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Olanzapine-d8

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    Olanzapine-d<sub>8</sub>
  • Olanzapine-d<sub>8</sub>
Cat No: 25447
Biochemicals - Isotopically Labeled Standards
Cayman

Olanzapine-d8 is intended for use as an internal standard for the quantification of olanzapine (Item No. 11937) by GC- or LC-MS. Olanzapine is an atypical antipsychotic that binds to dopamine D1, D2, and D4 receptors (Kis = 31, 11, and 27 nM, respecti...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2-methyl-4-(4-methyl-1-piperazinyl-2,2,3,3,5,5,6,6-d8)-10H-thieno[2,3-b][1,5]benzodiazepine
Correlated keywords:
  • deuterated deuterium LY170053 LY-170053 5HT 5HT2A 5HT2C 5HT3 anti-depressant psychotic
Product Overview:
Olanzapine-d8 is intended for use as an internal standard for the quantification of olanzapine (Item No. 11937) by GC- or LC-MS. Olanzapine is an atypical antipsychotic that binds to dopamine D1, D2, and D4 receptors (Kis = 31, 11, and 27 nM, respectively) as well as the serotonin (5-HT) receptor subtypes 5-HT2A, 5-HT2C, and 5-HT3 (Kis = 4, 11, and 57 nM, respectively).{21347} It also binds to M1 muscarinic acetylcholine, α1-adrenergic, and histamine H1 receptors (Kis = 2, 19, and 7 nM, respectively). Olanzapine (0.5 mg/kg, i.p.) decreases immobility time in the forced swim test in non-stressed and prenatally-stressed rats, indicating antidepressant-like activity.{42431} It also decreases the number of avoidances made in the conditioned avoidance response test in rats when administered at doses of 0.5 and 1 mg/kg.{42432} Formulations containing olanzapine have been used in the treatment of schizophrenia and bipolar disorder.
Size 500 µg
Shipping dry ice
CAS Number 1093380-13-2
Molecular Formula C17H12D8N4S
SMILES CN(C([2H])([2H])C1([2H])[2H])C([2H])([2H])C([2H])([2H])N1C2=NC3=CC=CC=C3NC4=C2C=C(C)S4
Molecular Weight 320,5
Formulation A solid
Purity ≥99% deuterated forms (d1-d8)
Custom Code 3822.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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