576-02-3 Usage
Description
MARITIMETIN, also known as a hydroxyaurone, is a chemical compound that features aurone substituted by hydroxy groups at positions 6, 7, 3', and 4' respectively. It is derived from natural sources and has potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
MARITIMETIN is used as a pharmaceutical compound for its potential therapeutic applications. Its hydroxy groups enable interactions with biopolymers and macromolecules, making it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
MARITIMETIN is used as an active ingredient in the cosmetic industry for its potential benefits to skin health and appearance. MARITIMETIN's ability to interact with biopolymers and macromolecules may contribute to its use in skincare products, potentially offering anti-aging, moisturizing, or protective properties.
Used in Research and Development:
MARITIMETIN is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure and functional groups make it an interesting subject for scientific investigation, which could lead to the discovery of new uses and applications in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 576-02-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 576-02:
(5*5)+(4*7)+(3*6)+(2*0)+(1*2)=73
73 % 10 = 3
So 576-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O6/c16-9-3-1-7(5-11(9)18)6-12-13(19)8-2-4-10(17)14(20)15(8)21-12/h1-6,16-18,20H/b12-6-
576-02-3Relevant articles and documents
Design, synthesis and biological activities of dihydroaurones
VENKATESWARLU, SOMEPALLI,MURTY, GANDROTU NARASIMHA,SATYANARAYANA, MEKA,SIDDAIAH, VIDAVALUR
, p. 1396 - 1402 (2021/06/09)
To widen aurones applicability in achromatic food and cosmetic applications, a series of dihydroaurones were designed to mimic natural aurones as well as synthetic aurones. Dihydroaurones have been synthesized from the corresponding aurones by hydrogenation. These dihydroaurones and their corresponding aurones were screened for antioxidant, anti-inflammatory and tyrosinase enzyme inhibitory activity. Synthesized dihydroaurones (3b-f) displayed superior antioxidant activity in superoxide free radical scavenging assay than the standard gallic acid. Dihydroaurones (3b-f) also exhibited significant tyrosinase enzyme inhibitory activity and two dihydroaurones (3h, 3j) showed promising 5-lipoxygenase inhibitory activity.
"On water" synthesis of aurones: First synthesis of 4,5,3',4',5'-pentamethoxy-6-hydroxyaurone from Smilax riparia
Venkateswarlu, Somepalli,Murty, Gandrotu Narasimha,Satyanarayana, Meka
, p. 303 - 314 (2017/06/19)
A simple and green method for the synthesis of aurones by condensation of benzofuranone with aromatic aldehyde in neat water has been developed. The main advantages of this protocol include good yields, absence of catalyst, reagent, organic solvent, work-up and chromatographic purification. 4,5,3',4',5'-Pentamethoxy-6-hydroxyaurone, isolated from Smilax riparia was synthesized for the first time from 3-benzyloxy-4,5-dimethoxybenzaldehyde in five steps. {figure presented}.
New aurone glucosides and new phenylpropanoid glucosides from Bidens pilosa
Sashida,Ogawa,Kitada,Karikome,Mimaki,Shimomura
, p. 709 - 711 (2007/10/02)
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