6-Gingerol

6-Gingerol Basic information
Product Name:6-Gingerol
Synonyms:1-(4'-HYDROXY-3'-METHOXYPHENYL)-5-HYDROXY-3-DECANONE;6-GINGEROL;[6]-GINGEROL, ZINGIBER OFFICINALE;(5s)-5-hydroxy-1-(4-hydroxy-3-methoxy-phenyl)decan-3-one;GINGEROL;GINGEROL [6];(S)-5-HYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL-3-DECANONE;5-HYDROXY-1-(4'-HYDROXY-3'-METHOXYPHENYL)-3-DECANONE
CAS:23513-14-6
MF:C17H26O4
MW:294.39
EINECS:607-241-6
Product Categories:chemical reagent;pharmaceutical intermediate;Aromatic Phenols;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Natural Plant Extract;The group of Ginerols;Elisa Kit-plant ELISA Kit;23513-14-6
Mol File:23513-14-6.mol
6-Gingerol Structure
6-Gingerol Chemical Properties
Melting point 31℃
Boiling point 453.0±35.0 °C(Predicted)
density 1.083±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility methanol: soluble1mg/mL, clear, colorless
pka10.02±0.20(Predicted)
form Pale yellow oil
color White to Light yellow
InChIInChI=1S/C17H26O4/c1-3-4-5-6-14(18)12-15(19)9-7-13-8-10-16(20)17(11-13)21-2/h8,10-11,14,18,20H,3-7,9,12H2,1-2H3/t14-/m0/s1
InChIKeyNLDDIKRKFXEWBK-AWEZNQCLSA-N
SMILESC(C1=CC=C(O)C(OC)=C1)CC(=O)C[C@@H](O)CCCCC
LogP2.485 (est)
CAS DataBase Reference23513-14-6(CAS DataBase Reference)
NIST Chemistry ReferenceGingerol(23513-14-6)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 26-36/37
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
RTECS HE0757000
HS Code 29145090
MSDS Information
ProviderLanguage
6-Gingerol English
6-Gingerol Usage And Synthesis
Chemical PropertiesLight yellow ceraceous solid
Uses[6]-Gingerol has been used:
  • to study its effects on transient receptor potential (TRP) channels
  • to study its effects on experimental models of non-alcoholic steatohepatitis
  • to determine its effects on microsomal prostaglandine E2 synthase 1 (mPGES-1), glycogen synthase kinase 3β (GSK-3β) and β-catenin pathway in A549 cell line
  • to analyse the effects of 6-Shogaol (6-SG) on diabetic nephropathy (DN) in db/db mice
Definition ChEBI:Gingerol is a beta-hydroxy ketone that is 5-hydroxydecan-3-one substituted by a 4-hydroxy-3-methoxyphenyl moiety at position 1; believed to inhibit adipogenesis. It is a constituent of fresh ginger. It has a role as an antineoplastic agent and a plant metabolite. It is a beta-hydroxy ketone and a member of guaiacols.
General Description6-Gingerol is a naturally occurring plant phenoland an active pungent constituent found in the rhizome of ginger, which is known to possess anti-inflammatory, anti-tumor and antioxidant properties and can hence, serve as a potential candidate in the treatment of cancer.
Biological Activity6-Gingerol is the major pharmacologically-active component of ginger. It is known to exhibit a variety of biological activities including anticancer, anti-inflammation, and anti-oxidation. 6-Gingerol has been found to possess anticancer activities via its effect on a variety of biological pathways involved in apoptosis, cell cycle regulation, cytotoxic activity, and inhibition of angiogenesis.
Biochem/physiol ActionsBioactive compound found in ginger (Zingiber officinale) with antioxidant activity, which functions as an anti-inflammatory and antitumor agent. [6]-Gingerol down regulates proinflammatory cytokine release by macrophages. It has been shown to inhibit COX-2 expression by blocking the activation of p38 MAP kinase and NF-κB in phorbol ester-stimulated mouse skin.
Anticancer Research6-Gingerol is a plant polyphenol and an active constituent of Zingiber officinale, whichshowed antioxidant, anti-inflammation, and antitumor properties. It has the capacityto inhibit NOS, TNF-α, and COX-2 enzymes which are regulated by NF-κB(Aggarwal and Shishodia 2004; Wang et al. 2012). It hinders the cell growth ofprostate, gastric, and breast cancer cells and suppresses the lung metastasis ofB16F10 melanoma. It exhibits antitumorigenic effect in human colorectal cancercells via upregulating NSAID-activated gene-1 (NAG-1) (Aggarwal et al. 2008). Italters ERK1/2/JNK/AP1 pathway and induces apoptosis in colon cancer cells in acaspase-dependent manner (Singh et al. 2016b). ROS levels were significantlyincreased in K562 and MOLT4 cells treated with gingerol, and apoptosis wasinduced in leukemia cells by mitochondrial pathway (Wang et al. 2012).
6-Gingerol Preparation Products And Raw materials
Cianidanol L-Epicatechin PHENYL RESIN Methoxy 6-Gingerol 4-Methoxyphenylacetone Anisole (Trifluoromethoxy)benzene PHENYL VALERATE 10-Gingerol p-Anisic acid p-Anisidine 5-hydroxy-1-(4-hydroxy-3-methoxy-cyclohexyl)decan-3-one GINGEROL, 6-(P),GINGEROL, 6-(P) p-Anisaldehyde CHLOROPHOSPHONAZO III Diphenylsilanediol Phenylacetic acid

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