ChemicalBook--->CAS DataBase List--->175519-16-1

175519-16-1

175519-16-1 Structure

175519-16-1 Structure
IdentificationBack 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 PropertiesBack 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 InformationBack 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]

TargetValue
Topo II
[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
Spectrum DetailBack Directory
[Spectrum Detail]

AG 7352 Hydrochloride(175519-16-1)1HNMR
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