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Related Concept Videos

Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
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Properties of Organometallic Compounds

Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
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Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...
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Antifungal Agents

Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to cholesterol contributes to...
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Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...

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Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay
11:14

Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay

Published on: November 10, 2013

Alkaloid-metal based anticancer agents.

Zhen-Feng Chen1, Yan-Cheng Liu, Ke-Bin Huang

  • 1State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004, P.R. China. chenzfubc@yahoo.com.

Current Topics in Medicinal Chemistry
|August 28, 2013
PubMed
Summary
This summary is machine-generated.

New alkaloid-metal complexes offer a promising alternative to platinum-based chemotherapy, showing improved anticancer activity and potential to overcome drug resistance. These novel agents are being explored for their therapeutic benefits.

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Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
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Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
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Last Updated: May 8, 2026

Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay
11:14

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Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
07:20

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents

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Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
09:33

Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling

Published on: March 20, 2018

Area of Science:

  • Medicinal Chemistry
  • Pharmacology
  • Oncology

Background:

  • Platinum-based anticancer drugs face challenges with significant side effects and acquired resistance.
  • Developing novel metal-based anticancer agents is crucial for improved therapeutic outcomes.
  • Alkaloid-metal complexes represent a promising new avenue for cancer treatment.

Purpose of the Study:

  • To review recent advancements in alkaloid-metal based anticancer agents.
  • To discuss the in vitro anticancer activities and mechanisms of action of these compounds.
  • To explore the future potential of hybrid alkaloid-metal complexes in overcoming multidrug resistance.

Main Methods:

  • Literature review of recent progress in alkaloid-metal anticancer agents.
  • Analysis of in vitro anticancer activities of various alkaloid-metal complexes.
  • Examination of the primary action mechanisms of these novel agents.

Main Results:

  • Alkaloid-metal complexes, including those with liriodenine, β-carboline, and quinolinoline, demonstrate significant in vitro anticancer activities.
  • These complexes offer a potential strategy to overcome acquired resistance associated with traditional chemotherapy.
  • The review highlights the diverse pharmacological properties and antitumor activities of these novel compounds.

Conclusions:

  • Alkaloid-metal complexes are a promising class of anticancer agents with potential to overcome limitations of current therapies.
  • Further development of hybrid alkaloid-metal complexes may offer new solutions for multidrug resistance (MDR).
  • These novel agents represent a significant advancement in the search for more effective cancer treatments.