色情影片

惭贰贰罢听翱鲍搁听贵础颁鲍尝罢驰
惭贰贰罢听翱鲍搁听厂迟补蹿蹿

Tony Barbosa, Ph.D.

Associate Professor of Chemistry
Email:
tony.barbosa@avemaria.edu
Phone:
(239) 280-1584
WhatsApp:
Office:
Henkels 3050

Tony Barbosa, Ph.D.

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Education

  • B.S., Chemistry, Providence College
  • M.S., Organic Chemistry, University of Rochester
  • Ph.D., Organic Chemistry, University of Rochester

About

Professional Experiences

Dr. Tony Barbosa is an Associate Professor of Chemistry and past Chair of the Department of Chemistry and Physics at 色情影片. At AMU, in addition to teaching chemistry/biochemistry courses, he works collaboratively with fellow faculty and students to design new treatments for Alzheimer's disease. Dr. Barbosa also holds a position outside the university as the Vice President of Research for where he oversees discovery efforts to develop breakthrough medicines, both small molecule and biologics, to treat solid tumors, lupus/lupus nephritis, kidney disease, muscular dystrophy, and inflammatory bowel diseases.

Dr. Barbosa has greater than twenty-five years of experience in drug discovery and development. He is the recipient of three NIH SBIR grants: 1R43AI179510 (2023) Integrin-Targeted Novel Oral Therapeutics for Lupus Nephritis - Co-Investigator ($306,500), 1R43AI100499 (2013) - Medicinal Chemistry Based Optimization of Lead Compounds Against Multiple Sclerosis ($600,000), and NIH Niche Assessment Program NIH1063TN (2014) for 1R43AI100499 (~$150,000). He is also the recipient of a Florida Cancer Innovation Fund grant to study the development of Myeloid-Targeted Immunotherapy to Treat Breast Cancer ($750,000, 2024) an Ed and Ethel Moore Alzheimer's Disease Research Program grant through the Florida State Department of Health 8AZ01 ($100,000). His focus has been in the fields of oncology and immunology & inflammation targeting diseases such as lupus/lupus nephritis, kidney disease, Alzheimer鈥檚 disease, pancreatic cancer, breast cancer, multiple sclerosis, rheumatoid arthritis, psoriasis and Crohn鈥檚 disease.

Prior to his time at Allosite Therapeutics, Dr. Barbosa was Director of Chemistry at Adhaere Pharmaceuticals where he led efforts which moved their immuno-oncology lead CD11b/CD18 (Mac-1) agonist up to clinical trials for solid tumors. () Adhaere Pharmaceuticals was then purchased by Gossamer Bio, Inc. which took the drug into clinical trials for pancreatic, esophageal, gastric, triple negative breast, castration-resistant prostate, and microsatellite stable colorectal cancers. Dr. Barbosa has extensive experience with medicinal chemistry efforts to balance optimization of efficacy, pharmacokinetics (PK) and ADME-T (adsorption, dissolution, metabolism, excretion and toxicity) properties.

Before working at Adhaere Pharma, Dr. Barbosa worked at Boehringer Ingelheim Pharmaceuticals on several classes of protein targets such as cell surface adhesion molecules (integrins), GPCRs and kinases where he is responsible for a SoPD (start of pre-development) for the integrin CD11a/CD18 (LFA-1) project. Dr. Barbosa then moved to a small pharmaceutical company, CGI Pharmaceuticals, where in addition to his in-house medicinal chemistry efforts, he was also responsible for designing scientific work for and communicating with outsourced partners internationally.

Dr. Barbosa works closely with students to help prepare them for their lives post-graduation. He has committed significant effort to organizing a web site, DrBarbosa.com, to guide students through their plans to apply for summer internships, enter graduate school, and attend medical school or other health related fields.

Family and Personal Info

Dr. Barbosa has been married for greater than 26 years to his wife, Valerie. He is also a proud father of four children. His oldest son, Antonio, is an assistant editor at EWTN in Alabama. His daughter, Grace Angel, is a graduate of AMU with a double major in Music and Accounting. He also has two teen age sons, Maximilian and John, with whom he spends time enjoying the outdoors.

