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HRID 1846411作成日:2026年10月25日

Amsacrine → 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone

https://huagongshe.com/reaction/1846411

反応式

関与物質

役割名称HCID仕込み量
反応物AmsacrineHCID 2179—
反応物(NE)-N-[1-[4-(furo[2,3-b]quinolin-4-ylamino)phenyl]ethylidene]hydroxylamineHCID 9572568—
反応物N-[4-[(E)-N-methoxy-C-methylcarbonimidoyl]phenyl]furo[2,3-b]quinolin-4-amineHCID 9572569—
生成物1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanoneHCID 404353—

反応手順

In addition, (E)-1-(4-(furo[2,3-b]quinolin-4-ylamino)phenyl)ethanone oxime (a hydroxyimino derivative of compound 1, referred to as compound 2 hereinafter) and (E)-1-(4-(furo[2,3-b]quinolin-4-ylamino)phenyl)ethanone O-methyloxime (a methoxyimino derivative of compound 1, referred to as compound 3 hereinafter) were also shown to have an antiproliferative potency comparable to that of amsacrine. The applicants even further found that compound 1 is able to induce mitotic arrest and apoptosis by binding to tubulin and inhibiting tubulin polymerization (Huang Y. T. et al. (2005), J. Med. Chem., 280:2771-2779).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08952033B2
出典データセットuspto-grants-2015_02
ORD IDord-4caf5da0fffc42b49fb31ac62b759575
出典メモuspto-grants-2015_02