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Picembrin 7-acetate is a natural flavonoid compound derived from plants in the Scrophulariaceae family, known for its antioxidant, anti-inflammatory, and neuroprotective properties. It has shown potential in the treatment of neurodegenerative diseases, cancer, and cardiovascular diseases due to its ability to modulate intracellular signaling pathways and reduce oxidative stress.

109592-60-1

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109592-60-1 Usage

Uses

Used in Pharmaceutical Industry:
Picembrin 7-acetate is used as a neuroprotective agent for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its neuroprotective effects make it a promising candidate for further research and development in the field of medicine.
Used in Cancer Therapy:
Picembrin 7-acetate is used as a potential therapeutic agent in cancer treatment. Its ability to modulate intracellular signaling pathways and reduce oxidative stress has led to research into its potential applications in cancer therapy.
Used in Cardiovascular Disease Treatment:
Picembrin 7-acetate is used as a potential therapeutic agent for the treatment of cardiovascular diseases. Its antioxidant and anti-inflammatory properties, along with its ability to modulate intracellular signaling pathways, make it a valuable compound for further exploration in the field of cardiovascular medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 109592-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109592-60:
(8*1)+(7*0)+(6*9)+(5*5)+(4*9)+(3*2)+(2*6)+(1*0)=141
141 % 10 = 1
So 109592-60-1 is a valid CAS Registry Number.

109592-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-5-Hydroxy-4-oxo-2-phenyl-3,4-dihydro-2H-chromen-7-yl acetate

1.2 Other means of identification

Product number -
Other names Formononetinacetat

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:109592-60-1 SDS

109592-60-1Relevant academic research and scientific papers

Reduction of flavanones by NaBH3CN in trifluoroacetic acid.

Lewin, G.,Bert, M.,Dauguet, J. C.,Dolley, J.,Menez, P. Le,et al.

, p. 939 - 944 (2007/10/02)

For our studies on the reduction of flavanones, we worked on flavanone itself and on some other derivatives, oxygenated on the B ring.Besides expected flavans and chalcanes, condensed compounds (dimers and trimers) are also obtained.Reaction begins with the reduction of carbonyl to methylene; all the other isolated products arise from the two possible and competitive reactions on the potential carbocation C-2 of the flavan system: a) reductive cleavage of heterocycle; b) electrophilic aromatic substitution.Reactivity of flavanones is correlated with substituents of B ring through their ?+ values. Key words: flavanones / sodium cyanoborhydride / trifluoroacetic acid / flavans / chalcanes / dimers

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