936-05-0
936-05-0
Chemical Structure
HMMNI
Synonym(s): Hydroxy Dimetridazole
- CAS 番号: 936-05-0
- Formula:C5H7N3O3
- Molecular Weight:157.13
IUPAC Name: (1-methyl-5-nitro-1H-imidazol-2-yl)methanol
InChIKey: JSAQDPJIVQMBAY-UHFFFAOYSA-N
SMILES: OCC1=NC=C([N+]([O-])=O)N1C
Biological Activity: HMMNI (Hydroxy dimetridazole) is a hydroxy metabolite of Dimetridazole (HY-B1244). Dimetridazole is a nitroimidazole class drug that combats protozoan infections[1][2].
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
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HMMNI | 99.91% | HMMNI (Hydroxy dimetridazole) is a hydroxy metabolite of Dimetridazole (HY-B1244). Dimetridazole is a nitroimidazole class drug that combats protozoan infections. | ||||||||||||||||||||
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HMMNI (Standard) | ≥98% | HMMNI (Standard) (Hydroxy Dimetridazole (Standard)) is the analytical standard of HMMNI (HY-W008216). This product is intended for research and analytical applications. HMMNI (Hydroxy dimetridazole) is a hydroxy metabolite of Dimetridazol (HY-B1244). Dimetridazole is a nitroimidazole class drug that combats protozoan infections. | ||||||||||||||||||||
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HMMNI-d3 | 99.90% | HMMNI-d3 (Hydroxy Dimetridazole-d3) is deuterium labeled HMMNI (HY-W008216). HMMNI (Hydroxy dimetridazole) is a hydroxy metabolite of Dimetridazol (HY-B1244). Dimetridazole is a nitroimidazole class agent that combats protozoan infections. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.84
HY-B1244Dimetridazole -
Similarity Score 0.82
HY-136440Hydroxymetronidazole -
Similarity Score 0.82
HY-B0318Metronidazole -
Similarity Score 0.82
HY-B0318SMetronidazole-13C2,15N2 -
Similarity Score 0.80
HY-135212Hydroxy ipronidazole -
Similarity Score 0.80
HY-B0318AMetronidazole hydrochloride -
Similarity Score 0.80
HY-B0565RRonidazole (Standard) -
Similarity Score 0.80
HY-151217RIpronidazole (Standard) -
Similarity Score 0.79
HY-136436ATernidazole -
Explore the MedChemAI to find more analogs
References
- [1]. Cronly M, et al. Rapid confirmatory method for the determination of 11 nitroimidazoles in egg using liquid chromatography tandem mass spectrometry. J Chromatogr A. 2009;1216(46):8101‐8109. [Content Brief]
- [2]. Walsh JS, et al., Structural alterations that differentially affect the mutagenic and antitrichomonal activities of 5-nitroimidazoles. J Med Chem. 1987 Jan;30(1):150-6. [Content Brief]
