About
Activity
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Excited to announce Pfizer's partnership with Triana Biomedicines! Looking forward to a productive partnership to impact patient lives. Thanks to…
Excited to announce Pfizer's partnership with Triana Biomedicines! Looking forward to a productive partnership to impact patient lives. Thanks to…
Liked by Chris O'Donnell
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Big news today for TRIANA! Announcing a research collaboration with Pfizer to Discover novel molecular glue degraders https://lnkd.in/exAGkn68
Big news today for TRIANA! Announcing a research collaboration with Pfizer to Discover novel molecular glue degraders https://lnkd.in/exAGkn68
Liked by Chris O'Donnell
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I am honored and humbled to share the most exciting news on today's FDA approval of Vorasidenib. https://lnkd.in/eXXXrye5 I am so grateful to having…
I am honored and humbled to share the most exciting news on today's FDA approval of Vorasidenib. https://lnkd.in/eXXXrye5 I am so grateful to having…
Liked by Chris O'Donnell
Experience & Education
Publications
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A facile synthesis of 2,3-azaisoindoline
Tetrahedron Lett. 2010, 51 (45), 5859-5860
https://doi.org/10.1016/j.tetlet.2010.08.091
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A General Route to the Synthesis of 1,5-Methano- and 1,5-Ethano-2,3,4,5-tetrahydro-1H-3-benzazepines
J. Org. Chem. 2004, 69, 5756
DOI: 10.1021/jo049122q
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A PTK7-targeted antibody-drug conjugate reduces tumor-initiating cells and induces sustained tumor regressions
Sci. Transl. Med. 2017, eaag2611
DOI: 10.1126/scitranslmed.aag2611
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Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active gamma-secretase inhibitor
J. Med. Chem. 2012, 55 (7), 3414-24
DOI: 10.1021/jm300094u
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Aza-Cope Rearrangement-Mannich Cyclizations for the Formation of Complex Tricyclic Amines: Stereocontrolled Total Synthesis of ()-Gelsemine
J. Am. Chem. Soc. 2005, 127, 18046
DOI: 10.1021/ja055710p
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Biosynthetic engineering and fermentation media development leads to gram-scale production of spliceostatin natural products in Burkholderia sp.
Metab. Eng. 2016, 33, 67-75
https://doi.org/10.1016/j.ymben.2015.11.003
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Cyclic Hydropyran Oligolides as Preorganized Ligand Arrays: Cumulative Effects of Structural Elements on Shape and Cation Binding
J. Am. Chem. Soc. 1995, 117, 12649
DOI: 10.1021/ja00155a035
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Cytotoxic spliceostatins from Burkholderia sp. and their semisynthetic analogs
Nat. Prod. 2014, 77 (8), 1864-1870
DOI: 10.1021/np500342m
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Design and synthesis of dihydrobenzofuran amides as orally bioavailable, centrally active γ-secretase modulators
Bioorg. Med. Chem. Lett. 2012, 22 (8), 2906-2911
https://doi.org/10.1016/j.bmcl.2012.02.059
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Design of Pyridopyrazine-1,6-dione γ-Secretase Modulators that Align Potency, MDR Efflux Ratio, and Metabolic Stability
ACS Medicinal Chemistry Letters 2015, 6 (5), 596-601
DOI: 10.1021/acsmedchemlett.5b00070
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Design, Synthesis, and Cytotoxic Evaluation of Novel Tubulysin Analogues as ADC Payloads.
