152464-78-3 Usage
General Description
Leachianone G is a chemical compound found in the plant Litchi chinensis, commonly known as lychee. It is a flavonoid with reported antioxidant, anti-inflammatory, and anticancer properties. Studies have shown that leachianone G has the potential to inhibit the growth of cancer cells, particularly in breast cancer and leukemia. Additionally, it has been found to reduce inflammation and protect against oxidative stress, which may be beneficial for overall health and disease prevention. Further research is needed to fully understand the potential therapeutic uses of leachianone G, but its natural occurrence in lychee suggests it could be a valuable source of bioactive compounds with health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 152464-78-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,6 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 152464-78:
(8*1)+(7*5)+(6*2)+(5*4)+(4*6)+(3*4)+(2*7)+(1*8)=133
133 % 10 = 3
So 152464-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O6/c1-10(2)3-5-13-15(23)8-16(24)19-17(25)9-18(26-20(13)19)12-6-4-11(21)7-14(12)22/h3-4,6-8,18,21-24H,5,9H2,1-2H3
152464-78-3Relevant articles and documents
8-Dimethylallylnaringenin 2′-hydroxylase, the crucial cytochrome P450 mono-oxygenase for lavandulylated flavanone formation in Sophora flavescens cultured cells
Yamamoto, Hirobumi,Yatou, Atsushi,Inoue, Kenichiro
, p. 671 - 676 (2001)
8-Dimethylallylnaringenin (8-DMAN) 2′-hydroxylase, which is indispensable for the formation of a lavandulylated flavanone, sophoraflavanone G, was detected in cell suspension cultures of Sophora flavescens. The enzyme catalyzes the 2′-hydroxylation of 8-D
Synthesis, biological evaluation of prenylflavonoids as vasorelaxant and neuroprotective agents
Dong, Xiaowu,Qi, Lingling,Jiang, Chaoyi,Chen, Jing,Wei, Erqing,Hu, Yongzhou
scheme or table, p. 3196 - 3198 (2010/03/03)
A series of prenylflavonoids with multiple hydroxyl groups were synthesized and evaluated for their vasorelaxant activities against rat aorta rings pre-contracted by phenylephrine (PE), as well as their neuroprotective effects against OGD induced PC12 cel
