Inventor

BOGER DALE L

US40 patents

⚠️ This page may combine multiple inventors who share the name “BOGER DALE L”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

BOGER DALE L

SCRIPPS RESEARCH INST

CBI analogs of CC-1065 and the duocarmycins

iso-CBI and iso-CI analogs of CC-1065 duocarmycins

Inhibitors of fatty acid amide hydrolase

Analogs of duocarmycin and cc-1065

ISO-CBI and ISO-CI analogs of CC-1065 and the duocarmycins

Analogs of CC-1065 and the duocarmycins

Template for solution phase synthesis of combination libraries

Inhibitors of oleamide hydrolase

Inhibitors of fatty acid amide hydrolase

Sandramycin analogs

Synthesis of CC-1065/duocarmycin analogs

Inhibitors of gap junction communication

MCBI analogs of CC-1065 and the duocarmycins

Combinatorial libraries of molecules and methods for producing same

Inhibitors of fatty acid amide hydrolase

Ningalin B analogs employable for reversing multidrug resistance

Methods for inhibiting angiogenesis and tumor growth

Inhibitors of oleamide hydrolase

Oxazole ketones as modulators of fatty acid amide hydrolase

Inhibitors of fatty acid amide hydrolase

Oxadiazole ketone inhibitors of fatty acid amide hydrolase

Inhibition of angiogenesis and tumor growth

Convergent synthesis of combinatorial library

Methods for inhibiting angiogenesis and tumor growth

Selective potentiation of serotonin receptor subtypes

Serotonin potentiation by oleamide analogs

Diprovocims: a new and potent class of TLR agonists

Neoseptins: small molecule adjuvants

N-(hydrophobe-substituted) vancosaminyl [Ψ-[C(=NH) NH] Tpg4] vancomycin and [Ψ-[CH2NH]Tpg4] vancomycin

Cyclic prodrugs of duocarmycin analogs

Tetracyclic inhibitors of fatty acid amide hydrolase

Process for antibody combining site-catalyzed SYN elimination in the formation of a CIS olefin

BOGER DALE L

Alpha-ketoheterocycles and methods of making and using

Glycopeptide antibiotic analogs effective against vancomycin-resistant bacterial strains

Alpha-keto heterocycles as FAAH inhibitors

10′-fluorinated Vinca alkaloids provide enhanced biological activity against MDR cancer cells

Substituted oxazole ketone modulators of fatty acid amide hydrolase

Tricyclic inhibitors of fatty acid amide hydrolase

ABIDE THERAPEUTICS INC

Pyrazole compounds and methods of making and using same

BRISTOL MYERS SQUIBB CO

Seco-cyclopropapyrroloindole compounds, antibody-drug conjugates thereof, and methods of making and use