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41 Results Found

  • Article
  • Open Access
18 Citations
10,605 Views
8 Pages

New Imide 5-HT1A Receptor Ligands – Modification of Terminal Fragment Geometry

  • Andrzej J. Bojarski,
  • Maria J. Mokrosz,
  • Beata Duszyńska,
  • Aneta Kozioł and
  • Ryszard Bugno

28 February 2004

Two sets of new o-methoxyphenylpiperazine (MPP; series a) and 1,2,3,4-tetrahydroisoquinoline (THIQ; series b) derivatives, containing various imide moietiesderived from NAN190, were synthesized and evaluated in vitro for their ability to bind tothe s...

  • Article
  • Open Access
2 Citations
6,154 Views
14 Pages

A simple and convenient synthesis of (–)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid is described, applying a combination of two synthetic methods: the Petasis reaction and Pomeranz–Fritsch–Bobbitt cyclization. Th...

  • Article
  • Open Access
8 Citations
6,880 Views
12 Pages

1 February 2013

We report herein an application of an α-amidoalkylation reaction, as an alternative efficient synthesis of 4-aryl- and 4-methyl-1,2,3,4-tetrahydroisoquinoline derivatives. The amides required for this purpose would result from reaction of aminoacetal...

  • Article
  • Open Access
2,757 Views
25 Pages

2 November 2022

Tetrahydroisoquinoline (THIQ) alkaloids and their derivatives have a structural similarity to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), a well-known neurotoxin. THIQs seem to present a broad range of actions in the brain, critically depend...

  • Article
  • Open Access
9 Citations
3,416 Views
10 Pages

A [3 + 2] 1,3-Dipolar cycloaddition of C,N-cyclic azomethine imines with allyl alkyl ketones has been achieved. The reaction proceeds under mild conditions and tolerates a wide range of functional groups. An array of tetrahydroisoquinoline derivative...

  • Article
  • Open Access
5 Citations
2,313 Views
18 Pages

Synthesis, Crystal Growth, and Computational Investigation of New Tetrahydroisoquinoline Derivatives Potent against Molecule Nitric Oxide Synthases

  • Youness El Bakri,
  • Shaaban K. Mohamed,
  • Atazaz Ahsin,
  • Subramani Karthikeyan,
  • Suzan Abuelhassan,
  • Abdu E. Abdel-Rahman,
  • Islam S. Marae,
  • Etify A. Bakhite,
  • Joel T. Mague and
  • Rashad Al-Salahi

26 July 2023

In the present work, we describe the synthesis of new tetrahydroisoquinoline derivatives and the crystal structures of two of them. Density functional theory (DFT) investigations at the B3LYP/6-31+G(d,p) level provided their structural reactivity and...

  • Article
  • Open Access
6 Citations
3,546 Views
23 Pages

Synthesis of Novel 1-Oxo-2,3,4-trisubstituted Tetrahydroisoquinoline Derivatives, Bearing Other Heterocyclic Moieties and Comparative Preliminary Study of Anti-Coronavirus Activity of Selected Compounds

  • Meglena I. Kandinska,
  • Nikola T. Burdzhiev,
  • Diana V. Cheshmedzhieva,
  • Sonia V. Ilieva,
  • Peter P. Grozdanov,
  • Neli Vilhelmova-Ilieva,
  • Nadya Nikolova,
  • Vesela V. Lozanova and
  • Ivanka Nikolova

3 February 2023

A series of novel 1-oxo-2,3,4-trisubstituted tetrahydroisoquinoline (THIQ) derivatives bearing other heterocyclic moieties in their structure were synthesized based on the reaction between homophthalic anhydride and imines. Initial studies were carri...

