N1-EthylpseudoUridine is an indispensable compound in the biomedical field, demonstrating profound applications encompass disease research, prevention and intervention. This exceptional substance exhibits unparalleled potential in studying viral onslaughts, malignant neoplasms and neurologic afflictions.
N1-BenzylpseudoUridine, a cutting-edge biomedical marvel, emerges as an ingenious solution to combat various ailments. Its remarkable prowess lies in its potential to exhibit antiviral properties, rendering it a captivating prospect for conquering RNA viruses. Additionally, its inhibitory effect on cancer cell proliferation makes it an alluring candidate for tailored therapeutic interventions. Scientists are diligently conducting further investigations to unleash its therapeutic potential against specific viral infections and malignant conditions, illuminating the path toward unprecedented medical breakthroughs.
N10-(Trifluoroacetyl)pteroic acid (CAS# 37793-53-6) is a derivative of Pteroic acid (P840110), both of which are used as reagents to synthesize target ligands, like Folic acid (F680300), that have the ability to deliver chemotherapeutic agents specifically to cancer cells.
N1,N3-Bis(cyanomethyl)pseudoUridine, a compound employed in the production of antiviral drugs aimed at combating viral infections spanning coronaviruses, designates a formidable inhibitor of viral RNA generation, disallowing virus replication. Elucidating its further capabilities, studies suggest this compound exhibits prospective implications in tumor therapy, acting as a growth-reducing agent for malignant cells.
N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamide is an impurity of Afatinib, which is a tyrosine kinase inhibitor used to treat non-small cell lung carcinoma (NSCLC).
N-[2-(4-oxo-4H-3,1-benzoxazin-2-yl)phenyl]-2-naphthalenesulfonamide, a profound small molecule inhibitor designed to target Cancerous Enzyme Carbonic Anhydrase IX (CAIX). This molecule is capable of exhibiting its potential therapeutic efficacy against various malignancies in numerous body sites including Breast, Prostate, and Kidney. This inhibitor is highly recommended due to its ability to repress the CAIX activity, a pivotal catalyst responsible for tumor inception, advancement, and invasion, rendering it a glimmer of hope as a Cancer treatment.
An impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor.
N-[[(1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl]carbonyl]glycine ethyl ester is a cooling compound and a derivative of the monoterpene (–)-menthol. Formulations containing WS5 have been used as cooling agents in toothpaste and hard candies, as well as skin creams and lotions.
N'-[(6-Methyl-2-pyridyl)methylene]pyrrolidine-1-carbothiohydrazide, a chemical entity with an aptitude for disrupting tumor metastasis, has recently proven to be quite efficacious. Its ability to suppress the growth of various cancerous cells has been demonstrated in numerous studies. When used judiciously, this agent could be quite promising in the treatment of cancer, opening up alternate therapeutic avenues.
An impurity of Acyclovir. Acyclovir is an antiviral drug used for the treatment of infections caused by herpes simplex virus and herpes zoster virus. It acts via inhibiting the production of virus' DNA.
N,N'-Ethylenebisoleamide is a compound with surfactant and emulsifying properties, extensively used in biomedicine. Its multipurpose functionality includes being an antifungal, anticancer and antiviral agent, and its feasibility against life-altering diseases such as HIV, influenza, and cancer are being researched.
N,N-Dimethyl-L-Tyrosine, a derivative of the amino acid tyrosine, has been a subject of interest in the research field due to its key role in elucidating amino acid metabolism. Additionally, it has been extensively studied for its precursor role in the synthesis of well-known neurotransmitters like dopamine and norepinephrine, thereby finding novel therapeutic applications in the treatment of neurodegenerative disorders such as Parkinson's disease and depression. The significance of this chemical compound could not be overstated in the realm of medicinal research.
N,N-dimethyldodecan-1-amine oxide is a frequently-used amine oxide surfactant. It is strongly hydrophilic, and it forms normal micelles and normal liquid crystalline phases.
N,N-Dimethyldecylamine N-oxide, commonly known as a tertiary amine oxide, is a surfactant used extensively in scientific research due to its unique properties as both a nonionic surfactant and a stabilizing agent in various aqueous and non-aqueous systems.
