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Treatment regimen for administration of phenylacetylglutamine, phenylacetylisoglutamine, and/or phenylacetate

InactiveUS6943192B2High plasma concentrationFull penetrationBiocidePeptide/protein ingredientsDiseasePhenylacetylglutamine
Herein is disclosed a method of treating neoplastic disease, including cancer, comprising administering a pharmaceutical composition, the pharmaceutical composition comprising a highly concentrated aqueous solution of phenylacetylglutamine and phenylacetylisoglutamine in a 4:1 ratio, at an infusion rate of from 100 mL / hr to 400 mL / hr. In a further embodiment, herein is also disclosed a method of treating neoplastic disease, including cancer, comprising administering a pharmaceutical composition, the pharmaceutical composition comprising a highly concentrated aqueous solution of phenylacetate and (phenylacetylglutamine or phenylacetylisoglutamine) in a 4:1 ratio, at an infusion rate of from 100 mL / hr to 400 mL / hr. Herein are also disclosed the pharmaceutical compositions used in the above methods.
Owner:BURZYNSKI STANISLAW R

Preparation of functionalized anionic polymerization initiators

A process for preparing a functionalized polymerization initiator, the process comprising combining a functionalized styryl compound and an organolithium compound.
Owner:BRIDGESTONE CORP

Biodegradable targetable microparticle delivery system

Copolymers designed for use as particulate carriers containing functionalizable amino acid subunits for coupling with targeting ligands are described. The copolymers are polyesters composed of α-hydroxy acid subunits such as D,L-lactide and pseudo-α-amino acid subunits which may be derived from serine or terpolymers of D,L-lactide and glycolide and pseudo-α-amino acid subunits which may be derived from serine. Stable vaccine preparations useful as delayed release formulations containing antigen or antigens and adjuvants encapsulated within or physically mixed with polymeric microparticles are described. The particulate carriers are useful for delivering agents to the immune system of a subject by mucosal or parenteral routes to produce immune responses, including antibody and protective responses.
Owner:SOKOLL KENNETH K +2

Methods of treating inflammation

InactiveUS20090105281A1Increase therapeutic indexReduction and/or alleviationBiocideOrganic active ingredientsRelated disorderInflammation
Owner:UNIV OF CONNECTICUT

N-myristoyl transferase inhibitors

ActiveUS9156811B2Improve permeabilityRapid onset of activityBiocideAntimycoticsN-myristoyltransferaseBiochemistry
Owner:UNIVERSITY OF DUNDEE

Novel screening method

InactiveUS20070077607A1Maintain functionPrevent extensive cell deathMicrobiological testing/measurementBiological material analysisLead compoundDrug
The present invention provides a method for identifying a drug-like compound, or lead compound for the development of a drug-like compound, which is capable of modulating cellular adhesion and / or cell survival comprising the step of testing said compound for an ability to modulate the binding of a complex of tissue transglutaminase and fibronectin to a heparan sulfate containing receptor. In particular, there is provided a method for identifying a compound for use in the curative and / or prophylactic treatment of a proliferative disorder or with efficacy in promoting wound healing and / or cell survival, and compounds identified by such methods.
Owner:ASTON UNIV
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