5 Results for "

endocrine therapy

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "endocrine therapy" in MCE Product Catalog:

Cat. No.: HY-163561
CAS No.: 1269199-96-3
CARM1-IN-6 is a potent CARM1 inhibitor that inhibits CARM1 enzymatic activity with an IC50 of 12.3 μM and a Kd of 0.6785 μM. CARM1-IN-6 suppresses oncogenic estrogen/ERα-target gene expression, activates type I interferon (IFN) and IFN-induced genes (ISGs), induces cell cycle arrest, and inhibits breast cancer cell proliferation both in vitro and in vivo. CARM1-IN-6 can be used for the research of breast cancer .
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Cat. No.: HY-W040270
CAS No.: 928292-69-7
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Amino-PEG10-amine, a PEG-based PROTAC linker used to combine two mono diethylstilbestrol (DES)-based ligands, provides an alternative strategy for preparing more selective and active ER antagonists for endocrine therapy of breast cancer .
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Cat. No.: HY-130411
CAS No.: 479200-82-3
Purity:  ≥95.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Amino-PEG11-amine, a PEG-based (12 units) PROTAC linker used to combine two mono diethylstilbestrol (DES)-based ligands, provides an alternative strategy for preparing more selective and active ER antagonists for endocrine therapy of breast cancer .
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Cat. No.: HY-176955
CAS No.: 2376991-14-7
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

ER degrader 12 (Example 1) is an estrogen receptor (ER) degrader with IC50 values for ERα and ERβ of 2.3 and 80.2 nM respectively (TR-FRET experiment). ER degrader 12 inhibits the proliferation of MCF-7 cells, with an IC50 of 1.53 nM. ER degrader 12 can be used for research on breast cancer .
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Cat. No.: HY-187225
Research Areas:  

Cancer

NCP07 is a PROTAC degrader targeting the coactivator-binding site (CBS) of ERα. NCP07 induces the formation of the ERα-NCP07-VHL ternary complex and promotes ERα degradation via the ubiquitin-proteasome system. NCP07 induces apoptosis and cell cycle arrest in endocrine therapy-resistant breast cancer cells. NCP07 inhibits the proliferation of wild-type and ESR1-mutant breast cancer cells. NCP07 is applicable to breast cancer-related research .
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