Chemistry Milestones Of 56621-48-8

There is still a lot of research devoted to this compound(SMILES:OC1=CC=C(N2CCNCC2)C=C1)COA of Formula: C10H14N2O, and with the development of science, more effects of this compound(56621-48-8) can be discovered.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 56621-48-8, is researched, SMILESS is OC1=CC=C(N2CCNCC2)C=C1, Molecular C10H14N2OJournal, Article, Bioorganic & Medicinal Chemistry Letters called Potent, selective, and orally active adenosine A2A receptor antagonists: Arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines, Author is Neustadt, Bernard R.; Hao, Jinsong; Lindo, Neil; Greenlee, William J.; Stamford, Andrew W.; Tulshian, Deen; Ongini, Ennio; Hunter, John; Monopoli, Angela; Bertorelli, Rosalia; Foster, Carolyn; Arik, Leyla; Lachowicz, Jean; Ng, Kwokei; Feng, Kung-I., the main research direction is pyrazolo triazolo pyrimidine arylpiperazine preparation adenosine receptor antagonist SAR.COA of Formula: C10H14N2O.

Antagonism of the adenosine A2A receptor offers great promise in the treatment of Parkinson’s disease. Employing the known pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine A2A antagonist SCH 58261 as a starting point, we identified the potent and selective (vs. A1) antagonist 11h (I), orally active in the rat haloperidol-induced catalepsy model. We further optimized this lead to the methoxyethoxyethyl ether 12a (SCH 420814), which shows broad selectivity, good pharmacokinetic properties, and excellent in vivo activity.

There is still a lot of research devoted to this compound(SMILES:OC1=CC=C(N2CCNCC2)C=C1)COA of Formula: C10H14N2O, and with the development of science, more effects of this compound(56621-48-8) can be discovered.

Reference:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem