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Search for dual function inhibitors for Alzheimer’s disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Aβ fibril formation inhibition capacity

Bioorganic & medicinal chemistry, 2006-01, Vol.14 (2), p.472-478

2006

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Antimicrobial Evaluation of Some Styryl Ketone Derivatives and Related Thiol Adducts

Journal of pharmaceutical sciences, 1994-04, Vol.83 (4), p.545-548

1994

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Mannich bases of phenolic azobenzenes possessing cytotoxic activity

European journal of medicinal chemistry, 1997-07, Vol.32 (7), p.583-594

1997

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Electrochemical biosensor for the interaction of DNA with the alkylating agent 4,4′-dihydroxy chalcone based on guanine and adenine signals

Journal of pharmaceutical and biomedical analysis, 2002-11, Vol.30 (4), p.1339-1346

2002

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Cytotoxic and inhibitory effects of 4,4′-dihydroxy chalcone (RVC-588) on proliferation of human leukemic HL-60 cells

Leukemia research, 2003, Vol.27 (1), p.57-64

2003

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Cytotoxicity of Some Azines of Acetophenone Derived Mono-Mannich Bases against Jurkat Cells

Biological and Pharmaceutical Bulletin, 2003, Vol.26(5), pp.631-637

2003

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Synthesis and biological activity of pyridinium-type acetylcholinesterase inhibitors

Journal of pharmacy and pharmacology, 2003-10, Vol.55 (10), p.1397-1404

2003

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Synthesis and stereochemistry of potentially powerful analgesics: 2,4-m-diaryl substituted 3,7-diazabicyclo(3,3,1)nonan-9-one-1,5-diesters

Archiv der Pharmazie (Weinheim), 1992-10, Vol.325 (10), p.657-663

1992

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Synthese und Stereochemie potentiell stark analgetischer 2,4-m-diarylsubstituierter 3,7-diazabicyclo[3.3.1]nonan-9-one-1,5-diester

Archiv der Pharmazie (Weinheim), 1992, Vol.325 (10), p.657-663

1992

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Cytotoxic activities of mono and bis Mannich bases derived from acetophenone against Renca and Jurkat cells

Pharmaceutica acta Helvetiae, 2000-04, Vol.74 (4), p.393-398

2000

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Antifungal activity of some mono, bis and quaternary Mannich bases derived from acetophenone

Arzneimittel-Forschung, 2001-01, Vol.51 (1), p.72

2001

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Effect of acetophenone derived Mannich bases on cellular glutathione level in Jurkat cells. A possible mechanism of action

Arzneimittel-Forschung, 2001, Vol.51 (8), p.679

2001

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Evaluation of the cytotoxicity of some Mannich bases of acetophenone against the EMT6 tumour

Pharmazie, 1990-10, Vol.45 (10), p.755-757

1990

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Evaluation of some azines of aminomethylacetophenones and related quaternary ammonium compounds versus the EMT6 tumour

Pharmazie, 1988-09, Vol.43 (9), p.614-616

1988

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Synthesis and stereochemistry of potentially powerful analgesics: 2,4-m-diaryl substituted 3,7-diazabicyclo(3,3,1)nonan-9-one-1,5-diesters

Archiv der Pharmazie (Weinheim), 1992-10, Vol.325 (10), p.657

1992

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In the Search for New Anticancer Drugs: 28. Synthesis and Evaluation of Highly Active Aminoxyl Labeled Amino Acid Derivatives Containing the [N;‐(2‐chloroethyl)‐N′‐nitrosoamino]carbonyl group

Journal of pharmaceutical sciences, 1994-07, Vol.83 (7), p.999-1005

1994

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In the search for new anticancer drugs. XXVIII: synthesis and evaluation of highly active aminoxyl labeled amino acid derivatives containing the [N'-(2-chloroethyl)-N'-nitrosoamino]carbonyl group

Journal of pharmaceutical sciences, 1994, Vol.83 (7), p.999-1005

1994

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8+a-Amyrin tetratriacontanoate, a new triterpene from Scolymus hispanicus

Pharmazie, 1989, Vol.44 (8)

1989

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Cytotoxicity of Mannich bases of alpha-arylidene-beta-ketoesters and related compounds against EMT6 mammary carcinoma cells

Drug design and delivery, 1990-12, Vol.7 (1), p.51

1990

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Syntheses and stability studies of some Mannich bases of acetophenones and evaluation of their cytotoxicity against Jurkat cells

