• Korean Journal of Plant Resources
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• v.21 no.4
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• pp.254-259
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• 2008

The radical scavenging activities of 9 medicinal plants on peroxynitrite ($ONOO^-$) and hydroxyl (${\cdot}OH$) radical were investigated using in vitro system. The water extracts of 9 medicinal plants showed the protective effect against $ONOO^-$ and ${\cdot}OH$ radical. In particular, Akebia quinata, Aster scaber, Cudrania tricuspidata, Diospyros kaki, Eriobotrya japonica, Lycium chinense, Parthenocissus tricuspidata and Polygonum aviculare exhibited $ONOO^-$-scavenging activity by about 50% at the concentration of $10{\mu}g/ml$. Although those $ONOO^-$-scavenging activities were lower than that of penicillamine (94.08${\pm}$3.04%) as a positive control, Eriobotrya japonica (89.87${\pm}$4.57%) was the most potent scavenger of $ONOO^-$ at the concentration of $10{\mu}g/ml$. Also, Diospyros kaki and Urtica angustifolia showed the strong${\cdot}$OH-scavenging activity than thiourea, positive control, at the concentration of lmg/ml. Our results indicate that 9medicinal plants may act as free radical scavengers and reduce damages caused by oxidative stress associated with $ONOO^-$ and${\cdot}$OH radical.

• Bulletin of the Korean Chemical Society
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• v.31 no.3
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• pp.570-576
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• 2010

A variety of ynamides undergo highly regio- and stereoselective radical addition of arenethiols with the aid of triethylborane as a radical initiator. The products, N-[(Z)-2-arylsulfanyl-1-alkenyl]amides, can be reduced with triethylsilane in trifluoroacetic acid to yield N-[2-(arylsulfanyl)alkyl]amides.

• Journal of the Korean Mathematical Society
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• v.38 no.6
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• pp.1117-1123
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• 2001

A ring is a DICC ring if every chain of right ideals in-dexed by the integers stabilizes to the left or to the right or to both sides. A counterexample is given to an assertion of karamzadeh and Motamedi that a transfinite power of the Jacobson radical of a right DICC ring is zero. we determine the behavior of the transfinite powers of the Jacobson radical relative to a torsion theory and consequently can obtain their correct behavior in the classical setting.

• Communications of the Korean Mathematical Society
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• v.12 no.3
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• pp.499-505
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• 1997

This paper is a continuation of [3]. We prove that if A is quasi-associative (resp. an implicative) ideal of a BCI-algebra X then the k-nil radical of A is a quasi-associative (resp. an implicative) ideal of X. We also construct the quotient algebra $X/[Z;k]$ of a BCI-algebra X by the k-nhil radical [A;k], and show that if A and B are closed ideals of BCI-algebras X and Y respectively, then

• Bulletin of the Korean Mathematical Society
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• v.41 no.4
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• pp.599-608
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• 2004

Let R be an associative ring with identity and J(R) be the Jacobson radical of R. In this paper we investigate the generalization of the Jacobson radical of R, J＊ (R) say. Also we study the rings that J＊(R) = J(R).

• Journal of the Korean Mathematical Society
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• v.57 no.6
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• pp.1389-1406
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• 2020

Let Λ be an Artin algebra and mod Λ the category of finitely generated right Λ-modules. We prove that the radical layer length of Λ is an upper bound for the radical layer length of mod Λ. We give an upper bound for the extension dimension of mod Λ in terms of the injective dimension of a certain class of simple right Λ-modules and the radical layer length of DΛ.

• Communications of the Korean Mathematical Society
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• v.20 no.1
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• pp.35-49
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• 2005

For an extension field K of k, a restriction homomorphism on Brauer k-group B(k) maps Brauer k-algebras to Brauer K- algebras by tensor product. A purpose of this work is to study the restriction map that sends radical (Schur) k-algebras to radical (Schur) K-algebras. And we ask an analogous question with respect to corestriction map on Brauer group B(K) that whether the corestriction map sends radical K-algebras to radical k-algebras.

• Proceedings of the Korean Biophysical Society Conference
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• 1998.06a
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• pp.25-25
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• 1998

Ascorbyl free radical reductase was purified from the white rot fungus, Pleurotus ostreatus. The enzyme contained FMN as a prosthetic group, which was reduced by NADH and reoxidized by ascorbyl free radical. Reduction of ascorbyl free radical by the enzyme was observed by EPR spectroscopy.(omitted)

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.320-320
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• 2006

The authors report the synthesis and radical ring-crossover polymerization of macrocycles with radically exchangeable dynamic covalent bonds. The macrocyclic compounds with alkoxyamine units were designed and synthesized by condensation from alkoxyamine-based diol and the corresponding acid chlorides in the presence of pyridine under high-dilution condition. The macrocycles can thermally polymerize by intermolecular radical crossover reaction. Furthermore, the poly(alkoxyamine)s depolymerized to the monomers principally by the intramolecular radical exchange process under high-dilution conditions.

• Journal of applied mathematics & informatics
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• v.6 no.3
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• pp.937-942
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• 1999

In this paper we will show that if [G($\chi$),$\chi$] D($\chi$) and [D($\chi$), G($\chi$)] lie in the nil radical of A for all $\chi$$\in$A, then either D or G maps A into the radical where D and G are derivations on a Banach algebra A.