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Documenti fondamentali

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Supelco

(S)-ar-Turmerone

analytical standard

Sinonimo/i:

(S)-2-Methyl-6-(4-methylphenyl)-2-hepten-4-one

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About This Item

Formula empirica (notazione di Hill):
C15H20O
Numero CAS:
Peso molecolare:
216.32
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:

Grado

analytical standard

Saggio

≥90.0% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

C[C@@H](CC(=O)\C=C(\C)C)c1ccc(C)cc1

InChI

1S/C15H20O/c1-11(2)9-15(16)10-13(4)14-7-5-12(3)6-8-14/h5-9,13H,10H2,1-4H3/t13-/m0/s1
NAAJVHHFAXWBOK-ZDUSSCGKSA-N

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Descrizione generale

(S)-ar-Turmerone is the major constituent of turmeric oil derived from turmeric[1], which can find pharmaceutical applications due to its antibacterial, anti-carcinogenic, insect-repellent, anti-oxidant and anti-fungal properties.[2][1]

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sun Young Park et al.
International immunopharmacology, 14(1), 13-20 (2012-06-26)
Amyloid β (Aβ) induces the production of neuroinflammatory molecules, which may contribute to the pathogenesis of numerous neurodegenerative diseases. Therefore, suppression of neuroinflammatory molecules could be developed as a therapeutic method. Aromatic (ar)-turmerone, turmeric oil isolated from Curcuma longa, has
Preparation of alginate nanocapsules containing turmeric oil
Lertsutthiwong P,et al.
Carbohydrate Polymers, 74, 209-214 (2008)
Mara E M Braga et al.
Journal of agricultural and food chemistry, 51(22), 6604-6611 (2003-10-16)
Turmeric extracts were obtained from two lots of raw material (M and S) using various techniques: hydrodistillation, low pressure solvent extraction, Soxhlet, and supercritical extraction using carbon dioxide and cosolvents. The solvents and cosolvents tested were ethanol, isopropyl alcohol, and
Mai Fujiwara et al.
Journal of natural products, 74(1), 86-89 (2010-12-30)
Biotransformation studies conducted on (+)-(S)-ar-turmerone (1) and (+)-(S)-dihydro-ar-turmerone (2) by the fungus Aspergillus niger have revealed that 1 was metabolized to give four oxidized metabolites, (+)-(7S)-hydroxydehydro-ar-todomatuic acid (3), (+)-(7S,10E)-12-hydroxydehydro-ar-todomatuic acid (4), (+)-(7S,10E)-7,12-dihydroxydehydro-ar-todomatuic acid (5), and (+)-(7S)-15-carboxy-9,13-epoxy-7-hydroxy-9,13-dehydro-ar-curcumene (6), and (+)-(S)-dihydro-ar-turmerone (2)
Mingjie Ji et al.
International journal of molecular medicine, 14(2), 253-256 (2004-07-16)
This study investigated the cytotoxic effect of ar-turmerone isolated from turmeric (Curcuma longa L) on the K562, L1210, U937 and RBL-2H3 cell lines by the MTT assay. Ar-turmerone exhibited potent cytotoxicity on these cancer cell lines. The IC50 values of

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Recensioni

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