University of South Carolina 1990 - 1993
Associates
University of Illinois at Urbana - Champaign 1985 - 1990
Doctorates, Doctor of Philosophy, Philosophy, Chemistry
University of Illinois at Urbana - Champaign 1983 - 1985
Bachelors, Bachelor of Science, Chemical Engineering
Ohio Wesleyan University 1980 - 1983
Bachelors, Bachelor of Arts, Chemistry
Kevin G. Pinney - Hewitt TX George R. Pettit - Paradise Valley AZ Vani P. Mocharla - Waco TX Maria del Pilar Mejia - Evanston IL Anupama Shirali - Pune, IN
Assignee:
Baylor University Arizona Disease Control Research Commission
Methoxy and ethoxy substituted 3-aroyl-2-arylbenzo[b]thiophenes and benzo[b]thiophene analogues are described for use in inhibiting tubulin polymerization. The compounds use for treating tumor cells is also described. Additional aspects described here are certain diaryl ether benzo[b]thiophene derivatives. Also described are particular analogs derived from dihydronaphthalene which have proven particularly effective. Certain new benzofuran analogs are described, as well as certain sulfur oxide benzo[b]thiophene analogs. Important compounds described herein include the first nitrogen-containing derivatives of combretastatin. These include nitro, amino and azide combrdtastatin derivatives.
Tubulin Binding Ligands And Corresponding Prodrug Constructs
Kevin G. Pinney - Hewitt TX Vani P. Mocharla - Waco TX Zhi Chen - Hamden CT Charles M. Garner - McGregor TX Anjan Ghatak - Waco TX James M. Dorsey - Waco TX
Assignee:
Baylor University - Waco TX
International Classification:
A61K 31075
US Classification:
514721, 568633, 564443, 558197
Abstract:
A diverse set of tubulin binding ligands have been discovered which are structurally characterized, in a general sense, by a semi-rigid molecular framework capable of maintaining arylâaryl, pseudo pi stacking distances appropriate for molecular recognition of tubulin. In phenolic or amino form, these ligands may be further functionalized to prepare phosphate esters, phosphate salts, and phosphoramidates capable of demonstrating selective targeting and destruction of tumor cell vasculature.
Indole-Containing And Combretastatin-Related Anti-Mitotic And Anti-Tubulin Polymerization Agents
Kevin Pinney - Woodway TX, US Feng Wang - Jeffersonville PA, US Mallinath Hadimani - Waco TX, US
Assignee:
Baylor University - Waco TX
International Classification:
A61K 31404 C07D20912
US Classification:
514419, 548491, 548492, 548469
Abstract:
Trimethoxyphenyl substituted indole ligands have been discovered which demonstrate impressive cytotoxicity as well as a remarkable ability to inhibit tubulin polymerization. Such compounds as well as related derivatives are excellent clinical candidates for the treatment of cancer in humans. In addition, certain of these ligands, as prodrugs, may well prove to be tumor selective vascular targeting and destruction chemotherapeutic agents or to have anti-angiogenesis activity resulting in the selective prevention and/or destruction of tumor cell vasculature.
Functionalized Stilbene Derivatives As Improved Vascular Targeting Agents
David J. Chaplin - Watlington, GB Robert Ronald Kane - Waco TX, US Kevin G. Pinney - Woodway TX, US Joseph Anthony Prezioso - Boston MA, US Klaus Edvardsen - Klampenborg, DK
Assignee:
Oxigene, Inc. - Waltham MA Baylor University - Waco TX
International Classification:
A61K031/661 C07F009/09
US Classification:
514114, 558166, 558169
Abstract:
Novel stilbenoid compounds and their prodrug forms are disclosed, which serve as potent vascular targeting agents useful for the treatment of solid tumor cancers and other diseases associated with unwanted neovascularization. The novel stilbenoid compounds are tubulin-binding stilbenoid analogs structurally related to combretastatin A-1 and combretastatin A-4. The prodrug forms serve as potent vascular targeting agents (VTAs) useful for the treatment of solid tumor cancers and diseases associated with retinal neovascularization.
