Chitrakar, Ravi team published research on Bioorganic & Medicinal Chemistry Letters in 2021 | 1603-41-4

1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, Recommanded Product: 2-Amino-5-methylpyridine

At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Recommanded Product: 2-Amino-5-methylpyridine.

Chitrakar, Ravi;Rawat, Deepa;Sistla, Ramakrishna;Vadithe, Lakshma Nayak;Subbarayappa, Adimurthy research published 《 Design, synthesis and anticancer activity of sulfenylated imidazo-fused heterocycles》, the research content is summarized as follows. The design, synthesis and study of anticancer properties of sulfenylated 2-phenylimidazo[1,2-a]pyridines I [R = H, Me, Cl, Ph; Ar = (E)-styryl, 4-methylsulfanylphenyl, 1-naphthyl, etc.; Ar1 = Ph, 4-ClPh, 1-naphthyl] and their analogs were prepared A set of twenty sulfenylated imidazo[1, 2-a]pyridine derivatives I were synthesized. Whereby elusive amendmented to the imidazo[1,2-a]pyridine motif confer dramatic changes in functional affinity of a novel action to modulate anticancer activity in seven different human cancer cell lines i.e.: MDA MB 231 (breast), HepG2 (liver), Hela (cervical), A549 (lung), U87MG (glioblastoma), SKMEL-28 (skin melanoma) and DU-145 (prostate) by employing MTT assay. Among the series, compounds I [R = H, Ar = 1-naphthyl, Ar1 = Ph; R = H, Ar = (E)-styryl, Ar1 = Ph; R = H, Ar = 4-methylsulfanylphenyl, Ar1 = Ph] showed potent activity towards human liver cancer cells HepG2. Cell cycle anal. results revealed that these compounds I [R = H, Ar = 1-naphthyl, Ar1 = Ph; R = H, Ar = (E)-styryl, Ar1 = Ph; R = H, Ar = 4-methylsulfanylphenyl, Ar1 = Ph] arrested the cell cycle at G2/M phase and induced apoptosis in human liver cancer cells HepG2. It was further confirmed by Hoechst staining, Measurement of mitochondrial membrane potential (ΔΨm) and Annexin V-FITC assay.

1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, Recommanded Product: 2-Amino-5-methylpyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem