Iriny B.

Principal Scientist at Iambic Therapeutics
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Contact Information
us****@****om
(386) 825-5501
Location
United States, US

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Simon P.

I had the pleasure of working with Iriny and would have no hesitation in recommending her as a diligent, hard working,very able yet modest chemist. Iriny exhibited full lab independence and always had exemplary productivity. She excels at the ability to produce synthetic output with minimal supervision, and would be a great asset to any team.

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Experience

    • United States
    • Biotechnology Research
    • 1 - 100 Employee
    • Principal Scientist
      • Oct 2021 - Present

    • United States
    • Biotechnology Research
    • 1 - 100 Employee
    • Research Scientist II
      • Aug 2021 - Oct 2021

    • Research Scientist I
      • Apr 2019 - Aug 2021

    • United States
    • Biotechnology Research
    • 100 - 200 Employee
    • Research Scientist
      • May 2018 - Apr 2019

  • Dart NeuroScience
    • Greater San Diego Area
    • Senior Associate Scientist
      • Oct 2011 - Feb 2018

      • Designed and advanced a lead compound from a library hit to pre-clinical candidate status. • Synthesized more than one thousand novel compounds to optimize the ADME and pharmacokinetics properties. • Optimized synthetic routes to prepare advanced intermediates to explore SAR of promising cores more efficiently through the library approach. • Independently designed and proposed new compound targets based on structure activity relationship and ADME data. • Demonstrated expertise in… Show more • Designed and advanced a lead compound from a library hit to pre-clinical candidate status. • Synthesized more than one thousand novel compounds to optimize the ADME and pharmacokinetics properties. • Optimized synthetic routes to prepare advanced intermediates to explore SAR of promising cores more efficiently through the library approach. • Independently designed and proposed new compound targets based on structure activity relationship and ADME data. • Demonstrated expertise in the targeting of challenging CNS targets. • Delivered gram quantities of advanced compounds on time for various in-vivo and in-vitro studies. • Regular presentation and discussion of synthesis, SAR and DMPK results within multidisciplinary meetings. Show less • Designed and advanced a lead compound from a library hit to pre-clinical candidate status. • Synthesized more than one thousand novel compounds to optimize the ADME and pharmacokinetics properties. • Optimized synthetic routes to prepare advanced intermediates to explore SAR of promising cores more efficiently through the library approach. • Independently designed and proposed new compound targets based on structure activity relationship and ADME data. • Demonstrated expertise in… Show more • Designed and advanced a lead compound from a library hit to pre-clinical candidate status. • Synthesized more than one thousand novel compounds to optimize the ADME and pharmacokinetics properties. • Optimized synthetic routes to prepare advanced intermediates to explore SAR of promising cores more efficiently through the library approach. • Independently designed and proposed new compound targets based on structure activity relationship and ADME data. • Demonstrated expertise in the targeting of challenging CNS targets. • Delivered gram quantities of advanced compounds on time for various in-vivo and in-vitro studies. • Regular presentation and discussion of synthesis, SAR and DMPK results within multidisciplinary meetings. Show less

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior Scientist
      • Sep 2003 - Aug 2011