Arzneimittel-Forschung, 2002-01, Vol.52 (8), p.628

2002

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Antimicrobial evaluation of some Mannich bases of acetophenones and representative quaternary derivatives

Arzneimittel-Forschung, 2002-01, Vol.52 (10), p.773

2002

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Charge densities of atoms of conjugated styryl ketones having activity against L1210 leukemia cells

Drug design and delivery, 1990-12, Vol.7 (1), p.45

1990

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Intramolecular cyclization and cytotoxicities of some Mannich bases of styryl ketones

European journal of medicinal chemistry, 1989, Vol.24 (4), p.379-383

1989

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Evaluation of the citotoxicity of some Mannich base of acetophenone againt the EMT6 tumour

Pharmazie, 1990, Vol.45 (10), p.755-757

1990

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ChemInform Abstract: In the Search for New Anticancer Drugs. Part 28. Synthesis and Evaluation of Highly Active Aminoxyl Labeled Amino Acid Derivatives Containing the (N′-(2-Chloroethyl)-N′-nitrosoamino)carbonyl Group

ChemInform, 1995-01, Vol.26 (1), p.no-no

1995

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Search for dual function inhibitors for Alzheimer’s disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Aβ fibril formation inhibition capacity

Antimicrobial Evaluation of Some Styryl Ketone Derivatives and Related Thiol Adducts

Mannich bases of phenolic azobenzenes possessing cytotoxic activity

Electrochemical biosensor for the interaction of DNA with the alkylating agent 4,4′-dihydroxy chalcone based on guanine and adenine signals

Cytotoxic and inhibitory effects of 4,4′-dihydroxy chalcone (RVC-588) on proliferation of human leukemic HL-60 cells

Cytotoxicity of Some Azines of Acetophenone Derived Mono-Mannich Bases against Jurkat Cells

Synthesis and biological activity of pyridinium-type acetylcholinesterase inhibitors

Synthesis and stereochemistry of potentially powerful analgesics: 2,4-m-diaryl substituted 3,7-diazabicyclo(3,3,1)nonan-9-one-1,5-diesters

Synthese und Stereochemie potentiell stark analgetischer 2,4-m-diarylsubstituierter 3,7-diazabicyclo[3.3.1]nonan-9-one-1,5-diester

Cytotoxic activities of mono and bis Mannich bases derived from acetophenone against Renca and Jurkat cells

Antifungal activity of some mono, bis and quaternary Mannich bases derived from acetophenone

Effect of acetophenone derived Mannich bases on cellular glutathione level in Jurkat cells. A possible mechanism of action

Evaluation of the cytotoxicity of some Mannich bases of acetophenone against the EMT6 tumour

Evaluation of some azines of aminomethylacetophenones and related quaternary ammonium compounds versus the EMT6 tumour

Synthesis and stereochemistry of potentially powerful analgesics: 2,4-m-diaryl substituted 3,7-diazabicyclo(3,3,1)nonan-9-one-1,5-diesters

In the Search for New Anticancer Drugs: 28. Synthesis and Evaluation of Highly Active Aminoxyl Labeled Amino Acid Derivatives Containing the [N;‐(2‐chloroethyl)‐N′‐nitrosoamino]carbonyl group

In the search for new anticancer drugs. XXVIII: synthesis and evaluation of highly active aminoxyl labeled amino acid derivatives containing the [N'-(2-chloroethyl)-N'-nitrosoamino]carbonyl group

8+a-Amyrin tetratriacontanoate, a new triterpene from Scolymus hispanicus

Cytotoxicity of Mannich bases of alpha-arylidene-beta-ketoesters and related compounds against EMT6 mammary carcinoma cells

Syntheses and stability studies of some Mannich bases of acetophenones and evaluation of their cytotoxicity against Jurkat cells

Antimicrobial evaluation of some Mannich bases of acetophenones and representative quaternary derivatives

Charge densities of atoms of conjugated styryl ketones having activity against L1210 leukemia cells

Intramolecular cyclization and cytotoxicities of some Mannich bases of styryl ketones

Evaluation of the citotoxicity of some Mannich base of acetophenone againt the EMT6 tumour

ChemInform Abstract: In the Search for New Anticancer Drugs. Part 28. Synthesis and Evaluation of Highly Active Aminoxyl Labeled Amino Acid Derivatives Containing the (N′-(2-Chloroethyl)-N′-nitrosoamino)carbonyl Group

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