No items found.
  • "Discerning the Impact of Non-Covalent Interactions via Simulated Crystal Growth: A Structural Study of Aromatic Esters" Boucher, Mairead; Bellia, Sophia; Howarth, Alexis; Collart, Anne; Musozoda , Muhammadiqboli ; Adu, Clinton; Guillet, Gary; Barbosa, Antonio; Fulvio, Pasquale ; Mirjafari, Arsalan; Zeller, Matthias; Hillesheim, Patrick Crystal Growth & Design, Submitted
  • 鈥淓xamining the Non-Covalent Interactions for Two Polymorphs of a 2,1,3-benzoxadiazole Derivative鈥 Katherine Standish, Matthias Zeller, Antonio J. Barbosa, and Patrick C. Hillesheim Crystals 2022, 12(8), 1143, 21pp., DOI: 10.3390/cryst12081143
  • 鈥淐ontrasting the Noncovalent Interactions of Aromatic Sulfonyl Fluoride and Sulfonyl Chloride Motifs via Crystallography and Hirshfeld Surfaces鈥 Sophia Bellia鈥, Lara I Teodoro鈥, Antonio J Barbosa鈥, Matthias Zeller鈥, Arsalan Mirjafari鈥, Patrick C Hillesheim ChemistrySelect 2022, 7(46), December 13, DOI: 10.1002/SLCT.202203797
  • 鈥淧yridinium 3-nitro颅benzoate鈥3-nitro颅benzoic acid鈥 Alexis Howarth, Tony J. Barbosa, Matthias Zeller and Patrick C. Hillesheim IUCrDATA ISSN: 2414-3146 Volume 6, Part 6, June 2021, x210581, DOI: 10.1107/S2414314621005812
  • 鈥淐hance and Indeterminism in Chemistry鈥, Third Annual Thomistic Philosophy and Natural Sciences Symposium, Thomistic Institute, Washington, D.C., June 16-20, 2021
  • 鈥淎lzheimer鈥檚 Update on Research and Treatments鈥, Interview on 鈥楳ade For Greatness鈥 on Maria Vision Television Station, September 21, 2021, 鈥
  • 鈥淚ntegrin agonists reduce infiltration of tumor-associated macrophages to promote T-cell mediated anti-tumor immunity鈥 Cancer Immunology Research February 2017 5(3 Supplement):B03-B03; DOI10.1158/2326-6074.TUMIMM16-B03
  • 鈥淎n integrin agonist suppresses breast cancer by reducing CD11b+ leukocytes, promoting anti-tumor immunity鈥 Cancer Research August 1 2016 76(15 Supplement) A17; DOI: 10.1158/1538-7445.TME16-A17
  • 鈥淎n integrin agonist suppresses breast cancer by reducing CD11b+ leukocytes, promoting antitumor immunity.鈥 An AACR Special Conference on The Function of Tumor Microenvironment in Cancer Progression, January 7-10, 2016, Hard Rock Hotel, San Diego, CA .
  • 鈥淒iscovery and Design of Novel Benzimidazolone Based Inhibitors of p38 MAP Kinase鈥 Bioorganic & Medicinal Chemistry Letters2006, 听16(24), 听6316-6320
  • 鈥淭oward the Development of a General Chiral Auxiliary. A Total Synthesis of (+)-Tetronolide via a Tandem Ketene-Trapping [4 + 2] Cycloaddition Strategy鈥 Journal of the American Chemical Society 听2006, 听128(32), 听10572-10588
  • 鈥淢icrowave-assisted synthesis of benzimidazolone libraries.鈥 听Abstracts of Papers, 228th ACS National Meeting, Philadelphia, PA, United States, August 22-26, 2004, ORGN-424.
  • 鈥淒iscovery and design of novel benzimidazolones as inhibitors of p38 MAP kinase.鈥 听Abstracts of Papers, 228th ACS National Meeting, Philadelphia, PA, United States, August 22-26, 2004, MEDI-218.
  • 鈥淎symmetric Lewis-acid-promoted thio-Claisen rearrangements of N,S-ketene acetals.鈥 听Book of Abstracts, 219th ACS National Meeting, San Francisco, CA, March 26-30, 2000, ORGN-014.
  • 鈥淚mprovement in physicochemical properties for a series of diaminopyrimidine based for PKC theta inhibitors.鈥 Bioorganic & Medicinal Chemistry Letters 听In Preparation.

