Inventor

STEINHAGEN HENNING

DE26 patents

⚠️ This page may combine multiple inventors who share the name “STEINHAGEN HENNING”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

STEINHAGEN HENNING

STEINHAGEN HENNING

Cyclic (aza)indolizinecarboxamides, their preparation and their use as pharmaceuticals

Cyclic azaindole-3-carboxamides, their preparation and their use as pharmaceuticals

Tartrate derivatives for use as coagulation factor IXa inhibitors

Cyclic indole-3-carboxamides, their preparation and their use as pharmaceuticals

Malonamide derivatives with antithrombotic activity

Isoserine derivatives for use as coagulation factor IXa inhibitors

HEINELT UWE

Triazolopyridazines as PAR1 inhibitors, production thereof, and use as medicaments

Triazolium salts as PAR1 inhibitors, production thereof, and use as medicaments

Triazolium salts as PAR1 inhibitors, production thereof, and use as medicaments

Triazolopyridazines as PAR1 inhibitors, production thereof, and use as medicaments

Imidazopyridazines as PAR1 inhibitors, production thereof, and use as medicaments

SF5 derivatives as PAR1 inhibitors, production thereof, and use as medicaments

GRUENENTHAL GMBH

Fluoromethyl-substituted pyrrole carboxamides

Fluoromethyl-substituted pyrrole carboxamides as CaV2.2 calcium channel blockers

Fluoromethyl-substituted pyrrole carboxamides iv

3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5H)-yl) derivatives II

3-oxo-tetrahydro-furo[3,2-B]pyrrol-4(5H)-yl) derivatives I

BAYER AG

Substituted phenylcyclohexane carboxylic acid amides and their use as adenosine uptake inhibitors

Substituted amidoalkyl-uracils and their use

Substituted phenylcyclohexanecarboxamides and their use

Substituted phenylcyclohexanecarboxamides and their use

Substituted amidoalkyl uracils and their use as inhibitors of the poly(adp-ribose) synthetase (PARS)

SANOFI SA

Tricyclic pyridyl-vinyl pyrroles as PAR1 inhibitors

Pyridylvinylpyrazoloquinolines as PAR1 inhibitors

BOCSKEI JOZSEF ZSOLT

Aryl- and heteroaryl-ethyl-acylguanidine derivatives, their preparation and their application in therapeutics

SANOFI AVENTIS

Pyrazolopyridine derivatives as inhibitors of β-Adrenergic receptor kinase 1