HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Amsacrine → 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Amsacrine | HCID 2179 | — |
| Edukt | (NE)-N-[1-[4-(furo[2,3-b]quinolin-4-ylamino)phenyl]ethylidene]hydroxylamine | HCID 9572568 | — |
| Edukt | N-[4-[(E)-N-methoxy-C-methylcarbonimidoyl]phenyl]furo[2,3-b]quinolin-4-amine | HCID 9572569 | — |
| Produkt | 1-(4-(Furo(2,3-b)quinolin-4-ylamino)phenyl)ethanone | HCID 404353 | — |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08952033B2 |
| Quelldatensatz | uspto-grants-2015_02 |
| ORD ID | ord-4caf5da0fffc42b49fb31ac62b759575 |
| Quellennotiz | uspto-grants-2015_02 |