Anti-Infective Drugs
Support for antibiotics, antivirals, and antifungal agents, with emphasis on parent-drug exposure, renal excretion, tissue penetration, stability, and infection-associated response markers.
View Category →Explore analytical support by therapeutic area, drug class, parent compound, metabolite, pathway, or service need. This library connects drug-centered research questions with LC-MS/MS quantification, MetID, PK exposure profiling, biomarker readouts, and customized method development.
Start from a parent compound or drug class, then connect to relevant metabolites and analytical needs.
Link drug exposure with pathway-associated readouts for mechanism and response interpretation.
Map study goals to quantification, MetID, PK support, DDI, or multi-analyte panel services.
This library category maps out our validated LC-MS/MS assay workflows across diverse therapeutic classes. Researchers can immediately review mature protocols tailored to their specific parent compound, target metabolites, and challenging biological matrices.
Start with the disease or therapeutic area most relevant to your study, such as oncology, anti-infective, CNS, cardiovascular, endocrine, or natural product research.
Narrow the scope to representative drug families, parent drugs, active metabolites, degradation products, or related pathway-associated analytes.
Connect your target analytes and matrices with quantification, MetID, parent-metabolite ratio analysis, DDI, PK support, or biomarker measurement.
Each reference entry delivers multi-dimensional pharmacokinetic and bioanalytical insights, evaluating target analytes from core parent drug clearance to downstream metabolite identification and biomarker pathways.
Use representative parent compounds as the starting point for drug-specific bioanalysis, PK support, and study planning.
Track major metabolites, active forms, inactive products, degradation products, and pathway-relevant intermediates.
Evaluate relevant matrices and exposure patterns across plasma, serum, urine, tissue, tumor, brain, bile, or cell samples.
Support metabolite identification through targeted LC-MS/MS, HRMS profiling, phase I/II characterization, and structural confirmation.
Connect drug exposure with mechanism-related readouts, including inflammatory, immune, hormone, metabolic, neural, and tumor markers.
Explore our tailor-made DMPK and bioanalytical screening strategies sorted by therapeutic area, addressing unique drug clearance mechanisms, tissue distribution profiles, and disease-specific biomarker readouts.
Support for antibiotics, antivirals, and antifungal agents, with emphasis on parent-drug exposure, renal excretion, tissue penetration, stability, and infection-associated response markers.
View Category →Analytical support for cytotoxic agents, targeted therapies, biologics, ADCs, and PROTACs, focusing on tumor exposure, active metabolites, pathway inhibition, and PK/PD-linked biomarkers.
View Category →Bioanalytical support for cardiovascular drug classes, including plasma exposure analysis, active metabolite quantification, CYP/transporter-related DDI assessment, and functional cardiovascular readouts.
View Category →Support for CNS-active compounds requiring plasma–brain exposure assessment, active metabolite analysis, neurotransmitter-related biomarkers, and low-level bioanalytical method development.
View Category →Services for NSAIDs, opioids, anesthetics, and controlled drug classes, including parent–metabolite ratio analysis, glucuronide metabolite quantification, and pain or inflammation-associated readouts.
View Category →Support for antidiabetic agents, thyroid-related drugs, steroid hormones, and metabolic disease compounds, linking drug exposure with hormone-axis and metabolic biomarker readouts.
View Category →High-sensitivity analytical support for immunosuppressive agents with narrow exposure ranges, CYP3A/P-gp interactions, metabolite monitoring needs, and immune pathway-related biomarkers.
View Category →Support for gastrointestinal and hepatobiliary drug studies involving hepatic metabolism, bile-related matrices, acid-suppression agents, bile acid-related analytes, and liver-associated biomarkers.
View Category →Analytical support for natural product-derived compounds, complex mixtures, phase II conjugates, gut microbiota-related metabolites, and low-abundance bioactive components.
View Category →Across therapeutic categories, Creative Proteomics can support quantitative, mechanistic, and method-development needs using LC-MS/MS, HRMS, targeted metabolomics, and matrix-aware bioanalytical workflows.
Parent-drug and metabolite quantification is often the primary entry point for DMPK studies. Assays can be designed around target analytes, expected concentration range, and matrix complexity.
Support for metabolite identification, phase I/phase II characterization, parent-metabolite ratio analysis, and reactive metabolite screening.
CYP inhibition, induction, time-dependent inhibition, and transporter interaction bioanalysis for mechanism-linked exposure questions.
Therapeutic class panels, preclinical PK panels, parent-metabolite panels, and high-sensitivity multiplex quantification.
Custom LC-MS/MS methods, HPLC-UV development, matrix-specific sample preparation, and full, partial, or cross-validation.
Whether the project starts from a known drug, investigational compound, metabolite, degradation product, or pathway biomarker, the workflow can be aligned with the target analyte and study objective.
Share the parent drug, compound class, metabolite, pathway, or biomarker of interest.
Clarify whether the study involves plasma, serum, urine, tissue, tumor, brain, bile, cell lysate, or another matrix.
Choose targeted LC-MS/MS, HRMS profiling, MetID, multi-analyte panels, or custom method development.
Optimize extraction, chromatography, mass transitions, calibration, LLOQ, precision, and matrix effects as needed.
Receive quantitative outputs, MetID interpretation, method notes, QC summaries, and project-specific reporting.
Share your matrix type, sample count, and expected range—feasibility routing will confirm whether direct quantification is fit-for-purpose or method development is recommended.
Want to browse compounds, matrices, and assay coverage? Explore the Library →