EL-102

CAS No. 1233948-61-2

EL-102( —— )

Catalog No. M33349 CAS No. 1233948-61-2

EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 135 Get Quote
5MG 217 Get Quote
10MG 350 Get Quote
25MG 527 Get Quote
50MG 716 Get Quote
100MG 1044 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    EL-102
  • Note
    Research use only, not for human use.
  • Brief Description
    EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.
  • Description
    EL-102 is a hypoxia-induced factor 1 (Hif1α) inhibitor. EL-102 induces apoptosis, inhibits tubulin polymerisation and shows activities against prostate cancer. EL-102 can be used for the research of cancer.
  • In Vitro
    EL-102 (0-120 nM; 72 h) inhibits prostate cancer cells proliferation in vitro.EL-102 (0-100 nM; 72 h) shows cytotoxicity to prostate cancer cell lines.EL-102 (10-100 nM; 24-72 h) induces cellular apoptosis and affects cell cycle.EL-102 (10-100 nM; 24-48 h) affects PARP cleavage in DU145 cells.EL-102 (5 nM; 0-60 min) inhibits tubulin polymerisation activity.EL-102 (0-100 nM; 1 hour) inhibits Hif1α protein expression.Cell Proliferation Assay Cell Line:CWR22, 22Rv1, DU145, PC-3, DLKP and DLKPA cell lines Concentration:0-120 nM Incubation Time:72 hours Result:Inhibited proliferation of CWR22, 22Rv1, DU145, PC-3, DLKP and doxorubicin-selected variant DLKPA cells with IC50s of 24, 21.7, 40.3, 37.0, 14.4 and 16.3 nM, respectively.Cell Cytotoxicity Assay Cell Line:CWR22, 22Rv1, DU145 and PC-3 cell lines Concentration:0-100 nM Incubation Time:72 hoursResult:Exibited cytotoxicity to prostate cancer cell lines, and showed no additive effect on the inhibition of cell viability with docetaxel.Apoptosis Analysis Cell Line:CWR22, 22Rv1, DU145, PC-3, DLKP and DLKPA cell lines Concentration:10 and 100 nM Incubation Time:24, 48 and 72 hours Result:Induced cell apoptosis to inhibits cell viability with a dose of 100 nM.Western Blot Analysis Cell Line:DU145 cell line Concentration:10 and 100 nM Incubation Time:24 and 48 hours Result:Increased PARP cleavage in DU145 cells and showed a more dramatic effect with docetaxel adding.Cell Cycle Analysis Cell Line:DU145 cell line Concentration:10 and 100 nM Incubation Time:24, 48 and 72 hours Result:Increased loss of cells from G1 phase and accumulated cells in G2/M phase.Western Blot Analysis Cell Line:Prostate cancer cells Concentration:10 , 50 and 100 nM Incubation Time:24 and 48 hours Result:Modestly inhibited Hif1α expression at doses of 50 and 100 nM in normoxia.
  • In Vivo
    EL-102 (12 and 15 mg/kg; p.o. 5-day on and 2-day off, from 13 to 37 days after tumour transplantation) potentiates effects of docetaxel in vivo.Animal Model:Nude mice with CWR22 xenografts Dosage:12 and 15 mg/kg Administration:Oral gavage; 12 and 15 mg/kg 5-day on and 2-day off; from 13 to 37 days after tumour transplantation Result:Showed no effect on tumor growth, but enhanced the effect of docetaxel on tumor .
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Microtubule Associated | HIF
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1233948-61-2
  • Formula Weight
    384.47
  • Molecular Formula
    C19H16N2O3S2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 36 mg/mL (93.64 mM )
  • SMILES
    COc1ccc(cc1)S(=O)(=O)Nc1cc(ccc1C)-c1csc(c1)C#N
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. A P Toner et al. The novel toluidine sulphonamide EL102 shows pre-clinical in vitro and in vivoactivity against prostate cancer and circumvents MDR1 resistance. Br J Cancer, 2013 Oct 15, 109(8): 2131-2141.?
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