Patents

  • Provisional Patent Application 鈥 鈥淐ompositions and Methods Involving Integrin Alpha3Beta1.鈥 PCT Int. 2022, 81pp.
  • WO2021061665A1 鈥 鈥淚ntegrin agonist prodrugs鈥 2021, 65pp.
  • WO2020205827A1 鈥 鈥淩eagents and assays using modified integrin domains.鈥, PCT Int. Appl., 2020, 84pp.
  • WO2018126072 A1 鈥 鈥淧reparation of heterocyclic integrin agonists for treatment of cancer.鈥 2018, 168pp.
  • WO2016201356 鈥 鈥淪olid Forms of (Z)-4-(5-((3-Benzyl-4-Oxo-2-Thioxothiazolidin-5-ylidene)Methyl)Furan-2-yl)Benzoic Acid.鈥 2016, 117 pp.
  • US Patent 9260415 鈥 鈥淗eteroaryl pyridone and aza-pyridone compounds with electrophilic functionality.鈥 Publication Date: February 16, 2016
  • US Patent 8748607 鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 Publication date: Jun 10, 2014
  • US Patent 8618107 鈥 鈥淧yridone and aza-pyridone compounds and methods of use.鈥 Publication date: December 31, 2013
  • US Patent 8598174 鈥 鈥淧yridazinones, Method of Making, and Method of Use Thereof.鈥 Publication date: Dec 3, 2013
  • US Patent 8575360 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid amides.鈥 Publication date: November 5, 2013
  • US Patent 8552205 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-alpha]imidazole-3-carboxylic acid amides.鈥 Publication date: October 8, 2013
  • US Patent 8455493鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 Publication date: Jun 4, 2013
  • WO2011140488 鈥 鈥淧reparation of pyridone and azapyridone compounds as Btk inhibitors for treating immune disorders, inflammation, cancer, and other Btk-mediated diseases.鈥 PCT Int. Appl, 2011, 511 pp.
  • WO2010141273 鈥 鈥淧reparation of 6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxamides as inhibitors of the interaction of ICAMs and leukointegrins.鈥 PCT Int. Appl., 2010, 131pp.
  • WO2010068810 鈥 鈥淐ertain substituted amides, method of making, and method of use thereof.鈥 PCT Int. Appl. 2010, 84 pp.
  • WO2010056875 鈥 鈥淧yridazinones and their use as BTK Inhibitors.鈥 PCT Int. Appl. 2010, 301 pp.
  • WO2010068257 鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 PCT Int. Appl. 2009, 305 pp.
  • WO2009070485 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-伪]imidazole-3- carboxylic acid amides.鈥 PCT Int. Appl. 2009, 322 pp.
  • WO2007076247 鈥 鈥淧reparation of pyrimidine derivatives useful as inhibitors of PKC-theta for treating various diseases.鈥 PCT Int. Appl. 2007, 99 pp.
  • WO2006014482 鈥 鈥淧yrimidine Derivatives Useful as Inhibitors of PKC-theta.鈥 PCT Int. Appl. 2006, 226 pp.
  • US2006025433 鈥 鈥淧reparation of pyrimidine derivatives as selective inhibitors of protein kinase C theta with therapeutic uses.鈥 U.S. Pat. Appl. Publ. 2006, 156 pp.
  • WO2004024699 鈥 鈥淧reparation of benzimidazolones as cytokine inhibitors for treating inflammation.鈥 PCT Int. Appl. 2004, 140 pp.

