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Finasteride
[CAS# 98319-26-7]

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Identification
Classification API >> Urinary system medication >> Other urinary system medication
Name Finasteride
Synonyms N-(2-methyl-2-propyl)-3-oxo-4-aza-5alpha-androst-1-ene-17beta-carboxamide; Proscar
Molecular Structure CAS # 98319-26-7, Finasteride, N-(2-methyl-2-propyl)-3-oxo-4-aza-5alpha-androst-1-ene-17beta-carboxamide, Proscar
Molecular Formula C23H36N2O2
Molecular Weight 372.55
CAS Registry Number 98319-26-7
EC Number 620-534-3
SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2C(=O)NC(C)(C)C)CC[C@@H]4[C@@]3(C=CC(=O)N4)C
Properties
Water solubility insoluble
Safety Data
Hazard Symbols symbol symbol symbol   GHS07;GHS08;GHS09 Danger    Details
Hazard Statements H302-H360-H360D-H372-H410    Details
Precautionary Statements P203-P260-P264-P270-P273-P280-P301+P317-P318-P319-P330-P391-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Specific target organ toxicity - repeated exposureSTOT RE1H372
Reproductive toxicityRepr.1BH360
Reproductive toxicityRepr.1BH360D
Reproductive toxicityRepr.2H361
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.1H302
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H312
Eye irritationEye Irrit.2H319
SDS Available
up Discovory and Applicatios
Finasteride is a synthetic 4-azasteroid compound that has significantly impacted the treatment of benign prostatic hyperplasia (BPH) and androgenetic alopecia (male pattern baldness). Developed in the late 1980s by the pharmaceutical company Merck, Finasteride was approved by the FDA in 1992 for BPH treatment and later in 1997 for treating hair loss in men.

The discovery of Finasteride originated from research into the role of androgens in prostate growth and hair loss. Scientists identified dihydrotestosterone (DHT), a potent androgen derived from testosterone by the action of the enzyme 5-alpha-reductase, as a critical factor in both conditions. DHT is essential for the development of male characteristics but its excessive production can lead to prostate enlargement and hair follicle miniaturization.

Finasteride works by inhibiting type II 5-alpha-reductase, the enzyme responsible for converting testosterone to DHT. By reducing DHT levels, Finasteride helps to shrink the enlarged prostate in BPH patients, alleviating urinary symptoms such as difficulty in starting urination, weak stream, and frequent urination. Clinical studies have shown that Finasteride significantly reduces the need for surgery in BPH patients and improves their quality of life.

In the context of androgenetic alopecia, Finasteride's inhibition of DHT helps to halt hair loss and stimulate hair regrowth. Hair follicles affected by DHT tend to shrink, leading to thinning hair and eventual hair loss. By lowering DHT levels, Finasteride allows hair follicles to recover, increasing hair count and improving hair density. It is one of the few medications that have been scientifically proven to be effective in treating male pattern baldness.

Apart from its primary uses, Finasteride has been studied for other potential applications. Research is ongoing into its effects on prostate cancer prevention, as DHT plays a role in prostate cancer development. Some studies suggest that Finasteride may reduce the incidence of low-grade prostate cancers, although its impact on high-grade cancer is still debated.

Finasteride's effectiveness and relatively mild side effect profile have made it a widely used treatment. However, potential side effects include sexual dysfunction, such as decreased libido and erectile dysfunction, which can persist even after discontinuation of the drug in some cases. Due to these concerns, it is crucial for patients to discuss the risks and benefits of Finasteride with their healthcare provider.

Overall, Finasteride represents a significant advancement in the treatment of BPH and androgenetic alopecia. Its ability to inhibit the production of DHT addresses the underlying cause of these conditions, providing relief and improving quality of life for many patients. The continued study and application of Finasteride highlight its importance in clinical medicine and potential for broader therapeutic uses.
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