18 Results for "

estrogen receptor 1

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "estrogen receptor 1" in MCE Product Catalog:

12
12 Cited Publications
Cat. No.: HY-B1100
CAS No.: 313-06-4
Estradiol cypionate is the 17β-cypionate ester of Estradiol, which inhibits ET-1 synthesis by acting on estrogen receptors .
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2
2 Cited Publications
Cat. No.: HY-P80663
Synonyms: ESR1; Era; Eralpha; estrogen receptor; Estradiol receptor; ER-alpha; estrogen receptor 1; NR3A1; ER; ESR; ESRA; estrogen receptor alpha

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, IP, ChIP

Reactivity:  

Human

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Cat. No.: HY-W005186
CAS No.: 19063-55-9
Synonyms: 6-Bromochromen-2-one
Target:  

17β-HSD

Research Areas:  

Infection

6-Bromocoumarin (compound 34) is a potential anti-bacterial agent, with no inhibition against 17β-HSD1. 6-Bromocoumarin exhibtis affinity for α and β estrogen receptors .
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Cat. No.: HY-B1100R
CAS No.: 313-06-4
Estradiol cypionate (Standard) is the analytical standard of Estradiol cypionate. This product is intended for research and analytical applications. Estradiol cypionate is the 17β-cypionate ester of Estradiol, which inhibits ET-1 synthesis by acting on estrogen receptors .
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Cat. No.: HY-132294A
CAS No.: 1953134-15-0
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

(1S,3R)-GNE-502 (compound 179) is a potent ERα degrader with an EC50 value of 13 nM against ERα in MCF7 HCS. (1S,3R)-GNE-502 can be used to research cancer related with estrogen receptor .
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Cat. No.: HY-P3833
CAS No.: 166664-90-0
Synonyms: Anti-estrogen
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

Yp537 is an estrogen receptor (ER) inhibitor that blocks dimerization of the human estrogen receptor .
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Cat. No.: HY-121351
CAS No.: 15130-85-5
Inokosterone is a potential agent target of estrogen receptor 1 in rheumatoid arthritis patients .
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Cat. No.: HY-121451
CAS No.: 523-31-9
Synonyms: DBzP
Research Areas:  

Others

Dibenzyl phthalate, a diaryl phthalate, is extensively used as a plasticizer to modify the properties of the synthetic resin substrates, resulting in the improvement of flexibility and durability of the end products. Dibenzyl phthalate is an endocrine-disrupting compound, and activates estrogen and androgen receptors .
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Cat. No.: HY-P80662
Synonyms: ESR1; Era; Eralpha; estrogen receptor; Estradiol receptor; ER-alpha; estrogen receptor 1; NR3A1; ER; ESR; ESRA; estrogen receptor alpha

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P80662A
Synonyms: ESR1; Era; Eralpha; estrogen receptor; Estradiol receptor; ER-alpha; estrogen receptor 1; NR3A1; ER; ESR; ESRA; estrogen receptor alpha

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P80663A
Synonyms: ESR1; Era; Eralpha; estrogen receptor; Estradiol receptor; ER-alpha; estrogen receptor 1; NR3A1; ER; ESR; ESRA; estrogen receptor alpha

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, IP, ChIP

Reactivity:  

Human

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Cat. No.: HY-P810664
Synonyms: ESR1; Era; Eralpha; estrogen receptor; Estradiol receptor; ER-alpha; estrogen receptor 1; NR3A1; ER; ESR; ESRA; estrogen receptor alpha

Host:  

Rabbit

Application:  

WB, ICC/IF, IF-Tissue, IHC-P

Reactivity:  

Human, Mouse

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Cat. No.: HY-139999
CAS No.: 3033849-90-7
Research Areas:  

Cancer

LCL-PEG3-N3 is a decoy oligonucleotide ligand for E3 ligase which can be used for developing chimeric molecules LCL-ER(dec), degrading the estrogen receptor . LCL-PEG3-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-139999A
CAS No.: 3033849-91-8
Research Areas:  

Cancer

LCL-PEG3-N3 (hydrochloride) is a decoy oligonucleotide ligand for E3 ligase which can be used for developing chimeric molecules LCL-ER(dec), degrading the estrogen receptor . LCL-PEG3-N3 (hydrochloride) is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-P81150
Synonyms: G Protein Coupled receptor 30; G-protein coupled receptor 30; G-protein coupled estrogen receptor 1; Membrane estrogen receptor; mER; Chemokine receptor-like 2; IL8-related receptor DRY12; Flow-induced endothelial G-protein coupled receptor 1; FEG-1; Lymphocyte-derived G-protein coupled receptor; LYGPR; GPCR-BR; CEPR; CMKRL2; DRY12; GPER.

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, ICC/IF, FC, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P3833A
Synonyms: Anti-estrogen TFA
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

Yp537 TFA is an estrogen receptor (ER) inhibitor that blocks dimerization of the human estrogen receptor .
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Cat. No.: HY-N13290
CAS No.: 91413-55-7
Synonyms: 10-CIEsra
10-Chloroestra-1,4-diene-3,17-dione (10-CIEsra) is a derivative of estrogen receptor .
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Cat. No.: HY-N17632
CAS No.: 73338-86-0
Moracin G is a plant-derived kinase modulator and receptor ligand that forms stable bindings with multiple key proteins (AKT1, COX2 and Estrogen receptor 1) and competitively inhibits the activity of specific kinases. By binding to MELK to disrupt cell cycle regulation, Moracin G impairs the survival and proliferation of cancer cells, induces cancer cell apoptosis, and thereby exerts anti-tumor potential. Moracin G can be used in research related to periodontitis and breast cancer .
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