Novartis institutes for biomedical research (nibr)
Nov 2018
Position:
Global head oncology and immuno-oncology chemistry at novartis institutes
Education
Degree:
Doctorates, Doctor of Philosophy
School / High School:
Dyson School of Design Engineering
1998 to 2000
Skills
Drug Discovery • Medicinal Chemistry • Drug Development • Drug Design • Purification • Organic Synthesis • Organic Chemistry • Pharmaceutical Industry • Life Sciences • Lead Change • High Throughput Screening • Chemistry • Lc Ms • Hplc • Lifesciences • Oncology • Clinical Development
Languages
French • English • German
Industries
Pharmaceuticals
Resumes
Global Head Oncology And Immuno-Oncology Chemistry At Novartis Institutes
Novartis Institutes For Biomedical Research (Nibr)
Global Head Oncology and Immuno-Oncology Chemistry at Novartis Institutes
Novartis Institutes For Biomedical Research (Nibr) Dec 2016 - Oct 2018
Director Medicinal Chemistry
Novartis Institutes For Biomedical Research (Nibr) Oct 2018 - Oct 2018
Novartis Leading Scientist
Novartis Institutes For Biomedical Research (Nibr) Jun 2011 - Nov 2016
Group Leader
Novartis Institutes For Biomedical Research (Nibr) Nov 2009 - Jun 2011
Senior Research Investigator
Education:
Dyson School of Design Engineering 1998 - 2000
Doctorates, Doctor of Philosophy
Imperial College London
Skills:
Drug Discovery Medicinal Chemistry Drug Development Drug Design Purification Organic Synthesis Organic Chemistry Pharmaceutical Industry Life Sciences Lead Change High Throughput Screening Chemistry Lc Ms Hplc Lifesciences Oncology Clinical Development
Sejal Patel - Lexington MA, US Justin Mao - North Reading MA, US Qian Lui - Malden MA, US Rui Zheng - Chestnut Hill MA, US Tyler Harrison - Somerville MA, US Rohit Duvadie - Arlington MA, US Xin Chen - Lexington MA, US Frederic Zecri - Brookline MA, US Jay Larrow - Cambridge MA, US Xuchun Zheng - Changshu, CN Yizong Zhou - Changshu, CN Jiong Ye - Changshu, CN Yiping Ding - Changshu, CN Yu Gai - Changshu, CN
The invention relates to compounds of formula (I):useful for treating disorders mediated by acyl coA-diacylglycerol acyl transferase 1 (DGAT1), e.g. metabolic disorders. The invention also provides methods of treating such disorders, and compounds and compositions etc. for their treatment.
Dihydro-Benzo-Oxazine And Dihydro-Pyrido-Oxazine Derivatives
Novartis AG - Basel, CH Sylvie CHAMOIN - Saint Louis, FR Pascal FURET - Thann, FR Klemens HOGENAUER - Oberwil, CH Konstanze HURTH - Lorrach, DE Christoph KALIS - Gundelfingen, DE Karen KAMMERTOENS - Village-Neuf, FR Ian LEWIS - Riehen, CH Henrik MOEBITZ - Freiburg, DE Alexander Baxter SMITH - Niffer, FR Nicolas SOLDERMANN - Village-Neuf, FR Romain WOLF - Schlierbach, FR Frederic ZECRI - Brookline MA, US
Assignee:
NOVARTIS AG - Basel
International Classification:
A61K 31/538 C07D 413/14
US Classification:
5142305, 544105
Abstract:
The invention relates to dihydro-benzo-oxazine and dihydro-pyrido-oxazine compounds of the formula (I) and/or pharmaceutically acceptable salts and/or solvates thereof,wherein Y, V, W, U, Q, R, R, Rand Rare as defined in the description. Such compounds are suitable for the treatment of a disorder or disease which is mediated by the activity of the PI3K enzymes.
