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- 保存条件:
Pure form: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
3-Methylsulfanylpropionic acid
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
646-01-5
- 规格:
10 mM * 1 mL/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥550.0 |
|---|---|---|---|
| 规格: | 100 mg | 产品价格: | ¥500.0 |
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3-(Methylthio)propionic acid
CAS No. : 646-01-5
MCE 国际站:3-(Methylthio)propionic acid
产品活性:3-(Methylthio)propionic acid是甲硫氨酸代谢的中间体。
研究领域:Anti-infection | Metabolic Enzyme/Protease
作用靶点:Fungal | Endogenous Metabolite
结构分类:酮、醛、酸
In Vitro: Methionine has consistently been shown to be the most toxic amino acid in experiments devised to assess the relative toxicity of dietary amino acids. 3-methylthiopropionate is an intermediate in methionine catabolism in rat and monkey liver in vitro. This pathway appears to account for a major portion of methionine oxidation in vitro. Cultures of Streptomyces lincolnensis accumulated 3-methylthioacrylic acid in amounts directly related to the concentration of methionine in the medium. The first intermediate in the pathway may be the keto acid, which is then oxidatively decarboxylated to 3-methylthiopropionic acid. The purified 3-MTPA has antifungal activity in assays using F. oxysporum as a model fungus. Daily measurements of shoot and root length shows severe inhibition of seed germination and root and shoot development at concentrations above 12mg for partially purified extracts. 3-methylthiopropionic acid ethyl ester possesses potential anticarcinogenic properties by inducing differentiation in well-differentiated colon cancer cells. Treatment of RCM-1 cells for 4 days with 3-methylthiopropionic acid ethyl ester between the doses of 0.25 and 2 mM progressively increases the percent area occupied by duct structures relative to the control, and also induces an increase in the number and the maximum diameter of the ducts in each culture plate.
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文献和实验Figure 4.11.2 Data from the scintillation counter are plotted as cpm (divided by 1 × 103 for convenience) versus reaction time for the substrates hydrocinnamic acid (open triangles) and indole‐3‐propionic acid
Characterization of Wild‐Type Excitatory Amino Acid Ion Channel Receptors
‐4‐isoxazole propionic acid ([3 H]AMPA; NEN Life Sciences) Test compounds Tissue solubilizer (e.g., Solvable; NEN Life Sciences
Pollen Development in Anthers of Arabidopsis
apart from the anthers. 10. Carefully remove excess Acetic Acid with a piece of filter paper and immediately add a drop of 1% Propionic Carmine to stain the chromosomes (see Hint #1). 11. Gently tap the preparation with a copper rod
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