Topotecan hydrochloride
CAS No. 119413-54-6
Topotecan hydrochloride( Hycamtin | NSC 609669 | SKF 104864A )
Catalog No. M10677 CAS No. 119413-54-6
Topotecan HCl (SKF 104864A; NSC 609669) is the first topoisomerase I-directed cytotoxic agent to enter clinical trials in the United States.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 27 | In Stock |
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| 10MG | 42 | In Stock |
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| 25MG | 66 | In Stock |
|
| 50MG | 98 | In Stock |
|
| 100MG | 132 | In Stock |
|
| 500MG | 327 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTopotecan hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionTopotecan HCl (SKF 104864A; NSC 609669) is the first topoisomerase I-directed cytotoxic agent to enter clinical trials in the United States.
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DescriptionTopotecan HCl (SKF 104864A; NSC 609669) is the first topoisomerase I-directed cytotoxic agent to enter clinical trials in the United States. (In Vitro):Topotecan Hydrochloride (SKF 104864A Hydrochloride) obviously inhibits proliferation of not only human glioma cells but also glioma stem cells (GSCs) in a dose- and time-dependent manner. According to the IC50 values at 24 h, 3 μM of Topotecan Hydrochloride is selected as the optimal administration concentration. In addition, Topotecan Hydrochloride induces cell cycle arrest in G0/G1 and S phases and promoted apoptosis. Results show that the cell viability is inhibited by Topotecan Hydrochloride in a dose-dependent manner. 2, 20 and 40 μM of Topotecan Hydrochloride obviously inhibits the cell viability compared with the control groups. The IC50 values of Topotecan Hydrochloride at 24 h are 2.73±0.25 μM of U251 cells, 2.95±0.23 μM of U87 cells, 5.46±0.41 μM of GSCs-U251 and 5.95±0.24 μM of GSCs-U87. Thus 3 μM of Topotecan Hydrochloride is selected as the optimal administration concentration in the subsequent experiments. (In Vivo):NUB-7 metastatic model, the animals belonging to all the 4 groups are sacrificed after 14 days treatment. Compared with the control, Low dose metronomic (LDM) Topotecan Hydrochloride and TP+Pazopanib (PZ) liver weights are significantly lower in TP+PZ-treated animals, compared with PZ. Microscopic tumors are visible in the livers of mice belonging to all the groups except TP+PZ confirming the ability of Topotecan Hydrochloride+PZ to control liver metastasis. In a previous dose-response study, the daily dose of oral metronomic Topotecan Hydrochloride (0.5, 1.0, and 1.5 mg/kg) causes greater reduction in microvascular density compared with weekly maximum-tolerated dose regimen (7.5 and 15 mg/kg) in an ovarian cancer model, but the mice treated with 1.5 mg/kg daily, oral Topotecan Hydrochloride show decreased food intake, and a lesser antitumor effect.
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In Vitro——
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In Vivo——
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SynonymsHycamtin | NSC 609669 | SKF 104864A
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PathwayCell Cycle/DNA Damage
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TargetTopoisomerase
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RecptorTopo I (DU-145 Luc cells)| Topo I (MCF-7 Luc cells)
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number119413-54-6
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Formula Weight457.92
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Molecular FormulaC23H24ClN3O5
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Purity>98% (HPLC)
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SolubilityWater: 92 mg/mL (200.91 mM); DMSO: 92 mg/mL (200.91 mM)
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SMILESCC[C@@]1(C2=C(COC1=O)C(=O)N3CC4=C(C3=C2)N=C5C=CC(=C(C5=C4)CN(C)C)O)O.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Caceres G, et al. anticancer Drugs. 2003, 14(7), 569-574.
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