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Loss of Carboxy Group as CO2: Decarboxylation of β-Ketoacids01:02

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Carboxylic acids, upon heating, undergo a decarboxylation reaction by releasing carbon dioxide gas. Monocarboxylic acids do not undergo decarboxylation easily. However, a silver salt of carboxylic acid reacts with bromine or iodine under high temperature to release carbon dioxide gas and forms halide with one less carbon. This reaction is called the Hunsdiecker reaction.
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IUPAC Nomenclature of Carboxylic Acids01:16

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IUPAC names of carboxylic acids are systematically derived following a few rules discussed below.
For acyclic saturated monocarboxylic acids, the longest hydrocarbon chain containing the –COOH carbon is identified as the parent chain. Then, the last -e of the parent hydrocarbon name is replaced with a suffix -oic acid.
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Carrier-Mediated Transport01:06

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Carrier-mediated transport is a pivotal process in drug absorption, particularly for lipid-insoluble drugs, and encompasses facilitated diffusion and active transport. Facilitated diffusion allows drugs to move along their concentration gradient without energy expenditure, while active transport utilizes ATP to drive drug movement against this gradient.
Active transport involves two types of membrane-spanning transporters: uptake and efflux. Uptake transporters are expressed in the small...
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Drug Absorption Mechanism: Carrier-Mediated Membrane Transport01:19

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Certain large, lipid-insoluble drug molecules that resemble amino acids, peptides, or glucose, require specialized carrier proteins to facilitate their diffusion across cell membranes. This transport can occur through either facilitated diffusion, which does not require energy input, or active transport, which does require energy input.
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Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives01:35

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Just like β-keto acids—which upon thermal decarboxylation form ketones—β-dicarboxylic acids undergo decarboxylation to generate monocarboxylic acids with the liberation of carbon dioxide.
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The ADP/ATP Carrier Protein01:42

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ADP/ATP carrier or AAC protein is the most abundant carrier protein in the inner mitochondrial membrane. It transports large quantities of ADP and ATP, equivalent to the average human body weight, every day. Among other transporters, ACC protein is one of the best-studied members of the mitochondrial carrier protein family. The ADP/ATP carrier protein comprises two transmembrane helices connected to a loop and a single alpha-helix on the matrix side. It switches between two conformational...
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Related Experiment Video

Updated: May 5, 2026

The Mesenteric Lymph Duct Cannulated Rat Model: Application to the Assessment of Intestinal Lymphatic Drug Transport
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The Mesenteric Lymph Duct Cannulated Rat Model: Application to the Assessment of Intestinal Lymphatic Drug Transport

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Monocarboxylic acid transport.

Andrew P Halestrap1

  • 1School of Biochemistry and The Bristol Heart Institute, University of Bristol, Bristol, United Kingdom.

Comprehensive Physiology
|November 23, 2013
PubMed
Summary
This summary is machine-generated.

Monocarboxylate transporters (MCTs) move key metabolic fuels like lactate across cell membranes. Their structure, function, and roles in disease and drug targeting are crucial for understanding cellular energy.

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Area of Science:

  • Biochemistry
  • Cell Biology
  • Physiology

Background:

  • Monocarboxylates (lactate, pyruvate, ketone bodies) are vital metabolic fuels.
  • Transport across plasma and mitochondrial membranes is essential for cellular metabolism.
  • Proton-linked MonoCarboxylate Transporters (MCTs) and Sodium-coupled MonoCarboxylate Transporters (SMCTs) facilitate this transport.

Purpose of the Study:

  • To review the characterization of MCTs, SMCTs, and the mitochondrial pyruvate carrier (MPC).
  • To discuss the molecular identity, structure, and function of these transporters.
  • To explore the regulation and physiological/pathological roles of monocarboxylate transport.

Main Methods:

  • Literature review of established research on monocarboxylate transporters.
  • Analysis of kinetic and specificity data for MCTs, SMCTs, and MPC.
  • Examination of structural models and regulatory mechanisms.

Main Results:

  • MCTs and SMCTs are well-defined, while MPC identity is less certain.
  • MCTs require specific glycoprotein partners (embigin, basigin) for activity.
  • Regulation occurs transcriptionally and post-transcriptionally, with examples in exercise and T-cells.
  • MCT4 is suited for lactate export and upregulated by hypoxia.

Conclusions:

  • Monocarboxylate transport is critical in various tissues and physiological states.
  • Dysregulation of these transporters is linked to disease.
  • MCTs represent promising therapeutic targets for cancer and drug delivery.