化工社化工社 化学情報印刷レポート · 研究参考用
Amsacrine → 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Amsacrine | HCID 2179 | — |
| 反応物 | (NE)-N-[1-[4-(furo[2,3-b]quinolin-4-ylamino)phenyl]ethylidene]hydroxylamine | HCID 9572568 | — |
| 反応物 | N-[4-[(E)-N-methoxy-C-methylcarbonimidoyl]phenyl]furo[2,3-b]quinolin-4-amine | HCID 9572569 | — |
| 生成物 | 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08952033B2 |
| 出典データセット | uspto-grants-2015_02 |
| ORD ID | ord-4caf5da0fffc42b49fb31ac62b759575 |
| 出典メモ | uspto-grants-2015_02 |