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A new method accurately measures molecular movement without complex modeling.

Keratin structure in hair is stable at pH 5-6 but disrupts between pH 6-7.

SCD1 inhibitors can cause skin issues in rodents.

Finasteride breaks down into new compounds under acidic conditions.

Cis-UCA can form new compounds without enzymes, and sulphide donors reduce its UVB-induced toxicity in skin cells.

The study successfully identified the structure of finasteride.

Finasteride, at doses of 5mg or higher, may negatively affect male fertility by reducing the expression of certain genes involved in sperm production.

4-azasteroids, including finasteride, can inhibit 5α-reductase, helping treat conditions like enlarged prostate and hair loss.

Finasteride forms three new products under acidic stress.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.

Divalproex sodium significantly improved headaches in two-thirds of patients.

Finasteride reduces sperm count and quality and alters hormone levels in mice.

Certain polyphenols may help treat skin pigmentation disorders.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

Permanent waving damages hair by disrupting its keratin structure.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Artificial sebum L closely mimics human sebum for drug delivery research.

Desolvation of finasteride depends on environment and technique.

New gel formulas without ethanol and propylene glycol, containing a minoxidil-methyl-β-cyclodextrin complex, have been created for treating hair loss.

Scientists made all eight versions of a compound called cyoctol, but found it's not an anti-androgen and it fully breaks down in the skin.

Loliolide from Scenedesmus deserticola may help with anti-aging.

Plant surfactants from quinoa and soybeans are effective, safe, and eco-friendly for shampoos.

Some natural compounds from Iris plants can block enzymes related to certain disorders, with a few affecting both targeted enzymes.

Minoxidil reacts to nitrosation 7 times more than phenol, mainly due to its -NH₂ groups, leading to the creation of N-nitrosominoxidil.

EPC-K is stable except at very acidic pH or when exposed to sunlight, and it can decompose in low ethanol concentrations.

A new, quick method accurately detects minoxidil in drugs and cosmetics.

Prenatal retinoic acid exposure did not affect mouse vibrissal follicle development.

Lotus corniculatus seed extract reduces oily skin by decreasing sebum production.

A new minoxidil-like substance, triaminodil, was found in an illegal hair growth supplement.

Researchers created 10 new compounds similar to cercidin, which could lead to new antibiotics.