6 Results for "

GDC0927

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "GDC0927" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-111484
CAS No.: 1642297-01-5
Purity:  99.98%
Synonyms: SRN-927
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

GDC-0927 (SRN-927) is a potent, non-steroidal, orally bioavailable, selective estrogen receptor antagonist .
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Cat. No.: HY-111484A
CAS No.: 1443983-36-5
Synonyms: SRN-927 Racemate
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

GDC-0927 Racemate (SRN-927 Racemate) is an estrogen receptor (ER) degrader that can effectively inhibit the activity of ER-α with an IC50 value of 0.2 nM and can be used in diseases related to estrogen receptors.
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Cat. No.: HY-111484R
CAS No.: 1642297-01-5
Synonyms: SRN-927 (Standard)
Research Areas:  

Cancer

GDC-0927 (Standard) is the analytical standard of GDC-0927 (HY-111484). This product is intended for research and analytical applications. GDC-0927 (SRN-927) is a potent, non-steroidal, orally bioavailable, selective estrogen receptor antagonist .
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Cat. No.: HY-120207
CAS No.: 1642297-53-7
Purity:  98.78%
Synonyms: (R)-SRN-927
Target:  

Estrogen Receptor/ERR

Research Areas:  

Others

(R)-GDC-0927 ((R)-SRN-927) is a (R)-enantiomer of GDC-0927 (HY-111484) .
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Cat. No.: HY-141551B
Target:  

Drug Isomer

Research Areas:  

Others

(R)-GNE-274 is a enantiomer of GNE-274. GNE-274 is a non-degrader that is structurally related to GDC-0927 (estrogen receptor degrader) .
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Cat. No.: HY-141551
CAS No.: 2369048-69-9
Purity:  98.00%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

GNE-274 is a structural analog of the ER degrader GDC-0927 and is a non-degrader. GNE-274 does not induce conversion of ER in breast cancer cell lines and functions as a partial ER agonist (partial ER agonist). GNE-274 increases the chromatin accessibility of ER-DNA binding sites, whereas GDC-0927 does not. GNE-274 is an effective ER ligand binding domain (LBD) inhibitor. GNE-274 can be used in cancer research.
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