ACS Medicinal Chemistry Letters 2016, 7, 999-1004
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Design, Synthesis, and Pharmacological Evaluation of a Novel Series of Pyridopyrazine-1,6-dione γ-Secretase Modulators
J. Med. Chem. 2014, 57 (3), 1046-1062
DOI: 10.1021/jm401782h
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Design, synthesis, and pharmacological evaluation of azetedine and pyrrolidine derivatives as dual norepinephrine reuptake inhibitors and 5-HT(1A) partial agonists
Bioorg. Med. Chem. Lett. 2011, 21 (2), 865-8
https://doi.org/10.1016/j.bmcl.2010.11.066
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Development of Solid-Phase Site-Specific Conjugation and Its Application toward Generation of Dual Labeled Antibody and Fab Drug Conjugates
Bioconjugate Chem. 2016, 27 (4), 1030-1039
DOI: 10.1021/acs.bioconjchem.6b00054
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Discovery and Characterization of a Novel Dihydroisoxazole Class of α-Amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) Receptor Potentiators
J. Med. Chem. 2013, 56 (22), 9180-9191
DOI: 10.1021/jm401274b
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Discovery of 4-(5-Methyloxazolo[4,5-b]pyridin-2-yl)-1,4-diazabicyclo[3.2.2]nonane (CP-810,123), a Novel α7 Nicotinic Acetylcholine Receptor Agonist for the Treatment of Cognitive Disorders in Schizophrenia: Synthesis, SAR Development, and in vivo Efficacy
J. Med. Chem. 2010, 53, 1222-1237
DOI: 10.1021/jm9015075
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Discovery of cytotoxic dolastatin 10 analogues with N-terminal modifications
J. Med. Chem. 2014, 57 (24), 10527-43
DOI: 10.1021/jm501649k
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High-throughput screening in embryonic stem cell-derived neurons identifies potentiators of alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate-type glutamate receptors
J. Biol. Chem. 2010, 285 (22), 17209-17
doi:10.1074/jbc.M109.098814
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Identification of a Potent, Highly Selective, and Brain Penetrant Phosphodiesterase 2A Inhibitor Clinical Candidate
J. Med. Chem. 2018, 61 (3), 1001-1018
DOI: 10.1021/acs.jmedchem.7b01466
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Identification of α7 nicotinic acetylcholine receptor agonists for their assessment in improving cognition in schizophrenia
RSC Drug Discovery Ser. 2011, 4 (Accounts in Drug Discovery), 332-362
http://dx.doi.org/10.1039/9781849731980-00332
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Investigational antibody drug conjugates for solid tumors
Expert Opin. Invest. Drugs 2011, 20, 1131-1149
https://doi-org.proxy1.athensams.net/10.1517/13543784.2011.582866
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Location matters: site of conjugation modulates stability and pharmacokinetics of antibody drug conjugates
Chem. Biol. 2013, 20 (2), 161-7
https://doi.org/10.1016/j.chembiol.2013.01.010
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Long-term tumor regression induced by an antibody-drug conjugate that targets 5T4, an oncofetal antigen expressed on tumor-initiating cells
Mol Cancer Ther 2013, 12 (1), 38-47
DOI: 10.1158/1535-7163.MCT-12-0603
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Metabolism-Directed Design of Oxetane-Containing Arylsulfonamide Derivatives as γ-Secretase Inhibitors
J. Med. Chem. 2011, 54, 7772-7783
DOI: 10.1021/jm200893p
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Molecular Basis of Valine-Citrulline-PABC Linker Instability in Site-Specific ADCs and Its Mitigation by Linker Design
Mol. Cancer Ther. 2016, 15 (5), 958-970
DOI: 10.1158/1535-7163.MCT-15-1004
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Multivalent peptidic linker enables identification of preferred sites of conjugation for a potent thialanstatin antibody drug conjugate.
PLoS One 2017, 12 (5), e0178452/1-e0178452/16
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Natural Product Splicing Inhibitors: A New Class of Antibody-Drug Conjugate (ADC) Payloads
Bioconjugate Chem. 2016, 27 (8), 1880-1888
DOI: 10.1021/acs.bioconjchem.6b00291
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New cytotoxic benzosuberene analogs. Synthesis, molecular modeling and biological evaluation
Bioorg. Med. Chem. Lett. 2013, 23 (24), 6688-6694
https://doi.org/10.1016/j.bmcl.2013.10.039
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Novel Anti-TM4SF1 Antibody-Drug Conjugates with Activity against Tumor Cells and Tumor Vasculature
Mol. Cancer Ther. 2015, 14 (8), 1868-1876
DOI: 10.1158/1535-7163.MCT-15-0188
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Optimization of Tubulysin Antibody-Drug Conjugates: A Case Study in Addressing ADC Metabolism
ACS Medicinal Chemistry Letters 2016, 7, 977-982
DOI: 10.1021/acsmedchemlett.6b00195
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RN927C, a site-specific trop-2 antibody-drug conjugate (ADC) with enhanced stability, is highly efficacious in preclinical solid tumor models
Mol. Cancer Ther. 2016, 15 (11), 2698-2708.
