1. Cell Cycle/DNA Damage Cytoskeleton
  2. Microtubule/Tubulin
  3. STA-9584

STA-9584 is a potent vascular disrupting agent (VDA) that targets tubulin. STA-9584 exhibits potent antitumor activity in mouse xenograft model by selectively targeting microvasculature at both the center and periphery of tumors. STA-9584 can be used for research in prostate and breast cancer.

For research use only. We do not sell to patients.

STA-9584

STA-9584 Chemical Structure

CAS No. : 906481-23-0

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Description

STA-9584 is a potent vascular disrupting agent (VDA) that targets tubulin. STA-9584 exhibits potent antitumor activity in mouse xenograft model by selectively targeting microvasculature at both the center and periphery of tumors. STA-9584 can be used for research in prostate and breast cancer[1].

In Vivo

STA-9584 (4.5 mg/kg, i.v., weekly for 2-3 weeks) induces significant tumor regressions in mouse prostate and breast xenograft models by selectively disrupting tumor microvasculature at both the center and periphery[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female BALB/c mice (7-12 weeks old) subcutaneously implanted with EMT6 cells[1]
Dosage: 4.5 mg/kg
Administration: i.v., weekly for 2 weeks
Result: Completely blocked blood flow in highly perfused tumor subregions within 4 h of drug administration.
Completely arrested tumor growth over this period with a single dose for 24 h.
Exhibited far more extensive cellular destruction throughout the entire tumor, including areas of fibrosis and dramatically reduced viable rim or surviving tumor zones.
Resulted in no detectable viable rim tissue in many tumor sections.
Increased microvasculature destruction and consequent apoptosis in peripheral regions of tumors.
Induced widespread disruption of tumor microvessels, characterized by decreased, patchy CD31 expression, loss of integrity, and thrombosis.
Decreased CD31 endothelial cells in the viable rim by 77%.
Animal Model: Female BALB/c nude mice (7-12 weeks old) subcutaneously implanted with PC-3 cells[1]
Dosage: 4.5 mg/kg
Administration: i.v., weekly for 3 weeks
Result: Induced significantly tumor regression (40%) compared with the control group.
Was well tolerated with minimal loss of body weight during the course of treatment.
Animal Model: Female CB-17/ Icr-Prkdcscid (SCID) mice (7-12 weeks old) subcutaneously implanted with MDA-MB-231 cells[1]
Dosage: 4.5 mg/kg
Administration: i.v., weekly for 3 weeks
Result: Resulted in 60% tumor regression.
Molecular Weight

540.01

Formula

C28H30ClN3O6

CAS No.
SMILES

O=C(NC1=CC(C2=C(C3=CC(OC)=C(OC)C(OC)=C3)ON=C2)=CC=C1OC)[C@@H](N)CC4=CC=CC=C4.Cl

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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STA-9584
Cat. No.:
HY-111170
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