Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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O126519-100mg
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100mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$9.90
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O126519-1g
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1g |
5
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$69.90
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O126519-5g
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5g |
4
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$231.90
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O126519-25g
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25g |
3
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$1,043.90
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O126519-100g
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100g |
1
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$3,755.90
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Non-selective 5-HT, dopamine, histamine and muscarinic antagonist
| Synonyms | NSC_4585 | Olanzapine Teva | 2-Methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e][1,4]diazepine | OLANZAPINE [INN] | 2-methyl-4-(4-methyl-1-piperazinyl)-5H-thieno[3,2-c][1,5]benzodiazepine | BDBM82479 | OLANZAPINE (USP MONOGRAPH) | OLANZAPINE [V |
|---|---|
| Specifications & Purity | Moligand™, ≥99% |
| Biochemical and Physiological Mechanisms | Olanzapine(Zyprexa) is a high affinity for 5-HT2 serotonin and D2 dopamine receptor antagonist. It has a higher affinity for 5-HT2 serotonin receptors than D2 dopamine receptors. Like most atypical antipsychotics, compared to the older typical ones, olanz |
| Storage Temp | Protected from light,Store at -20°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | AGONIST, ANTAGONIST |
| Mechanism of action | D2-like dopamine receptor antagonist |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
| Product Description |
Olanzapine is a high affinity for 5-HT2 serotonin and D2 dopamine receptor antagonist.Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Olanzapine is an atypical antipsychotic drug, widely used for the treatment of acute schizophrenia and psychotic conditions. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Benzodiazepines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzodiazepines |
| Alternative Parents | Thienodiazepines 2,3,5-trisubstituted thiophenes N-methylpiperazines N-arylated-2-aminothiophenes 1,4-diazepines Imidolactams Benzenoids Heteroaromatic compounds Trialkylamines Secondary amines Propargyl-type 1,3-dipolar organic compounds Carboxamidines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Benzodiazepine - Thieno-para-diazepine - 2,3,5-trisubstituted thiophene - Para-diazepine - N-methylpiperazine - N-alkylpiperazine - N-arylated-2-aminothiophene - 1,4-diazinane - Piperazine - 2-aminothiophene - Benzenoid - Imidolactam - Heteroaromatic compound - Thiophene - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Amidine - Carboxylic acid amidine - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Amine - Organopnictogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzodiazepines. These are organic compounds containing a benzene ring fused to either isomers of diazepine(unsaturated seven-member heterocycle with two nitrogen atoms replacing two carbon atoms). |
| External Descriptors | N-arylpiperazine - N-methylpiperazine - benzodiazepine |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 488202827 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488202827 |
| IUPAC Name | 2-methyl-4-(4-methylpiperazin-1-yl)-10H-thieno[2,3-b][1,5]benzodiazepine |
| INCHI | InChI=1S/C17H20N4S/c1-12-11-13-16(21-9-7-20(2)8-10-21)18-14-5-3-4-6-15(14)19-17(13)22-12/h3-6,11,19H,7-10H2,1-2H3 |
| InChIKey | KVWDHTXUZHCGIO-UHFFFAOYSA-N |
| Smiles | CC1=CC2=C(S1)NC3=CC=CC=C3N=C2N4CCN(CC4)C |
| Isomeric SMILES | CC1=CC2=C(S1)NC3=CC=CC=C3N=C2N4CCN(CC4)C |
| WGK Germany | 3 |
| RTECS | XJ9007750 |
| Molecular Weight | 312.43 |
| Beilstein | 7655141 |
| Reaxy-Rn | 7655141 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7655141&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | May 13, 2025 | O126519 | |
| Certificate of Analysis | Feb 17, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Jan 13, 2025 | O126519 | |
| Certificate of Analysis | Apr 30, 2024 | O126519 | |
| Certificate of Analysis | Apr 30, 2024 | O126519 | |
| Certificate of Analysis | Apr 30, 2024 | O126519 | |
| Certificate of Analysis | Oct 08, 2023 | O126519 | |
| Certificate of Analysis | Oct 08, 2023 | O126519 | |
| Certificate of Analysis | Dec 10, 2022 | O126519 | |
| Certificate of Analysis | Dec 10, 2022 | O126519 | |
| Certificate of Analysis | Dec 04, 2021 | O126519 |
| Solubility | DMSO 100 mg/ml 1eq. HCl 100 mg/ml;Soluble in Acetronitrile |
|---|---|
| Sensitivity | Heat & light sensitive |
| Melt Point(°C) | 192-196°C |
| Molecular Weight | 312.400 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 312.141 Da |
| Monoisotopic Mass | 312.141 Da |
| Topological Polar Surface Area | 59.100 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 432.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Huanhuan Yang, Cong Liu, Chuanhong Zhu, Yan Zheng, Juan Li, Qianyun Zhu, Hao Wang, Xiangming Fang, Quan Liu, Man Liang, Zilong Liu. (2023) Determination of ten antipsychotics in blood, hair and nails: Validation of a LC–MS/MS method and forensic application of keratinized matrix analysis. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 234 (115557). |
| 2. Kaikai Han, Jingjie Cui, Shaowei Chen, Tao Yu. (2023) Effects of olanzapine and lithium carbonate antipsychotic agents on dopamine oxidation. ANALYST, 148 (14): (3330-3340). |
| 3. Lingzhi Liang, Xia Ren, Junyi Xu, Yurong Ma, Yunlin Xue, Tao Zhuang, Guisen Zhang. (2022) Effect of Co-Treatment of Olanzapine with SEP-363856 in Mice Models of Schizophrenia. MOLECULES, 27 (8): (2550). |
| 4. Feifei Liang, Xiaofang Tan, Shuaishuai Hao, Wenwen Liu, Chenxin Duan, Guisen Zhang, Tao Zhuang, Yin Chen, Chao Hao. (2022) Synthesis and structural characterization of two novel olanzapine cocrystals with decreased or enhanced dissolution rate. JOURNAL OF MOLECULAR STRUCTURE, 1255 (132340). |
| 5. Cuilian Guo, Jinxin Liu, Huqun Li. (2021) Metformin ameliorates olanzapine-induced insulin resistance via suppressing macrophage infiltration and inflammatory responses in rats. BIOMEDICINE & PHARMACOTHERAPY, 133 (110912). |
| 6. Ting Jiang, Yingqiong Zhang, Mengru Bai, Ping Li, Wei Wang, Mingyang Chen, Zhiyuan Ma, Su Zeng, Hui Zhou, Huidi Jiang. (2019) Up-regulation of hepatic fatty acid transporters and inhibition/down-regulation of hepatic OCTN2 contribute to olanzapine-induced liver steatosis. TOXICOLOGY LETTERS, 316 (183). |
| 7. Lu Yang, Zijin Lin, Ruijing Mu, Wenhan Wu, Hao Zhi, Xiaodong Liu, Hanyu Yang, Li Liu. (2024) Neurons enhance blood–brain barrier function via upregulating claudin-5 and VE-cadherin expression due to glial cell line-derived neurotrophic factor secretion. eLife, (2024 Oct). |
| 8. Yuying Chen, Qingwei He, Huangjie Lu, Jie Yang, Jiongming Han, Ying Zhu, Ping Hu. (2024) Visualization and correlation of drug release of risperidone/clozapine microspheres in vitro and in vivo based on FRET mechanism. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 653 (123885). |