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fluticasone propionate

✓ Approved

Cantabria Labs · NR3C1 · Small Molecule

What is fluticasone propionate?

fluticasone propionate is a small molecule developed by Cantabria Labs. It is approved for therapeutic indications via topical.

Drug Profile

CompanyCantabria Labs
Drug ClassSmall Molecule
Molecular TargetNR3C1
RouteTopical
StatusApproved

Mechanism of Action

Molecular Targets

fluticasone propionate acts on 1 molecular target:

NR3C1nuclear receptor subfamily 3 group C member 1 (GR, GCCR)
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Therapeutic Indications

fluticasone propionate is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
InvestigationsDermatologic examination✓ Approved

Related Research Articles

PubMedMolecular therapy. Oncology2026-08-30

StagX1, an isoquinolinone compound, selectively targets CES1-positive Ewing sarcoma cells as a potential therapeutic agent.

Zhang Nenggang N, Gilbertson Scott R SR, Li Feng F, Pati Debananda D

StagX1 {ethyl 2-[[2-[2-[(2,3-dihydro-1,4-benzodioxin-6-yl)amino]-2-oxoethyl]-1,2-dihydro-1-oxo-5-isoquinolinyl]oxy]propanoate} is a derivative of isoquinolinone, possessing an ethyl propionate. StagX1 exhibits growth-inhibitory activity in multiple Ewing sarcoma cell lines. To advance StagX1 as a potential lead, we conducted experiments to examine its metabolism and stability in tissue culture media, plasma, liver microsomes, cells and mice. Our studies demonstrate that StagX1 is metabolically unstable and undergoes rapid hydrolysis to its corresponding acid metabolite (StagX1-acid) through cleavage of the ethyl ester group. We identified carboxylesterase 1 (CES1) as the primary enzyme responsible for this conversion. Notably, cells expressing CES1 are sensitive to StagX1, whereas CES1-deficient cells show minimal response, indicating that metabolic activation is required for its activity. In contrast, StagX1-acid is metabolically stable. These findings suggest that StagX1 functions as a prodrug that is enzymatically converted to its active metabolite, StagX1-acid, within cells. This metabolic conversion likely underlies its mechanism of action and contributes to its selective anticancer activity in Ewing sarcoma. Our findings provide insight into the metabolism of StagX1 and the role of CES1 in mediating its effects and demonstrate that StagX1 is a promising compound with growth inhibitory effects in CES1 positive Ewing sarcoma cells.

PubMedCureus2026-08-30

Real-World Efficacy and Safety of a Topical Salvia fruticosa Leaf Extract Rich in Carnosic Acid and Carnosol for Mild to Very Severe Facial Seborrheic Dermatitis: A 12-Year Retrospective Study.

Kallimanis Panagiotis P, Prodromidis Serafim S

Objective We aimed to evaluate the safety and efficacy of a cream (SDπ) containing S. fruticosa leaf extract rich in carnosic acid and carnosol in the treatment of facial seborrheic dermatitis (SD). Methods In this 12-year retrospective study, 10 patients (eight males, two females; age range, 40-78 years) with mild to very severe facial seborrheic dermatitis (mean baseline Seborrheic Dermatitis Area and Severity Index (SEDASI) score: 19; range, 10-60) applied SDπ cream once nightly as monotherapy. Follow-up ranged from 6 months to 5 years. Results All patients achieved complete disease clearance (SEDASI=0) within a mean of 7.7 days (range 3-15 days) with marked reduction in erythema, scaling, and rapid relief of pruritus. Remission persisted from 20 days to 10 months. Subsequent episodes responded to re-treatment in a shorter period (mean 4.8 days), while no relapses were observed during long-term maintenance therapy with nightly or alternate-night application. No local or systemic safety concerns were documented throughout treatment and the longitudinal follow-up period. Conclusions In this retrospective observational study, SDπ cream was associated with favorable clinical outcomes and good tolerability, suggesting that it may represent a promising natural topical monotherapy for facial seborrheic dermatitis. Although these findings are encouraging, prospective randomized controlled studies are required to confirm efficacy and long-term safety. To our knowledge, this work represents the first full-length retrospective report in the literature documenting the therapeutic role of S. fruticosa leaf extract rich in carnosic acid and carnosol in seborrheic dermatitis.

PubMedMicrobiome2026-08-30

Baseline gut microbiome and metabolome profiles predict weight loss after a structured lifestyle intervention.

Seethaler Benjamin B, Basrai Maryam M, Delzenne Nathalie M NM, Walter Jens J et al.

