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(Q105195036)
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5-Hydroxy-1-(4-hydroxy-3-methoxycyclohexyl)decan-3-one
group of stereoisomers with the chemical formula C₁₇H₃₂O₄
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Statements
instance of
group of stereoisomers
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subclass of
chemical compound
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mass
300.230059504
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₇H₃₂O₄
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canonical SMILES
O=C(CCC1CCC(O)C(OC)C1)CC(O)CCCCC
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found in taxon
Aframomum melegueta
1 reference
stated in
Termite antifeedant activity in Aframomum melegueta
Zingiber officinale
40 references
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[6]-gingerol induces Ca2+ mobilization in Madin-Darby canine kidney cells
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A new method for the determination of pungent compounds in ginger (Zingiber officinale)
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Antiallergic potential on RBL-2H3 cells of some phenolic constituents of Zingiber officinale (ginger).
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Antioxidant Effects of Some Ginger Constituents
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Application of two rapid techniques of column chromatography to separate the pungent principles of ginger,Zingiber officinale Roscoe
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A re-examination of gingerol, shogaol, and zingerone, the pungent principles of ginger (Zingiber officinale Roscoe)
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Bioassay-guided isolation and identification of antifungal compounds from ginger
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Changes in the amounts of [6]gingerol and derivatives during a culture cycle of ginger, Zingiber officinale
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Cholagogic effect of ginger and its active constituents
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Component of Zingiber officinale that improves the enhancement of small intestinal transport
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Diarylheptanoids from rhizomes ofZingiber officinale
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Extraction of ginger rhizome: partition constants and other equilibrium properties in organic solvents and in supercritical carbon dioxide
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Fresh organically grown ginger (Zingiber officinale): composition and effects on LPS-induced PGE2 production.
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Gastrointestinal motility enhancing effect of ginger and its active constituents
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Gingerdiol related compounds from the rhizomes of Zingiber officinale
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Gingerol Decreases after Processing and Storage of Ginger
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High Performance Liquid Chromatographic Determination of Pungent Gingerol Compounds of Ginger (Zingiber officinale Roscoe)
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High-performance liquid chromatographic separation of pungency components of ginger
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High-performance liquid chromatography–electrospray mass spectrometric analysis of pungent constituents of ginger
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Inhibition of Prostaglandin and Leukotriene Biosynthesis by Gingerols and Diarylheptanoids
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Isolation of 6-, 8-, and 10-Gingerol from Ginger Rhizome by HPLC and Preliminary Evaluation of Inhibition ofMycobacteriumaviumandMycobacteriumtuberculosis
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Isolation of Gingerols from Powdered Root Ginger by Countercurrent Chromatography
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Mutagen and anti-mutagen in ginger, Zingiber officinale
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Pungent compounds of ginger (Zingiber officinale roscoe) extracted by liquid carbon dioxide
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Stomachic principles in ginger. II. Pungent and anti-ulcer effects of low polar constituents isolated from ginger, the dried rhizoma of Zingiber officinale Roscoe cultivated in Taiwan. The absolute stereostructure of a new diarylheptanoid
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[Studies on the constituents of ginger (Zingiber officinale Roscoe) by GC-MS (author's transl)]
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The anti-ulcer effect in rats of ginger constituents
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Gingerol, a novel cardiotonic agent, activates the Ca2+-pumping ATPase in skeletal and cardiac sarcoplasmic reticulum
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Molluscicidal and antischistosomal activities of Zingiber officinale.
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Mutagenicity of gingerol and shogaol and antimutagenicity of zingerone in Salmonella/microsome assay.
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Genotoxic effect of 6-gingerol on human hepatoma G2 cells
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Ginger ingredients reduce viability of gastric cancer cells via distinct mechanisms
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Ginger inhibits cell growth and modulates angiogenic factors in ovarian cancer cells
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Increased growth inhibitory effects on human cancer cells and anti-inflammatory potency of shogaols from Zingiber officinale relative to gingerols.
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Multiple mechanisms are involved in 6-gingerol-induced cell growth arrest and apoptosis in human colorectal cancer cells.
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Stomachic principles in ginger. III. An anti-ulcer principle, 6-gingesulfonic acid, and three monoacyldigalactosylglycerols, gingerglycolipids A, B, and C, from Zingiberis Rhizoma originating in Taiwan
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Pharmacognostic studies on ginger and related drugs--part 1: five sulfonated compounds from Zingiberis rhizome (Shokyo)
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Crude Drug Processing by Far-infrared Treatment. II. Chemical Fluctuation of the Constituents during the Drying of Zingiberis Rhizoma
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Characterization of gingerol-related compounds in ginger rhizome (Zingiber officinale Rosc.) by high-performance liquid chromatography/electrospray ionization mass spectrometry
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Extraction of ginger (Zingiber officinale Roscoe) oleoresin with CO2 and co-solvents: a study of the antioxidant action of the extracts
Carum carvi
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Cuminum cyminum
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Illicium verum
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Myristica fragrans
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Piper nigrum
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
clove
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Zingiber
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Cinnamon
1 reference
stated in
Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents
Identifiers
InChI
InChI=1S/C17H32O4/c1-3-4-5-6-14(18)12-15(19)9-7-13-8-10-16(20)17(11-13)21-2/h13-14,16-18,20H,3-12H2,1-2H3
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InChIKey
ONQQLFWDTJJQKU-UHFFFAOYSA-N
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PubChem CID
42675
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
UniChem compound ID
1078219
1 reference
stated in
UniChem
KNApSAcK ID
C00062299
1 reference
based on heuristic
inferred from InChIKey
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