Compositions And Methods For Use In Targeting Vascular Destruction
Ronald W. Pero - Arlington VT, US David Sherris - Jamaica Plain MA, US Kevin G. Pinney - Woodway TX, US Vani P. Mocharla - Waco TX, US Zhi Chen - West Haven CT, US
Assignee:
Baylor University - Waco TX OXiGENE, Inc. - Waltham MA
Treatment of warm-blooded animals having a tumor or non-malignant hypervascularation, by administering a sufficient amount of a cytotoxic agent formulated into a phosphate prodrug form having substrate specificity for microvessel phosphatases, so that microvessels are destroyed preferentially over other normal tissues, because the less cytotoxic prodrug form is converted to the highly cytotoxic dephosphorylated form.
Tubulin Binding Agents And Corresponding Prodrug Constructs
Kevin G. Pinney - Woodway TX, US Vani P. Mocharla - San Diego CA, US Zhi Chen - Hamden CT, US Usha R. Ghatak, legal representative - West Bengal, IN Mallinath Hadimani - Waco TX, US Jimmy Kessler - Sugarland TX, US James M. Dorsey - Durham NC, US Klaus Edvardsen - Klampenborg, DK David J. Chaplin - Oxford, GB Joseph Prezioso - Boston MA, US
Assignee:
Oxigene, Inc. - Waltham MA Baylor University - Waco TX
International Classification:
A61K 31/075 C07C 41/00
US Classification:
514721, 568633
Abstract:
A diverse set of tubulin binding agents have been discovered which are structurally characterized, in a general sense, by a semi-rigid molecular framework capable of maintaining aryl-aryl, pseudo pi stacking distances appropriate for molecular recognition of tubulin. In phenolic or amino form, these ligands may be further functionalized to prepare phosphate esters, phosphate salts, phosphoramidates, and other prodrugs capable of demonstrating selective targeting and destruction of tumor cell vasculature.
Tubulin Binding Ligands And Corresponding Prodrug Constructs
Kevin G. Pinney - Woodway TX, US Vani P. Mocharla - Waco TX, US Zhi Chen - Hamden CT, US Charles M. Garner - Waco TX, US Mallinath Hadimani - Waco TX, US Raymond Kessler - Sugarland TX, US James M. Dorsey - Durham NC, US Klaus Edvardsen - Klampenborg, DK David J. Chaplin - Watlington, CA Joseph Prezioso - Boston MA, US Usha Ghatak, legal representative - Salt Lake City UT, US
Assignee:
Oxigene, Inc. - Watertown MA Baylor University - Waco TX
International Classification:
A61K 31/34 C07D 307/93
US Classification:
514469, 549468
Abstract:
A diverse set of tubulin binding agents have been discovered which are structurally characterized, in a general sense, by a semi-rigid molecular framework capable of maintaining aryl-aryl, pseudo pi stacking distances appropriate for molecular recognition of tubulin. In phenolic or amino form, these ligands may be further functionalized to prepare phosphate esters, phosphate salts, phosphoramidates, and other prodrugs capable of demonstrating selective targeting and destruction of tumor cell vasculature.
Functionalized Stilbene Derivatives As Improved Vascular Targeting Agents
David J. Chaplin - Watlington, GB Robert Ronald Kane - Waco TX, US Kevin G. Pinney - Woodway TX, US Joseph Anthony Prezioso - Boston MA, US Klaus Edvardsen - Klampenborg, DK
Assignee:
OXiGENE, Inc. - Waltham MA Baylor University - Waco TX
International Classification:
A61K 31/661 C07F 9/09
US Classification:
514114, 558 70, 558155, 558166, 558169
Abstract:
Novel stilbenoid compounds and their prodrug forms are disclosed, which serve as potent vascular targeting agents useful for the treatment of solid tumor cancers and other diseases associated with unwanted neovascularization. The novel stilbenoid compounds are tubulin-binding stilbenoid analogs structurally related to combretastatin A-1 and combretastatin A-4. The prodrug forms serve as potent vascular targeting agents (VTAs) useful for the treatment of solid tumor cancers and diseases associated with retinal neovascularization.
Denise Smario, Denise Hayes, Tricia Abens, Daniel Shotts, Pete Dell, Kevin Pinney, Gerald Haas, Dina Johnson, Michelle Grubbs, Beth Updike, Kyle Cox, Ronda Davis