  • Feature Paper
  • Article
  • Open Access
14 Citations
4,806 Views
18 Pages

New Tetrahydroisoquinoline Derivatives Overcome Pgp Activity in Brain-Blood Barrier and Glioblastoma Multiforme in Vitro

  • Iris Chiara Salaroglio,
  • Elena Gazzano,
  • Joanna Kopecka,
  • Konstantin Chegaev,
  • Costanzo Costamagna,
  • Roberta Fruttero,
  • Stefano Guglielmo and
  • Chiara Riganti

P-glycoprotein (Pgp) determines resistance to a broad spectrum of drugs used against glioblastoma multiforme (GB). Indeed, Pgp is highly expressed in GB stem cells and in the brain-blood barrier (BBB), the peculiar endothelium surrounding the brain....

  • Article
  • Open Access
6 Citations
2,876 Views
14 Pages

Enhanced Bioactivity of Quercetin–Tetrahydroisoquinoline Derivatives: Effect on Lipophilicity, Enzymes Inhibition, Antioxidant Potential, and Cytotoxicity

  • Marija Vučkovski,
  • Ana Filipović,
  • Milka Jadranin,
  • Lela Korićanac,
  • Jelena Žakula,
  • Bojan P. Bondžić and
  • Aleksandra M. Bondžić

5 December 2024

Quercetin, a well-known flavonoid with significant medicinal potential, was derivatized at the C8 position with a tetrahydroisoquinoline (THIQ) moiety, and physicochemical and pharmacological properties, inhibition potential, antioxidant activity, an...

  • Article
  • Open Access
4 Citations
10,481 Views
16 Pages

Coordination Compounds Based on 1,2,3,4-Tetrahydro-isoquinoline-3-carboxylic Acid

  • Petr Jansa,
  • Vladimír Macháček,
  • Petr Nachtigall,
  • Vladimír Wsól and
  • Markéta Svobodová

21 May 2007

Syntheses of 2,6-bis[((3S)-3-(methoxycarbonyl)-1,2,3,4-tetrahydroisoquinolin-2-yl)carbonyl]pyridine and its coordination compounds with Cu2+, Co2+, Co3+, or Fe3+ are described. By means of 1H- and 13C-NMR spectra it was proved that 2,6-bis[((3S)-3-(m...

  • Short Note
  • Open Access
2,735 Views
2 Pages

28 February 2006

As part of research programme directed to the synthesis of novel heterocyclic compounds pharmacologically interesting [1] via ring transformation of 1,2,4-triazine derivatives, we synthesized the title compounds 3 via two step process.[...]

  • Proceeding Paper
  • Open Access
1 Citations
3,188 Views
7 Pages

Searching for New Biologically Active Compounds Derived from Isoquinoline Alkaloids

  • Anna Kmieciak,
  • Marta Ćwiklińska,
  • Karolina Jeżak,
  • Afef Shili and
  • Marek P. Krzemiński

14 November 2020

Many isoquinoline alkaloids are biologically active compounds and successfully used as pharmaceuticals. Compounds belonging to the isoquinolines and tetrahydroisoquinolines (TIQs) can be used as anesthetics, antihypertensive drugs, antiviral agents,...

  • Article
  • Open Access
1 Citations
948 Views
18 Pages

Anticonvulsant Potential of 1-Aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines: Insights from Strychnine and Nicotine Models in In Vivo and In Silico Studies

  • Azizbek A. Azamatov,
  • Nilufar Z. Mamadalieva,
  • Asmaa A. Mandour,
  • Sherzod N. Zhurakulov,
  • Urkhiya K. Aytmuratova,
  • Valentina I. Vinogradova,
  • Fazliddin S. Jalilov and
  • Firuza M. Tursunkhodzhaeva

9 September 2025

Background: Epilepsy is a chronic, non-communicable brain disorder characterized by recurrent seizures. Some derivatives of 1,2,3,4-tetrahydroisoquinolines have demonstrated anticonvulsant effects. This study aims to investigate the effects of 33 der...

