Beijing University of Technology

Commonwealth Scientific and Industrial Research Organisation

Syngene Limited

Neuro Therapeutics Limited

Daratech Proprietary Limited

Duluxgroup (austrailia) Pty. Ltd

Australasian Drug Development Limited

Fpc Australia, Inc.

Monash University

William Roy Jackson

Andrea Jane Robinson

Maree Patricia Collis

Brad William Woonton

Milton Thomas William Hearn

Alan Duncan Robertson

Jim Patel

Bevyn Jarrott

Kirthi De Silva

Pankaj Maharjan

Alexander Serban

Christopher Henry Such

Jin Ling Chen

Frederick C Copp

Gottfried Lichti

Jomana Elaridi

Alan Frederick Elliott

Simon John Mountford

Philip Mark Beart

Paul A Horne

Daryl K Wood

Janine J Kibblewhite

Darren J Park

Glen B Deacon

Anthony G Flynn

Alan L Boura

Phillip Mark Beart

John D Cullen

Vijaya Bhaskar Kenche

Algirdas Kazimleras Serelis

Alexandra Papanikos

Kamani Rupika Subasinghe

Anjali Makarand Bhagwat

Milton T W Hearn

Clint Woodward

Nicolas Spiccia

Milton Tw Hearn

The present invention relates to a method for isolating proteins from a solution containing the proteins. The invention also relates to a method for the chromatographic separation of proteins. The present invention also relates to crosslinked hydroxylic polymer particles functionalized with temperature-responsive copolymer, and to methods of preparing such particles.

Temperature-responsive polymer particles in protein separation applications

The present invention provides processes for producing amine compounds. The amine compounds include diammonium compounds and amino acid derivatives.

Process for producing amine compounds

The present invention relates to methods for forming dicarba bridges in organic compounds. This involves the use of a pair of complementary metathesisable groups on the organic compound, and subjecting the compound to cross-metathesis under microwave radiation conditions. In an alternative, the compounds contain a turn-inducing group between the pair of cross-metathesisable groups to facilitate the cross-metathesis.

Methods for the synthesis of dicarba bridges in organic compounds

The present invention relates generally to affinity ligands and chemical affinity ligand-matrix conjugates for use as chromatographic adsorbents and methods which utilize the adsorbents in the purification of proteins by affinity chromatography. The affinity ligand-matrix conjugates of the present invention comprise ligands of general formula (I): wherein m represents an integer from 0-2, n represents an integer from 0-6, p represents an integer from 0-4, Rrepresents H or Calkyl, Ris an optional substituent, and X is the position at which the ligand is immobilized, optionally via a linker. 

Affinity ligands and methods for protein purification

The invention provides a method of preparing a crosslinked polymer, which method comprises polymerising branched polyunsaturated monomers by a metathesis polymerisation reaction, wherein the branched polyunsaturated monomers contain acyclic ethylenically unsaturated groups that are capable of undergoing polymerization by a metathesis reaction such that the metathesis polymerisation produces a crosslinked polymer and substantially no non-volatile ethylenically unsaturated by-products.

Crosslinking method

The present disclosure concerns compounds of formula (I) and pharmaceutically acceptable salts, hydrates, solvates, pharmaceutically acceptable derivatives, pro-drugs, tautomers and/or isomers thereof. The disclosure also relates to processes for the preparation of compounds according to formula (I), pharmaceutical or veterinary compositions containing such compounds or methods of treatment and/or prophylaxis of a condition or symptom that is inhibited, reduced or alleviated by opioid receptor activation 

Derivatives of morphine-like opioid compounds

This invention relates to compounds to formula (1) wherein B is optionally substituted aryl; Rand Rare the same or different and are independently selected from hydrogen or Calkyl; n is 1 or 2, preferably n is 1; m is 0 or 1; Ris hydrogen or acyl, Rand Rare the same or different and are independently selected from amino, alkylamino, dialkylamino, arylamino and C-Ccycloalkylamino; X and Y are independently selected from C, H or N provided at least one of X and Y is N; and salts thereof, solvates thereof, pharmaceutically acceptable derivatives thereof, prodrugs thereof, tautomers thereof and/or isomers thereof, and processes for their reparation and methods of treatment, pharmaceutical formulations and uses involving them.

Pharmaceutical agents

Arylalkylpiperazine compounds as antioxidants

Controlled release composition of biocide in an aqueous dispersion of

A process for preparing ferrous picrate comprising reacting picric acid in solution in a straight- or a branched-chain aliphatic alcohol with an iron carbonyl at a temperature between 10.degree. C. and 120.degree. C.

Manufacture of ferrous picrate

##STR1## A compound of general formula (I), wherein X=CH.sub.2, O, S or NR.sup.4, and Y=formula (II): where R.sup.1 =H, lower alkyl or an aryloxyalkyl group, wherein the aryl group is optionally substituted by alkyl, alkoxy, hydrogen, alkyl substituted by hydrogen, and n is an integer between 0 and 5, and Z=O, S or NR.sup.2 ; wherein R.sup.2 =H, lower alkyl, hydroxy, amino cyano or acyl, R.sup.3 =H, or lower alkyl, and R.sup.4 =H, lower alkyl, or lower acyl, and pharmaceutically acceptable salts thereof.

1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino-[1,2-a]azepino derivatives

Growing community of inventors

Camberwell, Australia

William Roy Jackson