No items found.
  • "Discerning the Impact of Non-Covalent Interactions via Simulated Crystal Growth: A Structural Study of Aromatic Esters" Boucher, Mairead; Bellia, Sophia; Howarth, Alexis; Collart, Anne; Musozoda , Muhammadiqboli ; Adu, Clinton; Guillet, Gary; Barbosa, Antonio; Fulvio, Pasquale ; Mirjafari, Arsalan; Zeller, Matthias; Hillesheim, Patrick Crystal Growth & Design, Submitted
  • 鈥淓xamining the Non-Covalent Interactions for Two Polymorphs of a 2,1,3-benzoxadiazole Derivative鈥 Katherine Standish, Matthias Zeller, Antonio J. Barbosa, and Patrick C. Hillesheim Crystals 2022, 12(8), 1143, 21pp., DOI: 10.3390/cryst12081143
  • 鈥淐ontrasting the Noncovalent Interactions of Aromatic Sulfonyl Fluoride and Sulfonyl Chloride Motifs via Crystallography and Hirshfeld Surfaces鈥 Sophia Bellia鈥, Lara I Teodoro鈥, Antonio J Barbosa鈥, Matthias Zeller鈥, Arsalan Mirjafari鈥, Patrick C Hillesheim ChemistrySelect 2022, 7(46), December 13, DOI: 10.1002/SLCT.202203797
  • 鈥淧yridinium 3-nitro颅benzoate鈥3-nitro颅benzoic acid鈥 Alexis Howarth, Tony J. Barbosa, Matthias Zeller and Patrick C. Hillesheim IUCrDATA ISSN: 2414-3146 Volume 6, Part 6, June 2021, x210581, DOI: 10.1107/S2414314621005812
  • 鈥淐hance and Indeterminism in Chemistry鈥, Third Annual Thomistic Philosophy and Natural Sciences Symposium, Thomistic Institute, Washington, D.C., June 16-20, 2021
  • 鈥淎lzheimer鈥檚 Update on Research and Treatments鈥, Interview on 鈥楳ade For Greatness鈥 on Maria Vision Television Station, September 21, 2021, 鈥
  • 鈥淚ntegrin agonists reduce infiltration of tumor-associated macrophages to promote T-cell mediated anti-tumor immunity鈥 Cancer Immunology Research February 2017 5(3 Supplement):B03-B03; DOI10.1158/2326-6074.TUMIMM16-B03
  • 鈥淎n integrin agonist suppresses breast cancer by reducing CD11b+ leukocytes, promoting anti-tumor immunity鈥 Cancer Research August 1 2016 76(15 Supplement) A17; DOI: 10.1158/1538-7445.TME16-A17
  • 鈥淎n integrin agonist suppresses breast cancer by reducing CD11b+ leukocytes, promoting antitumor immunity.鈥 An AACR Special Conference on The Function of Tumor Microenvironment in Cancer Progression, January 7-10, 2016, Hard Rock Hotel, San Diego, CA .
  • 鈥淒iscovery and Design of Novel Benzimidazolone Based Inhibitors of p38 MAP Kinase鈥 Bioorganic & Medicinal Chemistry Letters2006, 听16(24), 听6316-6320
  • 鈥淭oward the Development of a General Chiral Auxiliary. A Total Synthesis of (+)-Tetronolide via a Tandem Ketene-Trapping [4 + 2] Cycloaddition Strategy鈥 Journal of the American Chemical Society 听2006, 听128(32), 听10572-10588
  • 鈥淢icrowave-assisted synthesis of benzimidazolone libraries.鈥 听Abstracts of Papers, 228th ACS National Meeting, Philadelphia, PA, United States, August 22-26, 2004, ORGN-424.
  • 鈥淒iscovery and design of novel benzimidazolones as inhibitors of p38 MAP kinase.鈥 听Abstracts of Papers, 228th ACS National Meeting, Philadelphia, PA, United States, August 22-26, 2004, MEDI-218.
  • 鈥淎symmetric Lewis-acid-promoted thio-Claisen rearrangements of N,S-ketene acetals.鈥 听Book of Abstracts, 219th ACS National Meeting, San Francisco, CA, March 26-30, 2000, ORGN-014.
  • 鈥淚mprovement in physicochemical properties for a series of diaminopyrimidine based for PKC theta inhibitors.鈥 Bioorganic & Medicinal Chemistry Letters 听In Preparation.

