Boston University Boston, MA 1976 M.B.A.MIT Boston, MA 1967 Doctoral in ChemistryUniversity of New South Wales 1966 Doctoral in ChemistryBirmingham University 1965 Ph.D. in ChemistryBirmingham University Bachelor of Science in Chemistry
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
A cyanine dye having the formula wherein R -R are each independently selected from a group consisting of hydrogen, C -C alkyl group, and C -C alkyl group having a hydrophilic substituent thereon. R and R are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27904 C07D41704 C07D27762 C07D27760 C07D26352
US Classification:
548152
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 --R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27916 C07D24136 C07D41704 C07D27760 C07D40302
US Classification:
544 51
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27904 C07D41704 C07D27762 C07D27760 C07D26352
US Classification:
48152
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
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