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SX-682

Cat. No. M9821
SX-682 Structure
Synonym:

SX682

Size Price Availability Quantity
5mg USD 100  USD100 In stock
10mg USD 150  USD150 In stock
25mg USD 280  USD280 In stock
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Quality Control & Documentation
Biological Activity

SX-682 is a potent and selective CXCR1/2 allosteric inhibitor, it may be useful for castration-resistant prostate cancer. SX-682 can block tumor myeloid-derived suppressor cells (MDSCs) recruitment and enhance T cell activation and antitumor immunity. CXCR1 and CXCR2 chemokine receptors and their ligands (CXCL1/2/3/7/8) play an important role in tumor progression.

Chemical Information
Molecular Weight 467.2
Formula C19H14BF4N3O4S
CAS Number 1648843-04-2
Solubility (25°C) DMSO ≥ 120 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Lillian Sun, et al. JCI Insight. Inhibiting myeloid-derived suppressor cell trafficking enhances T cell immunotherapy

[2] Xin Lu, et al. Nature. Effective combinatorial immunotherapy for castration-resistant prostate cancer

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  Catalog
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Keywords: SX-682, SX682 supplier, CXCR, inhibitors, activators


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