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Amonafide Amonafide is a DNA intercalator and topoisomerase II inhibitor in clinical development for the treatment of neoplastic diseases. Antitumor agent. Group: Biochemicals. Alternative Names: 5-Amino-2-[2-(dimethylamino)ethyl]-1H-benz[de]isoquinoline-1,3(2H)-dione; FA 142; M-FA 142; MADE-FA 142; NCI 308847; NSC 308847; Nafidimide. Grades: Highly Purified. CAS No. 69408-81-7. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 2
Worldwide
Amonafide Amonafide is an imide derivative of naphthalic acid. Amonafide intercalates into DNA and inhibits topoisomerase II, resulting in protein-associated strand breaks and impaired DNA and RNA synthesis. Uses: Antineoplastic agents. Synonyms: Nafidimide; Quinamed; Xanafide. Grades: 0.98. CAS No. 69408-81-7. Molecular formula: C16H17N3O2. Mole weight: 283.33. BOC Sciences
Amonafide Amonafide is a topoisomerase II inhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding of Topo II to DNA. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AS1413. CAS No. 69408-81-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10982. MedChemExpress MCE
Amonafide L-malate Amonafide L-malate is the malate salt of amonafide, an imide derivative of naphthalic acid, with potential antineoplastic activity. Amonafide intercalates into DNA and inhibits topoisomerase II, resulting in DNA double-strand breaks (DSB) and inhibition of DNA replication and RNA synthesis. Synonyms: AS1413; AS 1413; AS-1413; XLS-001; XLS001; XLS001; Xanafide. CAS No. 618863-60-8. Molecular formula: C20H24N4O6. Mole weight: 416.43. BOC Sciences 2
Amonafide N-oxide Amonafide N-oxide. Group: Biochemicals. Alternative Names: 5-Amino-2-[2- (dimethyloxidoamino) ethyl]-1H-benz[de]isoquinoline-1, 3 (2H) -dione; 5-Amino-2-[2-(dimethylamino)ethyl]-1H-benz[de]isoquinoline-1,3(2H)-dione N-oxide. Grades: Highly Purified. CAS No. 112726-97-3. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C16H17N3O3. US Biological Life Sciences. USBiological 6
Worldwide
Amonafide N-oxide Amonafide N-oxide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-Amino-2-[2-(dimethyloxidoamino)ethyl]-1H-benz[de]isoquinoline-1,3(2H)-dione; 5-Amino-2-[2-(dimethylamino)ethyl]-1H-benz[de]isoquinoline-1,3(2H)-dione N-Oxide. Product Category: Heterocyclic Organic Compound. CAS No. 112726-97-3. Molecular formula: C16H17N3O3. Mole weight: 299.32. Product ID: ACM112726973. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 4
N-Acetyl Amonafide A metabolite of Amonafide. Group: Biochemicals. Alternative Names: N-[2-[2-(Dimethylamino)ethyl]-2,3-dihydro-1,3-dioxo-1H-benz[de]isoquinolin-5-yl]acetamide; MADE-FA 4512; N-Acetylamonafide. Grades: Highly Purified. CAS No. 69409-02-5. Pack Sizes: 2.5mg. US Biological Life Sciences. USBiological 1
Worldwide
N'-Desmethyl amonafide N'-Desmethyl amonafide. Group: Biochemicals. Alternative Names: 5-Amino-2-[2-(methylamino)ethyl]-1H-benz[de]isoquinoline-1,3(2H)-dione. Grades: Highly Purified. CAS No. 114991-16-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C15H15N3O2. US Biological Life Sciences. USBiological 7
Worldwide
Ethonafide Ethonafide is an anthracene-containing derivative of amonafide that belongs to the azonafide series of anticancer agents. The lack of cross-resistance in multidrug-resistant cancer cell lines and the absence of a quinone and hydroquinone moiety make ethonafide a potentially less cardiotoxic replacement for existing anthracene-containing anticancer agents. Ethonafide was cytotoxic against three human prostate cancer cell lines at nanomolar concentrations. Ethonafide was found to be better tolerated and more effective at inhibiting tumor growth compared with mitoxantrone in a human xenograft tumor regression mouse model. Mechanistically, we found that ethonafide inhibited topoisomerase II activity by stabilizing the enzyme-DNA complex, involving both topoisomerase IIalpha and -beta. In addition, ethonafide induced a potent G(2) cell cycle arrest in the DU 145 human prostate cancer cell line. By creating stable cell lines with decreased expression of topoisomerase IIalpha or -beta, we found that a decrease in topoisomerase IIalpha protein expression renders the cell line resistant to ethonafide. The decrease in sensitivity to ethonafide was associated with a decrease in DNA damage and an increase in DNA repair as measured by the neutral comet assay. These data demonstrate that ethonafide is a topoisomerase II poison and that it is topoisomerase IIalpha-specific in the DU 145 human prostate cancer cell line. Uses: Topoisomerase ii inhibitors. Synonyms: AMP-53; AMP 53; AMP53; 2-(2'-(Dimethylamino)ethyl)-1,2-dihydro-7-ethoxydibenz(de, H)isoquinoline-1,3-dione; 2-[2-(Dimethylamino)ethyl]-7-ethoxy-1H-dibenz[de,h]isoquinoline-1,3(2H)-dione. CAS No. 175293-23-9. Molecular formula: C22H22N2O3. Mole weight: 362.43. BOC Sciences 11
UNBS3157 UNBS3157 is a DNA intercalator, and a novel nonhematotoxic naphthalimide derivative with potent antitumor activity. Amonafide, a naphthalimide which binds to DNA by intercalation and poisons topoisomerase IIalpha, has demonstrated activity in phase II breast cancer trials, but has failed thus far to enter clinical phase III because of dose-limiting bone marrow toxicity. Synonyms: UNBS 3157; UNBS-3157. Grades: 98%. CAS No. 868962-26-9. Molecular formula: C19H17Cl3N4O4. Mole weight: 471.72. BOC Sciences 11

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