Average Co-Inventor Count = 5.98
ph-index = 10
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. Sanofi-a Ventis Deutschland Gmbh (18 from 1,827 patents)
2. Sanofi-aventis (15 from 389 patents)
3. Aventis Pharma Deutschland, Gmbh (9 from 330 patents)
4. Sanofi (7 from 1,451 patents)
5. Aventis Pharma S.a. (3 from 377 patents)
6. Genzyme Corporation (1 from 787 patents)
53 patents:
1. 11897876 - Isoxazolidines as RIPK1 inhibitors and use thereof
2. 9073975 - Cyclic peptides, their preparation and their use as inhibitors of the platelet adhesion
3. 8946212 - Annelated N-heterocyclic sulfonamides with oxadiazolone headgroup, processes for their preparation and their use as pharmaceuticals
4. 8716317 - Sulfonamides with heterocycle and oxadiazolone headgroup, processes for their preparation and their use as pharmaceuticals
5. 8673917 - 2-heteroaryl-pyrrolo [3,4-C]pyrrole derivatives, and use thereof as SCD inhibitors
6. 8580813 - Cyclic azaindole-3-carboxamides, their preparation and their use as pharmaceuticals
7. 8415336 - Cyclic (aza)indolizinecarboxamides, their preparation and their use as pharmaceuticals
8. 8344004 - Cyclic pyridyl-N-[1,3,4]-thiadiazol-2-yl-benzene sulfonamides, processes for their preparation and their use as pharmaceuticals
9. 8329725 - Annelated pyrrolidin sulfonamides with oxadiazolone headgroup, processes for their preparation and their use as pharmaceuticals
10. 8211885 - Cyclic indole-3-carboxamides, their preparation and their use as pharmaceuticals
11. 8153647 - Aryl- and heteroaryl-ethyl-acylguanidine derivatives, their preparation and their application in therapeutics
12. 8143242 - Malonamide derivatives with antithrombotic activity
13. 8088925 - Heteroaryl-carboxylic acid (sulfamoyl alkyl) amide-derivatives as factor Xa inhibitors
14. 8039481 - Tetrahydrofuran derivatives for use as inhibitors of matrix metalloproteinases
15. 8003677 - 2-heteroaryl-pyrrolo[3,4-c]pyrrole derivatives and their use as SCD inhibitors