103239-24-3 Usage
Uses
Used in Pharmaceutical Industry:
GLUTATHIONE DISODIUM SALT OXIDIZED FORM is used as a therapeutic target for the treatment of cancer. It plays a significant role in cellular redox pathways, which are often disrupted in cancer cells, leading to uncontrolled cell growth and proliferation. By targeting these pathways, glutathione disodium salt oxidized form can potentially help in the development of novel cancer treatments.
Additionally, GLUTATHIONE DISODIUM SALT OXIDIZED FORM can be used in other applications such as:
1. Antioxidant Supplement: It can be used as an antioxidant supplement to support the body's natural defense against oxidative stress and maintain overall health.
2. Detoxification: It can be used in detoxification processes to help the body eliminate harmful substances and toxins.
3. Skin Care: It can be used in the cosmetic industry for its antioxidant and skin-protective properties, promoting healthy skin and reducing signs of aging.
4. Immune System Support: It can be used to support the immune system by maintaining the balance of reactive oxygen species, which are essential for proper immune function.
5. Research Applications: It can be used in scientific research to study the role of glutathione in various biological processes and its potential therapeutic applications in different diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 103239-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103239-24:
(8*1)+(7*0)+(6*3)+(5*2)+(4*3)+(3*9)+(2*2)+(1*4)=83
83 % 10 = 3
So 103239-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H32N6O12S2.2Na/c21-9(19(35)36)1-3-13(27)25-11(17(33)23-5-15(29)30)7-39-40-8-12(18(34)24-6-16(31)32)26-14(28)4-2-10(22)20(37)38;;/h9-12H,1-8,21-22H2,(H,23,33)(H,24,34)(H,25,27)(H,26,28)(H,29,30)(H,31,32)(H,35,36)(H,37,38);;/q;2*+1/p-2/t9-,10-,11+,12+;;/m0../s1
103239-24-3Relevant academic research and scientific papers
Formation of Reducing Radicals on Radiolysis of Glutathione and Some Related Compounds in Aqueous Solution
Eriksen, Trygve,Fransson, Gunilla
, p. 1117 - 1122 (2007/10/02)
The .OH-induced oxidation of glutathione in basic aqueous solution has been found to produce the sulphur-centred radical GS. (GSSG.- and two reducing radicals.Decarboxylation, considered to be initiated by .OH radical addition to the nitrogen of the amino group on the γ-glutamyl unit, was found to be effective for methylated glutathione (GSMe) and ophthalmic acid (GMe) but of minor importance for glutathione.The G-values for the strongly reducing α-amino radicals formed on decarboxylation were found to be 3.3, 3.3, and 0.5 for GSMe, GME, and GSH, respectively, at pH 10.5.The formation of an additional strongly reducing radical with G=2.2 at pH 10.5 was demonstrated by measuring the electron-transfer to p-nitroacetophenone (PNAP).This radical is not formed from GSMe or GMe.We suggest that the underlying mechanism for the formation of this species is based on pH-dependent conformational changes of glutathione followed by .OH addition to the cysteine sulphur, or hydrogen abstraction from the CH2 group in the α-position to the sulphur leading to the formation of a reducing carbon-centred radical.
