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Carsten Spanka
Observed names:
C. SPANKA,
C. Spanka,
Spanka, C.,
Spanka, Carsten
Institution:
Novartis (Switzerland)
Observed institutions:
Scripps Research Institute,
Novartis (Switzerland),
Scripps Institution of Oceanography,
Universität Hamburg,
Princeton University,
Clausthal University of Technology,
Novartis Institutes for BioMedical Research
show all 7
ORCID:
0000-0003-0365-204X
Observed ORCID:
0000-0003-0365-204X
OpenAlex ID:
A5048812178
Oxysterols direct immune cell migration via EBI2
2011
·
Sébastien Hannedouche
, Juan Zhang
, et al.
·
Nature
·
509
Discovery of 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), A Potent and Selective Inhibitor of the Fibroblast Growth Factor Receptor Family of Receptor Tyrosine Kinase
2011
·
Vito Guagnano
, Pascal Furet
, et al.
·
Journal of Medicinal Chemistry
·
484
A segmented flow platform for on-demand medicinal chemistry and compound synthesis in oscillating droplets
2017
·
Ye-Jin Hwang
, Connor W. Coley
, et al.
·
Chemical Communications
·
91
N-Sulfonylanthranilic Acid Derivatives as Allosteric Inhibitors of Dengue Viral RNA-Dependent RNA Polymerase
2009
·
Zheng Yin
, Yen-Liang Chen
, et al.
·
Journal of Medicinal Chemistry
·
68
Solid-Phase Rhodium Carbenoid Reactions: An N−H Insertion Route to a Diverse Series of Oxazoles
2001
·
Bruce Clapham
, Carsten Spanka
, et al.
·
Organic Letters
·
61
Specific Activation of the Nuclear Receptors PPARγ and RORA by the Antidiabetic Thiazolidinedione BRL 49653 and the Antiarthritic Thiazolidinedione Derivative CGP 52608
1998
·
Irmgard Wiesenberg
, Michele Chiesi
, et al.
·
Molecular Pharmacology
·
50
A Tunable Hydrogel for Encapsulation and Controlled Release of Bioactive Proteins
2001
·
Mercedes Delgado
, Carsten Spanka
, et al.
·
Biomacromolecules
·
45
Preparation of New Microgel Polymers and Their Application as Supports in Organic Synthesis
2002
·
Carsten Spanka
, Bruce Clapham
, et al.
·
The Journal of Organic Chemistry
·
37
Piperidyl amides as novel, potent and orally active mGlu5 receptor antagonists with anxiolytic-like activity
2009
·
Carsten Spanka
, Ralf Glatthar
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
32
Improving the Oral Bioavailability of the Iron Chelator HBED by Breaking the Symmetry of the Intramolecular H-Bond Network
2000
·
Bernard Faller
, Carsten Spanka
, et al.
·
Journal of Medicinal Chemistry
·
27
Functionalized β-Thiolactams by Lewis Acid Catalyzed Addition of Alkynyl Silyl Sulfides to Azomethines
1997
·
Wolf-Rüdiger Förster
, Rainer Isecke
, et al.
·
Synthesis
·
27
Synthesis of Chiral Analoguesof FTY720 and its Phosphate
2003
·
Klaus Hinterding
, Sylvain Cottens
, et al.
·
Synthesis
·
23
The discovery of potent, orally bioavailable pyrazolo and triazolopyrimidine CXCR2 receptor antagonists
2013
·
David W. Porter
, Michelle Bradley
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
21
Application of Microgels as Polymer Supports for Organic Synthesis: Preparation of a Small Phthalide Library, a Scavenger, and a Borohydride Reagent
2002
·
Osamu Shimomura
, Bruce Clapham
, et al.
·
Journal of Combinatorial Chemistry
·
21
Synthesis of N-{4-[2-(2-Amino-5,6-dihydro-4(3H)-oxo-7H-pyrrolo[2,3-d]pyrimidin-6-yl)- ethyl]benzoyl}- l -glutamic Acid: A Ring-Contracted Analogue of 5,10-Dideaza-5,6,7,8-tetrahydrofolic Acid
1996
·
Edward C. Taylor
, Wendy B. Young
, et al.
·
The Journal of Organic Chemistry
·
16
Design and Synthesis of Metabolically Stable tRNA Synthetase Inhibitors Derived from Cladosporin
2018
·
Marion Rusch
, Arnaud Thevenon
, et al.
·
ChemBioChem
·
15
PDF
A Parallel Approach to the Discovery of Carrier Delivery Vehicles To Enhance Antigen Immunogenicity
2002
·
Mercedes Delgado
, Kyung Joo Lee
, et al.
·
Journal of the American Chemical Society
·
14
Developing Soluble Polymers for High-Throughput Synthetic Chemistry
2002
·
Carsten Spanka
, Paul Wentworth Jr
, et al.
·
Combinatorial Chemistry & High Throughput Screening
·
9
The Quest for β-Thiolactam Antibiotics
1997
·
Ernst Schaumann
, Ens Nieschalk
, et al.
·
Phosphorus, sulfur, and silicon and the related elements
·
9
Nucleophilic Addition of Lithiated Phenyl Trimethylsilylmethyl Sulfide to Activated Olefins. A Facile Synthesis of 2-(Functionally) Substituted Silylcyclopropanes
1986
·
Ernst Schaumann
, Carsten Friese
, et al.
·
Synthesis
·
9
Discovery of Amino Alcohols as Highly Potent, Selective, and Orally Efficacious Inhibitors of Leukotriene A4 Hydrolase
2023
·
Gebhard Thoma
, Christian Markert
, et al.
·
Journal of Medicinal Chemistry
·
8
Stabilizing Inactive Conformations of MALT1 as an Effective Approach to Inhibit Its Protease Activity
2020
·
Nicola Hughes
, Paul Erbel
, et al.
·
Advanced Therapeutics
·
8
Alkynyl Silyl Sulfides as Versatile Thioketene Equivalents
2014
·
Ernst Schaumann
, Carsten Spanka
·
Synlett
·
5
Category 3, Compounds with Four and Three Carbon Heteroatom Bonds
2006
·
R. L. Danheiser
, D. Bellus
, et al.
·
Thieme eBooks
·
5
Discovery of GJG057, a Potent and Highly Selective Inhibitor of Leukotriene C4 Synthase
2025
·
Gebhard Thoma
, Wolfgang Miltz
, et al.
·
Journal of Medicinal Chemistry
·
2
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Works count:
64
Citation count:
1,605
H-index:
15
I10-index:
17
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