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betamethasone dipropionate + salicyclic acid (Diprosalic)

✓ Approved

Merck & Co. · PTGS1 · Small Molecule

What is betamethasone dipropionate + salicyclic acid?

betamethasone dipropionate + salicyclic acid is a small molecule developed by Merck & Co.. It is approved for therapeutic indications via topical.

Drug Profile

Brand NamesDiprosalic
CompanyMerck & Co.
Drug ClassSmall Molecule
Molecular TargetPTGS1, PTGS2, TBXAS1
RouteTopical
StatusApproved

Mechanism of Action

Molecular Targets

betamethasone dipropionate + salicyclic acid acts on 3 molecular targets:

PTGS1prostaglandin-endoperoxide synthase 1 (COX3, PCOX1)
PTGS2prostaglandin-endoperoxide synthase 2 (GRIPGHS, hCox-2)
TBXAS1thromboxane A synthase 1 (CYP5, TXS)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

betamethasone dipropionate + salicyclic acid is developed for 3 unique indications across 2 therapeutic areas.

Therapeutic AreaConditionPhase
Skin and subcutaneous tissue disordersEczema✓ Approved
Hepatobiliary disordersHepatitis✓ Approved
Skin and subcutaneous tissue disordersPsoriasis✓ Approved

Related Research Articles

PubMedTrials2026-07-25

The World Health Organization Antenatal CorTicosteroids for Improving Outcomes in preterm Newborns (ACTION-III) trial-rationale for the selected lower steroid dose.

WHO ACTION Trials Collaborators

Antenatal corticosteroids (ACS), most commonly administered as betamethasone or dexamethasone, remain a cornerstone of care for women at risk of preterm birth. However, the standard 24-mg regimen introduced more than five decades ago has not undergone formal dose-finding evaluation. Emerging concerns regarding possible dose-related adverse effects, particularly among late preterm infants subsequently born at term, have renewed interest in optimizing corticosteroid exposure. Experimental data across species, supported by human pharmacokinetic analyses, indicate that fetal lung maturation is driven by sustained low corticosteroid concentrations rather than high peak levels. This commentary summarizes key experimental, pharmacokinetic, and modelling evidence that informed the selection of the lower-dose betamethasone phosphate regimen evaluated in the WHO ACTION-III trial and explains the scientific rationale for this dosing strategy. Pharmacokinetic modeling indicates that 2 mg betamethasone phosphate administered intramuscularly every 12 h for four doses achieves fetal concentrations within the 1 to 4 ng/mL range identified in experimental studies, while avoiding the supratherapeutic peaks observed with conventional regimens. The ACTION-III trial will evaluate whether this lower dose ACS regimen, chosen on the basis of carefully developed models and clinical studies, maintains clinical efficacy while potentially reducing unnecessary systemic corticosteroid exposure in women at risk of late preterm birth.Trial registration: ISRCTN11434567, registered on 7 June 2021.  https://www.isrctn.com/ISRCTN11434567?q=ACTION-III&filters=&sort=&offset=1&totalResults=1&page=1&pageSize=10 .

PubMedCureus2026-07-25

Economic Burden and Cost Differences Between Branded and Generic Topical Antifungals in India.

Dt Prateek P, Dongerkery Kavitha K, Deolekar Pradnya P, Dahibhate Atharva A et al.