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Selective Mesylation of Vicinal Diols: A Systematic Case Study
J. Org. Chem. 1998, 63, 8614
DOI: 10.1021/jo981532p
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Site Selection: a Case Study in the Identification of Optimal Cysteine Engineered Antibody Drug Conjugates
AAPS Journal 2017, 19 (4), 1123-1135
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Spliceostatin hemiketal biosynthesis in Burkholderia spp. is catalyzed by an iron/α-ketoglutarate-dependent dioxygenase
Proc. Natl. Acad. Sci. U. S. A. 2014, 111 (33), E3376-E3385
https://doi.org/10.1073/pnas.1408300111
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Synthesis and SAR studies of 1,4-diazabicyclo[3.2.2]nonane phenyl carbamates - subtype selective, high affinity α7 nicotinic acetylcholine receptor agonists
Bioorg. Med. Chem. Lett. 2009, 19 (16), 4747-4751
https://doi.org/10.1016/j.bmcl.2009.06.059
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Synthesis of 3-methoxy-9-(3,4,5-trimethoxyphenyl)-6,7-dihydro-5H-benzo[7]annulen-4-ol, a potent antineoplastic benzosuberene derivative for anti-cancer chemotherapy
Tetrahedron Lett. 2012, 53 (1), 64-66
https://doi.org/10.1016/j.tetlet.2011.10.145
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Synthesis of Cyclic Hydropyran Oligolides with Convergent Amine, Amide, Phosphonate and Furan Appendages
Tetrahedron Lett. 1997, 38, 2593
https://doi.org/10.1016/S0040-4039(97)00422-X
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Synthetic Approaches to the 2007 New Drugs
Mini Rev. Med. Chem. 2008, 8, 1526-48
DOI: 10.2174/138955708786786435
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Synthetic approaches to the 2008 new drugs
Mini-Rev. Med. Chem. 2009, 9 (14), 1655-1675
DOI: 10.2174/138955709791012201
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Synthetic approaches to the 2009 new drugs
Bioorg. Med. Chem. 2011, 19 (3), 1136-1154
https://doi.org/10.1016/j.bmc.2010.12.038
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Synthetic approaches to the 2010 new drugs
Bioorg. Med. Chem. 2012, 20 (3), 1155-1174
https://doi.org/10.1016/j.bmc.2011.12.049
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Synthetic approaches to the 2011 new drugs
Bioorg. Med. Chem. 2013, 21 (11), 2795-2825
https://doi.org/10.1016/j.bmc.2013.02.061
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Synthetic approaches to the 2012 new drugs
Bioorg. Med. Chem. 2014, 22 (7), 2005-2032
https://doi.org/10.1016/j.bmc.2014.02.017
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Synthetic approaches to the 2013 new drugs
Bioorg. Med. Chem. 2015, 23 (9), 1895-1922
https://doi.org/10.1016/j.bmc.2015.02.056
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Synthetic approaches to the 2014 new drugs
Bioorg. Med. Chem. 2016, 24 (9), 1937-1980
https://doi.org/10.1016/j.bmc.2016.03.004
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Synthetic Approaches to the New Drugs Approved During 2015
J. Med. Chem. 2017, 60 (15), 6480-6515
DOI: 10.1021/acs.jmedchem.7b00010
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Synthetic Approaches to the New Drugs Approved During 2015
J. Med. Chem. 2017, 60 (15), 6480-6515
DOI: 10.1021/acs.jmedchem.7b00010
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Template Macrolactonization of Trichloroethyl Ester Derivatives Catalyzed by Potassium Salts
J. Org. Chem. 1998, 63, 2715
DOI: 10.1021/jo970942v
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The Discovery and Characterization of the α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA) Receptor Potentiator N-{(3S,4S)-4-[4-(5-Cyano-2-thienyl)phenoxy]tetrahydrofuran-3-yl}propane-2-sulfonamide (PF-04958242)
J. Med. Chem. 2015, 58 (10), 4291-4308
DOI: 10.1021/acs.jmedchem.5b00300
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Thiophosgene
Encyclopedia of Reagents for Organic Synthesis, Leo A. Paquette, Ed.; Wiley, V7, p4881-3
DOI: 10.1002/047084289X.rt103
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Total Synthesis of ()-Gelsemine
Angew. Chem., Int. Ed. Eng. 1999, 38, 2934
DOI: 10.1002/(SICI)1521-3773(19991004)38:19<2934::AID-ANIE2934>3.0.CO;2-L
