
CAS 959605-90-4
:Formel:C19H21N3O
InChl:InChI=1S/C19H21N3O/c1-13-5-8-15(9-6-13)19-16(11-18(23)21(3)4)22-12-14(2)7-10-17(22)20-19/h5-10,12H,11H2,1-4H3/i3D3,4D3
InChI Key:ZAFYATHCZYHLPB-LIJFRPJRSA-N
SMILES:[2H]C([2H])([2H])N(C(=O)CC1=C(N=C2N1C=C(C=C2)C)C3=CC=C(C=C3)C)C([2H])([2H])[2H]
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Zolpidem-D6 0.1 mg/ml in Methanol
CAS:Kontrolliertes ProduktFormel:C192H6H15N3OFarbe und Form:ColourlessMolekulargewicht:313.43Zolpidem-d6
CAS:Kontrolliertes ProduktApplications Deuterated Zolpidem, a selective non-benzodiazepine GABAA receptor agonist. Sedative, hypnotic. Controlled substance (depresssant).
References Arbilla, S., et al.: Arch. Pharmacol., 330, 248 (1985), Cashman, J.N., et al.: Brit. J. Clin. Pharmacol., 21, 205 (1986)Formel:C192H6H15N3OFarbe und Form:NeatMolekulargewicht:313.43Zolpidem-d6 (100ug/ml in Methanol)
CAS:Kontrolliertes ProduktFormel:C192H6H15N3OFarbe und Form:Single SolutionMolekulargewicht:313.43Zolpidem-d6
CAS:Kontrolliertes ProduktZolpidem-d6 is a medicinal inhibitor that has been used in the treatment of cancer. It is an analog of other inhibitors that have been found to be effective against cancer cells. Zolpidem-d6 works by inhibiting the activity of kinases, which are proteins that regulate various cellular processes including cell growth and division. This inhibition leads to the induction of apoptosis, or programmed cell death, in tumor cells. Zolpidem-d6 has shown anticancer activity in Chinese hamster ovary cells and has also been detected in human urine samples. This drug may have potential as a therapeutic agent for the treatment of various types of cancer by targeting specific pathways involved in the cell cycle.Formel:C19H21N3OReinheit:Min. 95%Molekulargewicht:313.4 g/mol