  • Article
  • Open Access
9 Citations
3,203 Views
17 Pages

Evaluation of the Local Anesthetic Activity, Acute Toxicity, and Structure–Toxicity Relationship in Series of Synthesized 1-Aryltetrahydroisoquinoline Alkaloid Derivatives In Vivo and In Silico

  • Azizbek A. Azamatov,
  • Sherzod N. Zhurakulov,
  • Valentina I. Vinogradova,
  • Firuza Tursunkhodzhaeva,
  • Roaa M. Khinkar,
  • Rania T. Malatani,
  • Mohammed M. Aldurdunji,
  • Antonio Tiezzi and
  • Nilufar Z. Mamadalieva

4 January 2023

Isoquinoline alkaloids constitute one of the most common classes of alkaloids that have shown a pronounced role in curing various diseases. Finding ways to reduce the toxicity of these molecules and to increase their therapeutic margin is an urgent m...

  • Article
  • Open Access
3 Citations
6,582 Views
11 Pages

A simple procedure for the synthesis of 8-fluoro-3,4-dihydroisoquinoline is described below, based on a directed ortho-lithiation reaction. This key intermediate was then applied in various transformations. Fluorine–amine exchange afforded the...

  • Article
  • Open Access
32 Citations
9,415 Views
24 Pages

Synthesis and Contractile Activity of Substituted 1,2,3,4-Tetrahydroisoquinolines

  • Iliyan Ivanov,
  • Stoyanka Nikolova,
  • Dimo Aladjov,
  • Iliyana Stefanova and
  • Plamen Zagorchev

16 August 2011

A series of different 1-monosubstituted and 1,1-disubstituted 1,2,3,4-tetrahydro-isoquinolines was synthesized in high yields from different ketoamides. We have developed a convenient method for the synthesis of disubstituted derivatives by interacti...

  • Article
  • Open Access
14 Citations
4,435 Views
8 Pages

Acid Catalyzed Formation of C–C and C–S Bonds via Excited State Proton Transfer

  • Alessandro Strada,
  • Mattia Fredditori,
  • Giuseppe Zanoni and
  • Stefano Protti

The behavior of 2-naphthol and 7-bromo-2-naphthol as organic photoacids are exploited in organic synthesis for the preparation of benzyl sulfides (using a trichloroacetimidate derivative as the starting substrate) and polycyclic amines via acid catal...

  • Article
  • Open Access
12 Citations
3,568 Views
18 Pages

Synthesis, Molecular Docking, Molecular Dynamics Studies, and In Vitro Biological Evaluation of New Biofunctional Ketoprofen Derivatives with Different N-Containing Heterocycles

  • Stanimir Manolov,
  • Dimitar Bojilov,
  • Iliyan Ivanov,
  • Gabriel Marc,
  • Nadezhda Bataklieva,
  • Smaranda Oniga,
  • Ovidiu Oniga and
  • Paraskev Nedialkov

17 June 2023

Herein, we report the synthesis of four new hybrid molecules between ketoprofen or 2-(3-benzoylphenyl)propanoic acid and N-containing heterocyclic compounds, such as piperidine, pyrrolidine, 1,2,3,4-tetrahydroquinoline, and 1,2,3,4-tetrahydroisoquino...

  • Communication
  • Open Access
13 Citations
5,364 Views
12 Pages

7 March 2022

Herein we report the obtaining of 1-(3,4-dihydroquinolin-1(2H)-yl)-2- (4-isobutylphenyl)propan-1-one and its characterization. The newly obtained hybrid and its derivatives (hybrids of ibuprofen with 1,2,3,4-tetrahydroisoquinoline, and piperidine) we...

  • Feature Paper
  • Article
  • Open Access
2 Citations
3,828 Views
17 Pages

21 November 2023

Through the Lilly Open Innovation Drug Discovery program (OIDD), we discovered five cationic bis(aryltriazol-4-yl)methyl)-6,7-dimethoxytetrahydroisoquinolinium derivatives that effectively inhibit human nicotinamide N-methyltransferase. Compound...

