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1134639-23-8

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1134639-23-8 Usage

Chemical Properties

Yellow Solid

Uses

Protected Curcumin (C838500). 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 IκB 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.

Check Digit Verification of cas no

The CAS Registry Mumber 1134639-23-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,4,6,3 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1134639-23:
(9*1)+(8*1)+(7*3)+(6*4)+(5*6)+(4*3)+(3*9)+(2*2)+(1*3)=138
138 % 10 = 8
So 1134639-23-8 is a valid CAS Registry Number.

1134639-23-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Di-(tert-Butyl-dimethylsilyl) Curcumin

1.2 Other means of identification

Product number -
Other names (1E,4Z,6E)-1,7-bis[4-[tert-butyl(dimethyl)silyl]oxy-3-methoxyphenyl]-5-hydroxyhepta-1,4,6-trien-3-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1134639-23-8 SDS

1134639-23-8Downstream Products

1134639-23-8Relevant articles and documents

Influence of side-chain changes on histone deacetylase inhibitory and cytotoxicity activities of curcuminoid derivatives

Kumboonma, Pakit,Phaosiri, Chanokbhorn,Saenglee, Somprasong,Samankul, Arunta,Senawong, Gulsiri,Senawong, Thanaset,Somsakeesit, La-or,Yenjai, Chavi

supporting information, (2020/04/10)

Using curcuminoids as lead compounds, fifty-nine curcuminoid derivatives with different side chains at the phenolic moiety were synthesized. All compounds were investigated for their histone deacetylase (HDAC) inhibitory activities. The potent pan-HDAC in

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