Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 625-82-1, is researched, Molecular C6H9N, about Microtubule-Targeted Self-Assembly Triggers Prometaphase-Metaphase Oscillations Suppressing Tumor Growth, the main research direction is antimicrotubule mol self assembly metaphase oscillation antiproliferation; antimicrotubule; antiproliferation; cancer; molecular self-assembly; prometaphase−metaphase oscillation.Reference of 2,4-Dimethyl-1H-pyrrole.
Microtubules are highly strategic targets of cancer therapies. Small mol. antimitotic agents are so far the best chemotherapeutic medication in cancer treatment. However, the high rate of neuropathy and drug resistance limit their clin. usage. Inspired by the multicomponent-targeting feature of mol. self-assembly (MSA) overcoming drug resistance, we synthesized peptide-based rotor mols. that self-assemble in response to the surrounding environment to target the microtubule array. The MSAs self-adjust morphol. in response to the pH change and viscosity variations during Golgi-endosome trafficking, escape trafficking cargos, and eventually bind to the microtubule array phys. in a nonspecific manner. Such unrefined nano-bio interactions suppress regional tubulin polymerization triggering atypical prometaphase–metaphase oscillations to inhibit various cancer cells proliferating without inducing obvious neurotoxicity. The MSA also exerts potent antiproliferative effects in the s.c. cervix cancer xenograft tumor model equivalent to Cisplatin, better than the classic antimitotic drug Taxol.
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