Suzanne C. Aldous - Gillette NJ, US John Ziqi Jiang - Hillsborough NJ, US Jinqi Lu - Somerville NJ, US Liang Ma - Hillsborough NJ, US Lan Mu - Bedminster NJ, US Harry Randall Munson - Annandale NJ, US Jeffrey Stephen Sabol - Bridgewater NJ, US Sukanthini Thurairatnam - Bedminster NJ, US Christopher Loren Vandeusen - East Windsor NJ, US
Suzanne C Aldous - Gillette NJ, US Michael W Fennie - East Stroudsburg PA, US John Z Jiang - Hillsborough NJ, US Stanly John - Basking Ridge NJ, US Lan Mu - Basking Ridge NJ, US Brian Pedgrift - Flemington NJ, US James R Pribish - Piscataway NJ, US Barbara S Rauckman - Flemington NJ, US Jeffrey S Sabol - Bridgewater NJ, US Grzegorz T Stoklosa - Hillsborough NJ, US Sukanthini Thurairatnam - Bedminster NJ, US Christopher Loren Vandeusen - East Windsor NJ, US
Paul Wender - Menlo Park CA, US Jonathan Rothbard - Cupertino CA, US Lee Wright - Redwood City CA, US Erik Kreider - Sunnyvale CA, US Christopher VanDeusen - Columbus OH, US
Assignee:
CellGate, Inc. - Sunnyvale CA
International Classification:
A61K038/16 C12N015/85
US Classification:
514/012000, 435/455000
Abstract:
The present invention provides compositions and methods for enhancing transport of biologically active compounds across biological membranes and across and into animal epithelial or endothelial tissues. The composition includes a biologically active agent and a transport moiety. The transport moiety includes a structure selected from the group consisting of (ZYZ)Z, (ZY)Z, (ZYY)Z and (ZYYY)Z. Subunit “Z” is L-arginine or D-arginine, and subunit “Y” is an amino acid that does not comprise an amidino or guanidino moiety. Subscript “n” is an integer ranging from 2 to 10. The method for enhancing transport involves the administration of the aforementioned composition.
Bi-Directional Synthesis Of Oligoguanidine Transport Agents
Paul Wender - Menlo Park CA, US Christopher VanDeusen - Mountain View CA, US Kanaka Pattabiraman - Menlo Park CA, US Erin Pelkey - Phelps NY, US Theodore Jessop - Palo Alto CA, US
International Classification:
C07H005/06 C08B037/00
US Classification:
530/317000, 530/324000, 536/018700
Abstract:
Synthesis routes that can be adapted to large scale synthesis of oligoguanidine compounds such as oligoarginine compounds are described which use a perguanidinylation step to convert a group of -amino groups to the corresponding guanidinyl groups. These compounds find utility as transport agents. Modified oligoguanidine compounds are also described.
Bi-Directional Synthesis Of Oligoguanidine Transport Agents
Paul Wender - Menlo Park CA, US Christopher VanDeusen - East Windsor NJ, US Kanaka Pattabiraman - Palo Alto CA, US Erin Pelkey - Phelps NY, US Theodore Jessop - Princeton NJ, US
Synthesis routes that can be adapted to large scale synthesis of oligoguanidine compounds such as oligoarginine compounds are described which use a perguanidinylation step to convert a group of ω-amino groups to the corresponding guanidinyl groups. These compounds find utility as transport agents. Modified oligoguanidine compounds are also described.
Paul A. Wender - Menlo Park CA, US Jonathan B. Rothbard - Cupertino CA, US Lee Wright - Redwood City CA, US Erik L. Kreider - Sunnyvale CA, US Christopher L. VanDeusen - Columbus OH, US
International Classification:
A61K 38/16 A61K 38/10 A61K 38/08 A61P 43/00
US Classification:
514 12, 514 17, 514 16, 514 15, 514 14, 514 13
Abstract:
The present invention provides compositions and methods for enhancing transport of biologically active compounds across biological membranes and across and into animal epithelial or endothelial tissues. The composition includes a biologically active agent and a transport moiety. The transport moiety includes a structure selected from the group consisting of (ZYZ)Z, (ZY)Z, (ZYY)Z and (ZYYY)Z. Subunit “Z” is L-arginine or D-arginine, and subunit “Y” is an amino acid that does not comprise an amidino or guanidino moiety. Subscript “n” is an integer ranging from 2 to 10. The method for enhancing transport involves the administration of the aforementioned composition.
Christopher L. VANDEUSEN - East Windsor NJ, US Franz J. WEIBERTH - Ringoes NJ, US Harpal S. GILL - Lambertville NJ, US George LEE - Somerville NJ, US Andrea HILLEGASS - Nazareth PA, US
This invention is directed to a compound of formula (I):wherein R1, R2 and R3 are as defined herein, a pharmaceutical composition comprising the compound, intermediates and processes for making said compounds, and the use of the compound to treat allergic and/or inflammatory disorders, particularly disorders such as allergic rhinitis, asthma, chronic obstructive pulmonary disease (COPD) and age-related macular degeneration (AMD).
Chromene Derivatives As Inhibitors Of Tcr-Nck Interaction
Christopher Vandeusen (1989-1993), Joyce Hutchison (1953-1964)
Googleplus
Christopher Vandeusen
Lived:
Washington, DC Marysville, MI Ann Arbor, MI Detroit, MI Cambridge, MA
Work:
US Patent & Trademark Office - Patent Examiner (2009)
Education:
The George Washington University - Economics, University of Michigan - Materials Engineering
Relationship:
In_a_relationship
About:
I'm 25 and I live in DC. I work at the US Patent Office. I love music and am also mildy obsessed with: economics, Detroit, coffee, flying, most media, and swimming. Grad School: workin' on it.