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Curcumin-d6

Curcumin-d6 is listed under Stable Isotopes and is intended for analytical research, quality control and pharmaceutical reference standard applications. It is associated with Curcumin. The product is supplied by Clearsynth under CAT No. CS-T-51318. Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight and product enquiry details.

Product Specifications

Overview

"Labelled Curcumin . A natural phenolic compound. Potent anti-tumor agent having anti-inflammatory and anti-oxidant properties. Induces apoptosis in cancer cells and inhibits phorbol ester-induced protein kinase C (PKC) activity. Reported to inhibit production of inflammatory cytokines by peripheral blood monocytes and alveolar macrophages. Potent inhibitor of EGFR tyrosine kinase and IB kinase. Inhibits inducible nitric oxide synthase (iNOS), cycloxygenase and lipoxygenase. Easily penetrates into the cytoplasm of cells, accumulating in membranous structures such as plasma membrane, endoplasmic reticulum and nuclear envelope." "Srinivasan, et al, : J, Pharm, Pharmacol, , 5, 448 (1953), Tu, B, , et al, : J , Cell Biol, , 164, 341 (2004), Xu, G, , et al, : Biochemistry, 44, 9817"

CAS Number

1246833-26-0

Synonyms

Curcumin-d6

Molecular Formula

C 21 H 14 D 6 O 6

Molecular Weight

374.42

Additionnal Information

Curcumin-d6 is supplied with detailed characterization data compliant with regulatory guideline. Curcumin-d6 can be used for analytical method development, method validation (AMV), Quality Control (QC) application for Abbreviated New Drug Application (ANDA), or during commercial production of Curcumin.

Storage Conditions

Refer MSDS for complete information.

Applications Notes

"Labelled Curcumin . A natural phenolic compound. Potent anti-tumor agent having anti-inflammatory and anti-oxidant properties. Induces apoptosis in cancer cells and inhibits phorbol ester-induced protein kinase C (PKC) activity. Reported to inhibit production of inflammatory cytokines by peripheral blood monocytes and alveolar macrophages. Potent inhibitor of EGFR tyrosine kinase and IB kinase. Inhibits inducible nitric oxide synthase (iNOS), cycloxygenase and lipoxygenase. Easily penetrates into the cytoplasm of cells, accumulating in membranous structures such as plasma membrane, endoplasmic reticulum and nuclear envelope." "Srinivasan, et al, : J, Pharm, Pharmacol, , 5, 448 (1953), Tu, B, , et al, : J , Cell Biol, , 164, 341 (2004), Xu, G, , et al, : Biochemistry, 44, 9817"

HSN Code

38229010

Hazard Compound

Refer MSDS for accurate information.

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