Phillip Dan Cook - Fallbrook CA Haoyun An - Carlsbad CA Tingmin Wang - San Marcos CA Muthiah Manoharan - Carlsbad CA
Assignee:
ISIS Pharmaceuticals, Inc. - Carlsbad CA
International Classification:
C07H 2100
US Classification:
536 253
Abstract:
The present invention is directed to nucleoside monomers wherein the 3â-O atom is replaced with a methylene group. The present invention also provides oligomers comprising a plurality of such monomers which are linked by methylenephosphonate linkages. Further, methods of preparing monomers and oligomers according to the present invention are provided.
C3²-Methylene Hydrogen Phosphonate Oligomers And Related Compounds
The present invention is directed to nucleoside monomers wherein the 3â-O atom is replaced with a methylene group. The present invention also provides oligomers comprising a plurality of such monomers which are linked by methylene phosphonate linkages. Further, methods of preparing monomers and oligomers according to the present invention are provided.
Phillip Dan Cook - Escondido CA Haoyun An - Encinitas CA
Assignee:
ISIS Pharmaceuticals, Inc. - Carlsbad CA
International Classification:
G01N 3353
US Classification:
435 71, 546298
Abstract:
Compositions comprising novel chemical libraries are prepared. The compositions of the present invention are useful as antibacterial and other pharmaceutical agents and as intermediates for preparation of other pharmaceutical agents. In addition, compounds of the present invention are useful as research reagents.
Conformationally restricted 2â, 4â-bridged nucleoside analogues are described herein. The compounds can be prepared by cyclization at C2â and C4â of nucleosides through a linker or linking molecule. These novel nucleosides have a desired, locked sugar pucker and are potentially useful as pharmaceutical ingredients, and especially for use in treatment of HCV.
Inhibitors For De Novo-Rna Polymerases And Methods Of Identifying Targets For Same
Nanhua Yao - Irvine CA, US Haoyun An - Carlsbad CA, US Todd Appleby - Laguna Niguel CA, US Shahul Nilar - Irvine CA, US Yili Ding - Fountain Valley CA, US Zhi Hong - Aliso Viejo CA, US
A polymerase inhibitor has first moiety coupled to a second moiety via an optional linker in which the first moiety binds to an initiation nucleotide binding site of a polymerase and forms at least two hydrogen bonds with an RNA template strand that is associated with the polymerase, and in which the second moiety comprised a compound that binds to a site proximal to the nucleotide binding site of the polymerase and thereby increases the affinity of the polymerase inhibitor to the polymerase.
C3′ -Methylene Hydrogen Phosphonate Oligomers And Related Compounds
The present invention is directed to nucleoside monomers wherein the 3′-O atom is replaced with a methylene group. The present invention also provides oligomers comprising a plurality of such monomers which are linked by methylene phosphonate linkages. Further, methods of preparing monomers and oligomers according to the present invention are provided.
Weijian Zhang - Irvine CA, US William Ricketts - Irvine CA, US Haoyun An - Carlsbad CA, US Zhi Hong - Aliso Viejo CA, US
Assignee:
Valeant Research & Development - Costa Mesa CA
International Classification:
C07D 275/03 A61K 31/425
US Classification:
548206, 548213, 548214, 514372
Abstract:
Substituted isothiazole compounds and compositions are provided, wherein particularly preferred compositions and methods are directed towards inhibition of various protein kinases (especially MEK and/or ERK). Consequently, particularly preferred methods include treatment of diseases associated with abnormality in MEK and/or ERK function.
Granlen LLC since Jan 2009
President
Acea Biosciences Mar 2004 - Dec 2008
Director of Chemistry and Pharmaceuticals
ACON Laboratories & Azure Institute Mar 2004 - Oct 2006
Director of Chemistry
Valeant Pharmaceuticals Feb 2001 - Mar 2004
Head of Chemistry Department
ICN Pharmaceuticals Feb 2001 - 2003
Associate Director of Chemistry
Education:
University of Virginia 1993 - 1995
postdoc, Synthetic Organic and Bioorganic ChemistryAccomplished total synthesis of three natural and new anti-tumor antibiotics Bleomycins in 48 steps each; Synthesized natural product alkylresorcinols as DNA cleaving agents; Synthesized dinucleotide (pdCpA), and amino-acylated dinucleotides for protein modification.
Brigham Young University 1988 - 1992
Ph. D., Synthetic Organic Chemistry
Zhengzhou University 1977 - 1985
MS, Chemistry
Skills:
Medicinal synthetic combinatorial bioorganic and physical organic chemistry formulation pharmaceutical science and drug quality Natural product total synthesis small molecule heterocyclic macrocyclic organo-phosphorus carbohydrate glycopeptide nucleoside nucleotide triphosphate prodrug amino acid chemistry area immunogens bioreagents superchelating agents Anticancer antimitotic antimetabolic antiviral anti-TB antibacterial and antisense areas
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