33262-29-2
33262-29-2
Chemical Structure
Dibenzothiophene-d8
- CAS No.: 33262-29-2
- Formula:C12D8S
- Molecular Weight:192.31
IUPAC Name: dibenzo[b,d]thiophene-d8
InChIKey: IYYZUPMFVPLQIF-PGRXLJNUSA-N
SMILES: [2H]C1=C2C3=C([2H])C([2H])=C([2H])C([2H])=C3SC2=C([2H])C([2H])=C1[2H]
Biological Activity: Dibenzothiophene-d8 is the deuterium labeled Dibenzothiophene (HY-B0973). Dibenzothiophene is an orally active and a noncompetitive CYP1A inhibitor. Dibenzothiophene inhibits CYP1A-mediated EROD activity with Km of 0.592 μM. Dibenzothiophene interacts with the AHR pathway. Dibenzothiophene enhances the embryotoxicity of β-naphthoflavone (HY-114740). Dibenzothiophene shows acute toxicity in mice. Dibenzothiophene is mainly used for the study of the mechanism of developmental toxicity in organisms[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Dibenzothiophene-d8 | 99.3% | Dibenzothiophene-d8 is the deuterium labeled Dibenzothiophene (HY-B0973). Dibenzothiophene is an orally active and a noncompetitive CYP1A inhibitor. Dibenzothiophene inhibits CYP1A-mediated EROD activity with Km of 0.592 μM. Dibenzothiophene interacts with the AHR pathway. Dibenzothiophene enhances the embryotoxicity of β-naphthoflavone (HY-114740). Dibenzothiophene shows acute toxicity in mice. Dibenzothiophene is mainly used for the study of the mechanism of developmental toxicity in organisms. | ||||||||||||||||||||
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Dibenzothiophene (Standard) | ≥98% | Dibenzothiophene (Standard) is the analytical standard of Dibenzothiophene (HY-B0973). This product is intended for research and analytical applications. Dibenzothiophene is an orally active and a noncompetitive CYP1A inhibitor. Dibenzothiophene inhibits CYP1A-mediated EROD activity with Km of 0.592 μM. Dibenzothiophene interacts with the AHR pathway. Dibenzothiophene enhances the embryotoxicity of β-naphthoflavone (HY-114740). Dibenzothiophene shows acute toxicity in mice. Dibenzothiophene is mainly used for the study of the mechanism of developmental toxicity in organisms. | ||||||||||||||||||||
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Dibenzothiophene | 99.92% | Dibenzothiophene is an orally active and a noncompetitive CYP1A inhibitor. Dibenzothiophene inhibits CYP1A-mediated EROD activity with a Km of 0.592 μM. Dibenzothiophene interacts with the AHR pathway. Dibenzothiophene enhances the embryotoxicity of β-naphthoflavone (HY-114740). Dibenzothiophene shows acute toxicity in mice. Dibenzothiophene is mainly used for the study of the mechanism of developmental toxicity in organisms. | ||||||||||||||||||||
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9-Phenanthrol | 98.57% | 9-Phenanthrol (9-Hydroxyphenanthrene) is a selective TRPM4 inhibitor with an IC50 of 17 μM. 9-Phenanthrol has no inhibitory activity on TRPM5, TRPC6, and CFTR. 9-Phenanthrol can be used for the research of ischemia-reperfusion injury. | ||||||||||||||||||||
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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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Phenanthrene (Standard) | 99.57% | Phenanthrene (Standard) is the analytical standard of Phenanthrene. This product is intended for research and analytical applications. Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment. | ||||||||||||||||||||
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Dibenzo[b,d]furan | 99.95% | Dibenzo[b,d]furan is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Thioxanthone | 98.31% | Thioxanthone is a powerful photocatalyst for organic reactions. Thioxanthone mediates energy transfer, single-electron transfer, and hydrogen atom transfer processes. As a photoredox catalyst, Thioxanthone is used in nickel-catalyzed self-coupling reactions of aryl halides, arylation reactions of H-phosphine oxides/H-phosphites, decarbonylation reactions of cyclopropenones, and reactions generating acyl radicals from aromatic aldehydes. | ||||||||||||||||||||
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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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Phenanthridine | Phenanthridine is an aldehyde oxidase 1 (AOX1) substrate, with oxidation by hAOX1 yielding phenanthridone when molecular oxygen, ferricyanide, or dichlorophenolindophenol serves as electron acceptor. | |||||||||||||||||||||
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Phenanthrene-13C6 | 99.9% | Phenanthrene-13C6 is the 13C labeled Phenanthrene (HY-B1727). Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment. | ||||||||||||||||||||
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Phenanthrene-13C2 | Phenanthrene-13C2 is the 13C-labeled Phenanthrene (HY-B1727). Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment. | |||||||||||||||||||||
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