Identification | Back Directory | [Name]
AG 7352 Hydrochloride | [CAS]
175519-16-1 | [Synonyms]
AG 7352 Hydrochloride SNS-595 Hydrochloride Vosaroxin Hydrochloride Voreloxin (SNS-595) HCl Voreloxin (Hydrochloride) Vosaroxin hydrochloride salt Voreloxin(SNS-595)hydrochloride Vosaroxin hydrochloride >=98% (HPLC) SNS-595 HYDROCHLORIDE; VOSAROXIN HYDROCHLORIDE; AG 7352 HYDROCHLORIDE 1,8-Naphthyridine-3-carboxylic Acid, 1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-, monohydrochloride (3S-trans)-1,4-Dihydro-7-[3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid monohydrochloride | [Molecular Formula]
C18H20ClN5O4S | [MDL Number]
MFCD00946608 | [MOL File]
175519-16-1.mol | [Molecular Weight]
437.9 |
Chemical Properties | Back Directory | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in DMSO | [form ]
Solid | [color ]
White to gray | [optical activity]
[α]/D +42 to +52°, c =1 in 0.1 M NaOH | [Water Solubility ]
H2O: 1mg/mL, clear (warmed) |
Hazard Information | Back Directory | [Uses]
Voreloxin Hydrochloride is a first-in-class topoisomerase II inhibitor that intercalates DNA and induces site-selective DNA DSB, G2 arrest, and apoptosis. | [Biological Activity]
Voreloxin hydrochloride (SNS-595, Vosaroxin) is a potent Topoisomerase II inhibitor with broad-spectrum antitumor activity. Phase 2. | [in vivo]
Voreloxin (20 mg/kg, i.v.) alone results in 80% reduction in bone marrow cellularity of CD-1 mice by administration one dose every 4 days repeated twice (q4d ×2). voreloxin at 10 mg/kg in combination with cytarabine causes ablation of the marrow, dilation of sinusoids, and infiltration of adipocytes in mice. Voreloxin (20 mg/kg, i.v.) combined with cytarabine causes a reversible decrease in myeloid and lymphoid cells in bone marrow and peripheral blood CD-1 mice. voreloxin (10 mg/kg, q4d ×2) and cytarabine in combination causes reversible neutropenia with a more modest impact on platelets CD-1 mice[2]. | [target]
| [IC 50]
Topoisomerase II | [References]
[1] Hotinski AK, et al. Vosaroxin is a novel topoisomerase-II inhibitor with efficacy in relapsed and refractory acute myeloid leukaemia. Expert Opin Pharmacother. 2015 Jun;16(9):1395-402. DOI:10.1517/14656566.2015.1044437 [2] Scatena CD, et al. Voreloxin, a first-in-class anticancer quinolone derivative, acts synergistically with cytarabine in vitro and induces bone marrow aplasia in vivo. Cancer Chemother Pharmacol. 2010 Oct;66(5):881-8. DOI:10.1007/s00280-009-1234-z [3] Walsby EJ, et al. The topoisomerase II inhibitor voreloxin causes cell cycle arrest and apoptosis in myeloid leukemia cells and acts in synergy with cytarabine. Haematologica. 2011 Mar;96(3):393-9. DOI:10.3324/haematol.2010.032680 |
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Company Name: |
SPIRO PHARMA
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Tel: |
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Website: |
www.spiropharma.com.cn |
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