  • Abstract
  • Open Access
749 Views
2 Pages

Employing Mechanochemistry in the Synthesis of N-Ibuprofen-Substituted 1,2,3,4-Tetrahydroisoquinolines

  • Stanimir Manolov,
  • Diyana Dimitrova,
  • Iliyan Ivanov and
  • Dimitar Bojilov

Mechanochemistry has emerged as a potential alternative for organic transformations, leveraging substrate availability, stability, and reduced solvent use. Its high efficiency and eco-friendly profile have garnered significant attention, particularly...

  • Article
  • Open Access
3 Citations
2,675 Views
8 Pages

A mild and efficient strategy for the synthesis of tricyclic 1,2,4-oxadiazolines-fused tetrahydro-isoquinolines derivatives via [3 + 2] cycloaddition reaction is reported. The reactions provided the functionalized tricyclic 1,2,4-oxadiazolines in hig...

  • Review
  • Open Access
2 Citations
3,034 Views
14 Pages

30 August 2023

This report reviews the most important lipase-catalyzed strategies for the preparation of pharmaceutically and chemically important tetrahydroisoquinoline and tetrahydro-β-carboline enantiomers through O-acylation of the primary hydroxy group, N...

  • Article
  • Open Access
8 Citations
3,369 Views
19 Pages

Design, Radiosynthesis and Preliminary Biological Evaluation in Mice of a Brain-Penetrant 18F-Labelled σ2 Receptor Ligand

  • Rareş-Petru Moldovan,
  • Daniel Gündel,
  • Rodrigo Teodoro,
  • Friedrich-Alexander Ludwig,
  • Steffen Fischer,
  • Magali Toussaint,
  • Dirk Schepmann,
  • Bernhard Wünsch,
  • Peter Brust and
  • Winnie Deuther-Conrad

The σ2 receptor (transmembrane protein 97), which is involved in cholesterol homeostasis, is of high relevance for neoplastic processes. The upregulated expression of σ2 receptors in cancer cells and tissue in combination with the antiproliferative p...

  • Review
  • Open Access
35 Citations
5,976 Views
34 Pages

Marine-Derived Macrocyclic Alkaloids (MDMAs): Chemical and Biological Diversity

  • Hanan I. Althagbi,
  • Walied M. Alarif,
  • Khalid O. Al-Footy and
  • Ahmed Abdel-Lateff

17 July 2020

The curiosity and attention that researchers have devoted to alkaloids are due to their bioactivities, structural diversity, and intriguing chemistry. Marine-derived macrocyclic alkaloids (MDMAs) are considered to be a potential source of drugs. Trab...

  • Article
  • Open Access
2 Citations
2,175 Views
15 Pages

Amphiphilic Fluorescein Triazoles: Synthesis and Visible-Light Catalysis in Water

  • Alina Artemenko,
  • Elza Sultanova,
  • Diana Mironova,
  • Aliya Akhatova,
  • Ekaterina Bondareva,
  • Daut Islamov,
  • Konstantin Usachev,
  • Svetlana Solovieva,
  • Vladimir Burilov and
  • Igor Antipin

11 September 2024

Triazole derivatives of fluorescein-containing N,N-dimethylaminopropyl fragments and their ammonium salts were synthesized with yields of 74–85%. The resulting compounds exhibit fluorescent properties in the green region of the visible spectrum...

  • Article
  • Open Access
18 Citations
6,787 Views
16 Pages

16 June 2014

As part of our continuing research on isoquinoline acaricidal drugs, this paper reports the preparation of a series of the 2-aryl-1-cyano-1,2,3,4-tetrahydroisoquinolines with various substituents on the N-phenyl ring, their in vitro acaricidal activi...