India's pharmaceutical market is characterized by a significant presence of both generic and branded drugs, particularly for common ailments such as superficial mycoses (SFMs), which pose a substantial public health and economic burden. Patients in tropical countries like India, which have common superficial mycoses, need prolonged treatment because of their recurrence rates after initial treatment and due to incomplete therapy. Given the high variability in drug pricing and the imperative for cost-effective healthcare, a pharmacoeconomic analysis comparing generic and branded topical antifungals in India is crucial to inform prescribing practices and optimize resource allocation. The price comparison of various topical antifungal medications from different brands was conducted by using the latest information from the "Monthly Index of Medical Specialties" August to October 2025, and 1mg online pharmacy and Jan Aushadhi website. The study calculated the total expenses for 30 mL and 30 g dosage forms, which included cream, ointment, lotion, eye drops, and shampoo products of each drug brand. We conducted a comparison between different drug brands through their cost ratio, and percentage cost variation (PCV) analysis was done, keeping generic medicines prices (retrieved from the Jan Aushadhi website) as baseline values. The data analysis showed a significant variation in the costs of different brands of topical antifungals in the Indian market. After analysis, we identified itraconazole 1% ointment to have the highest cost variation at 8335.1%, followed by clotrimazole dusting powder (4740%). Ketoconazole 2% cream, bifonazole 1% lotion, and sertaconazole shampoo showed the smallest variation at 3.29%, 3.5%, and 11.3%, respectively. When generic and branded topical antifungals were compared, the highest cost variation was seen for clotrimazole 1% cream (3431.7%), and the least variation was observed for ketoconazole 2% powder (135.4%). When combination topical antifungals were compared, the highest percentage cost variation of 1479.4% was seen for clotrimazole 1%w/w and beclomethasone dipropionate 0.025%w/w cream, and the least percentage cost variation of 38.8% was seen for terbinafine (1% w/w) + ciprofloxacin (1% w/w) + metronidazole (1% w/w) + clobetasol (0.05% w/w). The market for topical antifungal agents demonstrates substantial price variation among available products. Regulatory authorities, pharmaceutical manufacturers, and clinicians must collaborate to achieve optimal reductions in drug costs. Strict implementation of cost regulation policies, along with increased awareness among clinicians regarding the rational selection of cost-effective therapies, is essential.

PubMedCanadian journal of ophthalmology. Journal canadien d'ophtalmologie2026-07-25

Bisphosphonates and glaucoma: a pharmacovigilance signal detection analysis using the FAERS database.

Zhang Yan Y, Huang Yi Hong YH, Xiao Yan Ling YL, Zhu Xin Xing XX et al.

To detect and characterize disproportionality signals between individual bisphosphonates and glaucoma subtypes using the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS). A retrospective pharmacovigilance disproportionality analysis. Participant data were drawn from adverse event reports from the FAERS database (Q1 2004-Q1 2025). Disproportionality analysis was conducted using the reporting odds ratio (ROR), proportional reporting ratio (PRR), and Bayesian confidence propagation neural network (BCPNN). Adverse events were coded using Medical Dictionary for Regulatory Activities (version 27.1). A significant signal required ≥3 cases and meeting thresholds (ROR 95% CI lower limit >1, PRR ≥2 with χ² ≥4, or BCPNN IC025 >0). Among 539 reports, significant disproportionality signals were identified for alendronic acid (ROR = 2.42; 95% CI: 2.18-2.70) and pamidronic acid (ROR = 2.23; 95% CI: 1.69-2.93) at the group level. Subtype-level signals included alendronic acid with open-angle glaucoma (ROR = 5.67) and normal-tension glaucoma (ROR = 4.60); pamidronic acid with open-angle glaucoma (ROR = 8.62); and risedronic acid with angle-closure glaucoma (ROR = 2.93). Median time-to-onset varied from 10 days (risedronic acid) to 1579 days (pamidronic acid). This pharmacovigilance analysis identifies distinct disproportionality signals linking specific bisphosphonates to different glaucoma subtypes, with heterogeneous time-to-onset patterns. The findings highlight potential safety signals warranting further clinical and mechanistic investigation.

PubMedBritish journal of pharmacology2026-07-25

Rosemary metabolite carnosic acid opens Kv1.1 via its voltage sensor and corrects Kv1.1-linked episodic ataxia in mice.

Manville Rían W RW, Yoshimura Ryan F RF, Nguyen Hanh A HA, Zhao Ruiming R et al.