      • Contributed to many projects in different therapeutic areas, including Diabetes, Ophthalmology and Oncology. • Designed, synthesized and purified compounds as well as interpretation of appropriate analytical data (NMR, LC/MS, EA, HPLC). • Optimization of key reactions. • Delivered compounds on time for in vivo studies which involved multistep (>10) synthesis. • Utilized structure activity relationship, HTS hits, and medicinal chemistry principles to design synthetic targets… Show more • Contributed to many projects in different therapeutic areas, including Diabetes, Ophthalmology and Oncology. • Designed, synthesized and purified compounds as well as interpretation of appropriate analytical data (NMR, LC/MS, EA, HPLC). • Optimization of key reactions. • Delivered compounds on time for in vivo studies which involved multistep (>10) synthesis. • Utilized structure activity relationship, HTS hits, and medicinal chemistry principles to design synthetic targets for lead discovery. • Optimization of structures to address issues of target potency, selectivity, and animal pharmacokinetics. • Utilized PMC approach, and the microwave reactor to increase productivity and to explore the SAR of a series in a timely manner. • Optimized and screened palladium-catalyzed coupling reactions to enable library production. • Managed outsourced projects through proposing viable synthetic routes, and keeping the project team updated with the progress of the outsourced packets frequently. • Contributed to patent applications through preparation of the experimental details and interpretation of analytical data. • Communication of chemistry progress to the project team through regular presentations in meetings and contributing to the monthly report. • Participated in ISO/OHSAS audit interview to ensure safe and clean environment at the work place. Show less • Contributed to many projects in different therapeutic areas, including Diabetes, Ophthalmology and Oncology. • Designed, synthesized and purified compounds as well as interpretation of appropriate analytical data (NMR, LC/MS, EA, HPLC). • Optimization of key reactions. • Delivered compounds on time for in vivo studies which involved multistep (>10) synthesis. • Utilized structure activity relationship, HTS hits, and medicinal chemistry principles to design synthetic targets… Show more • Contributed to many projects in different therapeutic areas, including Diabetes, Ophthalmology and Oncology. • Designed, synthesized and purified compounds as well as interpretation of appropriate analytical data (NMR, LC/MS, EA, HPLC). • Optimization of key reactions. • Delivered compounds on time for in vivo studies which involved multistep (>10) synthesis. • Utilized structure activity relationship, HTS hits, and medicinal chemistry principles to design synthetic targets for lead discovery. • Optimization of structures to address issues of target potency, selectivity, and animal pharmacokinetics. • Utilized PMC approach, and the microwave reactor to increase productivity and to explore the SAR of a series in a timely manner. • Optimized and screened palladium-catalyzed coupling reactions to enable library production. • Managed outsourced projects through proposing viable synthetic routes, and keeping the project team updated with the progress of the outsourced packets frequently. • Contributed to patent applications through preparation of the experimental details and interpretation of analytical data. • Communication of chemistry progress to the project team through regular presentations in meetings and contributing to the monthly report. • Participated in ISO/OHSAS audit interview to ensure safe and clean environment at the work place. Show less

    • Research Associate
      • Jan 2000 - Sep 2003

      • Contributed to multiple kinase projects including c-Met as a key team player through synthesis, purification, and characterization of novel chemical entities. • Investigated reaction routes for construction of patented, novel c-Met kinase inhibitors. • Designed synthetic routes and executed the synthesis of analogs for lead optimization. • Purified final compounds through flash chromatography, preparative HPLC or crystallization. • Characterized final compounds, using HPLC, NMR… Show more • Contributed to multiple kinase projects including c-Met as a key team player through synthesis, purification, and characterization of novel chemical entities. • Investigated reaction routes for construction of patented, novel c-Met kinase inhibitors. • Designed synthetic routes and executed the synthesis of analogs for lead optimization. • Purified final compounds through flash chromatography, preparative HPLC or crystallization. • Characterized final compounds, using HPLC, NMR, and LC/MS for purity, before submitting for biochemical screening. • Contributed over 300 compounds to support the medicinal chemistry effort in different projects. Show less • Contributed to multiple kinase projects including c-Met as a key team player through synthesis, purification, and characterization of novel chemical entities. • Investigated reaction routes for construction of patented, novel c-Met kinase inhibitors. • Designed synthetic routes and executed the synthesis of analogs for lead optimization. • Purified final compounds through flash chromatography, preparative HPLC or crystallization. • Characterized final compounds, using HPLC, NMR… Show more • Contributed to multiple kinase projects including c-Met as a key team player through synthesis, purification, and characterization of novel chemical entities. • Investigated reaction routes for construction of patented, novel c-Met kinase inhibitors. • Designed synthetic routes and executed the synthesis of analogs for lead optimization. • Purified final compounds through flash chromatography, preparative HPLC or crystallization. • Characterized final compounds, using HPLC, NMR, and LC/MS for purity, before submitting for biochemical screening. • Contributed over 300 compounds to support the medicinal chemistry effort in different projects. Show less

Education

  • Alexandria University
    BS, Chemistry
    1992 - 1996

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