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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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L126613-10mg
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10mg |
3
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$53.90
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L126613-50mg
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50mg |
3
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$129.90
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L126613-100mg
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100mg |
3
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$195.90
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L126613-250mg
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250mg |
3
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$441.90
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L126613-1g
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1g |
3
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$1,587.90
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L126613-5g
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5g |
2
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$7,144.90
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L126613-10g
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10g |
1
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$12,859.90
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L126613-25g
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25g |
5
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$28,934.90
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L126613-100g
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100g |
2
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$104,162.90
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Protein synthesis inhibitor. Potent oxazolidinone antibiotic.
| Synonyms | cid_441401 | s1408 | SMR000466335 | FT-0642294 | LINEZOLID [JAN] | LINEZOLID [USAN] | N-(((S)-3-(3-Fluoro-4-morpholinophenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide | N-{[(5S)-3-[3-fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide |
|---|---|
| Specifications & Purity | Moligand™, ≥99% |
| Biochemical and Physiological Mechanisms | Linezolid is a synthetic antibiotic used for the treatment of serious infections caused by Gram-positive bacteria that are resistant to several other antibiotics. A member of the oxazolidinone class of drugs, linezolid is active against most Gram-positive |
| Storage Temp | Store at 2-8°C |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | INHIBITOR |
| Mechanism of action | Bacterial 70S ribosome inhibitor |
| 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 |
Linezolid is a synthetic antibiotic used for the treatment of serious infections.((only for scientific research) ) |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Oxazinanes |
| Subclass | Morpholines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylmorpholines |
| Alternative Parents | Aniline and substituted anilines Dialkylarylamines Fluorobenzenes Oxazolidinones Aryl fluorides Acetamides Carbamate esters Secondary carboxylic acid amides Organic carbonic acids and derivatives Dialkyl ethers Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organofluorides Organopnictogen compounds Carbonyl compounds Organic oxides |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Phenylmorpholine - Aniline or substituted anilines - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Oxazolidinone - Benzenoid - Oxazolidine - Acetamide - Carbamic acid ester - Secondary carboxylic acid amide - Tertiary amine - Amino acid or derivatives - Carboxamide group - Carbonic acid derivative - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Amine - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenylmorpholines. These are aromatic compounds containing a morpholine ring and a benzene ring linked to each other through a CC or a CN bond. |
| External Descriptors | organofluorine compound - acetamides - morpholines - oxazolidinone |
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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 | 488189784 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488189784 |
| IUPAC Name | N-[[(5S)-3-(3-fluoro-4-morpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide |
| INCHI | InChI=1S/C16H20FN3O4/c1-11(21)18-9-13-10-20(16(22)24-13)12-2-3-15(14(17)8-12)19-4-6-23-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1 |
| InChIKey | TYZROVQLWOKYKF-ZDUSSCGKSA-N |
| Smiles | CC(=O)NCC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCOCC3)F |
| Isomeric SMILES | CC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCOCC3)F |
| WGK Germany | 3 |
| RTECS | AC2720000 |
| Molecular Weight | 337.35 |
| Reaxy-Rn | 9426017 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9426017&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 | Oct 30, 2024 | L126613 | |
| Certificate of Analysis | Jun 15, 2024 | L126613 | |
| Certificate of Analysis | Jun 15, 2024 | L126613 | |
| Certificate of Analysis | May 25, 2024 | L126613 | |
| Certificate of Analysis | Mar 25, 2024 | L126613 | |
| Certificate of Analysis | Mar 19, 2024 | L126613 | |
| Certificate of Analysis | Mar 19, 2024 | L126613 | |
| Certificate of Analysis | Mar 19, 2024 | L126613 | |
| Certificate of Analysis | Mar 19, 2024 | L126613 | |
| Certificate of Analysis | Mar 19, 2024 | L126613 | |
| Certificate of Analysis | Feb 22, 2024 | L126613 | |
| Certificate of Analysis | Feb 22, 2024 | L126613 | |
| Certificate of Analysis | Mar 16, 2023 | L126613 | |
| Certificate of Analysis | May 25, 2022 | L126613 | |
| Certificate of Analysis | May 12, 2022 | L126613 | |
| Certificate of Analysis | May 12, 2022 | L126613 |
| Solubility | Soluble in water (<1 mg/mL at 25 °C), ethanol (8 mg/mL at 25 °C), chloroform, methanol, and DMSO (68 mg/mL at 25 °C). |
|---|---|
| Sensitivity | Air Sensitive |
| Melt Point(°C) | 179 °C |
| Molecular Weight | 337.350 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 337.144 Da |
| Monoisotopic Mass | 337.144 Da |
| Topological Polar Surface Area | 71.100 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 472.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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. Chong-Fa Lai, Wei-Bin Xiao, Hua-Cheng Yan, Hui Yang, Lu-Xia Wang, Hui Guan, Qiu-ju Peng, Zhi-Rong Deng, Jian-Wen Chen, Lin-Kun An, Lei Shi. (2020) ZTW-41, a Potent Indolizinoquinoline-5,12-Dione Derivative Against Drug-Resistant Staphylococci and Enterococci Bacteria. Microbial Drug Resistance, 26 (2): (100-109). |
| 2. Tingting Liu, Xiaomin Chen, Guanxuanzi Zhang, Jing Zhao, Qian Lu, Fang Wang, Hongxia Li, Bing Liu, Ping Zhu. (2025) An LCMS/MS method for the simultaneous determination of ten antimicrobials and its application in critically ill patients. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 252 (116489). |
| 3. Shuai Dong, Xingyuan Bai, Bin Chen, Minzhe Fan, Qi Liu, Yubo Zhao, Linsen Li*, Dan Zhu. (2025) Panzerina lanata accelerates methicillin-resistant Staphylococcus aureus eradication by promoting migration and activation of neutrophils. Frontiers in Pharmacology, 15 |