92-84-2
92-84-2
Chemical Structure
Phenothiazine
Synonym(s): Thiodiphenylamine
- CAS 番号: 92-84-2
- Formula:C12H9NS
- Molecular Weight:199.28
IUPAC Name: 10H-phenothiazine
InChIKey: WJFKNYWRSNBZNX-UHFFFAOYSA-N
SMILES: C12=CC=CC=C1NC3=C(C=CC=C3)S2
Biological Activity: Phenothiazine is an antibiotic which has insecticidal, fungicidal, antibacterial and anthelmintic activities. Phenothiazine also can be used for the research of neurological diseases[1][2].
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
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Phenothiazine | 99.90% | Phenothiazine is an antibiotic which has insecticidal, fungicidal, antibacterial and anthelmintic activities. Phenothiazine also can be used for the research of neurological diseases. | ||||||||||||||||||||
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Phenothiazine (Standard) | ≥98% | Phenothiazine (Standard) is the analytical standard of Phenothiazine. This product is intended for research and analytical applications. Phenothiazine is an antibiotic which has insecticidal, fungicidal, antibacterial and anthelmintic activities. Phenothiazine also can be used for the research of neurological diseases. | ||||||||||||||||||||
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Phenothiazine-d8 | 99.0% | Phenothiazine-d8 is the deuterium labeled Phenothiazine. Phenothiazine is an antibiotic which has insecticidal, fungicidal, antibacterial and anthelmintic activities. Phenothiazine also can be used for the research of neurological diseases. | ||||||||||||||||||||
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Phenoxazine | 99.90% | Phenoxazine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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9-Aminophenanthrene | 99.74% | 9-Aminophenanthrene is a type of polycyclic aromatic amine compound, which can be used as a fluorescent labeling reagent for free fatty acids (FFA). | ||||||||||||||||||||
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Iminodibenzyl | 99.98% | Iminodibenzyl is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Iminostilbene | 99.66% | Iminostilbene is a chemical precursor of carbamazepine. Additionally, Iminostilbene is an orally active inhibitor of PKM2 (Pyruvate Kinase M2) and COX2 (Cyclooxygenase-2). Iminostilbene exerts its effects by inhibiting PKM2 and its interaction with HIF-1α and STAT3, reducing COX2 and iNOS expression, and decreasing LPS-induced release of IL-1β, IL-6, TNF-α, and MCP-1, thereby suppressing macrophage-mediated inflammatory responses and improving myocardial ischemia/reperfusion (MI/R) injury. Iminostilbene holds promise for research in inflammation regulation, cardiovascular diseases (such as MI/R injury), and macrophage-mediated immune-related diseases. | ||||||||||||||||||||
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Diphenylamine hydrochloride | 99.92% | Diphenylamine hydrochloride (N-Phenylaniline hydrochloride) is an antihyperglycemic agent with oral activity and a common structure in non-steroidal anti-inflammatory drugs (NSAIDs) that uncouples oxidative phosphorylation in mitochondria, leading to a decrease in hepatic cell ATP levels and causing liver cell damage. Diphenylamine hydrochloride is also an industrial antioxidant, a dyeing mordant, and is used in agriculture as an antifungal and antibacterial agent. | ||||||||||||||||||||
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Thianthrene (Standard) | ≥98% | Thianthrene (Standard) is the analytical standard of Thianthrene. This product is intended for research and analytical applications. Thianthrene is a potent and orally active inhibitor of Leishmania donovani pteridine reductase 1 (PTR1). Thianthrene is a sulfur-containing tricyclic molecule distributed widely within the macro-structure of hydrocarbon fossil fuels. Thianthrene inhibits the intracellular amastigotes of Leishmania donovani (IC50 = 23 μM). Thianthrene has a moderate anthelmintic activity. Thianthrene appears to inhibit RNA function and subsequent protein production. Thianthrene can stimulate liver regeneration in vivo. | ||||||||||||||||||||
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Diphenyl sulfide | 99.71% | Diphenyl sulfide is an additive for organic photovoltaic devices. Diphenyl sulfide modulates vertical composition distribution of PTB7-Th:PC71BM photoactive layers, promoting enrichment of PTB7-Th at the upper surface and PC71BM at the bottom. Diphenyl sulfide promotes ordered molecular packing and crystallinity of PTB7-Th:PC71BM photoactive layers, including more compact π−π stacking of PTB7-Th. Diphenyl sulfide improves exciton dissociation, charge transport, and charge collection in PTB7-Th:PC71BM-based inverted polymer solar cells. Diphenyl sulfide acts as a solvent additive to improve the photovoltaic performance of inverted organic photovoltaic devices. | ||||||||||||||||||||
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9-Anthracenamine | 9-anthracenamine is an end-capping agent. 9-anthracenamine caps both ends of polyrotaxanes and free PPG chains to avoid dethreading. | |||||||||||||||||||||
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9,10-Dihydroacridine | 99.75% | 9,10-Dihydroacridine is a chain-terminating antioxidant that can inhibit lipid peroxidation by capturing peroxide free radicals (LOO•). | ||||||||||||||||||||
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2-Chlorophenothiazine | 2-Chlorophenothiazine is a phenothiazine derivative. 2-Chlorophenothiazine has the activity of inhibiting DNA, RNA and protein synthesis. 2-Chlorophenothiazine is an intermediate in the synthesis of Chlorpromazine (HY-12708) and Perphenazine (HY-A0077). | |||||||||||||||||||||
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References
- [1]. Jun-hua Xiao, et al. Xiao JH, Zhang YL, Ding LL, Feng XL, Wang JL. Effects of isoliensinine on proliferation of porcine coronary arterial smooth muscle cells induced by phenylephrine. Yao Xue Xue Bao. 2005 Feb;40(2):105-10. [Content Brief]
- [2]. Mitchell SC, et, al. The toxicity of phenothiazine. Drug Metabol Drug Interact. 1994;11(3):201-35. [Content Brief]
