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90281-65-5

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90281-65-5 Usage

General Description

(S-benzylcysteinyl)glycine benzyl ester is a chemical compound that is derived from the amino acids cysteine and glycine. It is a benzyl ester, meaning that it contains a benzyl group attached to the ester functional group. (S-benzylcysteinyl)glycine benzyl ester has potential applications in the fields of pharmaceuticals and biochemistry due to its ability to modulate oxidative stress and inflammation. It may also have antioxidant properties and could be used in research related to the regulation of cellular redox balance. Additionally, (S-benzylcysteinyl)glycine benzyl ester has been studied for its potential role in mitigating the effects of certain diseases and conditions, such as cardiovascular disease and neurodegenerative disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 90281-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,8 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90281-65:
(7*9)+(6*0)+(5*2)+(4*8)+(3*1)+(2*6)+(1*5)=125
125 % 10 = 5
So 90281-65-5 is a valid CAS Registry Number.

90281-65-5Relevant articles and documents

Artificial model for cystathionine β-synthase: Efficient β-replacement reaction with thiols employing a novel pyridoxal model compound having an imidazole function

Miyashita, Kazuyuki,Murafuji, Hidenobu,Iwaki, Hiroshi,Yoshioka, Eito,Imanishi, Takeshi

, p. 4873 - 4879 (2007/10/03)

As a second-generation pyridoxal model compound for cystathionine β-synthase, we designed a novel model compound having an ionophore function and an imidazole function, application of which to the β-replacement reaction with various thiols smoothly took place to give S-substituted cysteines. Peptides having a serine-O-carbonate residue at the N-terminal position were also converted to the corresponding peptides having an S-substituted cysteine residue under the catalytic conditions of the novel pyridoxal model compound.

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