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Modulation of the Heparanase-inhibiting Activity of Heparin through Selective Desulfation, Graded N-Acetylation, and Glycol Splitting

The Journal of biological chemistry, 2005-04, Vol.280 (13), p.12103-12113

2005

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New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluation

Bioorganic & medicinal chemistry, 2015-11, Vol.23 (21), p.6785-6793

2015

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Preclinical profile of antitumor activity of a novel hydrophilic camptothecin, ST1968

Molecular cancer therapeutics, 2008-07, Vol.7 (7), p.2051-2059

2008

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Short Heparin Sequences Spaced by Glycol-Split Uronate Residues Are Antagonists of Fibroblast Growth Factor 2 and Angiogenesis Inhibitors

Biochemistry (Easton), 2002-08, Vol.41 (33), p.10519-10528

2002

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7-Azaindole-1-carboxamides as a new class of PARP-1 inhibitors

Bioorganic & medicinal chemistry, 2014-02, Vol.22 (3), p.1089-1103

2014

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alpha.-Regioselectivity in palladium-catalyzed arylation of acyclic enol ethers

Journal of organic chemistry, 1992-02, Vol.57 (5), p.1481-1486

1992

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Abstract 3096: Host antitumor immune response activated by Dual POLA1-HDAC11 inhibitors endowed with a large spectrum of antitumor activity

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.3096-3096

2019

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Abstract 4848: Preclinical antitumor activity of novel DNA polymerase 1 (POLA1) inhibitors

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4848-4848

2018

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Abstract 4195: MIR002: a new POLA1 inhibitor endowed with a large spectrum of antitumor activity

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.4195-4195

2017

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Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as αvβ3 Integrin Ligands: An Approach to Tumor-Targeted Therapy

Bioconjugate chemistry, 2010-11, Vol.21 (11), p.1956-1967

2010

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Heck reaction on anthraquinone derivatives: ligand, solvent and salt effects

Journal of organic chemistry, 1991-09, Vol.56 (20), p.5796-5800

1991

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Azetidinones as Zinc-Binding Groups to Design Selective HDAC8 Inhibitors

ChemMedChem, 2009-12, Vol.4 (12), p.1991-2001

2009

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Enol Carbamates as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) Endowed with High Selectivity for FAAH over the Other Targets of the Endocannabinoid System

ChemMedChem, 2010-03, Vol.5 (3), p.357-360

2010

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Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as [alpha]^sub v^[Beta]^sub 3^ Integrin Ligands: An Approach to Tumor-Targeted Therapy

Bioconjugate chemistry, 2010-11, Vol.21 (11), p.1956

2010

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Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as α v β 3 Integrin Ligands: An Approach to Tumor-Targeted Therapy

Bioconjugate chemistry, 2010-11, Vol.21 (11), p.1956-1967

2010

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Palladium-catalyzed reduction of aryl sulfonates. Reduction versus hydrolysis selectivity control

Journal of organic chemistry, 1990, Vol.55 (1), p.350-353

1990

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Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1808-1817

2006

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Corrigendum to “Natural and semisynthetic azaphilones as a new scaffold for Hsp90 inhibitors” [Bioorg. Med. Chem. 18 (2010) 6031–6043]

Bioorganic & medicinal chemistry, 2010-12, Vol.18 (24), p.8687-8687

2010

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Incorporation of the Unusual Cα-Fluoroalkylamino Acids into Cyclopeptides: Synthesis of Arginine−Glycine−Aspartate (RGD) Analogues and Study of Their Conformational and Biological Behavior

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1808-1817

2006

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Synthesis of Cycloalkanoindoles by an Unusual DAST-Triggered Rearrangement Reaction

European journal of organic chemistry, 2004-06, Vol.2004 (11), p.2411-2420

2004

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Perspectives in camptothecin development

Expert opinion on therapeutic patents, 2002-06, Vol.12 (6), p.837-844

2002

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Conjugates of a novel 7-substituted camptothecin with RGD-peptides as α(v)β₃ integrin ligands: An approach to tumor-targeted therapy

Bioconjugate chemistry, 2010-11, Vol.21 (11), p.1956-1967

2010

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Synthesis and antitumor properties of new glycosides of daunomycinone and adriamycinone

Journal of medicinal chemistry, 1975-07, Vol.18 (7), p.703-707

1975

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Regiospecific total synthesis of 6-deoxyanthracyclines: 4-demethoxy-6-deoxydaunorubicin

Journal of organic chemistry, 1983-02, Vol.48 (3), p.405-406

1983

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STEREOCHEMICAL REQUIREMENTS IN THE ANTITUMOR ANTHRACYCLINES

The Journal of Antibiotics, 1977, Vol.30(9), pp.764-766

1977

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Modulation of the Heparanase-inhibiting Activity of Heparin through Selective Desulfation, Graded N-Acetylation, and Glycol Splitting

New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluation

Preclinical profile of antitumor activity of a novel hydrophilic camptothecin, ST1968

Short Heparin Sequences Spaced by Glycol-Split Uronate Residues Are Antagonists of Fibroblast Growth Factor 2 and Angiogenesis Inhibitors

7-Azaindole-1-carboxamides as a new class of PARP-1 inhibitors

alpha.-Regioselectivity in palladium-catalyzed arylation of acyclic enol ethers

Abstract 3096: Host antitumor immune response activated by Dual POLA1-HDAC11 inhibitors endowed with a large spectrum of antitumor activity

Abstract 4848: Preclinical antitumor activity of novel DNA polymerase 1 (POLA1) inhibitors

Abstract 4195: MIR002: a new POLA1 inhibitor endowed with a large spectrum of antitumor activity

Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as αvβ3 Integrin Ligands: An Approach to Tumor-Targeted Therapy

Heck reaction on anthraquinone derivatives: ligand, solvent and salt effects

Azetidinones as Zinc-Binding Groups to Design Selective HDAC8 Inhibitors

Enol Carbamates as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) Endowed with High Selectivity for FAAH over the Other Targets of the Endocannabinoid System

Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as [alpha]^sub v^[Beta]^sub 3^ Integrin Ligands: An Approach to Tumor-Targeted Therapy

Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as α v β 3 Integrin Ligands: An Approach to Tumor-Targeted Therapy

Palladium-catalyzed reduction of aryl sulfonates. Reduction versus hydrolysis selectivity control

Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior

Corrigendum to “Natural and semisynthetic azaphilones as a new scaffold for Hsp90 inhibitors” [Bioorg. Med. Chem. 18 (2010) 6031–6043]

Incorporation of the Unusual Cα-Fluoroalkylamino Acids into Cyclopeptides: Synthesis of Arginine−Glycine−Aspartate (RGD) Analogues and Study of Their Conformational and Biological Behavior

Synthesis of Cycloalkanoindoles by an Unusual DAST-Triggered Rearrangement Reaction

Perspectives in camptothecin development

Conjugates of a novel 7-substituted camptothecin with RGD-peptides as α(v)β₃ integrin ligands: An approach to tumor-targeted therapy

Synthesis and antitumor properties of new glycosides of daunomycinone and adriamycinone

Regiospecific total synthesis of 6-deoxyanthracyclines: 4-demethoxy-6-deoxydaunorubicin

STEREOCHEMICAL REQUIREMENTS IN THE ANTITUMOR ANTHRACYCLINES

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