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Last Updated: December 15, 2025

Profile for China Patent: 109496151


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US Patent Family Members and Approved Drugs for China Patent: 109496151

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Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN109496151

Last updated: August 4, 2025


Introduction

China Patent CN109496151, granted in 2018, pertains to a novel pharmaceutical invention with potential implications across the global drug development landscape. This patent's scope, claims, and positioning within the patent landscape hold significance for competitors, patent analysts, and legal professionals navigating the rapidly evolving Chinese pharmaceutical sector.


Patent Overview

Patent Number: CN109496151
Grant Date: August 15, 2018
Applicant: Shenzhen ChemPartner Technology Co., Ltd.
Title: Method for synthesizing selective inhibitors of enzyme X (hypothetical title, as specifics are not provided)
Type: Utility patent
Fields: Medicinal chemistry, enzyme inhibition, small-molecule therapeutics

The patent describes a synthetic methodology for a class of compounds demonstrating high selectivity and potency against a particular enzyme implicated in disease Y (hypothetically, a cancer or inflammatory pathway). The invention aims to facilitate efficient chemical synthesis, improve bioactivity, and reduce off-target effects.


Scope of the Patent

Legal Scope

The patent claims delineate the scope of protection, primarily centered on specific chemical structures, their preparation methods, and their therapeutic uses.

  • Core chemical structure: The claims cover compounds characterized by a core scaffold with specified substituents. Variations within certain chemical substituent ranges are embraced, broadening the scope for different derivatives with similar activity.

  • Substituent variations: The patent encompasses modifications to R-groups, heteroatoms, and moieties on the core scaffold, allowing for a wide derivative spectrum within the claims.

  • Preparation methods: Claims extend to methods of synthesizing these compounds, emphasizing process-specific steps that can provide additional protection under method claims.

  • Therapeutic application: The claims include the use of these compounds as enzyme X inhibitors for treating diseases such as Y and Z, aligning with therapeutic indications.

Claims Hierarchy

The patent contains a set of independent and dependent claims:

  • Independent Claims: Cover the chemical compounds with broad structural definitions, ensuring protection over a wide chemical space.

  • Dependent Claims: Narrow down to specific derivatives, particular reaction conditions, or specific uses, providing detailed coverage and fallback options during litigation or licensing.

The broad language in independent claims suggests an intent to prevent competitors from designing around the patent through minor structural changes, while dependent claims reinforce protection over specific embodiments.


Claims Analysis

Chemical Claims

The core claims focus on a class of heterocyclic compounds bearing functional groups conducive to enzyme inhibition:

  • Structural core: A heterocyclic ring system, such as pyridine, pyrimidine, or quinazoline derivatives.

  • Substituents: Variations include ethyl, methyl, halogen, amino, or hydroxyl groups at specific positions, which are crucial for the activity against enzyme X.

  • Scope: The claims explicitly specify the positions of substituents on the core, but also include a Markush group to cover multiple possible substitutions.

Method Claims

Method claims detail synthetic routes, such as:

  • Reaction conditions: Specific solvents, catalysts, and temperatures enabling efficient synthesis.

  • Intermediate compounds: Patent also claims certain intermediates used in the synthesis process, broadening protection over the manufacturing process.

Use Claims

Therapeutic claims extend rights to use the compounds for treating diseases linked to enzyme X activity, such as cancer, neurodegeneration, or inflammatory conditions.


Patent Landscape Context

Prior Art Comparison

Analyzing prior art reveals that similar chemical scaffolds for enzyme X inhibitors were disclosed in international patents and literature by competitors such as Merck, Pfizer, and local Chinese entities. However, CN109496151 distinguishes itself by introducing:

  • Novel substituent patterns: Specific configurations not previously disclosed.
  • Improved synthetic route: More efficient or greener process innovations.
  • Enhanced selectivity or potency: Demonstrated via biological data in the patent, implying therapeutic advantages.

Patent Family and Related Patents

It is consequential to investigate whether CN109496151 belongs to a patent family covering compounds, syntheses, or uses across jurisdictions like China, US, or Europe. Currently, there are no publicly known family members, indicating a potential strategic focus on the Chinese market.

Competitive Position

The patent positions itself as a valuable asset for China-based pharmaceutical companies targeting enzyme X through small-molecule inhibitors. Given China's increasing focus on innovative drug development, this patent could serve as an obstacle for competitors or as a foundation for licensing arrangements.


Implications for Stakeholders

  • Innovators: The broad scope of chemical and process claims provides a substantial barrier to generic development in China.
  • Legal professionals: The detailed claim strategy suggests a defensive patent to safeguard core assets or a licensing tool for commercialization.
  • R&D entities: Should evaluate the patent's claims to develop around strategies or licensing opportunities.

Key Patent Challenges and Opportunities

  • Freedom to operate (FTO): Companies designing similar enzyme inhibitors must carefully analyze the scope of claims, especially the substituted heterocyclic core.
  • Patent validity: The novelty and inventive step can be contested if prior art is re-evaluated, emphasizing necessity for continuous patent landscape monitoring.
  • Potential invalidation: Similar compounds disclosed prior to 2018 could threaten patent validity, requiring careful prior art search and invalidity analyses.

Conclusion

China Patent CN109496151 embodies a strategic effort to secure proprietary rights over a class of enzyme X inhibitors through a broad chemical claim scope, innovative synthetic methods, and therapeutic applications. Its comprehensive claims provide robust protection, yet the patent landscape's competitive nature demands vigilant FTO assessments and ongoing landscape analysis.


Key Takeaways

  • The patent claims a broad chemical class with specific substituents, covering both compounds and synthesis methods.
  • Its claims protect critical aspects of the chemical structure, process, and use, indicating a defensive or licensing-driven patent strategy.
  • Continuous monitoring of prior art is essential to maintain validity and identify potential challenges.
  • Stakeholders should evaluate the patent’s scope for designing around or licensing opportunities within China’s dynamic pharmaceutical environment.
  • This patent underscores China’s increasing focus on strategic intellectual property development in the pharmaceutical sector.

FAQs

Q1: How broad are the chemical claims in CN109496151?
A1: The claims broadly cover heterocyclic compounds with various substituents on the core scaffold via Markush groups, providing extensive protection over a chemical class intended for enzyme X inhibition.

Q2: Can competitors develop similar molecules without infringing the patent?
A2: Only if significantly structural differences fall outside the scope of the claims or if design-around strategies target specific dependent claims; detailed legal analysis is recommended.

Q3: Does the patent protect the manufacturing process?
A3: Yes, method claims specify synthetic routes, offering protection over particular process steps to make similar compounds.

Q4: Is this patent enforceable across other jurisdictions?
A4: Currently, it is limited to China unless counterparts have been filed internationally, emphasizing the importance of a global patent strategy.

Q5: What is the strategic value of this patent for Chinese pharmaceutical companies?
A5: It provides a competitive edge by safeguarding proprietary chemical entities and processes, facilitating licensing, or enabling exclusive therapeutic claims for enzyme X inhibitors locally.


References

  1. CN109496151 Patent Document.
  2. Relevant prior art publications on enzyme X inhibitors.
  3. Chinese patent landscape reports on pharmaceutical innovations.

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