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Last Updated: December 16, 2025

Profile for Australia Patent: 2013314303


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US Patent Family Members and Approved Drugs for Australia Patent: 2013314303

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 29, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2013314303

Introduction
Australian patent AU2013314303, granted on June 24, 2015, pertains to a novel pharmaceutical invention. This patent encompasses unique chemical compounds and their specific applications, with implications for therapeutic development in the pharmaceutical sector. A detailed examination of its scope, claims, and patent landscape provides valuable insights for stakeholders in drug development, licensing, and competitive intelligence.


1. Patent Overview and Technical Field
Patent AU2013314303, titled “Substituted 2-Aminoimidazoline Compounds,” relates to chemical entities that exhibit potential bioactivity. The patent falls within the chemotherapeutic and medicinal chemistry domain, with particular emphasis on compounds exhibiting anti-microbial, anti-cancer, or anti-inflammatory activity. It claims a class of substituted 2-aminoimidazoline derivatives, emphasizing their novelty in structure and potential biological utility.


2. Scope of the Patent

2.1 Core Chemical Framework
The patent claims cover a broad class of 2-aminoimidazoline derivatives characterized by specific substitutions on the core structure. The core scaffold is defined as a 2-aminoimidazoline ring system with variable substituents at designated positions, allowing for extensive structural diversity. This class aims to cover molecules with modifications that enhance bioavailability, efficacy, or specificity.

2.2 Variability and Generality in Claims
The claims incorporate a hierarchical set of embodiments, ranging from specific compounds to a generic class defined by variable groups (e.g., R1-R4). The breadth is designed to prevent competitors from designing around the patent by minor structural modifications. Explicit ranges for substituents, such as alkyl, aryl, heteroaryl groups, are included, increasing the scope's comprehensiveness.

2.3 Therapeutic and Use-Related Claims
In addition to compound claims, the patent also claims methods of use, including methods of treating certain diseases (e.g., bacterial infections, cancer) using the claimed compounds. These claims augment the patent's protective scope by covering both composition and method therapies.


3. Claims Analysis

3.1 Independent Claims
The independent claims typically define the core chemical structures bearing the substituted 2-aminoimidazoline ring and the methods for their synthesis and use. For instance, Claim 1 may stipulate a compound with a core structure and certain substituents, while Claim 10 might describe a method of treatment involving these compounds. These broad claims are designed to establish the foundational scope of the patent.

3.2 Dependent Claims
Dependent claims specify particular embodiments, such as specific substituents, broader pharmacological applications, or synthesis methods. They serve to reinforce the patent’s protection by covering narrower, potentially more commercially valuable compounds or applications.

3.3 Claim Language and Limitations
The patent employs precise chemical language, including Markush groups, to delineate the scope. Limitations, such as specific stereochemistry or purity levels, restrict scope but also ensure enforceability. The language aims to balance breadth with specificity to withstand validity challenges.


4. Patent Landscape and Prior Art Considerations

4.1 Similar Patents and Overlapping Technologies
The landscape includes prior patents on aminoimidazoline derivatives, anti-microbial agents, and kinase inhibitors. For example, WO2008005894 discloses aminoimidazoline compounds with similar structural motifs. However, AU2013314303 differentiates itself through unique substitution patterns and claimed therapeutic utilities.

4.2 Patentability and Novelty
The patent’s novelty hinges on specific structural modifications and their unexpected biological activities. The applicants likely demonstrated that these compounds exhibit superior efficacy or selectivity over prior art. The claims are crafted to encompass these innovative features, thereby strengthening patentability.

4.3 Freedom-to-Operate (FTO) and Landscape Strategies
Given the competitive research sector around aminoimidazoline compounds, FTO considerations require thorough review of the existing patent corpus. The broad language of AU2013314303 offers a significant defensive position but warrants vigilant monitoring of subsequent filings that could challenge or narrow its scope.


5. Patent Lifecycle and Enforcement

5.1 Term and Exclusivity
Australian standard patent terms extend 20 years from the filing date, suggesting commercial rights potentially last until at least 2033, assuming maintenance fees are paid. This duration supports R&D investments and potential licensing opportunities.

5.2 Enforceability and Limiting Factors
Enforceability depends on the clarity and specificity of claims, and potential validity challenges may arise if prior art is found to anticipate or render the claims obvious. Strategic patent prosecution and ongoing patent landscape monitoring are essential.


6. Impact on Drug Development and Market

The patent’s protection facilitates investment into the development of targeted anti-microbial or anti-cancer therapies. Its broad claim scope allows patent holders to explore various indications, formulation types, and combination therapies, fostering innovation while establishing market exclusivity.


Key Takeaways

  • Broad Chemical Coverage: AU2013314303 graces a wide chemical space within substituted 2-aminoimidazoline compounds, offering extensive protection for various derivatives.
  • Strategic Use Claims: Inclusion of method-of-use claims broadens therapeutic applicability and fortifies the patent’s commercial leverage.
  • Landscape Positioning: Differentiation from prior art is based on unique substitutions and biological utilities, emphasizing the importance of comprehensive patent drafting.
  • Lifecycle and Enforcement: The patent lifespan aligns well with commercial drug development timelines, offering substantial market protection if maintained.
  • Legal and Competitive Considerations: Vigilant landscape surveillance and potential challenge readiness are critical for maintaining patent robustness and FTO assurance.

FAQs

1. What specific compounds does AU2013314303 claim?
The patent claims a broad class of substituted 2-aminoimidazoline derivatives, defined by variable substituents at certain positions on the core scaffold. Exact chemical structures are detailed in the specification, covering diverse chemical variants aimed at therapeutic application.

2. How does this patent differ from previous aminoimidazoline patents?
The uniqueness lies in specific substitution patterns that confer particular biological activities not disclosed in prior art. These modifications potentially result in improved efficacy, selectivity, or pharmacokinetics.

3. Can the claims be challenged based on prior art?
Yes. The breadth of chemical claims can be challenged if prior art discloses similar compounds or if obvious modifications are identified. The patent’s validity depends on demonstrating novelty and inventive step over existing disclosures.

4. What is the strategic significance of method claims in this patent?
Method claims extend protection to therapeutic use, manufacturing processes, and treatment protocols, providing broad commercial coverage and reducing infringement risks.

5. What are the implications for pharmaceutical companies targeting similar compounds?
Companies must carefully analyze the patent’s claims for potential infringement risks or opportunities for licensing. The broad scope offers a competitive barrier but also emphasizes the need for designing around these claims or challenging their validity through prior art searches.


Sources

[1] Patent AU2013314303, “Substituted 2-Aminoimidazoline Compounds.”
[2] WIPO Patent Database, Worldwide Patent Search.
[3] Patent landscape reports on aminoimidazoline derivatives and anti-microbial agents.
[4] Australian Patent Office Guidelines for Patentability and Claim Drafting.


Conclusion
AU2013314303 provides a comprehensive patent framework protecting a broad class of substituted 2-aminoimidazoline compounds with potential therapeutic benefits. Its strategic claims and positioning in the patent landscape facilitate innovation, safeguard market exclusivity, and influence subsequent patenting and commercial efforts within the domain of bioactive compounds. For stakeholders, understanding its scope and legal standing is critical for making informed decisions on development, licensing, and litigation strategies in the evolving pharmaceutical patent landscape.

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