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- Fulvestrant (ICI 182,780)
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- Estrogen/progestogen Receptor
- Fulvestrant (ICI 182,780)
Fulvestrant (ICI 182,780)
Size | Price | Stock | Qty |
---|---|---|---|
10mM (in 1mL DMSO) | $55.00 | In stock | |
25mg | $50.00 | In stock | |
100mg | $100.00 | In stock | |
Fulvestran is a newer type of estrogen receptor (ER) antagonist with IC50 value of 9.4 nM [1].
Fulvestrant treatment caused a significant decrease in MDM2 protein expression in human breast cancer cell lines MCF7 and T47D, and that the reduction of MDM2 correlated with the decrease in ER expression [1].
Fulvestrant enhances the sensitivity of human breast cancer cells to chemotherapeutic drugs. CompuSyn analyses showed that combined use of doxorubicin, paclitaxel or etoposide with fulvestrant resulted in different degrees of synergism in MCF7 and T47D cell lines tested. Besides, Combination of fulvestrant and chemotherapeutic drugs induces altered cell cycle distribution, apoptosis, and senescence [1].
References:
[1] Dolfi SC1,?J?ger AV2,?Medina DJ1,?Haffty BG3,?Yang JM4,?Hirshfield KM5.Fulvestrant treatment alters MDM2 protein turnover and sensitivity of human breast carcinoma cells to chemotherapeutic drugs. Cancer Lett.?2014 Apr 18. pii: S0304-3835 (14) 00215-8.
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- 1. Peng Wang, Li-Na Jiang, et al. "Estradiol-induced inhibition of endoplasmic reticulum stress normalizes splenic CD4 + T lymphocytes following hemorrhagic shock." Sci Rep. 2021 Apr 5;11(1):7508. PMID:33820957
- 2. Bai Y, Shen W, et al. "Combined detection of estrogen and tumor markers is an important reference factor in the diagnosis and prognosis of lung cancer." J Cell Biochem. 2018 Sep 14. PMID:30216488
- 3. McDermott MS, Chumanevich AA, et al. "Inhibition of CDK8 mediator kinase suppresses estrogen dependent transcription and the growth of estrogen receptor positive breast cancer." Oncotarget. 2017 Feb 21;8(8):12558-12575. PMID:28147342
- 4. Li, Han, et al. "Triptolide inhibits human breast cancer MCF-7 cell growth via downregulation of the ERα-mediated signaling pathway." Acta Pharmacologica Sinica (2015). PMID:25864647
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 606.77 |
Cas No. | 129453-61-8 |
Formula | C32H47F5O3S |
Solubility | ≥30.35 mg/mL in DMSO; insoluble in H2O; ≥58.9 mg/mL in EtOH |
Chemical Name | (7R,8R,9S,13S,14S,17S)-13-methyl-7-[9-(4,4,5,5,5-pentafluoropentylsulfinyl)nonyl]-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol |
SDF | Download SDF |
Canonical SMILES | CC12CCC3C(C1CCC2O)C(CC4=C3C=CC(=C4)O)CCCCCCCCCS(=O)CCCC(C(F)(F)F)(F)F |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Cell experiment [1]: | |
Cell lines |
T47D and MCF7 breast cancer cell lines |
Preparation method |
The solubility of this compound in DMSO is >30.3 mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37°C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20°C for several months. |
Reacting condition |
1 μM, 10 μM, 66 h |
Applications |
Treatment of ER+ human breast cancer cell lines, MCF7 and T47D cells with fulvestrant caused a significant decrease in MDM2 protein expression. Treatment with fulvestrant for 16 h or 66 h does not alter MDM2 mRNA level. Fulvestrant (1 μM, 16 h) facilitated degradation of MDM2 protein and shortened half-life of this protein (27 min vs. 42 min in T47D cells; 80 min vs. 180 min in MCF7 cells). Treatment with fulvestrant (5 μM, 72 h) increased the G1 population. |
Animal experiment [2]: | |
Animal models |
Nude mice bearing MCF-7 and Br10 human breast cancers |
Dosage form |
s.c. injection; 5 mg; 4 weeks |
Application |
Fulvestrant substantially reduced tumor growth. |
Clinical Trials [3]: | |
Clinical Trials |
Postmenopausal women with advanced breast cancer |
Dosage form |
Intramuscular injection; 250 mg as a once-monthly (one × 5 mL), |
Application |
Fulvestrant is an additional, effective, and well-tolerated treatment for advanced breast cancer in postmenopausal women whose disease progressed on prior endocrine therapy. |
Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
References: [1] Dolfi SC1, Jger AV2, Medina DJ1, Haffty BG3, Yang JM4, Hirshfield KM5.Fulvestrant treatment alters MDM2 protein turnover and sensitivity of human breast carcinoma cells to chemotherapeutic drugs. Cancer Lett. 2014 Apr 18. pii: S0304-3835 (14) 00215-8. [2] Wakeling A E, Dukes M, Bowler J. A potent specific pure antiestrogen with clinical potential [J]. Cancer research, 1991, 51 (15): 3867-3873. [3] Howell A, Robertson J F R, Quaresma Albano J, et al. Fulvestrant, formerly ICI 182,780, is as effective as anastrozole in postmenopausal women with advanced breast cancer progressing after prior endocrine treatment [J]. Journal of Clinical Oncology, 2002, 20 (16): 3396-3403. |
Quality Control & MSDS
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