Patents

  • Provisional Patent Application 鈥 鈥淐ompositions and Methods Involving Integrin Alpha3Beta1.鈥 PCT Int. 2022, 81pp.
  • WO2021061665A1 鈥 鈥淚ntegrin agonist prodrugs鈥 2021, 65pp.
  • WO2020205827A1 鈥 鈥淩eagents and assays using modified integrin domains.鈥, PCT Int. Appl., 2020, 84pp.
  • WO2018126072 A1 鈥 鈥淧reparation of heterocyclic integrin agonists for treatment of cancer.鈥 2018, 168pp.
  • WO2016201356 鈥 鈥淪olid Forms of (Z)-4-(5-((3-Benzyl-4-Oxo-2-Thioxothiazolidin-5-ylidene)Methyl)Furan-2-yl)Benzoic Acid.鈥 2016, 117 pp.
  • US Patent 9260415 鈥 鈥淗eteroaryl pyridone and aza-pyridone compounds with electrophilic functionality.鈥 Publication Date: February 16, 2016
  • US Patent 8748607 鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 Publication date: Jun 10, 2014
  • US Patent 8618107 鈥 鈥淧yridone and aza-pyridone compounds and methods of use.鈥 Publication date: December 31, 2013
  • US Patent 8598174 鈥 鈥淧yridazinones, Method of Making, and Method of Use Thereof.鈥 Publication date: Dec 3, 2013
  • US Patent 8575360 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid amides.鈥 Publication date: November 5, 2013
  • US Patent 8552205 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-alpha]imidazole-3-carboxylic acid amides.鈥 Publication date: October 8, 2013
  • US Patent 8455493鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 Publication date: Jun 4, 2013
  • WO2011140488 鈥 鈥淧reparation of pyridone and azapyridone compounds as Btk inhibitors for treating immune disorders, inflammation, cancer, and other Btk-mediated diseases.鈥 PCT Int. Appl, 2011, 511 pp.
  • WO2010141273 鈥 鈥淧reparation of 6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxamides as inhibitors of the interaction of ICAMs and leukointegrins.鈥 PCT Int. Appl., 2010, 131pp.
  • WO2010068810 鈥 鈥淐ertain substituted amides, method of making, and method of use thereof.鈥 PCT Int. Appl. 2010, 84 pp.
  • WO2010056875 鈥 鈥淧yridazinones and their use as BTK Inhibitors.鈥 PCT Int. Appl. 2010, 301 pp.
  • WO2010068257 鈥 鈥淚midazopyrazine SYK Inhibitors.鈥 PCT Int. Appl. 2009, 305 pp.
  • WO2009070485 鈥 鈥淒erivatives of 6,7-dihydro-5H-imidazo[1,2-伪]imidazole-3- carboxylic acid amides.鈥 PCT Int. Appl. 2009, 322 pp.
  • WO2007076247 鈥 鈥淧reparation of pyrimidine derivatives useful as inhibitors of PKC-theta for treating various diseases.鈥 PCT Int. Appl. 2007, 99 pp.
  • WO2006014482 鈥 鈥淧yrimidine Derivatives Useful as Inhibitors of PKC-theta.鈥 PCT Int. Appl. 2006, 226 pp.
  • US2006025433 鈥 鈥淧reparation of pyrimidine derivatives as selective inhibitors of protein kinase C theta with therapeutic uses.鈥 U.S. Pat. Appl. Publ. 2006, 156 pp.
  • WO2004024699 鈥 鈥淧reparation of benzimidazolones as cytokine inhibitors for treating inflammation.鈥 PCT Int. Appl. 2004, 140 pp.

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