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Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
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Combination Therapies and Personalized Medicine02:50

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Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

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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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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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Dopamine receptor antagonists, also known as antipsychotic agents, are critical in managing chemotherapy-induced vomiting. These antiemetic agents block dopamine receptors in the chemoreceptor trigger zone (CTZ), inhibiting signal transmission to the vomiting center. Antipsychotic agents encompass phenothiazines (PTZ), butyrophenones, benzamides, and thienobenzodiazepines (Zyprexa), which are utilized for their antiemetic and sedative properties.
Phenothiazines, such as prochlorperazine...
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Cancer Therapies02:49

Cancer Therapies

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Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
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Microwave-Assisted Preparation of 1-Aryl-1H-pyrazole-5-amines
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Current Developments in the Pyran-Based Analogues as Anticancer Agents.

Parul Grover1, Monika Bhardwaj2,3, Lovekesh Mehta4

  • 1KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad 201206, India.

Anti-Cancer Agents in Medicinal Chemistry
|November 22, 2021
PubMed
Summary
This summary is machine-generated.

Pyran derivatives show significant potential as anti-cancer agents. This review details pyran-based compounds, exploring their efficacy in various cancer models and their role in drug discovery.

Keywords:
HeterocyclesIC<sub>50</sub>anti-cancercell linecytotoxicitypyran

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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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Area of Science:

  • Medicinal Chemistry
  • Organic Chemistry
  • Pharmacology

Background:

  • Heterocyclic compounds are crucial for novel drug discovery, particularly for cancer treatment.
  • Oxygen-containing heterocycles, especially pyran derivatives, exhibit significant pharmacological activities.
  • Pyran, a six-membered oxygen-containing ring, is a privileged structure with diverse biological properties.

Purpose of the Study:

  • To review recent advancements in pyran-based derivatives as anti-cancer agents.
  • To consolidate research on the anti-cancer potential of various pyran structures.
  • To highlight the therapeutic promise of pyran scaffolds in oncology.

Main Methods:

  • Comprehensive literature review of pyran derivatives in cancer research.
  • Analysis of in vitro (cell-based) and in vivo (animal-based) studies.
  • Inclusion of molecular docking studies and natural pyran-containing anticancer compounds.

Main Results:

  • Pyran derivatives demonstrate broad-spectrum anti-cancer properties against diverse cancer types.
  • Evidence from in vitro, in vivo, and computational studies supports their efficacy.
  • Natural compounds incorporating pyran structures also exhibit anti-cancer activity.

Conclusions:

  • Pyran-based compounds represent a promising class of anti-cancer therapeutics.
  • Further research into pyran derivatives can lead to novel cancer drug candidates.
  • The privileged nature of the pyran scaffold facilitates the development of effective anti-cancer agents.