Sechenov School
Home › Pharmacology › Aromatic Compounds in Pharmacology

Aromatic Compounds in Pharmacology

For medical students2 min readUpdated 2026-10-10

Aromatic compounds in pharmacology are a group of antiseptic and disinfectant agents whose chemical structure is based on a benzene ring. The main representative of the class is phenol, while other agents are its derivatives or complex mixtures containing this substance.

Structural baseA benzene ring that determines the chemical and pharmacological properties of the entire group.
Spectrum of actionActive against vegetative forms of microbes, but demonstrates extremely weak activity against spores.
Triclosan targetThe enoyl-reductase enzyme (encoded by the *fabI* gene), which is involved in lipid biosynthesis.
Main reference standardPhenol—the base substance acting as the active component of complex products.

Basic Characteristics and Phenol

All pharmacological agents in this group share a common structural feature: the presence of a benzene ring. The primary reference representative of the class is phenol (also known in medical practice as carbolic acid). All other agents discussed here are classified either as its derivatives or as complex multi-ingredient products containing phenol as the active substance.

Phenol's antimicrobial spectrum has clear boundaries: it exerts a strong lethal effect on vegetative forms of microorganisms, yet shows weak activity against bacterial spores. In modern medicine, the use of pure phenol is strictly limited. It is used exclusively for the disinfection of inanimate environmental objects. It is employed to process medical instruments, hospital linens, room surfaces, and various household items. At the same time, phenol retains its significance as an active component within complex products such as tar and ichthammol.

Products of Natural Raw Material Distillation

This category includes complex mixtures obtained through thermal distillation.

  1. Birch tar (Pix Betulae). By origin, this is a product of birch bark distillation. It possesses a triple pharmacological effect: antimicrobial, insecticidal (effective as an anti-pediculosis agent), and local irritant. The main indications for its prescription are various skin pathologies, such as eczema, psoriasis, and neurodermatitis. In clinical practice, tar is rarely used in pure form; instead, it is included in well-known combination drugs, such as Wilkinson's ointment and Vishnevsky balsamic liniment.
  1. Ichthammol (Ichthyol). Unlike birch tar, ichthammol is a product of oil shale distillation. Its pharmacological profile is broader, encompassing antimicrobial, antiseptic, pronounced anti-inflammatory, keratoplastic, and local anesthetic effects. Methods of application depend on the medical specialty:
  2. In dermatology, ichthammol is used in the form of ointments and pastes to treat burns, erysipelas, and eczema.
  3. In gynecology and proctology, the drug is prescribed as suppositories for inflammatory processes of the pelvic organs, including disorders of the rectum and female reproductive organs.

Synthetic Phenol Derivatives

Chemically modified aromatic compounds include resorcinol and triclosan.

Resorcinol chemically represents meta-dioxybenzene. The mechanism of its antimicrobial action lies in its ability to cause protein coagulation, which directly leads to the death of vegetative microbial forms. The drug is indicated for bacterial and fungal skin infections, including eczema, seborrhea, and conditions accompanied by severe pruritus.

Triclosan is a chlorine-containing derivative of phenol distinguished by extremely high antibacterial activity. Its mechanism of action differs fundamentally from resorcinol: triclosan inhibits lipid biosynthesis within the bacterial cell. The specific target for the drug is the enoyl-reductase enzyme encoded by the fabI gene. Notably, mutation of the fabI gene in microorganisms can lead to the development of resistance to triclosan.

Applications of triclosan include:

Mnemonic

To quickly memorize the origin of natural preparations: Tar = Tree (birch bark), Ichthammol = Interred/Inorganic shale (Isund/fossil shales).

Frequently asked questions

Can pure phenol be used for wound care?

No, pure phenol is used exclusively for disinfecting environmental objects: surgical instruments, linens, premises, and household items.

What is the difference between the mechanisms of action of resorcinol and triclosan?

Resorcinol causes non-specific coagulation of microbial proteins. Triclosan acts selectively: it inhibits lipid biosynthesis by blocking the enoyl-reductase enzyme.

Why can resistance to triclosan develop?

Bacterial resistance arises as a result of a mutation in the fabI gene, which encodes the drug's target enzyme (enoyl-reductase), thereby preventing the antiseptic from binding to its target.

Go deeper

More topics in Pharmacology

DipyridamoleDoxazosinAntimicrobial Therapy Selection by PathogenDrugs for Trichomoniasis and GiardiasisVitamin-Like Compounds and Plant VitaminsAmitriptylineClopidogrelRenin-Angiotensin System Inhibitors: Pharmacology and Mechanism of ActionPentazocineMast Cell StabilizersGold CompoundsValidolPharmacology →