Elacestrant dihydrochloride
Elacestrant dihydrochloride Basic information
- Product Name:
- Elacestrant dihydrochloride
- Synonyms:
-
- Elacestrant dihydrochloride
- (R)-6-(2-(ethyl(4-(2-(ethylamino)ethyl)benzyl)amino)-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol dihydrochloride
- RAD1901 HCl salt
- (6R)-6-[2-(Ethyl{4-[2-(ethylamino)ethyl]benzyl}amino)-4-methoxyphenyl]-5,6,7,8-tetrahydro-2-naphthalenol dihydrochloride
- Elacestrant 2HCl
- RAD-1901
- RAD1901 dihydrochloride
- RAD 1901 2HCl
- CAS:
- 1349723-93-8
- MF:
- C30H40Cl2N2O2
- MW:
- 531.5568
- EINECS:
- 215-871-3
- Product Categories:
-
- API
- Mol File:
- 1349723-93-8.mol
Elacestrant dihydrochloride Chemical Properties
- solubility
- DMSO:100.0(Max Conc. mg/mL);188.13(Max Conc. mM)
H2O:50.0(Max Conc. mg/mL);94.06(Max Conc. mM) - form
- Solid
- color
- White to off-white
- InChIKey
- TVTRJGWMKDMZSN-AAZDGHFONA-N
- SMILES
- N(C1C=C(OC)C=CC=1[C@@H]1CCC2=CC(O)=CC=C2C1)(CC)CC1C=CC(CCNCC)=CC=1.Cl |&1:9,r|
Elacestrant dihydrochloride Usage And Synthesis
Uses
Elacestrant (RAD1901) dihydrochloride is an orally available and selective estrogen receptor degrader (SERD) with IC50s of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant dihydrochloride also can inhibit growth of ER+ breast cancer cell lines in vitro and in vivo[1][2].
in vivo
Elacestrant dihydrochloride (0.3-120 mg/kg; p.o.; single daily for 40 days) antagonizes E2-mediated uterine stimulation in a dose-dependent manner in vivo[1].
Elacestrant dihydrochloride (30, 60 mg/kg; p.o.; single daily for 4 weeks) induces complete tumor growth inhibition in mice[2].
Tumor growth inhibition is maintained for 4 weeks after Elacestrant dihydrochloride withdrawal[2].
| Animal Model: | MCF7 cell line xenograft model of mice[2]. |
| Dosage: | 30, 60 mg/kg |
| Administration: | Oral administration; single daily for 4 weeks. |
| Result: | Inhibited growth of tumor. |
References
[1] Garner F, et al. RAD1901: a novel, orally bioavailable selective estrogen receptor degrader that demonstrates antitumor activity in breast cancer xenograft models. Anticancer Drugs. 2015 Oct;26(9):948-56. DOI:10.1097/CAD.0000000000000271
[2] Bihani T, et al. Elacestrant (RAD1901), a Selective Estrogen Receptor Degrader (SERD), Has Antitumor Activity in Multiple ER+ Breast Cancer Patient-derived Xenograft Models. Clin Cancer Res. 2017 Aug 15;23(16):4793-4804. DOI:10.1158/1078-0432.CCR-16-2561
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