72598-34-6 Usage
Chemical class
Pyrazinone
Contains a pyrazinone ring
The compound has a five-membered nitrogen-containing ring.
Hydroxyl and methyl groups attached
The pyrazinone ring has hydroxyl (-OH) and methyl (-CH3) groups attached in specific positions.
Potential medicinal properties
The unique structure and functional groups of the compound may have biological and therapeutic activities.
Valuable for pharmaceutical research
The compound could be used in drug development and investigation of its potential uses.
Further investigation and applications
The specific structure and properties make it valuable for various fields, such as medicinal chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 72598-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72598-34:
(7*7)+(6*2)+(5*5)+(4*9)+(3*8)+(2*3)+(1*4)=156
156 % 10 = 6
So 72598-34-6 is a valid CAS Registry Number.
72598-34-6Relevant articles and documents
New Furanone Derivatives and Alkaloids from the Co-Culture of Marine-Derived Fungi Aspergillus sclerotiorum and Penicillium citrinum
Bao, Jie,Wang, Jie,Zhang, Xiao-Yong,Nong, Xu-Hua,Qi, Shu-Hua
, (2017/03/27)
Six new compounds including two furanone derivatives sclerotiorumins A and B (1 and 2), one novel oxadiazin derivative sclerotiorumin C (3), one pyrrole derivative 1-(4-benzyl-1H-pyrrol-3-yl)ethanone (4), and two complexes of neoaspergillic acid aluminiumneohydroxyaspergillin (5) and ferrineohydroxyaspergillin (6) were isolated from the co-culture of marine-derived fungi Aspergillus sclerotiorum and Penicillium citrinum. Compound 3 was the first natural 1,2,4-oxadiazin-6-one. Compound 5 showed significant and selective cytotoxicity against human histiocytic lymphoma U937 cell line (IC50?=?4.2?μm) and strong toxicity towards brine shrimp (LC50?=?6.1?μm), and oppositely increased the growth and biofilm formation of Staphylococcus aureus.
