1750-12-5
1750-12-5
Chemical Structure
AHMT
- CAS. Nr.: 1750-12-5
- Formula:C2H6N6S
- Molecular Weight:146.17
IUPAC Name: (Z)-4-amino-5-hydrazono-1,2,4-triazolidine-3-thione
InChIKey: RDIMQHBOTMWMJA-UHFFFAOYSA-N
SMILES: S=C(N/1N)NNC1=N\N
Biological Activity: AHMT is an aldehyde-specific and aldehyde-reactive colorimetric detection reagent. AHMT detects the formation of Phenylacetaldehyde in high-throughput screening for engineered anti-Markovnikov oxidation activity. AHMT serves as a formaldehyde detection reagent to detect formaldehyde produced in the Methanethiol oxidase reaction[1][2][3].
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AHMT | 98.0% | AHMT is an aldehyde-specific and aldehyde-reactive colorimetric detection reagent. AHMT detects the formation of Phenylacetaldehyde in high-throughput screening for engineered anti-Markovnikov oxidation activity. AHMT serves as a formaldehyde detection reagent to detect formaldehyde produced in the Methanethiol oxidase reaction. | ||||||||||||||||||||
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AHMT (Standard) | ≥98% | AHMT (Standard) is the analytical standard of AHMT (HY-D0906). This product is intended for research and analytical applications. AHMT is an aldehyde-specific and aldehyde-reactive colorimetric detection reagent. AHMT detects the formation of Phenylacetaldehyde in high-throughput screening for engineered anti-Markovnikov oxidation activity. AHMT serves as a formaldehyde detection reagent to detect formaldehyde produced in the Methanethiol oxidase reaction. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.62
HY-W0129913-Mercapto-1,2,4-triazole -
Similarity Score 0.55
HY-W0275921H-1,2,4-Triazol-3-amine -
Similarity Score 0.55
HY-W110148SAmitrole-13C,15N2 -
Similarity Score 0.54
HY-W1049797(4H-1,2,4-Triazole-3,5-diyl)dimethanol -
Similarity Score 0.54
HY-W010407SCyanuric acid-13C3 -
Similarity Score 0.54
HY-Y1117RMelamine (Standard) -
Similarity Score 0.54
HY-Y1117SMelamine-15N3 -
Similarity Score 0.54
HY-Y1117S1Melamine-13C3 -
Similarity Score 0.54
HY-Y1117S2Melamine-15N3,13C3 -
Explore the MedChemAI to find more analogs
References
- [1]. Upp D M, Mateljak I, Mendez-Sanchez D, et al. Promiscuous fungal peroxygenase from Chaetomium globosum by directed evolution[J]. iScience, 2026, 29(10): 117534.
- [2]. Schlemminger H, et al. Evolutionary Conservation of the Copper-Dependent Thiol Oxidase Activity of Selenium-Binding Proteins[J]. Antioxidants, 2026, 15(9): 1148.
- [3]. Krafczyk N, et al. Hepatic methanethiol oxidase (MTO) activity of mice requires adequate dietary supply of copper. Redox biology. 2026 Sep 06;97:104384.
