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108997-30-4

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108997-30-4 Usage

Description

(E)-1,3-bis(4-hydroxyphenyl)prop-2-en-1-one, commonly known as curcumin, is a naturally-occurring chemical compound derived from the spice turmeric. It is celebrated for its anti-inflammatory, antioxidant, and anti-cancer properties, and has been a subject of extensive research for its potential therapeutic effects on a variety of diseases and health conditions.

Uses

Used in Pharmaceutical Applications:
Curcumin is utilized as a therapeutic agent for its anti-inflammatory and antioxidant properties, making it a potential treatment for conditions such as arthritis, diabetes, and neurodegenerative disorders. Its anti-cancer properties are also being explored for its potential to combat various types of cancer.
Used in Heart Health Applications:
Curcumin is used as a supplement to promote heart health due to its ability to improve cardiovascular function and reduce the risk of heart-related diseases.
Used in Cognitive Function Applications:
It is also recognized for its potential to improve cognitive function, making it a candidate for use in treatments for neurodegenerative conditions that affect cognitive abilities.
Used in Food Industry:
In the food industry, curcumin is used as a natural preservative and coloring agent, capitalizing on its ability to enhance the visual appeal and shelf life of various food products.
Overall, (E)-1,3-bis(4-hydroxyphenyl)prop-2-en-1-one, or curcumin, is a versatile compound with a wide range of applications across different industries, primarily due to its health-promoting and medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 108997-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,9 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108997-30:
(8*1)+(7*0)+(6*8)+(5*9)+(4*9)+(3*7)+(2*3)+(1*0)=164
164 % 10 = 4
So 108997-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O3/c16-13-6-1-11(2-7-13)3-10-15(18)12-4-8-14(17)9-5-12/h1-10,16-17H/b10-3+

108997-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1,3-Bis(4-hydroxyphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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:108997-30-4 SDS

108997-30-4Relevant articles and documents

Liquid crystalline epoxy thermosets

Giamberini,Amendola,Carfagna

, p. 9 - 22 (1995)

Rigid rod epoxy compounds can be cured in liquid crystalline structure. The so obtained networks exhibit better mechanical properties with respect to the isotropic ones. The mesogenic character of the epoxy compounds appears more crucial than the molecular geometry of the curing agent in developing liquid crystallinity. The curing temperature plays an important role in affecting the state of order of the thermosets.

4,4'-DIHYDROXYCHALCONE FROM THE HEARTWOOD OF CHAMAECYPARIS OBTUSA

Ohashi, Hideo,Ido, Yoshimi,Imai, Takanori,Yoshida, Kazumasa,Yasue, Moritami

, p. 3993 - 3994 (1988)

A new chalcone, 4,4'-dihydroxychalcone was isolated from the heartwood of Chamaecyparis obtusa.The structure was elucidated by direct comparison with a synthetic sample.

A simple and highly efficient method for the synthesis of chalcones by using borontrifluoride-etherate

Narender,Papi Reddy

, p. 3177 - 3180 (2007)

Chalcones are secondary metabolites of terrestrial plants, precursors for the biosynthesis of flavonoids and exhibit various biological activities. Condensation of substituted acetophenones (2a-12a) with various aromatic aldehydes (1b-7b) in the presence of BF3-Et2O at room temperature gave chalcones in 75-96% yield.

Discovery of isoliquiritigenin analogues that reverse acute hepatitis by inhibiting macrophage polarization

Yang, Junjie,Hu, Fanjie,Guo, Chengjun,Liang, Yuqing,Song, Haiying,Cheng, Kui

, (2021/06/15)

Screening a natural product library of 850 compounds yield isoliquiritigenin as an effective anti-inflammatory agent by inhibiting the production of pro-inflammatory NO induced by Pam3CSK4, while its activity accompanied by toxicity. Further studies obtained the optimized isoliquiritigenin derivative SMU-B14, which can inhibit Pam3CSK4 triggered toll-like receptor 2 (TLR2) signaling with low toxicity and high potency. Preliminary mechanism studies indicated that SMU-B14 worked through TLR2/MyD88, phosphorylation of IKKα/β, leading to the reduce degradation of NF-κB related IKBα and p65 complex, then inhibited the production of inflammatory cytokines, such as TNF-α, IL-6, IL-1β both in human and murine cell lines. Subsequent polarization experiments showed SMU-B14 significant reversed the polarization of M1 phenotype primary macrophage activated by Pam3CSK4 in vitro, and reduced the infiltration of neutrophil and polarization of M1-type macrophage, decreased serum alanine transaminase (ALT), as a result protected liver from being injured in vivo. In summary, we obtained an optimized lead compound SMU-B14 and found it functionally blocked TLR2/MyD88/NF-κB signaling pathway to down-regulate the production of inflammatory cytokines resulted significant liver protection property.

Chalcones and Chalcone-mimetic Derivatives as Notch Inhibitors in a Model of T-cell Acute Lymphoblastic Leukemia

Quaglio, Deborah,Zhdanovskaya, Nadezda,Tobajas, Gloria,Cuartas, Viviana,Balducci, Silvia,Christodoulou, Michael S.,Fabrizi, Giancarlo,Gargantilla, Marta,Priego, Eva-María,Carmona Pestania, álvaro,Passarella, Daniele,Screpanti, Isabella,Botta, Bruno,Palermo, Rocco,Mori, Mattia,Ghirga, Francesca,Pérez-Pérez, María-Jesús

supporting information, p. 639 - 643 (2019/04/25)

Based on hit-likeness and chemical diversity, a number of chalcones and chalcone-mimetic compounds were selected as putative Notch inhibitors. The evaluation of the antiproliferative effect combined with the inhibition of Notch1 expression in KOPTK1 cell line identified compound 18, featuring a tetrahydronaphthalene-based scaffold, as a new promising Notch-blocking agent.

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