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1,2,3‐Triazole hybrids as anticancer agents: A review

Archiv der Pharmazie (Weinheim), 2022-01, Vol.355 (1), p.e2100158-n/a

Alam, Mohammad Mahboob

2022

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1,2,4,5‐Tetraoxane derivatives/hybrids as potent antimalarial endoperoxides: Chronological advancements, structure−activity relationship (SAR) studies and future perspectives

Medicinal research reviews, 2024-09, Vol.44 (5), p.2266-2290

2024

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[1, 2-Bis(2, 6-difluoro-3-hydroxyphenyl)ethylene-diamine]platinum(II) Complexes, Compounds for the Endocrine Therapy of Breast Cancer - Mode of Action I: Antitumor Activity Due to the Reduction of the Endogenous Estrogen Level

Archiv der Pharmazie (Weinheim), 2004-06, Vol.337 (6), p.335-348

2004

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1,3,5-Trisubstituted Pyrazoles as Potent Negative Allosteric Modulators of the mGlu 2/3 Receptors

ChemMedChem, 2017-06, Vol.12 (12), p.905-912

2017

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1,3‐Bis(aryloxy)propan‐2‐ols as potential antileishmanial agents

Chemical biology & drug design, 2017-11, Vol.90 (5), p.981-986

2017

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1,3-Diaryl-2-propenones and 2-Benzylidene-1,3-indandiones: A Quest for Compounds Displaying Greater Toxicity to Neoplasms than Normal Cells

Archiv der Pharmazie (Weinheim), 2010-09, Vol.343 (9), p.535-541

2010

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1,3-Dioxolane-based ligands as rigid analogues of naftopidil: structure-affinity/activity relationships at alpha1 and 5-HT1A receptors

ChemMedChem, 2009-03, Vol.4 (3), p.393

2009

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1,5‐Benzoxazepines as a unique and potent scaffold for activity drugs: A review

Archiv der Pharmazie (Weinheim), 2021-12, Vol.354 (12), p.e2100224-n/a

2021

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1,8‐Naphthalimide: A Potent DNA Intercalator and Target for Cancer Therapy

Chemical record, 2017-10, Vol.17 (10), p.956-993

2017

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1,8-Naphthyridine Derivatives: A Review of Multiple Biological Activities

Archiv der Pharmazie (Weinheim), 2015-12, Vol.348 (12), p.837-860

2015

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1-Amino-3-(1H-1,2,3-triazol-1-yl)propylphosphonates as Acyclic Analogs of Nucleotides

Archiv der Pharmazie (Weinheim), 2014-07, Vol.347 (7), p.496-505

2014

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1-Arylsulfonyl-5-(N-hydroxyacrylamide)indolines Histone Deacetylase Inhibitors Are Potent Cytokine Release Suppressors

Chembiochem : a European journal of chemical biology, 2013-07, Vol.14 (10), p.1248-1254

2013

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1-Cyclohexyl-4-(4-arylcyclohexyl)piperazines: Mixed σ and human Δ(8)-Δ(7) sterol isomerase ligands with antiproliferative and P-glycoprotein inhibitory activity

ChemMedChem, 2011-01, Vol.6 (1), p.73

2011

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1‐cyclohexyl‐x‐methoxybenzene derivatives, novel psychoactive substances seized on the internet market. Synthesis and in vivo pharmacological studies in mice

Human psychopharmacology, 2017-05, Vol.32 (3), p.n/a

2017

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1-methyl-4-phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase

Journal of neuroscience research, 2006-02, Vol.83 (2), p.233-242

2006

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10-, 12-, and 29-hydroxybullatacinones: new cytotoxic annonaceous acetogenins from Annona bullata Rich (Annonaceae)

Natural toxins, 1994, Vol.2 (2), p.49-55

1994

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The 10th and 11th residues of short length N-terminal PTH(1-12) analogue are important for its optimum potency

The journal of peptide research, 2004-07, Vol.64 (1), p.25-32

2004

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(2,2-Diphenyl-[1,3]oxathiolan-5-ylmethyl)-(3-phenyl-propyl)-amine: a potent and selective 5-HT(1A) receptor agonist

ChemMedChem, 2009-02, Vol.4 (2), p.196-203

2009

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2,3-Dihydro-1,2-Diphenyl-substituted 4H-Pyridinone Derivatives as New Anti Flaviviridae Inhibitors

Chemical biology & drug design, 2011-06, Vol.77 (6), p.441-449

2011

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2,3‐Dihydro‐1‐Benzofuran Derivatives as a Series of Potent Selective Cannabinoid Receptor 2 Agonists: Design, Synthesis, and Binding Mode Prediction through Ligand‐Steered Modeling

