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- B5e7fc04f2f6f908b78e8df49d354a911 NCIT_P378 "NCI" @default.
- B5e7fc04f2f6f908b78e8df49d354a911 type Axiom @default.
- B5e7fc04f2f6f908b78e8df49d354a911 annotatedProperty IAO_0000115 @default.
- B5e7fc04f2f6f908b78e8df49d354a911 annotatedSource NCIT_C29553 @default.
- B5e7fc04f2f6f908b78e8df49d354a911 annotatedTarget "The tartrate salt of an imidazopyridine with non-benzodiazepine benzodiazepine-receptor agonist and sedative-hypnotic activities. Zolpidem binds selectively to the alpha 1 subunit of the omega-1 (BZ1) receptor of the gamma-aminobutyric acid type A (GABA-A) receptor-chloride ionophore complex, thereby opening neuronal chloride channels, hyperpolarizing neuronal cell membranes, and inhibiting neuronal firing. In contrast, benzodiazepines non-selectively bind to and activate all omega receptor subtypes, exhibiting anticonvulsant and myorelaxant activities in addition to a sedative-hypnotic activity." @default.