Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Amsacrine → 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Amsacrine | HCID 2179 | — |
| 반응물 | (NE)-N-[1-[4-(furo[2,3-b]quinolin-4-ylamino)phenyl]ethylidene]hydroxylamine | HCID 9572568 | — |
| 반응물 | N-[4-[(E)-N-methoxy-C-methylcarbonimidoyl]phenyl]furo[2,3-b]quinolin-4-amine | HCID 9572569 | — |
| 생성물 | 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone | HCID 404353 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08952033B2 |
| 출처 데이터셋 | uspto-grants-2015_02 |
| ORD ID | ord-4caf5da0fffc42b49fb31ac62b759575 |
| 출처 메모 | uspto-grants-2015_02 |