Chemodex

Olanzapine

CHF 95.00
In stock
CDX-O0143-G0011 gCHF 95.00
CDX-O0143-G0055 gCHF 380.00
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Product Details
Synonyms 2-Methyl-4-(4-methyl-1-piperazinyl)- 10H-thieno[2,3-b][1,5]benzodiazepine; LY-170053
Product Type Chemical
Properties
Formula

C17H20N4S

MW 312.43
CAS 132539-06-1
RTECS XJ9007750
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance Yellow powder.
Solubility Soluble in DMSO (10mg/ml) or DMF.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key KVWDHTXUZHCGIO-UHFFFAOYSA-N
Smiles CN(CC1)CCN1C2=NC(C=CC=C3)=C3NC4=C2C=C(C)S4
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Olanzapine is a 5-HT2 serotonin and D1/D2 dopamine receptor antagonist, that binds to dopamine D1, D2, and D4 receptors (Ki=31, 11, and 27 nM, respectively) as well as the serotonin (5-HT) receptor subtypes 5-HT2A, 5-HT2C and 5-HT3 (Ki=4, 11, and 57 nM, respectively). It also binds to M1 muscarinic acetylcholine, α1-adrenergic and histamine H1 receptors (Ki=2, 19, and 7 nM, respectively). Olanzapine is an atypical antipsychotic that displays anticholinergic properties. Olanzapine shows antidepressant-like activity. Formulations containing olanzapine have been used in the treatment of schizophrenia and bipolar disorder and for the prevention and treatment of chronic nausea and chemotherapy-induced nausea and vomiting.

Product References

(1) N.A. Moore, et al.; J. Pharmacol. Exp. Ther. 262, 545 (1992) | (2) F.P. Bymaster, et al.; Neuropsychopharmacol. 14, 87 (1996) | (3) G.D. Tollefson & C.C. Taylor; CNS Drug Reviews 6, 303 (2000) | (4) E. Nowakowska, et al.; Pharmacol. Rep. 66, 404 (2014) | (5) D.M. Ashby, et al.; Behav. Pharmacol. 26, 133 (2015) | (6) C. Fonte, et al.; Crit. Rev. Oncol. Hematol. 95, 214 (2015)

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