Endoxifen E-isomer hydrochloride

≥98%

Reagent Code: #56903
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CAS Number 1197194-61-8

science Other reagents with same CAS 1197194-61-8

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Weight 409.95 g/mol
Formula C₂₅H₂₈ClNO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Endoxifen E-isomer hydrochloride is the hydrochloride salt of the (E)-stereoisomer of endoxifen, the primary active metabolite of tamoxifen responsible for most of its therapeutic effects in breast cancer treatment. It is primarily utilized in oncology research and investigational therapies for estrogen receptor-positive (ER+) breast cancer. As a potent selective estrogen receptor modulator (SERM), it potently inhibits the growth of ER+ breast cancer cells by antagonizing estrogen receptor signaling. This compound supports therapeutic strategies to reduce cancer recurrence risk and improve survival rates. It is also explored in personalized medicine, tailored to patient genetics (e.g., CYP2D6 polymorphisms) and metabolism. In research, it aids in studying estrogen receptor signaling mechanisms and resistance to hormonal therapies.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿5,877.00
inventory 5mg
10-20 days ฿23,499.00

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Endoxifen E-isomer hydrochloride
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Endoxifen E-isomer hydrochloride is the hydrochloride salt of the (E)-stereoisomer of endoxifen, the primary active metabolite of tamoxifen responsible for most of its therapeutic effects in breast cancer treatment. It is primarily utilized in oncology research and investigational therapies for estrogen receptor-positive (ER+) breast cancer. As a potent selective estrogen receptor modulator (SERM), it potently inhibits the growth of ER+ breast cancer cells by antagonizing estrogen receptor signaling. Thi

Endoxifen E-isomer hydrochloride is the hydrochloride salt of the (E)-stereoisomer of endoxifen, the primary active metabolite of tamoxifen responsible for most of its therapeutic effects in breast cancer treatment. It is primarily utilized in oncology research and investigational therapies for estrogen receptor-positive (ER+) breast cancer. As a potent selective estrogen receptor modulator (SERM), it potently inhibits the growth of ER+ breast cancer cells by antagonizing estrogen receptor signaling. This compound supports therapeutic strategies to reduce cancer recurrence risk and improve survival rates. It is also explored in personalized medicine, tailored to patient genetics (e.g., CYP2D6 polymorphisms) and metabolism. In research, it aids in studying estrogen receptor signaling mechanisms and resistance to hormonal therapies.

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