  • Abstract
  • Open Access
801 Views
2 Pages

Synthesis of N-Flurbiprofen-Substituted 1,2,3,4-Tetrahydroisoquinolines

  • Diyana Dimitrova,
  • Stanimir Manolov,
  • Iliyan Ivanov and
  • Dimitar Bojilov

Isoquinoline alkaloids constitute a substantial category of natural products, among which 1,2,3,4-tetrahydroisoquinoline (THIQ) holds significance. THIQ-based compounds, whether natural or synthetic, showcase a wide array of biological activities, de...

  • Article
  • Open Access
10 Citations
5,036 Views
20 Pages

Selective Anticancer Therapy Based on a HA-CD44 Interaction Inhibitor Loaded on Polymeric Nanoparticles

  • José M. Espejo-Román,
  • Belén Rubio-Ruiz,
  • Victoria Cano-Cortés,
  • Olga Cruz-López,
  • Saúl Gonzalez-Resines,
  • Carmen Domene,
  • Ana Conejo-García and
  • Rosario M. Sánchez-Martín

Hyaluronic acid (HA), through its interactions with the cluster of differentiation 44 (CD44), acts as a potent modulator of the tumor microenvironment, creating a wide range of extracellular stimuli for tumor growth, angiogenesis, invasion, and metas...

  • Article
  • Open Access
6 Citations
2,608 Views
20 Pages

Targeting Alzheimer’s Disease: Evaluating the Efficacy of C-1 Functionalized N-Aryl-Tetrahydroisoquinolines as Cholinergic Enzyme Inhibitors and Promising Therapeutic Candidates

  • Dunja Jovanović,
  • Ana Filipović,
  • Goran Janjić,
  • Tamara Lazarević-Pašti,
  • Zdravko Džambaski,
  • Bojan P. Bondžić and
  • Aleksandra M. Bondžić

14 January 2024

We have synthesized 22 C-1 functionalized-N-aryl-1,2,3,4-tetrahydroisoquinoline derivatives showing biological activities towards cholinergic enzymes. Synthesis was performed using visible-light-promoted photo-redox chemistry, starting from a common...

  • Feature Paper
  • Article
  • Open Access
4 Citations
2,713 Views
15 Pages

Point-Substitution of Phenylalanine Residues of 26RFa Neuropeptide: A Structure-Activity Relationship Study

  • Benjamin Lefranc,
  • Karima Alim,
  • Cindy Neveu,
  • Olivier Le Marec,
  • Christophe Dubessy,
  • Jean A. Boutin,
  • Julien Chuquet,
  • David Vaudry,
  • Gaëtan Prévost and
  • Jérôme Leprince
  • + 3 authors

16 July 2021

26RFa is a neuropeptide that activates the rhodopsin-like G protein-coupled receptor QRFPR/GPR103. This peptidergic system is involved in the regulation of a wide array of physiological processes including feeding behavior and glucose homeostasis. He...

  • Article
  • Open Access
25 Citations
4,311 Views
10 Pages

Penicamide A, A Unique N,N′-Ketal Quinazolinone Alkaloid from Ascidian-Derived Fungus Penicillium sp. 4829

  • Senhua Chen,
  • Minghua Jiang,
  • Bin Chen,
  • Jintana Salaenoi,
  • Shah-Iram Niaz,
  • Jianguo He and
  • Lan Liu

5 September 2019

Previously unreported N,N′-ketal quinazolinone enantiomers [(−)-1 and (+)-1] and a new biogenetically related compound (2), along with six known compounds, 2-pyrovoylaminobenzamide (3), N-(2-hydroxypropanoyl)-2 amino benzoic acid amide (4...

  • Article
  • Open Access
5 Citations
3,440 Views
24 Pages

Design, Synthesis and Biological Evaluation of Novel and Potent Protein Arginine Methyltransferases 5 Inhibitors for Cancer Therapy

  • Yixuan Tang,
  • Shihui Huang,
  • Xingxing Chen,
  • Junzhang Huang,
  • Qianwen Lin,
  • Lei Huang,
  • Shuping Wang,
  • Qihua Zhu,
  • Yungen Xu and
  • Yi Zou

6 October 2022

Protein arginine methyltransferases 5 (PRMT5) is a clinically promising epigenetic target that is upregulated in a variety of tumors. Currently, there are several PRMT5 inhibitors under preclinical or clinical development, however the established cli...