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Tumor Cells Chronically Treated with a Trastuzumab-Maytansinoid Antibody-Drug Conjugate Develop Varied Resistance Mechanisms but Respond to Alternate Treatments
Mol. Cancer Ther. 2015, 14 (4), 952-963
DOI: 10.1158/1535-7163.MCT-14-0862
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Use of the Intramolecular Heck Reaction for Forming Congested Quaternary Carbon Stereocenters. Stereocontrolled Total Synthesis of ()-Gelsemine
J. Am. Chem. Soc. 2005, 127, 18054
DOI: 10.1021/ja055711h
More activity by Chris
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Great to see #STORMTherapeutics featured in Labiotech.eu's summary of 'Six epigenetics companies making strides in 2024', highlighting STORM's…
Great to see #STORMTherapeutics featured in Labiotech.eu's summary of 'Six epigenetics companies making strides in 2024', highlighting STORM's…
Liked by Chris O'Donnell
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We are delighted to share that #STORMTherapeutics is featured in the Medical Technology Magazine 'ASCO 2024 unveils practice - changing research in…
We are delighted to share that #STORMTherapeutics is featured in the Medical Technology Magazine 'ASCO 2024 unveils practice - changing research in…
Liked by Chris O'Donnell
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I think they are on to something good here! Great job to the team at Storm!!
I think they are on to something good here! Great job to the team at Storm!!
Shared by Chris O'Donnell
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📰 News alert 📰 #STORM presented interim Phase 1 clinical data on its first-in-class lead product #STC15 at the American Society of Clinical…
📰 News alert 📰 #STORM presented interim Phase 1 clinical data on its first-in-class lead product #STC15 at the American Society of Clinical…
Liked by Chris O'Donnell
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I am pleased to share the latest edition of the "Synthetic Approaches..." annual drug review is now out in J. Med. Chem. I remember reading this…
I am pleased to share the latest edition of the "Synthetic Approaches..." annual drug review is now out in J. Med. Chem. I remember reading this…
Liked by Chris O'Donnell
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PFIZER MED DESIGN PUBLICATION: I've always loved the arrow push on a 1,3-dipolar cycloaddition, so I really couldn't resist this paper from our La…
PFIZER MED DESIGN PUBLICATION: I've always loved the arrow push on a 1,3-dipolar cycloaddition, so I really couldn't resist this paper from our La…
Liked by Chris O'Donnell
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Who makes the world go round? These two do! Thanks for bringing your A-Game EVERY day. @Christine(Wenzel)Petersen @HeatherHamilton
Who makes the world go round? These two do! Thanks for bringing your A-Game EVERY day. @Christine(Wenzel)Petersen @HeatherHamilton
Liked by Chris O'Donnell
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Congratulations Simon Kerry and Ali Tavassoli!
Congratulations Simon Kerry and Ali Tavassoli!
Liked by Chris O'Donnell
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Delighted to have Curve Therapeutics join our portfolio companies and to be joining the Board of Directors. So looking forward to working with this…
Delighted to have Curve Therapeutics join our portfolio companies and to be joining the Board of Directors. So looking forward to working with this…
Liked by Chris O'Donnell
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SKY-0515 is a small molecule RNA splicing modifier developed through our novel SKYSTAR® platform. Having successfully advanced through single…
SKY-0515 is a small molecule RNA splicing modifier developed through our novel SKYSTAR® platform. Having successfully advanced through single…
Liked by Chris O'Donnell
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I'm a judge at this year's BWB Awards! Learn more about this year's awards and submit your free nomination towards 10 life science categories by…
I'm a judge at this year's BWB Awards! Learn more about this year's awards and submit your free nomination towards 10 life science categories by…
Liked by Chris O'Donnell
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