Search Results - "Schnur, R C"
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erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships
Published in Journal of medicinal chemistry (15-09-1995)“…Overexpression of the erbB-2 oncogene has been linked to poor prognosis in breast, ovarian, and gastric cancers. Naturally occurring benzoquinoid ansamycin…”
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Binding of benzoquinoid ansamycins to p100 correlates with their ability to deplete the erbB2 gene product p185
Published in Biochemical and biophysical research communications (30-06-1994)“…Several benzoquinoid ansamycins, e.g., herbimycin A and geldanamycin, have been widely used as inhibitors of tyrosine kinases. We recently reported that…”
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3
Spiro Hydantoin Aldose Reductase Inhibitors
Published in Journal of medicinal chemistry (01-01-1988)“…Sorbitol formation from glucose, catalyzed by the enzyme aldose reductase, is believed to play a role in the development of certain chronic complications of…”
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Inhibition of the oncogene product p185erbB-2 in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives
Published in Journal of medicinal chemistry (01-09-1995)“…The erbB-2 oncogene encodes a transmembrane protein tyrosine kinase which plays a pivotal role in signal transduction and has been implicated when…”
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In vitro microbiological characterization of novel cyclic homopentapeptides, CP-101,680 and CP-163,234, for animal health use
Published in Journal of antibiotics (1999)“…Two cyclic homopentapeptides, CP-101,680 and CP-163,234 [6a-(3',4'-dichlorophenylamino) analogs of viomycin and capreomycin, respectively], were identified as…”
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N-(5-fluorobenzothiazol-2-yl)-2-guanidinothiazole-4-carboxamide. A novel, systemically active antitumor agent effective against 3LL Lewis Lung carcinoma
Published in Journal of medicinal chemistry (01-03-1991)“…N-(5-Fluorobenzothiazol-2-yl)-2-guanidinothiazole-4-carboxam ide (1) is a member of a series of amides found to substantially increase lifespan in mice bearing…”
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Improved glucose tolerance in rats treated with oxazolidinediones
Published in Journal of medicinal chemistry (01-05-1986)“…5-(2-Chloro-6-methoxyphenyl)oxazolidine-2,4-dione (49) is the most potent agent selected from a series of 5-substituted oxazolidinediones that were found to…”
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Quantitative structure-activity relationships of antitumor guanidinothiazolecarboxamides with survival enhancement for therapy in the 3LL Lewis lung carcinoma model
Published in Journal of medicinal chemistry (01-07-1991)“…Guanidinothiazolecarboxamides (GTCs) are a novel class of antitumor agents found to be systemically active against experimental pulmonary metastases of 3LL…”
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9
Rotationally restricted mimics of rigid molecules: nonspirocyclic hydantoin aldose reductase inhibitors
Published in Journal of medicinal chemistry (01-06-1989)“…Sorbinil (1), a spirocyclic hydantoin, is a potent inhibitor of the enzyme aldose reductase. Simulation of the rigid spirocyclic ring orientation found in…”
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10
erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships
Published in Journal of medicinal chemistry (01-09-1995)Get full text
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Depletion of p185erbB2, Raf-1 and mutant p53 proteins by geldanamycin derivatives correlates with antiproliferative activity
Published in Cancer chemotherapy and pharmacology (1997)“…Recently, it has been shown that geldanamycin (GA), a benzoquinone ansamycin, is able to deplete mutant p53, p185erbB2 and Raf-1 proteins in cancer cells…”
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13
Dehydrations with N-methyl-N,N'-di-tert-butylcarbodiimidium ion
Published in Journal of the American Chemical Society (01-01-1975)Get full text
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14
Depletion of the erbB-2 gene product p185 by benzoquinoid ansamycins
Published in Cancer research (Chicago, Ill.) (15-05-1994)“…Herbimycin A, a benzoquinoid ansamycin, is widely used as an inhibitor of tyrosine kinases. We have examined the effects of herbimycin A and several analogues…”
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15
Synthesis of novel 1,3-oxazino[6,5-b]indole-2,4-(3H,9H)-dione and 2H-1,3,5-oxadiazino[3,2-a]indole-2,4-(3H)-dione from oxindoles
Published in Journal of heterocyclic chemistry (01-03-1992)“…Two novel tricyclic ring systems were designed as serine protease inhibitors and synthesized from oxindoles; the first series,…”
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Synthesis of novel 1H-imidazo[5,1-B][3]benzazepine-1,3(2H)-dione and pyrimido[6,1-B][3]benzazepine-1,3,4(2H)-trione
Published in Journal of heterocyclic chemistry (01-05-1990)“…Two novel tricyclic ring systems derived from 3‐benzazepines were synthesized; the first, a 6,7,5‐ring, 1H‐imidazo[5,1‐b][3]benzazepine‐1,3(2H)‐dione was…”
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Spiro oxazolidinedione aldose reductase inhibitors
Published in Journal of medicinal chemistry (01-12-1982)“…Spiro oxazolidinediones (2) derived from five- and six-membered ring aralkyl ketones are potent aldose reductase inhibitors in vitro and in vivo. Their novel…”
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Synthesis of 1,2-dihydro-1-oxo-3H-3benzazepine and 3-acyl derivatives
Published in Journal of organic chemistry (1989)Get full text
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Inhibition of the oncogene product p185 super(erbB-2) in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives
Published in Journal of medicinal chemistry (01-01-1995)“…The erbB-2 oncogene encodes a transmembrane protein tyrosine kinase which plays a pivotal role in signal transduction and has been implicated when…”
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Journal Article -
20
Quantitative structure-activity relationships of antitumor guanidinothiazole-carboxamides with survival enhancement for therapy in the 3LL Lewis lung carcinoma model
Published in Journal of medicinal chemistry (01-01-1991)“…Guanidinothiazole-carboxamides (GTCs) are a novel class of antitumor agents found to be systemically active against experimental pulmonary metastases of 3LL…”
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