Episodic ataxia type 1 (EA1) is an autosomal dominant neurological disorder caused primarily by loss-of-function mutations in the voltage-gated potassium channel Kv1.1 (KCNA1). Small molecules that restore Kv1.1 activity hold promise as targeted therapies for EA1, yet current pharmacological strategies remain limited. Two electrode voltage-clamp electrophysiology and the Xenopus laevis oocyte expression system were used to study effects of carnosic acid, a phenolic diterpene from Salvia rosmarinus (rosemary) leaf extract on Kv1.1-linked EA1 mutant channels. We assessed ataxia therapeutic efficacy by comparing performance of Kcna1+/+ and Kcna1E283K/+ mice, a model of human EA1, on a balance beam under isoproterenol challenge in the absence or presence of 0.3-mg·kg-1 carnosic acid. Rosemary leaf extract and rosemary metabolite carnosic acid are efficacious Kv1.1 openers. Carnosic acid fully or partially corrects heterozygous, heteromeric Kv1.1 EA1 mutant channel activity in vitro and restores normal function in Kv1.1E283K/+ mice at 0.3 mg·kg-1. Experimental validation of unbiased in silico docking reveals carnosic acid occupies a binding pocket between the S1 and S4 helices of the voltage-sensing domain (VSD) of Kv1.1. Finally, we determined the chemical properties that endow carnosic acid with the ability to open Kv1.1 channels. Our findings uncover a Kv1.1 opener with the potential to reverse EA1 and other Kv1.1-linked disorders.

PubMedPoultry science2026-07-25

Dietary glutamine modulates egg albumen and yolk composition in laying quails: effects of age.

Tomaszewska Ewa E, Kasperek Kornel K, Drabik Kamil K, Puzio Iwona I et al.

This study evaluated the effects of dietary l-glutamine (Gln) supplementation on egg composition and amino acid profiles in laying Japanese quail (Coturnix japonica). A total of 320 birds were assigned to four dietary treatments containing 0.0%, 0.5%, 1.0%, or 1.5% Gln for 12 wk. Eggs were collected at 12 and 19 wk of age, representing the early and late stages of the peak laying period, for analyses of yolk and albumen composition. Dietary Gln supplementation significantly affected the concentration of several amino acids in both yolk and albumen, although the response depended on bird age and Gln inclusion level. The effects were more pronounced in late peak-lay birds and were generally greatest at moderate supplementation levels (0.5% or 1.0% Gln). In albumen, increasing dietary Gln was associated with selective changes in amino acid composition, whereas yolk amino acid responses showed more evident age-dependent patterns. Proximate composition of egg fractions was affected to a lesser extent than amino acid profiles. Overall, the results indicate that dietary Gln modulates amino acid deposition in egg components in an age-dependent manner rather than uniformly enhancing egg nutritional value. This study demonstrates for the first time that dietary Gln supplementation can alter yolk and albumen amino acid profiles in laying quail, supporting its role as a dietary factor influencing amino acid deposition during different stages of lay.

PubMedTalanta2026-07-25

Towards selective fluorimetric nanospheres sensor for perfluorooctanoic acid anions.

Jelińska Aldona A, Kalisz Justyna J, Maksymiuk Krzysztof K, Michalska Agata A

A fluorimetric approach allowing monitoring of perfluorooctanoic acid anions concentration changes in solution is proposed. The sensing mechanism explored is based on interactions of perfluorooctanoic anions with Nile red dye on the interface of organic liquid (plasticizer) and aqueous solution embedded within the polymeric nanospheres. In the presence of perfluorooctanoic acid a new emission band appears at approximately 660 nm, accompanied by a decrease in the emission characteristic for Nile Red in the organic phase (observed in the absence of the analyte) at ca 600 nm. The ratio of emission intensities recorded was increasing for increasing analyte concentration in the solution within the range from 0.1 to 400 ppm. Interestingly, this behaviour was observed only for perfluorooctanoic acid anions, offering selectivity over other perfluoroalkyl compounds bearing longer side chains, tested in parallel (perfluoroundecanoate and perfluorotetradecanoate anions). Other relatively lipophilic inorganic anions tested (ClO4- or PF6-) were also able to interact with Nile Red within the spheres, as proven by emission spectra change, however at much higher concentrations compared to that of perfluorooctanoic acid anions.

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