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Chemico-Biological Interactions | 1981

Characterization of 2,3-bis(chloromethyl)-1,4-naphthoquinone induced mitochondrial swelling.

Ronald S. Pardini; Margaret A. Tilka; Chris A. Pritsos; Ai Jeng Lin; Alan C. Sartorelli

Mitochondrial swelling induced by 2,3-bis(chloromethyl)-1,4-naphthoquinone (CMNQ) was found to be a non-energy linked, oxygen and sulfhydryl-dependent, substrate-independent, osmotic process, that lack cation specificity. Swelling was inhibited by cysteine and DTNB, and the CMNQ induced swelling resulted in a decrease in mitochondrial reactive sulfhydryl groups; thus, mitochondrial sulfhydryl interaction was mandatory in the CMNQ swelling process. The non-enzymatic reaction of CMNQ with cysteine but not cystine resulted in the consumption of oxygen, implicating sulfhydryl redox activity in the swelling process. High level of tocopherol and histidine depressed the CMNQ induced swelling, suggesting that free radicals and singlet oxygen are important in the CMNQ induced swelling process. These findings support the proposition that CMNQ interacts with mitochondrial reductase systems and sulfhydryl groups in such a way as to generate superoxide radical which subsequently may dismute to H2O2 and produce .OH and possibly singlet oxygen. These toxic oxygen species may be responsible for the CMNQ-promoted sulfhydryl depletion and mitochondrial swelling.


Journal of Medicinal Chemistry | 1972

Potential bioreductive alkylating agents. 1. Benzoquinone derivatives.

Ai Jeng Lin; Lucille A. Cosby; Charles W. Shansky; Alan C. Sartorelli


Archive | 1976

Potential Bioreductive Alkylating Agents

Ai Jeng Lin; Lucille A. Cosby; Alan C. Sartorelli


Journal of Medicinal Chemistry | 1973

Potential bioreductive alkylating agents. 2. Antitumor effect and biochemical studies of naphthoquinone derivatives

Ai Jeng Lin; Ronald S. Pardini; Lucille A. Cosby; Brian J. Lillis; Charles W. Shansky; Alan C. Sartorelli


Journal of Medicinal Chemistry | 1975

Potential bioreductive alkylating agents. 5. Antineoplastic activity of quinoline-5,8-diones, naphthazarins, and naphthoquinones.

Ai Jeng Lin; Brian J. Lillis; Alan C. Sartorelli


Biochemical Pharmacology | 1976

Potential bioreductive alkylating agents--vi. Determination of the relationship between oxidation-reduction potential and antineoplastic activity.

Ai Jeng Lin; Alan C. Sartorelli


Journal of Medicinal Chemistry | 1976

Potential bioreductive alkylating agents. 7. Antitumor effects of phenyl-substituted 2-chloromethyl-3-phenyl-1,4-naphthoquinones

Ai Jeng Lin; Alan C. Sartorelli


Journal of Organic Chemistry | 1973

2,3-Dimethyl-5,6-bis(methylene)-1,4-benzoquinone. Active intermediate of bioreductive alkylating agents

Ai Jeng Lin; Alan C. Sartorelli


Journal of Medicinal Chemistry | 1974

Potential bioreductive alkylating agents. 3. Synthesis and antineoplastic activity of acetoxymethyl and corresponding ethyl carbamate derivatives of benzoquinones.

Ai Jeng Lin; Charles W. Shansky; Alan C. Sartorelli


Journal of Medicinal Chemistry | 1974

Potential antitumor agents. 9. 2-Formyl(m-amino)phenylpyridine thiosemicarbazones.

Krishna C. Agrawal; Ai Jeng Lin; Barbara A. Booth; Wheaton; Alan C. Sartorelli

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