ChemMedChem, 2009-10, Vol.4 (10), p.1615-1629

2009

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2-(4'-Chlorophenyl)benzothiazole is a potent inducer of cytochrome P450IA1 in a human and a mouse cell line: anomalous correlation between protein and mRNA induction

European journal of biochemistry, 1989-04, Vol.181 (1), p.143-148

1989

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(2,4-cis)-asimicinone and (2,4-trans)-asimicinone: two novel bioactive ketolactone acetogenins from Asimina triloba (Annonaceae)

Natural toxins, 1996, Vol.4 (3), p.128-134

1996

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2,4‐Disubstituted 5‐Nitroimidazoles Potent against Clostridium difficile

ChemMedChem, 2019-03, Vol.14 (5), p.561-569

2019

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2-Amino[1,2,4]triazolo[1,5-c]quinazolines and Derived Novel Heterocycles: Syntheses and Structure-Activity Relationships of Potent Adenosine Receptor Antagonists

ChemMedChem, 2016-10, Vol.11 (20), p.2272-2286

2016

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1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H 3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition

1,2,3‐Triazole hybrids as anticancer agents: A review

1,2,4,5‐Tetraoxane derivatives/hybrids as potent antimalarial endoperoxides: Chronological advancements, structure−activity relationship (SAR) studies and future perspectives

[1, 2-Bis(2, 6-difluoro-3-hydroxyphenyl)ethylene-diamine]platinum(II) Complexes, Compounds for the Endocrine Therapy of Breast Cancer - Mode of Action I: Antitumor Activity Due to the Reduction of the Endogenous Estrogen Level

1,3,5-Trisubstituted Pyrazoles as Potent Negative Allosteric Modulators of the mGlu 2/3 Receptors

1,3‐Bis(aryloxy)propan‐2‐ols as potential antileishmanial agents

1,3-Diaryl-2-propenones and 2-Benzylidene-1,3-indandiones: A Quest for Compounds Displaying Greater Toxicity to Neoplasms than Normal Cells

1,3-Dioxolane-based ligands as rigid analogues of naftopidil: structure-affinity/activity relationships at alpha1 and 5-HT1A receptors

1,5‐Benzoxazepines as a unique and potent scaffold for activity drugs: A review

1,8‐Naphthalimide: A Potent DNA Intercalator and Target for Cancer Therapy

1,8-Naphthyridine Derivatives: A Review of Multiple Biological Activities

1-Amino-3-(1H-1,2,3-triazol-1-yl)propylphosphonates as Acyclic Analogs of Nucleotides

1-Arylsulfonyl-5-(N-hydroxyacrylamide)indolines Histone Deacetylase Inhibitors Are Potent Cytokine Release Suppressors

1-Cyclohexyl-4-(4-arylcyclohexyl)piperazines: Mixed σ and human Δ(8)-Δ(7) sterol isomerase ligands with antiproliferative and P-glycoprotein inhibitory activity

1‐cyclohexyl‐x‐methoxybenzene derivatives, novel psychoactive substances seized on the internet market. Synthesis and in vivo pharmacological studies in mice

1-methyl-4-phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase

10-, 12-, and 29-hydroxybullatacinones: new cytotoxic annonaceous acetogenins from Annona bullata Rich (Annonaceae)

The 10th and 11th residues of short length N-terminal PTH(1-12) analogue are important for its optimum potency

(2,2-Diphenyl-[1,3]oxathiolan-5-ylmethyl)-(3-phenyl-propyl)-amine: a potent and selective 5-HT(1A) receptor agonist

2,3-Dihydro-1,2-Diphenyl-substituted 4H-Pyridinone Derivatives as New Anti Flaviviridae Inhibitors

2,3‐Dihydro‐1‐Benzofuran Derivatives as a Series of Potent Selective Cannabinoid Receptor 2 Agonists: Design, Synthesis, and Binding Mode Prediction through Ligand‐Steered Modeling

2-(4'-Chlorophenyl)benzothiazole is a potent inducer of cytochrome P450IA1 in a human and a mouse cell line: anomalous correlation between protein and mRNA induction

(2,4-cis)-asimicinone and (2,4-trans)-asimicinone: two novel bioactive ketolactone acetogenins from Asimina triloba (Annonaceae)

2,4‐Disubstituted 5‐Nitroimidazoles Potent against Clostridium difficile

2-Amino[1,2,4]triazolo[1,5-c]quinazolines and Derived Novel Heterocycles: Syntheses and Structure-Activity Relationships of Potent Adenosine Receptor Antagonists

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