standard polar	2025-10-23	2241.04
Gas Chromatography	Fucitol_TMS_28	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2351.1
Gas Chromatography	Fucitol_TMS_29	C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2717.41
Gas Chromatography	Fucitol_TMS_30	C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2694.23
Gas Chromatography	Fucitol_TMS_31	C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1725.19

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Proteobacteria	1		Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0240315

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Fucitol

METLIN ID

Not Available

PubChem Compound

25032396

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Showing metabocard for Fucitol (MMDBc0000723)

MOL for #<Metabolite:0x00007f2e5204b6e0>

3D MOL for #<Metabolite:0x00007f2e5204b6e0>

3D SDF for #<Metabolite:0x00007f2e5204b6e0>

3D-SDF for #<Metabolite:0x00007f2e5204b6e0>

PDB for #<Metabolite:0x00007f2e5204b6e0>

3D PDB for #<Metabolite:0x00007f2e5204b6e0>

SMILES for #<Metabolite:0x00007f2e5204b6e0>

INCHI for #<Metabolite:0x00007f2e5204b6e0>

Structure for #<Metabolite:0x00007f2e5204b6e0>

3D Structure for #<Metabolite:0x00007f2e5204b6e0>