Average Co-Inventor Count = 7.26
ph-index = 6
The patent ph-index is calculated by counting the number of publications for which an author has been cited by other authors at least that same number of times.
Company Filing History:
1. Aeterna Zentaris Gmbh (9 from 36 patents)
2. Arzneimittelwerk Dresden Gmbh (5 from 39 patents)
3. Elbion Ag (4 from 9 patents)
4. Zentaris Gmbh (2 from 22 patents)
5. Zentaris Ag (2 from 20 patents)
6. Biotie Therapies Corporation (1 from 28 patents)
7. Ae Zentaris Gmbh (1 from 1 patent)
8. Æterna Zentaris Gmbh (2 patents)
24 patents:
1. 8937068 - Pyridopyrazine derivatives and their use
2. 8604196 - Modulating signal transduction pathways with 1-ethyl-3-[3-(1-methyl-1H-pyrazol-4-yl)-pyrido[2.3-B]pyrazine-6-yl]thiourea
3. 8541462 - Tetrahydrocarbazole derivatives as ligands of G-protein coupled receptors
4. 8536332 - Modulating signal transduction pathways with substituted pyridol [2,3-b] pyrazines
5. 8507486 - Pyridopyrazine derivatives, process of manufacturing and uses thereof
6. 8461178 - Naphthyridine derivatives and the use thereof as kinase inhibitors
7. 8394801 - Quinoxaline derivatives and their use for treating benign and malignant tumour disorders
8. 8217042 - Pyridopyrazines and their use as modulators of kinases
9. 8202883 - Substituted pyrido[2,3-b]pyrazine compounds as modulators of tyrosine kinases
10. 8148546 - Tetrahydrocarbazole derivatives as ligands of G-protein coupled receptors
11. 8067456 - Tetrahydrocarbazole derivatives having improved biological action and improved solubility as ligands of G-protein coupled receptors (GPCPs)
12. 7683074 - 7-azaindoles, their use as inhibitors of phosphodiesterase 4, and a method for synthesizing them
13. 7419987 - 7-azaindoles, their use as inhibitors of phosphodiesterase 4, and a method for synthesizing them
14. 7378522 - Quinoline, isoquinoline and phthalazine derivatives as antagonists of the gonadotropin-releasing hormone
15. 7375127 - Tetrahydrocarbazole derivatives having improved biological action and improved solubility as ligands of G-protein coupled receptors (GPCRs)