GLPBio

Elacestrant dihydrochloride (RAD1901 dihydrochloride)

Catalog No.: GC32696Purity:>99.50%Synonyms: RAD1901 dihydrochloride
Elacestrant-Dihydrochlorid (RAD1901-Dihydrochlorid) (RAD1901-Dihydrochlorid) ist ein oral verfÜgbarer selektiver Östrogenrezeptor-Degrader (SERD) mit IC50-Werten von 48 und 870 nM fÜr ER&7#945; bzw. ERβ.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Elacestrant dihydrochloride (RAD1901 dihydrochloride)
Cas No.: 1349723-93-8
10mM (in 1mL DMSO)In Stock
$213.00
1
1mgIn Stock
$83.00
1
5mgIn Stock
$177.00
1
10mgIn Stock
$293.00
1
25mgIn Stock
$482.00
1
50mgIn Stock
$680.00
1
100mgIn Stock
$888.00
1

Zitate (Citations)

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  • Nature cover
    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

Beschreibung (Description)

Elacestrant dihydrochloride (RAD1901 dihydrochloride) is a novel, orally bioavailable selective estrogen receptor (ER) degrader with IC50 of 48nM and 870nM for ERα and ERβ, respectively. Estrogen and estrogen receptor (ER) are important drivers of breast tumorigenesis and breast cancer progression. Elacestrant dihydrochloride can specifically bind to and degrade estrogen receptors, making it a potent antagonist of estrogen receptor-positive breast cancer cell proliferation[1].

In vitro, treatment with Elacestrant dihydrochloride (10⁻15–10⁻6M; 48h) dose-dependently inhibited MCF-7 cell proliferation in the presence of 10pM E₂, with an IC₅₀ value of 4.2nM[1]. Elacestrant dihydrochloride (0-1µM; 24 or 48h) dose-dependently induced estrogen receptor (ER) degradation and inhibited estrogen-mediated signaling and growth in multiple ER+ cell lines, including MCF-7 and T47D[2].

In vivo, oral administration of Elacestrant dihydrochloride (0.1, 0.3, 1, and 3mg/kg/d; 4 weeks) produced a dose-dependent and statistically significant suppression of ovariectomy-induced bone loss in female SD rats[1]. Elacestrant dihydrochloride (0.01-10mg/kg/d; p.o.; 3 days) dose-dependently reversed E₂ (0.01mg/kg)-induced uterine stimulation, including increases in uterine wet weight and endometrial epithelial thickness[1]. Elacestrant dihydrochloride (0.3, 1, 3, 10, 30, and 120mg/kg/day; p.o.; 40 days) dose-dependently inhibited tumor growth in the MCF-7 xenograft model, with no adverse effect on body weight[1]. Elacestrant dihydrochloride (120mg/kg/d; p.o.; 54 days) effectively crossed the blood-brain barrier and significantly prolonged survival in the MCF-7 intracranial xenograft mouse model[1].

References:
[1] Garner F, Shomali M, Paquin D, Lyttle CR, Hattersley G. RAD1901: a novel, orally bioavailable selective estrogen receptor degrader that demonstrates antitumor activity in breast cancer xenograft models. Anticancer Drugs. 2015;26(9):948-956.
[2] Bihani T, Patel HK, Arlt H, 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;23(16):4793-4804.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

MCF-7

Preparation Method

MCF-7 cells were plated at 10000 cells/well in 96-well culture plates in MEM with 10% fetal bovine serum, and they were allowed to adhere for 48h. Thereafter, the cultures were washed with serum-free MEM and incubated in 100μl serum-free MEM. After 72h, the medium was removed and replaced with 2% charcoal-stripped FBS–MEM containing 10pM E2 with either Elacestrant dihydrochloride or additional E2 at concentrations ranging from 10−15 to 10−6M. The medium was removed after 48h of incubation.

Reaction Conditions

10−15 to10−6M; 48h

Applications

Treatment of cells with Elacestrant dihydrochloride in the presence of 10pM E2 resulted in a dose-dependent decrease in proliferation, with an IC50 value of 4.2nM. Importantly, Elacestrant dihydrochloride treatment (0.1pM to 1µM) did not stimulate proliferation in the absence of E2, and resulted in significant inhibition of basal cell proliferation, which was observed at doses of 10nM and above.
Animal experiment [1]:

Animal models

Female Sprague–Dawley rats

Preparation Method

Elacestrant dihydrochloride was stored as a dry powder, formulated for use as a homogenous suspension in 0.5% (w/v) methylcellulose in deionized water. Ovariectomy was performed on anesthetized adult female Sprague–Dawley rats, with sham surgery as a control. Following surgery, ovariectomized rats were treated once daily for 4 weeks with vehicle, E2 (0.01mg/kg), or Elacestrant dihydrochloride (0.1, 0.3, 1, and 3mg/kg), administered by oral gavage. Animals in the sham surgery group were vehicle treated. All animals were killed by carbon dioxide inhalation 24h after the final dose.

Dosage form

0.1, 0.3, 1, and 3mg/kg/d; p.o.; 4w

Applications

Following ovariectomy, untreated (vehicle control) rats experienced a decrease in bone mineral density both in the entire femur and in the lumbar spine compared with baseline. Treatment with Elacestrant dihydrochloride resulted in a dose-dependent and statistically significant suppression of ovariectomy-induced bone loss.

References:
[1] Garner F, Shomali M, Paquin D, Lyttle CR, Hattersley G. RAD1901: a novel, orally bioavailable selective estrogen receptor degrader that demonstrates antitumor activity in breast cancer xenograft models. Anticancer Drugs. 2015;26(9):948-956.

Produktdokumente (Product Documents)

Purity:>99.50%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
1349723-93-8
Synonyme
RAD1901 dihydrochloride
SMILES
OC1=CC=C2C[C@H](C3=CC=C(OC)C=C3N(CC)CC4=CC=C(CCNCC)C=C4)CCC2=C1.[H]Cl.[H]Cl
Summenformel
C30H40Cl2N2O2
Molekulargewicht
531.56
Löslichkeit
DMSO : 17.6 mg/mL (33.11 mM)
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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