Obesity remains a global health challenge, and responses to lifestyle-based weight-loss interventions are heterogeneous. Here, we evaluate a one-year structured lifestyle program in 50 adults with obesity (mean BMI 42 ± 7.0 kg/m2), integrating clinical, microbiome, and metabolomic profiling, to identify predictors of weight-loss success and metabolic improvement (ClinicalTrials.gov: NCT01344525). The intervention included a 3-month very low-calorie formula diet (approximately 850 kcal/day), a 3-month transition phase from a formula diet to a balanced diet (approximately 1000 kcal/day), and a 6-month maintenance period in which the participants followed a balanced diet (gradually increasing to a maximum of 2000 kcal/day). Following the intervention, the participants exhibited marked reductions in body weight, body fat percentage, C-reactive protein, and glycated hemoglobin. Longitudinal analyses revealed that shifts in the gut microbiota composition were associated with changes in clinical and anthropometric data, as well as gut barrier function. An increased abundance of Lachnospiraceae was associated with improved gut barrier function; the relationship was mediated by fecal butyrate and propionate. Multivariate analyses revealed that serum baseline levels of diacylphosphatidylcholine C40:1 predicted postintervention BMI, indicating that this metabolite could serve as a biomarker of weight loss success. A random forest model incorporating baseline microbial and clinical features was used to predict weight loss and clinical improvements with high accuracy. Our findings elucidate the interplay between the gut microbiota and host metabolism during weight loss and highlight the potential utility of baseline profiling to achieve a high success rate in personalized obesity treatment. Video Abstract.

PubMedMedical mycology journal2026-08-30

Inflammatory-Type Tinea Corporis from Trichophyton mentagrophytes Animal Type 3 with Suspected Infection from a Guinea Pig.

Hosoi Misato M, Tsuchihashi Hitoshi H, Hiruma Masataro M, Taguchi Nobuyuki N et al.

An adlescent girl was bitten on the right middle finger while attempting to intervene in a fight among her three pet guinea pigs. She was initially treated by a local physician without improvement and was subsequently referred to the Department of Dermatology at our hospital. Direct microscopic examination of scales and crusts with KOH was positive, and she was diagnosed with tinea corporis. The isolated fungus was morphologically identified as belonging to the Trichophyton mentagrophytes complex, and topical luliconazole cream was administered. Molecular analysis based on the DNA sequence of the nuclear ribosomal internal transcribed spacer (ITS) 1 region revealed that the isolate belonged to ITS type II, corresponding to T. mentagrophytes animal type 3. These findings strongly suggested zoonotic transmission from the pet guinea pigs. This appears to be one of the very few reported cases of T. mentagrophytes animal type 3 isolated from a human lesion.

PubMedDrug delivery and translational research2026-08-30

Biodegradable furylacryloyl-modified hyaluronan: in vivo evaluation and its use as a nanofibrous drug delivery system.

Brtková Barbora B, Bártová Tereza T, Piskláková Lenka L, Šimek Matěj M et al.

Furylacryloyl-modified hyaluronan (F-HA) has emerged as an appropriate material for the fabrication of UV-crosslinkable, water-stable nanofibrous scaffolds with preserved porosity. However, the safety profile and in vivo applicability of F-HA have not yet been established. In this study, we present biological assessment of F-HA, including biodegradation studies and its first in vivo evaluation in C57BL/6J mice following both intravenous and intraperitoneal administration. The results demonstrate good tolerability under the tested conditions and confirm biodegradability. Additionally, we confirm the ability of composite nanofibers consisting of F-HA with established nanofiber-forming polymers, to incorporate active pharmaceutical ingredients (API), while retaining their porous structure and favorable mechanical properties. Importantly, the incorporation of F-HA alters the release profile of embedded API. Using octenidine dihydrochloride (OCT) as a model compound, we demonstrate sustained release from F-HA/lauroyl hyaluronan (L-HA) nanofibrous scaffolds in biologically relevant protein-containing media, while retaining its structural integrity, thus supporting its suitability for biomedical applications. These findings highlight the potential of F-HA as a versatile platform for the development of advanced nanofibrous biomaterials with translational relevance in topical wound healing and drug delivery.

PubMedOrvosi hetilap2026-08-30

[Modern treatment of androgenetic alopecia].

Rózsa Petra P, Kemény Lajos L, Gyulai Rolland R

Androgenetic alopecia is the most common hair loss, characterized by a chronic and progressive course and a significant psychosocial burden. The aim of this study was to provide a comparative analysis of current international guidelines and expert consensus statements on the treatment of androgenetic alopecia and to summarize their applicability in clinical practice. A literature search was performed in the PubMed database to identify English-language guidelines and expert recommendations published between 2015 and 2025. The included documents were analyzed narratively and compared based on therapeutic approaches. Conventional treatments, including topical minoxidil and 5-alpha-reductase inhibitors, remain the cornerstone of therapy. More recent recommendations increasingly support the use of low-dose oral minoxidil and dutasteride; however, their position varies across guidelines. The role of procedural therapies also differs, mainly due to limited evidence. Differences between recommendations are primarily driven by variability in levels of evidence and the evolving new therapies. In clinical practice, an individualized, multimodal treatment strategy combined with regular follow-up is essential. The management of androgenetic alopecia is a rapidly evolving field requiring personalized therapeutic decisions. In clinical practice, a personalized combined treatment strategy and regular follow-up are of paramount importance. Orv Hetil. 2026; 167(35): 1385-1393.

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