Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Imre Weisz"'
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Akademický článek
Novel Suicide Ligands of Tubulin Arrest Cancer Cells in S-Phase
Autor: Ashley Davis, Jian-Dong Jiang, Kim M. Middleton, Yue Wang, Imre Weisz, Yi-He Ling, J. George Bekesi
Publikováno v: Neoplasia: An International Journal for Oncology Research, Vol 1, Iss 6, Pp 498-507 (1999)
It is presently accepted that the mechanism of action for all anti-tumor tubulin ligands involves the perturbation of microtubule dynamics during the G2/M phase of cell division and subsequent entry into apoptosis 1]. In this report, we challenge the
Externí odkaz: https://doaj.org/article/a50b2ecb1bf943a38df1ca3817ae2a9c
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2
Novel Suicide Ligands of Tubulin Arrest Cancer Cells in S-Phase
Autor: Imre Weisz, Yue Wang, J. George Bekesi, Yi-He Ling, Ashley Davis, Kim Middleton, Jian-Dong Jiang
Publikováno v: Neoplasia: An International Journal for Oncology Research, Vol 1, Iss 6, Pp 498-507 (1999)
It is presently accepted that the mechanism of action for all anti-tumor tubulin ligands involves the perturbation of microtubule dynamics during the G2/M phase of cell division and subsequent entry into apoptosis 1]. In this report, we challenge the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebd823e05ccff2bb197be4194ef3b227
http://www.sciencedirect.com/science/article/pii/S1476558699800037
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Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives
Autor: Imre Wolf, John Roboz, J. George Bekesi, Jozsef Szabo, Imre Weisz
Publikováno v: Bioorganic & Medicinal Chemistry Letters. 8:3241-3244
Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino-carboxylic esters and alpha-amino a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::973edd5b71edebdd3ef1ccfaee9ab5a0
https://doi.org/10.1016/s0960-894x(98)00593-9
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4
Acidic coupling and aminolytic TFA cleavage approaches in a new synthesis of an l- m-sarcolysin containing antitumor tripeptide ester
Autor: Imre Weisz, John Roboz, J. George Bekesi
Publikováno v: Tetrahedron Letters. 37:563-566
l -prolyl- l -m-[bis(chloroethyl)amino]-phenylalanyl- l -norvaline ethyl ester hydrochloride, 4 (and its 3 H and 14 C doublylabeled version) was synthesized starting with reacting unprotected l -m-sarcolysin, 1 , with TFA-Pro-Cl in an acidic system t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::80a7e62737a875f26b75b883bc3f7fd6
https://doi.org/10.1016/0040-4039(95)02261-9
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ChemInform Abstract: Synthesis of Diacylamines and the Preparation of α-Amino-acylureas, a New Type of α-Amino Acid Derivatives
Autor: Jozsef Szabo, John Roboz, Imre Wolf, Imre Weisz, J. George Bekesi
Publikováno v: ChemInform. 30
Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino-carboxylic esters and α-amino acid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff9578a4cc86283475f84c6bf708135b
https://doi.org/10.1002/chin.199910207
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Inhibition of human hepatocellular carcinoma by L-proline-m-bis (2-chloroethyl) amino-L-phenylalanyl-L-norvaline ethyl ester hydrochloride (MF13) in vitro and in vivo
Autor: Qiong-Ying Hu, George Bekesi, Dan-Qing Song, Jian-Dong Jiang, Yan-Ling Wang, Jiannong Li, Imre Weisz
Publikováno v: International journal of oncology. 25(5)
A new anticancer tripeptide, L-proline-m-bis (2-chloroethyl) amino-L-phenylalanyl-L-norvaline ethyl ester hydrochloride (MF13), was investigated for its activity and mechanism in human hepatocellular carcinoma (HCC) cell lines. MF13 showed antiprolif
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a6281cf797ad8b0b7310ec858580ed
https://pubmed.ncbi.nlm.nih.gov/15492817
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Derivate der Piperidincarbinole, I: Über die Phenyl‐piperidyl‐(2)‐carbinole
Autor: Antal Dudäs, Imre Weisz
Publikováno v: Chemische Berichte. 94:412-414
Die Konfiguration der beiden diastereomeren Racemate des Phenyl-piperidyl-(2)-carbinols wurde bewiesen und eine Methode zur Darstellung des threo-Racemats erythro-Racemat beschrieben.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d78cb2749fc3818a3c7c80473361d7ca
https://doi.org/10.1002/cber.19610940218
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