Lipids And Lipid Compositions For The Delivery Of Active Agents
- BASEL, CH Delai CHEN - Cambridge MA, US Gabriel GAMBER - Cambridge MA, US Andrew GEALL - Cambridge MA, US Kevin LOVE - Somerville MA, US Thomas ZABAWA - Cambridge MA, US Frederic ZECRI - Cambridge MA, US
This invention provides for a compound of formula (I):or a pharmaceutically acceptable salt thereof, wherein R-R, L, n and p are defined herein. The compounds of formula (X) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
Novel Fatty Acids And Their Use In Conjugation To Biomolecules
- Basel, CH Avirup BOSE - Marlborough MA, US Alexandra Marshall BRUCE - Cambridge MA, US Alokesh DUTTAROY - Marlborough MA, US Chikwendu IBEBUNJO - Newton MA, US Aaron KANTER - Somerville MA, US Louise Clare KIRMAN - Swampscott MA, US Changgang LOU - Somerville MA, US Aimee Richardson USERA - Winchester MA, US Ken YAMADA - Brookline MA, US Jun YUAN - Boston MA, US Frederic ZECRI - Brookline MA, US
The invention provides a conjugate comprising a biomolecule linked to a fatty acid via a linker wherein the fatty acid has the following Formulae A1, A2 or A3:
- Basel, CH Paulo Fernandes Gomes Dos Santos - Basel, CH Nadege Graveleau - Basel, CH Christina Hebach - Basel, CH Klemens Hoegenauer - Basel, CH Gregory John Hollingworth - Horsham, GB Alexander Baxter Smith - Basel, CH Nicolas Soldermann - Basel, CH Frank Stowasser - Basel, CH Ross Sinclair Strang - Basel, CH Nicola Tufilli - Basel, CH Anette von Matt - Basel, CH Romain Wolf - Basel, CH Frederic Zecri - Cambridge MA, US
Assignee:
Novartis AG - Basel
International Classification:
C07D 471/04 A61K 31/519 A61K 31/5377
Abstract:
The invention relates to substituted tetrahydro-pyrido-pyrimidine derivatives of the formula (I),wherein Y, R, Rand m are as defined in the description. Such compounds are suitable for the treatment of a disorder or disease which is mediated by the activity of the PI3K enzymes.
Novel 3' End Caps, 5' End Caps And Combinations Thereof For Therapeutic Rna
- Basel, CH Scott Louis COHEN - Burlington MA, US John Louis DIENER - Cambridge MA, US Christian GAMPE - Watertown MA, US James ROACHE - Cambridge MA, US Amy WHITE - Somerville MA, US Sarah Louise WILLIAMS - Livermore CA, US Jun YUAN - Boston MA, US Frederic ZECRI - Brookline MA, US
The disclosure relates to nucleic acids that contain modifications at the 5′-end, 3′-end or 5′-end and 3′-ends, and compounds that can be used to make the modified nucleic acids are disclosed. The modified nucleic acids have improved expression, lower immunogenicity and improved stability compared to unmodified nucleic acids.
Lipids And Lipid Compositions For The Delivery Of Active Agents
- Basel, CH Delai Chen - Cambridge MA, US Gabriel Grant Gamber - Cambridge MA, US Andrew Geall - Cambridge MA, US Kevin Love - Somerville MA, US Thomas Zabawa - Cambridge MA, US Frederic Zecri - Cambridge MA, US
This invention provides for a compound of formula (I):or a pharmaceutically acceptable salt thereof, wherein R-R, n, p, Land Lare defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
Tetrahydro-Pyrido-Pyrimidine Derivatives As Pi3Kdelta Inhibitors
- Basel, CH Paulo Fernandes Gomes Dos Santos - Basel, CH Nadege Graveleau - Hesingue, FR Christina Hebach - Meunchenstein, CH Klemens Hoegenauer - Oberwil, CH Gregory John Hollingworth - Kent, GB Alexander Baxter Smith - Niffer, FR Nicolas Soldermann - Village-Neuf, FR Frank Stowasser - Murg, DE Ross Sinclair Strang - Hagenthal le Bas, FR Nicola Tufilli - Moehlin, CH Anette von Matt - Biel-Benken, CH Romain Wolf - Schlierbach, FR Frederic Zecri - Brookline MA, US
International Classification:
C07D 471/04 A61K 31/519 A61K 31/5377
Abstract:
The invention relates to substituted tetrahydro-pyrido-pyrimidine derivatives of the formula (I),wherein Y, R1, R2 and m are as defined in the description. Such compounds are suitable for the treatment of a disorder or disease which is mediated by the activity of the PI3K enzymes.
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