1219803-41-4
1219803-41-4
Chemical Structure
Phenothiazine-d8
- CAS No.: 1219803-41-4
- Formula:C12HD8NS
- Molecular Weight:207.32
IUPAC Name: 10H-phenothiazine-1,2,3,4,6,7,8,9-d8
InChIKey: WJFKNYWRSNBZNX-PGRXLJNUSA-N
SMILES: [2H]C1=C2SC3=C([2H])C([2H])=C([2H])C([2H])=C3NC2=C([2H])C([2H])=C1[2H]
Biological Activity: 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[1][2].
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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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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 | 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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Structural Analogs
-
Similarity Score 0.82
HY-Y17492-Chlorophenothiazine -
Similarity Score 0.76
HY-W014120RThianthrene (Standard) -
Similarity Score 0.74
HY-34463Phenoxazine -
Similarity Score 0.72
HY-W1291559,10-Dihydroacridine -
Similarity Score 0.71
HY-B2131Iminodibenzyl -
Similarity Score 0.71
HY-N7064Iminostilbene -
Similarity Score 0.65
HY-N7133Diphenylamine hydrochloride -
Similarity Score 0.64
HY-W016174Diphenyl sulfide -
Similarity Score 0.64
HY-W1121999-Anthracenamine -
Explore the MedChemAI to find more analogs
References
- [1]. Gao YQ, et al. Isolation and Characterization of Antifungal Metabolites from the Melia azedarach-Associated Fungus Diaporthe eucalyptorum. J Agric Food Chem. 2020 Feb 26;68(8):2418-2425. [Content Brief]
- [2]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
