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[6]-Gingerol - 10mM in DMSO, high purity , CAS No.23513-14-6

  • 10mM in DMSO
Item Number
G422764
Grouped product items
SKUSizeAvailabilityPrice Qty
G422764-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$90.90

Apoptotic, antioxidant and anti-inflammatory agent. SERCA activator.

Basic Description

Synonyms6-Gingerol|gingerol|23513-14-6|[6]-Gingerol|(6)-Gingerol|(S)-(+)-[6]Gingerol|(S)-(6)-Gingerol|(S)-5-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one|(5S)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one|1391-73-7|3-Decanone, 5-hydroxy-1-(4-hydroxy-3-met
Specifications & Purity10mM in DMSO
Biochemical and Physiological MechanismsApoptotic, antioxidant and anti-inflammatory agent. SERCA activator (EC 50 = 4 μM, Ca 2+ ATPase in cardiac sarcoplasmic reticulum). Inhibts COX-2 expression. Blocks p38 MAP kinase activation. Shows antiangiogenic effects in vivo. Orally active.
Storage TempStore at -80°C
Shipped InIce chest + Ice pads
Product Description

Gingerol, a phenolic substance and a potent cardiotonic agent isolated from the rhizome of ginger, has been shown to stimulate the Ca2+-pumping activity of sarcoplasmic reticulum (SR) of rabbits in a concentration-dependent manner. It was noted that Gingerol specifically activated SERCA (Ca2+-ATPase of cardiac and skeletal SR). Additional research has shown Gingerol to inhibit platelet aggregation via suppression of thromboxane production. Gingerol blocked ATP release from platelets induced by adrenaline and adenosine 5-diphosphate and prevented secondary aggregation. It has been demonstrated that Gingerol contains antioxidant and antiinflammatory characteristics and could significantly inhibit 7,12-dimethylbenz[a]anthracene-induced skin papillomagenesis in mice. Furthermore, Gingerol has been noted as an agonist of the capsaicin-activated VR1 (vanilloid receptor) and in leukemia cell studies it has been shown to have apoptotic properties.

Associated Targets

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (5S)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one
INCHI InChI=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
InChi Key NLDDIKRKFXEWBK-AWEZNQCLSA-N
Canonical SMILES CCCCCC(CC(=O)CCC1=CC(=C(C=C1)O)OC)O
Isomeric SMILES CCCCC[C@@H](CC(=O)CCC1=CC(=C(C=C1)O)OC)O
WGK Germany 3
RTECS HE0757000
PubChem CID 442793
UN Number 2811
Molecular Weight 294.39

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SensitivityLight & heat sensitive.

Safety and Hazards(GHS)

Pictogram(s) GHS06
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H301:Toxic if swallowed

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P301+P310:IF SWALLOWED: Immediately call a POISON CENTER/doctor/...

WGK Germany 3
RTECS HE0757000

Related Documents

Solution Calculators