  • Article
  • Open Access
7 Citations
2,833 Views
17 Pages

Design, Synthesis, and Biological Evaluation of Marine Lissodendrins B Analogues as Modulators of ABCB1-Mediated Multidrug Resistance

  • Chaoming Wang,
  • Jinman Zhang,
  • Xianfeng Wei,
  • Mengke Yang,
  • Weiping Ma,
  • Rilei Yu,
  • Ming Liu and
  • Tao Jiang

20 May 2023

Multidrug resistance (MDR) caused by ATP-Binding Cassette Subfamily B Member 1 (ABCB1, P-glycoprotein, P-gp) is a major barrier for the success of chemotherapy in clinics. In this study, we designed and synthesized a total of 19 Lissodendrins B analo...

  • Article
  • Open Access
705 Views
10 Pages

Effects of a Synthetic Isoquinoline Derivative Against Ichthyophthirius multifiliis In Vivo and In Vitro in Grass Carp (Ctenopharyngodon idella)

  • Xianqi Peng,
  • Xialian Bu,
  • Weisong Ma,
  • Jinbiao Jiao,
  • Xiaohong Huang,
  • Yu Zhao,
  • Jian Zhu,
  • Lei Huang,
  • Jing Chen and
  • Jiayun Yao
  • + 2 authors

21 October 2025

White spot disease, caused by the parasitic Ichthyophthirius multifiliis, induces mortality exceeding 80% in intensive aquaculture systems, resulting in global annual losses of >$1 billion. Current chemical controls (e.g., formaldehyde) face envir...

  • Article
  • Open Access
11 Citations
3,534 Views
20 Pages

15 December 2022

A dysregulation of the cell-death mechanism contributes to poor prognosis in lung cancer. New potent chemotherapeutic agents targeting apoptosis-deregulating molecules have been discovered. In this study, 22-(4-pyridinecarbonyl) jorunnamycin A (22-(4...

  • Article
  • Open Access
27 Citations
5,760 Views
15 Pages

Renieramycin T Induces Lung Cancer Cell Apoptosis by Targeting Mcl-1 Degradation: A New Insight in the Mechanism of Action

  • Korrakod Petsri,
  • Supakarn Chamni,
  • Khanit Suwanborirux,
  • Naoki Saito and
  • Pithi Chanvorachote

21 May 2019

Among malignancies, lung cancer is the major cause of cancer death. Despite the advance in lung cancer therapy, the five-year survival rate is extremely restricted due to therapeutic failure and disease relapse. Targeted therapies selectively inhibit...

  • Article
  • Open Access
2 Citations
1,759 Views
22 Pages

28 February 2025

The tetrahydroisoquinoline skeleton is a pharmacologically significant core structure containing chiral centers, making enantiomeric separation crucial due to the potentially distinct biological effects of each enantiomer. In this study, laudanosine...

  • Review
  • Open Access
100 Views
15 Pages

Consensus Molecules Associated with Parkinson’s Disease

  • Sara Eyal,
  • Shira Alfasi,
  • Karin Ben Zaken,
  • Ibrahim O. Sawaid,
  • Lior Segev,
  • Samuel Mesfin,
  • Pnina Frankel,
  • Rahaf Ezzy,
  • Trishna Saha-Detroja and
  • Abraham O. Samson
  • + 3 authors

Parkinson’s disease (PD) has been associated with some types of food and drugs. Here, we query PubMed for the association of PD with foods and drugs, using a list of 217,776 compounds derived from the Human Metabolome Database (HMDB). To calcul...