N,N'-Difurfuryloxamide, an organic compound of paramount significance used as a crucial forerunner in the creation of sundry medicines and pharmaceuticals. Distinguished by its notable anti-inflammatory and antimicrobial traits, it exhibits extensive promise as an agent amenable for treating multiple ailments like gingivitis and periodontitis.
N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine, also called 2-Ethylaminoatrazine, under the IUPAC name 2-Ethylaminoatrazine, can be used as insecticide and herbicide.
N,N-diethyl-2-((6-methylpyridin-2-yl)methylene)hydrazinecarbothioamide, a chemically-complex compound, is gaining recognition in biomedicine as a viable drug candidate for treating a range of ailments. Notably, research suggests that it possesses considerable anti-inflammatory, analgesic, and antioxidant activity that could hold promise in combatting conditions such as arthritis and other inflammatory disorders. Nevertheless, comprehensive studies are necessary to ascertain its optimal therapeutic capacity.
An impurity of Levofloxacin, which is as efficacious as or more efficacious than that with ciprofloxacin in systemic as well as pyelonephritis infections in mice.
N,N'-bis-(2-Chloroethyl)urea is an indispensable compound in the field of biomedicine manifesting remarkable cytotoxic characteristics. Its application extends to diverse cancer types, encompassing lymphoma, leukemia and solid tumors, owing to its potent chemotherapeutic attributes.
N,N,N,N-Tetraacetyl Chitotetraose is an intriguing biomedical compound with prodigious prowess in the research of immunology and pioneering drug delivery systems.
N-(Quinoxalin-2-yl)-4-(quinoxalin-2-ylamino)benzenesulfonamide, an intriguing chemical substance, has garnered interest in the biomedical domain as a plausible remedy for assorted cancer types. This compound exerts its therapeutic effects by curbing certain enzymes and provoking apoptosis in malignant cells, thereby causing their demise. Although promising, further scientific investigations and clinical deliberations are fundamental to ascertain its potency and risk profiles.
N-(Formyl amidino)-N-β-D-ribofuranosylurea is a formidable antiviral compound extensively applied in the biomedical sector, exhibiting exceptional qualities in the research of impeding the proliferation of designated viruses like influenza and herpes viruses.
An impurity of Sulfamethoxazole, which is an antibiotic and a structural analog of para-aminobenzoic acid (PABA). It competes with PABA to bind to dihydropteroate synthetase to inhibit the synthesis of dihydrofolic acid.
N-(2-Methoxy-5-methylphenyl)-acetamide, a chemical compound of interest, has potential applications in biomedical research as a putative analgesic, anti-inflammatory and antipyretic agent, as well as in the treatment of neurodegenerative diseases such as Parkinson's and Alzheimer's. Coherent research is warranted to ascertain its full pharmaceutical potential.
N-(2-Aminoethyl)piperazine-1,4-diethylamine, a compound utilized in the biomedical sector, holds promise in the treatment of select cancer and neurological ailments. Demonstrating efficacy as a targeted therapeutic agent for distinct tumor varieties, this product has displayed encouraging outcomes in preliminary research investigations.
One of the impurities of Vonoprazan, which is a potassium-competitive acid blocker and has been found to be effective in the treatment of gastroduodenal ulcer and reflux esophagitis.
An impurity of Valdecoxib. Valdecoxib is a non-steroidal anti-inflammatory drug (NSAID) used for the treatment of osteoarthritis, rheumatoid arthritis, etc. Valdecoxib exhibits a selectively inhibitory effect of cyclooxygenase-2.
N 0924 hydrochloride is a dopamine (DA) receptor agonist that is the less active enantiomer of N-0437 in comparison with the opposite (S)-(-)-enantiomer, Rotigotine.
Myristyl acetate, a fragrance ingredient ubiquitous in cosmetics and personal care products, and also present in food as a flavoring agent, has been of considerable interest in the pharmaceutical industry. Its therapeutic properties against a variety of disorders, including psoriasis and eczema, have been investigated, as has its insecticidal potential.
