Undecenoic acid 2% / Dibrompropamidine isetionate 0.15% cream
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 2 · 1998–2025
Showing the 50 most relevant studies, sorted by most relevant.
Susana Fernandes, Anabela Borges, Inês B. Gomes, et al.
Food Research International, 2023
Shengyu Dai, Changle Chen
Macromolecules, 2018
Hua Wei, Xianzheng Zhang, Han Cheng, et al.
Journal of controlled release : official journal of the Controlled Release Society, 2006
V. Rahman, Sayeed Mukhtar, W. H. Ansari, et al.
European journal of medicinal chemistry, 2005
Suman Rana, Suman Rana, Neena G. Shetake, et al.
Dalton transactions, 2016
A. M. Api, D. Belsito, D. Botelho, et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2018
K. Padmaja, B. Rao, R. K. Reddy, et al.
Industrial Crops and Products, 2012
Hiroki Takeshita, Akito Nishiyama, Xiuxiu Wang, et al.
Biomacromolecules, 2025
Biobased polyesters, recyclable sustainable polymers derived from renewable feedstock, are promising alternatives to petroleum-based polymers. The crystallization behavior, crystal structure, and supramolecular structures of a series of biobased long-chain aliphatic polyesters, consisting of a diester of 10-undecenoic acid with isosorbide (IS), isomannide (IM), and butanediol (BD) as the midsegments, were studied by various scattering methods and Raman spectroscopy. Polyesters containing butanediol-type midsegments (C18BD) participated in the crystallization by being incorporated into the orthorhombic polyethylene crystal lamellae. The polyesters containing isosorbide- and isomannide-type midsegments (C18IS, C18IM) were excluded from the crystal lamellae and inhibited the formation of orthorhombic crystals; the lamellar thickness was thus determined by the length of the methylene chains between the midsegments. An introduction of these midsegments (IS, IM) led to formation of some loose structures even in the molten state; acceleration of the nucleation led to a heterogeneous nucleation-like crystallization behavior, and the final spherulite size was finer.
Abstract licence: CC BY-NC-ND
C.A. Ospina-Delacruz, V. Castillo-Gallardo, D. Ariza-Flores, et al.
Materials Letters, 2023
Mai Toan, Jaehyouk Choi, Hang Thi Ngo, et al.
Polymers, 2024
Recent advancements in polymer materials have enabled the synthesis of bio-based monomers from renewable resources, promoting sustainable alternatives to fossil-based materials. This study presents a novel zwitterionic surfactant, SF, derived from 10-undecenoic acid obtained from castor oil through a four-step reaction, achieving a yield of 78%. SF has a critical micelle concentration (CMC) of 1235 mg/L, slightly higher than the commercial anionic surfactant Rhodacal DS-4 (sodium dodecyl benzene sulfonate), and effectively stabilizes monomer droplets, leading to excellent conversion and stable latex formation. The zwitterionic groups in SF enhance adhesion to hydrophilic substrates (glass, stainless steel, and skin). Films produced with SF exhibit outstanding water resistance, with only 18.48% water uptake after 1800 min, compared to 81% for the control using Rhodacal DS-4. Notably, SF maintains low water uptake across various concentrations, minimizing water penetration. Thus, the synthesized SF demonstrates improved adhesive properties and excellent water resistance in emulsion polymerization applications, highlighting its potential as a sustainable, high-performance alternative to petrochemical surfactants.
Abstract licence: CC BY
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.